{"title":"Asymmetric Organocatalysts","description":"\u003cp\u003e\u003cstrong\u003eAsymmetric Organocatalysts\u003c\/strong\u003e — mencakup katalis organik kiral seperti turunan prolina, tiourea, dan asam amino sederhana yang bekerja tanpa logam untuk mengarahkan pembentukan produk dengan selektivitas stereokimia tinggi. Struktur kiralnya dirancang untuk berinteraksi secara terarah dengan substrat lewat ikatan hidrogen atau pembentukan enamin\/iminium.\u003c\/p\u003e\u003cp\u003eAsymmetric Organocatalysts dipakai kimiawan sintesis dalam reaksi aldol, Michael, dan Mannich asimetris untuk menghasilkan senyawa kiral dengan enansioselektivitas terkontrol, termasuk pada tahap awal sintesis molekul kompleks di laboratorium riset akademik maupun industri bahan baku farmasi. Turunan tiourea bifungsional sering dipakai bersama gugus amina untuk mengaktifkan substrat elektrofilik dan nukleofilik secara simultan.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0179280\"\u003eTCI A0179 56-41-7 L-Alanine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570112414\"\u003eTCI B5701 848821-76-1 (S)-alpha,alpha-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0177276\"\u003eTCI A0177 338-69-2 D-Alanine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b588212651\"\u003eTCI B5882 948595-00-4 (R)-Bis[3,5-bis(trifluoromethyl)phenyl](pyrrolidin-2-yl)methanol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t419555944\"\u003eTCI T4195 67123-97-1 H-DL-Tic-OH\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b661113567\"\u003eTCI B6611 848821-61-4 (2S)-2-[Bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilyl)oxy]methyl]pyrrolidine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t308054612\"\u003eTCI T3080 1089663-51-3 N-(2-Thiophenesulfonyl)-L-prolinamide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b680413721\"\u003eTCI B6804 620960-26-1 1-[3,5-Bis(trifluoromethyl)phenyl]-3-[(1R,2R)-2-(dimethylamino)cyclohexyl]thiourea\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan konfigurasi enansiomer (R atau S), kemurnian optik (ee), serta gugus fungsi pendamping seperti trifluorometil atau silil yang memengaruhi selektivitas dan kelarutan katalis. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Organocatalysts [Catalysis], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-condensation-organocatalysts\"\u003eCondensation Organocatalysts\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-organocatalysts-others-catalysis\"\u003eOrganocatalysts (Others) [Catalysis]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-organocatalysts-catalysis\"\u003eOrganocatalysts [Catalysis]\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b570112414","title":"TCI B5701 848821-76-1 (S)-alpha,alpha-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-alpha,alpha-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol is a chiral reagent widely used in asymmetric synthesis to produce compounds with specific stereochemical configurations. This compound plays a critical role in laboratory settings where precise control over molecular structure is essential. It is particularly valuable in research focused on creating enantiomerically pure substances, which are crucial in pharmaceutical and biochemical applications. Its unique molecular structure allows for selective interactions with substrates, enhancing the efficiency of complex chemical reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature makes it a preferred choice for researchers aiming to achieve high enantioselectivity in synthetic processes. Its ability to act as a chiral catalyst or ligand enables the selective modification of molecules without interfering with the reaction pathway. This characteristic is vital for the development of bioactive compounds with specific pharmacological properties. Additionally, its stability under controlled conditions ensures consistent performance in various experimental setups, making it a reliable tool for both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in scientific research related to pharmacology, food chemistry, and materials science. It supports the development of new compounds with targeted biological activities, contributing to advancements in drug discovery and chemical innovation. Its application is widespread across research institutions and universities, where it is utilized to enhance the precision and effectiveness of synthetic processes in organic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research due to its high enantioselectivity and ability to produce chiral compounds with specific stereochemistry.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules in medicinal chemistry where precise molecular configuration is essential for biological activity.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis of complex molecules in academic research settings requiring controlled stereochemical outcomes.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chiral catalytic systems in chemical engineering for industrial-scale production of enantiomerically pure products.\u003c\/li\u003e\n\u003cli\u003eExploration of new materials in polymer science where chiral structures influence material properties and functionality.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 848821-76-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation and supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of materials that are chemically inert to prevent degradation. Due to its chiral nature, it is important to handle the compound with care to avoid contamination or cross-contamination with other substances. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the material. Proper ventilation should be maintained in the workspace to ensure safe handling and minimize exposure risks. Regular monitoring of storage conditions is advised to ensure the compound remains effective for its intended applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085898068186,"sku":"TCI2510B570112414","price":3005000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5701.jpg?v=1767092687"},{"product_id":"tci2510b588212651","title":"TCI B5882 948595-00-4 (R)-Bis[3,5-bis(trifluoromethyl)phenyl](pyrrolidin-2-yl)methanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-Bis[3,5-bis(trifluoromethyl)phenyl](pyrrolidin-2-yl)methanol is a chiral reagent widely used in asymmetric synthesis to produce compounds with specific optical properties. This compound plays a crucial role in chemical reactions that require precise control over stereochemistry, making it an essential tool in modern laboratory settings. Its chiral nature allows it to selectively influence reaction pathways, leading to the formation of desired enantiomers with high efficiency. This compound is particularly valuable in pharmaceutical and organic chemistry research, where the stereochemistry of a molecule can significantly affect its biological activity.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique structure, featuring trifluoromethyl groups, contributes to its distinct electronic and reactive properties. These groups enhance the molecule's ability to interact selectively with other chiral components in a reaction, improving the overall yield and reducing the formation of byproducts. Its high chiral purity and stability under controlled conditions make it a preferred choice for researchers aiming to achieve precise stereochemical outcomes. The compound’s effectiveness in asymmetric catalysis is further supported by its compatibility with a variety of reaction conditions and reagents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and pharmacologists working on the development of new compounds with specific biological activities. Its application in drug synthesis and organic chemistry research is widespread due to its ability to enhance reaction efficiency and provide precise stereochemical control. As a key component in chiral synthesis, it supports the advancement of pharmaceutical and chemical research in the region, offering a reliable and high-quality option for laboratory use.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the selective formation of enantiomers with high stereocontrol.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is widely used in drug development to create compounds with specific optical properties, enhancing their biological activity and efficacy.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its unique electronic properties make it suitable for various organic reactions requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Development: It serves as a key reagent in the design and testing of new chiral catalysts for industrial and academic applications.\u003c\/li\u003e\n\u003cli\u003eBiologically Active Compound Synthesis: Its ability to influence reaction pathways makes it valuable in the synthesis of compounds with specific therapeutic applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 948595-00-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers made of materials that are chemically inert to prevent any unwanted reactions. Due to its chiral nature and potential reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation should be maintained in the laboratory when working with this compound to ensure a safe working environment. All handling should be conducted in a controlled setting to minimize exposure and ensure compliance with standard laboratory safety protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085908160730,"sku":"TCI2510B588212651","price":2399000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085908193498,"sku":"TCI2510B588212652","price":7295000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5882_2471edf7-857a-4fb7-a9a8-57bcdf9634fd.jpg?v=1767863728"},{"product_id":"tci2510b661113567","title":"TCI B6611 848821-61-4 (2S)-2-[Bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilyl)oxy]methyl]pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6611, with the CAS number 848821-61-4, is a complex chiral compound that plays a vital role in asymmetric synthesis. This material is specifically designed for use in chemical laboratories where precise control over stereochemistry is essential. Its unique molecular structure allows it to act as a chiral reagent, facilitating the synthesis of enantiomerically pure compounds. In the context of modern organic chemistry, this compound is indispensable for achieving high enantioselectivity in various reactions.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes of TCI B6611 is its highly complex chiral architecture, which enables it to interact selectively with specific substrates. This property makes it an ideal choice for researchers aiming to develop efficient and targeted synthetic pathways. The compound’s stability under certain conditions further enhances its utility, allowing for consistent performance in laboratory settings. Its ability to direct chemical reactions with high specificity is a major factor in its popularity among chemists working in the field of asymmetric synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI B6611 is widely used in organic chemistry research, particularly in the development of bioactive compounds and pharmaceuticals. It is a preferred tool for academic and industrial researchers who require precise control over stereochemical outcomes. Its application extends to various areas of chemical synthesis, making it a valuable asset in both academic and applied research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in organic chemistry laboratories for the production of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules and pharmaceuticals requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eResearch in chiral catalysis and ligand design for advanced synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eInvestigation of reaction mechanisms involving chiral reagents and substrates.\u003c\/li\u003e\n\u003cli\u003eSupport for academic and industrial research in drug discovery and chemical innovation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 848821-61-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its complex molecular structure, it is important to handle it with care to avoid contamination or degradation. Laboratory personnel should ensure proper ventilation when working with this material. Always follow standard safety protocols for handling chiral compounds, including the use of personal protective equipment. The compound is not known to be hazardous under normal storage conditions, but it is advisable to follow general chemical safety guidelines to ensure safe handling and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085950202074,"sku":"TCI2510B661113567","price":6790000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6611.jpg?v=1767094028"},{"product_id":"tci2510b692713811","title":"TCI B6927 131180-57-9 (S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol is a chiral compound used in asymmetric synthesis to produce molecules with specific optical properties. This material plays a crucial role in laboratories where precise control over stereochemistry is required. It is commonly employed in reactions that demand chiral catalysts or ligands to enhance the efficiency and accuracy of chemical synthesis. Its unique molecular structure makes it a valuable reagent in the development of pharmaceuticals and complex organic compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature allows for high selectivity in chemical reactions, minimizing the formation of by-products and improving the yield of the desired compound. Its molecular framework includes methoxy groups and a pyrrolidine ring, which contribute to its reactivity and specificity in various synthetic pathways. These features make it a preferred choice for researchers aiming to achieve controlled stereochemical outcomes. The compound's ability to influence reaction pathways with minimal side reactions is a key factor in its widespread use in advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely utilized by chemists in educational institutions and research organizations. It is an essential component in the development of new pharmaceutical compounds and complex molecules. Its role in pharmacological and biochemical research underscores its importance in the scientific community. The compound is often used in studies that require precise optical control, making it a staple in modern chemical synthesis practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound is used to control the stereochemistry of products, offering high enantioselectivity in complex reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development benefits from this compound's ability to selectively produce desired stereoisomers, which is crucial for drug efficacy and safety.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research relies on its chiral properties to facilitate the synthesis of complex molecules with specific optical configurations.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies utilize this compound to explore enzyme-substrate interactions and molecular recognition processes in biological systems.\u003c\/li\u003e\n\u003cli\u003eAdvanced synthetic methodologies incorporate this compound to achieve controlled stereochemical outcomes in multi-step chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 131180-57-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Proper ventilation is essential when handling the material to minimize exposure to vapors. Due to its chiral nature, it is important to maintain strict purity standards to ensure consistent results in chemical reactions. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Regular monitoring of storage conditions is advised to maintain its integrity and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085961212122,"sku":"TCI2510B692713811","price":8959000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6927.jpg?v=1767094392"},{"product_id":"tci2510c001513929","title":"TCI C0015 3144-16-9 (+)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0015 (+)-10-Camphorsulfonic Acid, CAS 3144-16-9, is a strong, optically active sulfonic acid built on the camphor framework. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallisation. The compound also serves as a convenient solid Brønsted acid catalyst for protection and deprotection steps, and as an ion-pairing additive in chromatography. AMI Scientific offers this TCI product in 25 g, 100 g, and 500 g pack sizes; because it is hygroscopic, keep the container tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYan et al. (1999). Thermoelectric Properties of Alternatively Layered Films of Polyaniline and (±)-10-Camphorsulfonic Acid-Doped Polyaniline. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1999.1217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1999.1217\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085966127322,"sku":"TCI2510C001513929","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4468000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0015.jpg?v=1767094558"},{"product_id":"tci2510c034714413","title":"TCI C0347 485-71-2 Cinchonidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0347 Cinchonidine, CAS 485-71-2, is a cinchona alkaloid that has long served as a workhorse reagent in asymmetric synthesis. Its quinoline ring, basic quinuclidine nitrogen, and secondary hydroxyl group at a stereogenic centre allow it to act simultaneously as a chiral base and a hydrogen-bond donor. It is applied as an organocatalyst, as a chiral modifier for heterogeneous hydrogenation catalysts, as a resolving agent for racemic acids, and as a starting material for cinchona-derived phase transfer catalysts and ligands. AMI Scientific offers this TCI product in 25 g and 100 g packs, with lot-specific data available from the manufacturer.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2018). Synthesis of (+)-Cinchonidine. \u003cem\u003eSynfacts\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0037-1611233\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0037-1611233\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBeresford (2004). Enantioselective Addition of Diethylzinc to N‐Diphenylphosphinoylimines Employing Cinchonidine and Cinchonine as Chiral Ligands.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200446025\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200446025\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLindholm et al. (2003). Hydrosilylation of Cinchonidine and 9‐O‐TMS‐Cinchonidine with Triethoxysilane: Application of 11‐(Triethoxysilyl)‐10,11‐dihydrocinchonidine as a Chiral Modifier in the Enantioselective Hydrogenation of 1‐Phenylpropane‐1,2‐dione.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200318077\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200318077\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085991456986,"sku":"TCI2510C034714413","price":2273000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085991489754,"sku":"TCI2510C034714414","price":6790000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0347.jpg?v=1767095063"},{"product_id":"tci2510c034814415","title":"TCI C0348 24302-67-8 Cinchonidine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0348 Cinchonidine Dihydrochloride, CAS 24302-67-8, is the dihydrochloride salt of the cinchona alkaloid cinchonidine. Salt formation changes its handling profile compared with the free base, generally improving solubility in aqueous and more polar media while remaining convenient to weigh and store. The cinchona framework retains the stereogenic centres responsible for chiral induction, so the compound serves as an organocatalyst precursor, a starting material for cinchona-derived ligands and phase transfer catalysts, and a reagent in enantiomer separation studies. AMI Scientific supplies this TCI product in a 25 g pack; store it tightly closed, away from moisture, and consult the manufacturer's Safety Data Sheet before use.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085991522522,"sku":"TCI2510C034814415","price":1389000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0348.jpg?v=1767095067"},{"product_id":"tci2510c034914416","title":"TCI C0349 524-61-8 Cinchonidine Sulfate Dihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCinchonidine Sulfate Dihydrate (TCI C0349, CAS 524-61-8) is a cinchona alkaloid salt widely used as an organocatalyst and chiral resolving agent. Its quinuclidine nitrogen and secondary hydroxyl group create a well-defined chiral environment that supports asymmetric transformations at laboratory scale. Researchers also rely on it to form diastereomeric salts with racemic carboxylic acids for classical resolution by crystallisation. AMI Scientific supplies this product in a 25 g pack for research and industrial laboratories in Indonesia, and users should always consult the official TCI safety data sheet before handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085991555290,"sku":"TCI2510C034914416","price":1213000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0349.jpg?v=1767095071"},{"product_id":"tci2510c035014417","title":"TCI C0350 118-10-5 Cinchonine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCinchonine (TCI C0350, CAS 118-10-5) is a naturally occurring cinchona alkaloid and one of the most established chiral catalysts in asymmetric synthesis. Because it behaves as a pseudo-enantiomer of cinchonidine, the two are frequently paired to access opposite stereochemical outcomes within the same reaction system. It also serves as a starting scaffold for chiral phase-transfer catalysts and as a resolving agent for racemic acids. AMI Scientific offers this TCI product in 25 g and 200 g packs to suit both small-scale studies and more intensive synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBartók et al. (2005). Enantioselective hydrogenation of ethyl pyruvate catalysed by cinchonine-modified Pt\/Al2O3: tilted adsorption geometry of cinchonine. \u003cem\u003eCatalysis Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10562-004-3449-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10562-004-3449-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHuaizhi et al. (2000). Study on Adsorption Properties of Cinchonine Loaded Resin to Mo and V by ICP-AES. \u003cem\u003eAnalytical Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00032710008543172\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00032710008543172\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eXi et al. (2013). Cinchonine and thiourea. \u003cem\u003eChemical Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c3cc40825f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c3cc40825f\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085991620826,"sku":"TCI2510C035014417","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"200g","offer_id":48085991653594,"sku":"TCI2510C035014418","price":7850000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0350.jpg?v=1767095075"},{"product_id":"tci2510c097215327","title":"TCI C0972 35963-20-3 (-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0972 (-)-10-Camphorsulfonic Acid (CAS 35963-20-3) is a crystalline chiral sulfonic acid available in 25 g, 100 g, and 500 g pack sizes. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallization. The compound also serves as a strong Brønsted acid catalyst for acetal formation, deprotection, and related transformations. Store it tightly sealed in a cool, dry place and wear gloves and eye protection when weighing, as the solid is corrosive.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSong et al. (2013). Improved thermoelectric performance of PEDOT:PSS film treated with camphorsulfonic acid. \u003cem\u003eJournal of Polymer Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10965-013-0316-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10965-013-0316-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086040969434,"sku":"TCI2510C097215327","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086041002202,"sku":"TCI2510C097215328","price":3458000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086041034970,"sku":"TCI2510C097215329","price":10600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0972.jpg?v=1767096117"},{"product_id":"tci2510c272817583","title":"TCI C2728 1440939-88-7 N-[(9S)-8alpha-Cinchonan-9-yl]quinoline-8-sulfonamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-[(9S)-8alpha-Cinchonan-9-yl]quinoline-8-sulfonamide is a specialized chemical compound widely used in catalytic and organic reactions within laboratory settings. This compound plays a crucial role in facilitating chemical transformations by acting as an organocatalyst. Its unique structure combines elements of quinoline and cinchona, which contribute to its catalytic efficiency. This compound is particularly valuable in research environments where precise and effective catalytic performance is required. Its ability to interact selectively with substrates makes it a preferred choice for complex chemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure allows for specific interactions with various substrates, enhancing reaction efficiency and selectivity. Its stability under standard laboratory conditions ensures consistent performance across different experimental setups. Additionally, the compound exhibits good solubility in common organic solvents, making it versatile for a wide range of applications. These properties make it a reliable and efficient tool for researchers working in organic chemistry and catalysis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in academic and research institutions for advanced chemical experiments. Its application is particularly relevant in studies involving asymmetric catalysis and oxidation reactions. Due to its effectiveness and reliability, it is a valuable resource for scientists and researchers aiming to achieve high-quality results in their experiments. Its availability through AMI Scientific ensures that Indonesian researchers have access to this essential chemical for their work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Catalysis: This compound is ideal for asymmetric catalysis due to its chiral structure, enabling the selective synthesis of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eOxidation Reactions: Its catalytic properties make it suitable for oxidation reactions, where it facilitates the conversion of substrates with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: The compound is widely used in organic synthesis for its ability to promote complex chemical transformations with minimal side reactions.\u003c\/li\u003e\n\u003cli\u003eGreen Chemistry Initiatives: Its efficiency and selectivity align with green chemistry principles, reducing waste and improving reaction sustainability.\u003c\/li\u003e\n\u003cli\u003eResearch and Development: It is a key component in R\u0026amp;D projects requiring precise and effective catalytic performance in diverse chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1440939-88-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it away from incompatible substances to avoid any potential chemical interactions. Proper labeling of storage containers is essential for safe handling and easy identification. Regular monitoring of storage conditions ensures the compound remains in optimal condition for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086194094298,"sku":"TCI2510C272817583","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2728.jpg?v=1767098697"},{"product_id":"tci2510d213022189","title":"TCI D2130 112022-83-0 (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2130, (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine, is a chiral catalyst belonging to the oxazaborolidine family, widely known among synthetic chemists as the CBS catalyst. The compound is used together with a hydride source such as borane to carry out enantioselective reduction of prochiral ketones, delivering secondary alcohols in which one configuration predominates. Its role in the laboratory is strategically important because many bioactive molecules and active pharmaceutical ingredients display the desired activity in only one enantiomeric form, making control of chirality a fundamental requirement in modern synthesis.\u003c\/p\u003e\n\u003cp\u003eThe properties that lead chemists to select this catalyst are its ability to provide high selectivity under relatively mild reaction conditions, its effectiveness in substoichiometric amounts, which conserves material, and the fact that the products it generates are straightforward to separate during post-reaction work-up. The bicyclic framework, bearing two bulky phenyl groups at the 5-position, creates a well-defined steric environment around the boron atom, and it is precisely this environment that directs the approach of hydride to one face of the ketone. Because the catalyst is available both as the (R) form and as its enantiomeric counterpart, the chemist can choose which configuration of the alcohol product to obtain.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this catalyst is typically used in organic synthesis and medicinal chemistry research groups at universities, in research institutes, and in pharmaceutical development laboratories where a defined stereochemical outcome is required. It is generally applied on a small preparative scale, in method development and route-scouting work, and in the preparation of chiral intermediates and reference standards, where reagent quantities are modest and consistent enantioselectivity matters more than throughput.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnantioselective reduction of prochiral ketones — the defined steric environment around boron directs hydride delivery to a single ketone face, giving secondary alcohols with one dominant configuration.\u003c\/li\u003e\n\u003cli\u003eSynthesis of chiral pharmaceutical intermediates — many active pharmaceutical ingredients are active in only one enantiomeric form, so a catalyst that controls configuration is essential to the route.\u003c\/li\u003e\n\u003cli\u003ePreparation of chiral secondary alcohol building blocks — the alcohol products serve as stereochemically defined starting points for further transformations in multi-step synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eAsymmetric synthesis method development — the catalyst works under relatively mild conditions and in substoichiometric amounts, making it economical for screening and optimising reduction protocols.\u003c\/li\u003e\n\u003cli\u003eAccess to a chosen product configuration — because both the (R) form and its enantiomer are available, chemists can select which enantiomeric alcohol a given synthetic route produces.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 112022-83-0\u003c\/li\u003e\n\u003cli\u003eChemical name: (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the tightly closed original container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from moisture, heat, and sources of ignition, and follow the storage conditions printed on the manufacturer's label and safety data sheet. Keep the material in its original container or in a clean, dry, well-sealed vessel that is compatible with boron-containing reagents; transfer under an inert atmosphere where the laboratory protocol calls for it. Handle only in a functioning fume hood, wearing safety glasses, chemically resistant gloves, and a laboratory coat. Because the compound is used together with borane-type hydride sources, keep it separate from water, alcohols, oxidising agents, and other incompatible chemicals. Label all working containers clearly, minimise exposure of the material to air and humidity during weighing, and dispose of residues and contaminated consumables in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086496968922,"sku":"TCI2510D213022189","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086497001690,"sku":"TCI2510D213022190","price":5376000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2130.jpg?v=1767104260"},{"product_id":"tci2510d213122191","title":"TCI D2131 112022-81-8 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2131 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine is a chiral oxazaborolidine catalyst and the enantiomeric counterpart of the (R) variant. As a member of the CBS class of catalysts, it is used together with borane as the hydride source to reduce prochiral ketones into chiral secondary alcohols, delivering the opposite product configuration compared with its paired catalyst. The availability of both enantiomers is precisely what makes this catalyst system so useful in synthesis laboratories, because researchers can select the desired direction of chiral induction simply by switching catalysts, without having to redesign the entire synthetic route.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that lead researchers to choose this catalyst are its high level of enantioselectivity across a wide range of ketone types, the small catalyst loading required because it operates catalytically rather than stoichiometrically, and reaction conditions that are relatively mild, so other functional groups on the substrate molecule generally remain intact. The rigid bicyclic framework, bearing two bulky phenyl groups, forms a well-defined steric pocket around the boron atom, and it is this pocket that controls the orientation of the ketone as it coordinates. The generally straightforward post-reaction workup is a further practical advantage.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this catalyst is typically used in academic and industrial research settings where a single enantiomer of a secondary alcohol is required, such as asymmetric synthesis studies, the preparation of chiral intermediates, and method development work. Because both enantiomeric forms of the catalyst are available, laboratories can run comparative experiments on the same substrate and obtain either product configuration, which supports teaching, publication-oriented research, and process development on a laboratory scale.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric reduction of prochiral ketones — used with borane as hydride source to deliver chiral secondary alcohols with high enantioselectivity across many ketone classes.\u003c\/li\u003e\n\u003cli\u003ePreparation of chiral intermediates — provides access to a defined alcohol configuration for downstream synthetic steps without redesigning the overall route.\u003c\/li\u003e\n\u003cli\u003eEnantiomer-selection studies — pairing this (S) catalyst with the (R) variant allows either product configuration to be obtained on the same substrate.\u003c\/li\u003e\n\u003cli\u003eMethodology and route development — the small catalytic loading and mild conditions make it practical for screening reduction conditions on sensitive, multifunctional substrates.\u003c\/li\u003e\n\u003cli\u003eTeaching and demonstration of stereocontrol — the rigid bicyclic structure with two bulky phenyl groups clearly illustrates how a steric pocket around boron governs ketone orientation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D2131\u003c\/li\u003e\n\u003cli\u003eCAS number: 112022-81-8\u003c\/li\u003e\n\u003cli\u003eChemical name: (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes and storage: available in the pack sizes offered by the manufacturer; store according to the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this catalyst in its original tightly closed container, in a cool, dry, and well-ventilated area away from moisture, direct sunlight, and heat sources, and follow the specific storage conditions printed on the manufacturer's label and safety data sheet. Oxazaborolidine catalysts are generally moisture-sensitive, so handling under dry, inert conditions and minimising exposure to air during weighing is advisable. Use appropriate personal protective equipment, including gloves, safety glasses, and a laboratory coat, and carry out transfers in a fume hood. Keep the material separate from incompatible substances, and consult the safety data sheet before use and for disposal guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086497067226,"sku":"TCI2510D213122191","price":1692000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086497099994,"sku":"TCI2510D213122192","price":5603000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2131.jpg?v=1767104264"},{"product_id":"tci2510d236522550","title":"TCI D2365 22348-32-9 (R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific optical properties. This reagent plays a crucial role in organic chemistry laboratories, where precise control over stereochemistry is essential. Its unique structure allows it to act as a chiral catalyst or ligand, guiding chemical reactions toward desired enantiomers. This makes it indispensable in applications requiring high selectivity and specificity.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chiral nature and molecular complexity make it a preferred choice for researchers aiming to achieve high optical purity in their products. Its two phenyl groups contribute to its distinct optical properties, enhancing its effectiveness in asymmetric reactions. This reagent is particularly favored in scenarios where controlling the stereochemistry of the final product is critical. Its reliability and performance in various synthetic pathways have made it a staple in advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical, biochemical, and material science research. It supports the development of new drugs, bioactive compounds, and functional materials by enabling precise stereochemical control. Its application in both academic and industrial research settings highlights its importance in advancing chemical innovation within the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research to produce enantiomerically pure drug candidates with enhanced therapeutic effects.\u003c\/li\u003e\n\u003cli\u003eChiral ligand in catalytic reactions for the selective synthesis of complex organic molecules with defined stereochemistry.\u003c\/li\u003e\n\u003cli\u003eOptical resolution processes in the production of high-purity chiral compounds used in biotechnology and fine chemical manufacturing.\u003c\/li\u003e\n\u003cli\u003eStructural analysis in organic chemistry laboratories to study the stereochemical behavior of reaction intermediates.\u003c\/li\u003e\n\u003cli\u003eDevelopment of chiral materials in material science for applications in sensors, coatings, and advanced polymer technologies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 22348-32-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on the specific product formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to maintain the integrity of the compound during handling to ensure consistent performance in synthetic reactions. Proper labeling and storage conditions are essential to preserve its chemical stability and effectiveness. Laboratory personnel should wear appropriate personal protective equipment when handling this material to ensure safety and compliance with standard chemical handling protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086537666778,"sku":"TCI2510D236522550","price":3913000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086537699546,"sku":"TCI2510D236522551","price":13149000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2365.jpg?v=1767104675"},{"product_id":"tci2510d272923054","title":"TCI D2729 65283-60-5 (R)-(-)-6,6'-Dibromo-1,1'-bi-2-naphthol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(-)-6,6'-Dibromo-1,1'-bi-2-naphthol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific optical properties. This reagent plays a crucial role in laboratory settings where precise control over stereochemistry is essential. It is commonly employed in reactions that require chiral catalysts or ligands to direct the formation of enantiomerically pure products. Its unique molecular structure enables it to act as a highly selective reagent in complex organic synthesis processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature and structural complexity make it a preferred choice for researchers aiming to achieve high enantiomeric excess in their reactions. Its two bromo groups positioned at the 6 and 6' positions of the bi-naphthol framework contribute to its specificity in stereoselective reactions. This makes it particularly valuable in applications where stereochemical control is critical, such as in pharmaceutical and agrochemical research. Its ability to influence reaction pathways with minimal side reactions enhances its utility in advanced synthetic strategies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in organic chemistry research, especially in asymmetric synthesis and drug development. It is a key component in studies focused on creating chiral molecules with specific biological activities. Many research institutions and universities in Indonesia rely on this reagent to advance their understanding of stereochemistry and catalytic processes. Its application is particularly relevant in the development of new therapeutic agents and functional materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the selective formation of enantiomerically pure products.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is used in drug development to produce chiral compounds with specific biological activities, crucial for creating effective therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Researchers use it to explore stereoselective reactions and understand the impact of chirality on molecular behavior.\u003c\/li\u003e\n\u003cli\u003eCatalyst Development: Its structural properties make it suitable for designing and testing new chiral catalysts in synthetic processes.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Applications: It contributes to the synthesis of functional materials with controlled stereochemistry, enhancing their performance in various industrial uses.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 65283-60-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chiral nature, it is essential to handle it with care to avoid any unintended racemization or loss of optical purity. Proper labeling and storage conditions are crucial to ensure its effectiveness in laboratory applications. Always follow standard safety protocols when handling chiral reagents to maintain a safe and efficient research environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086580265178,"sku":"TCI2510D272923054","price":4240000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2729.jpg?v=1767105245"},{"product_id":"tci2510d273023055","title":"TCI D2730 80655-81-8 (S)-(+)-6,6'-Dibromo-1,1'-bi-2-naphthol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2730 (S)-(+)-6,6'-Dibromo-1,1'-bi-2-naphthol is the enantiomeric counterpart of the brominated BINOL series and a key reagent in asymmetric synthesis. The molecule consists of two naphthol units joined at the 1,1' positions, so rotation between the rings is hindered and a stable axial chirality is maintained at ordinary laboratory working temperatures. The two opposing hydroxyl groups form a chiral pocket capable of binding metals or acting as an organocatalyst scaffold, while the two bromine atoms at the 6 and 6' positions open the way to further structural elaboration.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that leads researchers to select this material is its availability as a single enantiomer of (S) configuration, which allows the direction of chiral induction in a reaction to be reversed without altering any other condition. Comparing results obtained with the (R) and (S) series is the most direct way to demonstrate that the selectivity of a reaction is genuinely controlled by the catalyst. The bromine substituents lower the electron density of the aromatic framework, influencing the acidity of phosphate derivatives while also providing reactive sites for cross-coupling. The rigid binaphthyl backbone keeps the geometry of the chiral pocket consistent.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on asymmetric catalysis, where the (S) enantiomer is ordered alongside the (R) form so that both directions of chiral induction can be examined in the same study. It is handled in synthetic organic chemistry laboratories as a starting scaffold for preparing chiral ligands and organocatalysts, and it serves method-development work where enantioselectivity must be established with confidence rather than assumed.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChiral ligand synthesis: the two hydroxyl groups form a defined chiral pocket that binds metal centres, making this compound a direct precursor for ligands used in enantioselective transformations.\u003c\/li\u003e\n\u003cli\u003eOrganocatalyst preparation: the rigid binaphthyl backbone serves as a scaffold for chiral phosphate and related organocatalysts, with the bromine substituents tuning the acidity of the derived catalyst.\u003c\/li\u003e\n\u003cli\u003eCross-coupling elaboration: bromine atoms at the 6 and 6' positions provide reactive handles for cross-coupling chemistry, allowing systematic extension of the binaphthol core into larger structures.\u003c\/li\u003e\n\u003cli\u003eControl experiments in asymmetric catalysis: as the single (S) enantiomer, it reverses the direction of chiral induction while every other reaction condition is held unchanged.\u003c\/li\u003e\n\u003cli\u003eSelectivity verification studies: comparing outcomes between the (R) and (S) series is the most direct demonstration that observed selectivity is genuinely controlled by the catalyst rather than the substrate.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 80655-81-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eChemical name: (S)-(+)-6,6'-Dibromo-1,1'-bi-2-naphthol\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in TCI standard research-scale packaging; please confirm the required pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a cool, dry place in a tightly closed original container, protected from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the material in its original tightly closed container in a cool, dry place away from direct light and moisture, since prolonged exposure to air and light is undesirable for phenolic aromatic compounds. Amber glass or the supplier's original packaging is suitable, and containers should be resealed promptly after each use to preserve enantiomeric integrity. Handle inside a fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust when weighing. Use clean, dry spatulas to prevent cross-contamination between the (S) and (R) series, label all secondary containers clearly with configuration and CAS number, and consult the manufacturer's safety data sheet before use and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086580297946,"sku":"TCI2510D273023055","price":3458000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086580330714,"sku":"TCI2510D273023056","price":10298000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2730.jpg?v=1767105249"},{"product_id":"tci2510d273523063","title":"TCI D2735 112068-01-6 (S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. This reagent plays a crucial role in laboratories where precise control over molecular structure is essential, particularly in pharmaceutical and organic chemistry research. Its chiral nature allows it to act as a catalyst or ligand, enhancing reaction efficiency by directing the formation of desired enantiomers. This makes it an indispensable tool for scientists aiming to achieve high selectivity in complex chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique properties, including its optical activity and ability to selectively interact with substrates, make it a preferred choice in advanced chemical applications. Its molecular structure enables it to influence reaction pathways in a way that traditional reagents cannot, offering enhanced control over product stereochemistry. This selectivity is vital for the development of pharmaceuticals, where the correct enantiomer can significantly impact the efficacy and safety of a drug. Its versatility in various synthetic strategies further solidifies its position as a key reagent in modern chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used by researchers and pharmaceutical industries for the development of new compounds, testing of catalysts, and studies on asymmetric reactions. Its application is particularly relevant in academic and industrial settings where precision and efficiency in chemical synthesis are paramount. It supports both educational and research initiatives, contributing to the advancement of chemical sciences in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound is used to produce chiral molecules with high enantiomeric purity, making it ideal for pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003eChiral ligand applications benefit from its ability to selectively influence reaction pathways, enhancing the efficiency of catalytic processes in organic chemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drugs with specific stereochemical configurations, ensuring optimal biological activity and safety.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments rely on its optical activity to study reaction mechanisms and stereochemical outcomes in complex chemical transformations.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical sciences employs this compound to explore advanced synthetic methods and improve the selectivity of chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 112068-01-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which can affect its stability. In a laboratory setting, proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the material to ensure safety. It is important to keep the compound in a well-ventilated area and follow standard chemical safety protocols. Regular monitoring of storage conditions will help ensure the compound remains effective for its intended applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086580592858,"sku":"TCI2510D273523063","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086580625626,"sku":"TCI2510D273523064","price":5224000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2735.jpg?v=1767105257"},{"product_id":"tci2510d281023158","title":"TCI D2810 111795-43-8 (R)-3,3'-Dibromo-1,1'-bi-2-naphthol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-3,3'-Dibromo-1,1'-bi-2-naphthol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemistry and desired biological activity. This reagent plays a crucial role in organic chemistry laboratories, particularly in the development of enantiomerically pure compounds. Its application extends to pharmaceutical and biochemical research, where precise control over molecular structure is essential for drug development and functional molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique structure, featuring two bromine atoms at the 3 and 3’ positions of the bi-2-naphthol framework, contributes to its high reactivity and compatibility with chiral catalysts. This structural feature allows it to effectively participate in asymmetric catalytic reactions, enhancing enantioselectivity. Its aromatic nature and functional groups make it a versatile tool for synthetic chemists aiming to achieve high stereocontrol in complex molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research focused on organic chemistry, pharmacology, and biochemistry. It supports the development of new compounds with potential applications in medicine and industry. Many research institutions and universities in Indonesia rely on this material for advanced synthetic processes and experimental studies requiring high precision and selectivity.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research due to its ability to produce enantiomerically pure compounds with high selectivity.\u003c\/li\u003e\n\u003cli\u003eChiral ligand applications in catalytic reactions that require precise stereochemical control for drug molecule development.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis of complex molecules where stereochemistry plays a critical role in determining biological activity.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies involving chiral compounds that mimic natural molecules and interact with biological targets.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the design and synthesis of novel therapeutic agents with improved efficacy and reduced side effects.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 111795-43-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard chemical supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and maintain its chemical integrity. Due to its brominated structure, it may react with certain materials, so it should be handled with care and stored in a compatible container such as glass or high-density polyethylene. Laboratory personnel should ensure proper ventilation when working with this compound and avoid exposure to open flames or high temperatures. Regular monitoring of storage conditions is advised to ensure the material remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086589178074,"sku":"TCI2510D281023158","price":4619000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086589210842,"sku":"TCI2510D281023159","price":14738000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2810.jpg?v=1767105396"},{"product_id":"tci2510d281123160","title":"TCI D2811 119707-74-3 (S)-3,3'-Dibromo-1,1'-bi-2-naphthol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-3,3'-Dibromo-1,1'-bi-2-naphthol is a chiral compound widely used in asymmetric synthesis to produce molecules with defined stereochemistry. This material plays a crucial role in organic chemistry laboratories, particularly in the development of pharmaceuticals, industrial chemicals, and bioactive compounds. Its unique structure allows it to act as a chiral reagent or catalyst, enabling precise control over the stereochemical outcome of chemical reactions. In research settings, it is essential for creating enantiomerically pure products, which are vital in drug development and advanced chemical synthesis. The compound's ability to influence reaction pathways makes it a valuable tool for scientists aiming to achieve high selectivity and yield in complex synthetic processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature and structural complexity are key factors that make it a preferred choice in asymmetric synthesis. Its ability to interact selectively with other reactants ensures that only the desired stereoisomer is formed, reducing the need for additional purification steps. This characteristic is especially important in the production of pharmaceuticals, where the stereochemistry of a molecule can significantly affect its biological activity. Additionally, its stability under various reaction conditions enhances its utility in a wide range of chemical processes. These properties make it a reliable and effective component in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-3,3'-Dibromo-1,1'-bi-2-naphthol is commonly used in research related to organic chemistry, drug discovery, and materials science. It is frequently employed in academic institutions and research centers to support the development of new compounds and to meet the growing demand for chiral pharmaceuticals. Its application is also seen in the production of specialty chemicals and in studies focused on improving synthetic efficiency and product purity.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound is used to produce enantiomerically pure compounds, which are essential in pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003eChiral catalyst development benefits from this material's ability to influence reaction stereochemistry, making it ideal for creating new catalytic systems.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research utilizes this compound to explore stereochemical control in complex synthetic pathways, enhancing the efficiency of chemical processes.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects rely on this reagent to synthesize bioactive molecules with specific stereochemical configurations, improving the effectiveness of potential therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production uses this compound to create specialty chemicals with defined chiral properties, meeting the needs of various manufacturing sectors.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 119707-74-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical integrity. In laboratory settings, proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the material to ensure safety. The compound is not flammable, but it should be handled with care to avoid contamination. It is important to store it in a well-ventilated area and keep it away from incompatible substances to prevent any adverse reactions. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086589243610,"sku":"TCI2510D281123160","price":4013000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086589276378,"sku":"TCI2510D281123161","price":14107000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2811.jpg?v=1767105400"},{"product_id":"tci2510d318523441","title":"TCI D3185 155155-73-0 (2R,5R)-2,5-Diphenylpyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(2R,5R)-2,5-Diphenylpyrrolidine is a chemical compound widely used as an organocatalyst in various chemical reactions within the laboratory. This compound plays a crucial role in accelerating chemical reactions without undergoing degradation, ensuring efficient and accurate results. Its unique molecular structure, featuring two phenyl groups attached to carbon atoms at positions 2 and 5 of the pyrrolidine ring, makes it highly effective in catalytic processes. It is particularly valuable in asymmetric reactions and catalytic systems that require substrate activation. Due to its stability and reactivity, it is a key component in many synthetic and analytical procedures.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure provides it with several advantageous properties that make it a preferred choice in laboratory settings. Its stability in various solvents and resistance to degradation under typical reaction conditions contribute to its reliability. Additionally, its ability to interact with a wide range of substrates enhances its versatility in different chemical applications. The compound's non-toxic nature compared to other chemical catalysts also makes it safer for use in laboratory environments, reducing potential health and safety risks. These characteristics collectively make it a reliable and efficient choice for researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (2R,5R)-2,5-Diphenylpyrrolidine is commonly used in chemical research, especially in catalysis and organic synthesis. It is frequently employed in academic and industrial settings to facilitate complex reactions and improve reaction yields. Its widespread use in research institutions and universities highlights its importance in advancing chemical studies in the region. The compound's reliability and effectiveness make it an essential tool for chemists working in various fields of study.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis reactions benefit from its ability to selectively activate substrates, enhancing enantioselectivity and yield.\u003c\/li\u003e\n\u003cli\u003eCatalytic activation in organic reactions is supported by its stable molecular structure and reactivity with diverse substrates.\u003c\/li\u003e\n\u003cli\u003eSynthetic chemistry applications leverage its role in promoting efficient and selective chemical transformations under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry processes utilize its stability and non-toxic properties for reliable and safe experimental outcomes.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it for scalable and reproducible catalytic reactions in production settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 155155-73-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and potential degradation. Due to its non-toxic nature, it is generally safe to handle, but standard laboratory precautions should still be followed, such as wearing appropriate personal protective equipment. It is important to ensure that the storage area is well-ventilated and free from incompatible materials. Proper handling and storage conditions help preserve the compound's integrity and ensure its safe use in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086603038938,"sku":"TCI2510D318523441","price":16380000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3185.jpg?v=1767105764"},{"product_id":"tci2510d347523760","title":"TCI D3475 2010983-27-2 6,10-Dibenzyl-N,N'-dimethyl-N,N,N',N'-tetrakis(4-methylbenzyl)-1,4-dioxaspiro[4.5]decane-(2R,3R)-diylbis(methylammonium) Bis(tetrafluoroborate) [=(R,R)-TaDiAS-2nd]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3475, catalogue name 6,10-Dibenzyl-N,N'-dimethyl-N,N,N',N'-tetrakis(4-methylbenzyl)-1,4-dioxaspiro[4.5]decane-(2R,3R)-diylbis(methylammonium) Bis(tetrafluoroborate), also written (R,R)-TaDiAS-2nd, is a second-generation chiral catalyst from the TaDiAS family: a tartaric acid–derived quaternary bis-ammonium salt designed specifically for asymmetric synthesis. Its full name describes a spiroacetal framework carrying two stereocentres of R,R configuration together with two positively charged ammonium centres, each balanced by a tetrafluoroborate anion. Catalysts of this type function as chiral phase-transfer catalysts, shuttling nucleophilic anions from an aqueous phase into an organic phase while simultaneously directing their attack from one face only.\u003c\/p\u003e\n\u003cp\u003eThe property that gives this reagent its high value in the laboratory is the presence of two ammonium centres within a single molecule, which creates a tight chiral pocket around the ion pair. Four 4-methylbenzyl groups, together with the two benzyl groups on the spiro skeleton, assemble a firmly defined steric environment, so a substrate can only approach comfortably through one particular orientation and the reaction delivers product with high enantiomeric excess. The tetrafluoroborate counter-anion is weakly coordinating, leaving the ammonium centres available to organise the reacting ion pair rather than being tied up by their own counter-ion.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this catalyst is typically used in university research groups, graduate methodology projects, and pharmaceutical or fine-chemical development work where a single enantiomer of a target molecule is required. It is normally handled at small scale on the bench, in catalytic loadings, within biphasic reaction systems set up for asymmetric alkylation and related transformations. Because it is supplied as a defined single stereoisomer, it also serves as a dependable reference catalyst when a group is validating or comparing asymmetric methods.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric phase-transfer alkylation — the bis-ammonium structure carries nucleophilic anions into the organic phase while its chiral pocket forces attack from a single face, giving high enantioselectivity.\u003c\/li\u003e\n\u003cli\u003eEnantioselective synthesis of chiral building blocks — the fixed (2R,3R) configuration of the spiroacetal backbone allows researchers to target one predictable enantiomeric series throughout a synthetic route.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical intermediate development — a defined single-stereoisomer catalyst supports work where only one enantiomer of an active molecule is biologically relevant and the other must be suppressed.\u003c\/li\u003e\n\u003cli\u003eAsymmetric catalysis methodology research — the second-generation TaDiAS design, with four 4-methylbenzyl and two benzyl groups, makes it a useful probe of how steric bulk controls stereochemical outcome.\u003c\/li\u003e\n\u003cli\u003eReference catalyst for comparative screening — because its structure, stereochemistry and CAS identity are unambiguous, it serves as a benchmark against which newly prepared chiral catalysts can be measured.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2010983-27-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eChemical class: tartaric acid–derived quaternary bis-ammonium salt with bis(tetrafluoroborate) counter-anions\u003c\/li\u003e\n\u003cli\u003eStereochemistry: single defined stereoisomer, (2R,3R) configuration, (R,R)-TaDiAS-2nd\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in TCI research-scale catalogue packs; please confirm the required pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the tightly closed original container in a cool, dry place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry place, protected from moisture and away from direct sunlight and sources of heat. As an ionic quaternary ammonium salt, it should be kept from prolonged exposure to humid air; a desiccator or a sealed secondary container is appropriate for opened packs, and weighing is best done quickly with clean dry spatulas to avoid caking. Handle in a fume hood using safety glasses, gloves, and a laboratory coat, and avoid generating or inhaling dust. Keep the container clearly labelled, return it to storage immediately after use, and follow the manufacturer's safety data sheet together with your institution's chemical waste procedures for disposal of residues and contaminated solvents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086617817306,"sku":"TCI2510D347523760","price":2953000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086617850074,"sku":"TCI2510D347523761","price":10272000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3475.jpg?v=1767106148"},{"product_id":"tci2510d347623762","title":"TCI D3476 2135524-59-1 6,10-Dibenzyl-N,N'-dimethyl-N,N,N',N'-tetrakis(4-methylbenzyl)-1,4-dioxaspiro[4.5]decane-(2S,3S)-diylbis(methylammonium) Bis(tetrafluoroborate) [=(S,S)-TaDiAS-2nd]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3476 is a chiral catalyst belonging to the diquaternary ammonium salt class, derived from a tartrate-based framework and widely known by the designation (S,S)-TaDiAS-2nd. The compound is supplied as a bis(tetrafluoroborate) salt bearing two positively charged ammonium centers attached to a 1,4-dioxaspiro[4.5]decane skeleton of (2S,3S) configuration. In the laboratory, this material functions as a chiral phase-transfer catalyst — a substance that shuttles anionic species from an aqueous or solid phase into the organic phase while establishing a chiral environment that directs the formation of one enantiomer predominantly. Its role is central to modern asymmetric synthesis research.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this catalyst a preferred choice are the combination of a rigid tartrate framework with bulky 4-methylbenzyl and benzyl groups arranged around the ammonium centers. This densely packed steric arrangement creates a chiral pocket that effectively differentiates the two approach faces of a substrate, so that the enantiomeric selectivity obtained can be high even when the catalyst is used in small quantities. The tetrafluoroborate anion contributes good solubility in organic solvents together with non-coordinating character, which keeps the counter-ion from interfering with the reactive intermediates that form during the catalytic cycle.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in university and institutional research groups working on asymmetric synthesis, medicinal chemistry, and the preparation of enantiomerically enriched building blocks. It is generally used at small scale on the bench, where a single package supports many exploratory reactions and catalyst-screening experiments. Researchers commonly handle it as part of methodology development studies, thesis work, and publication-oriented projects that require reliable stereochemical control rather than bulk production.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric phase-transfer alkylation — the diquaternary ammonium centers transport enolate anions into the organic phase while the rigid chiral pocket steers the alkylating agent to a single face of the substrate.\u003c\/li\u003e\n\u003cli\u003eEnantioselective synthesis of amino acid derivatives — the tartrate-derived framework provides the facial discrimination needed to build stereocenters adjacent to carbonyl groups with strong enantiomeric preference.\u003c\/li\u003e\n\u003cli\u003eMethodology development in asymmetric catalysis — researchers screen this catalyst against other chiral ammonium salts to establish structure-selectivity relationships within the TaDiAS family of catalysts.\u003c\/li\u003e\n\u003cli\u003ePreparation of enantiomerically enriched building blocks — small catalyst loadings can deliver chiral intermediates for downstream medicinal chemistry work without requiring stoichiometric chiral auxiliaries.\u003c\/li\u003e\n\u003cli\u003eTeaching and demonstration of chiral phase-transfer principles — the well-defined (2S,3S) configuration makes it a clear illustration of how catalyst stereochemistry translates into product enantioselectivity in graduate-level laboratory courses.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 2135524-59-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eChemical class: diquaternary ammonium salt, bis(tetrafluoroborate) counter-ion, (2S,3S) configuration\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the research-scale unit sizes offered by the manufacturer; please confirm the current packaging option when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly closed in a cool, dry place away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry location, protected from moisture and away from direct sunlight or heat sources. As an ammonium salt, the material is best kept in its original tightly sealed bottle or transferred to a well-sealed amber glass container with a chemically resistant closure; a desiccator or dry cabinet is advisable if the laboratory environment is humid. Weigh and transfer the solid inside a fume hood using clean, dry spatulas to avoid contamination and moisture uptake. Wear safety glasses, gloves, and a laboratory coat during handling, avoid the generation of dust, and wash hands thoroughly after use. Consult the manufacturer's safety data sheet before first use and follow institutional procedures for chemical waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086617882842,"sku":"TCI2510D347623762","price":2953000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086617915610,"sku":"TCI2510D347623763","price":10272000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3476.jpg?v=1767106152"},{"product_id":"tci2510d384324231","title":"TCI D3843 848821-58-9 (S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThe TCI D3843, with CAS number 848821-58-9, is a chiral reagent known as (S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether. This compound plays a crucial role in asymmetric synthesis, where it acts as a chiral catalyst or ligand to facilitate the formation of chiral molecules. In laboratory settings, it is widely used to produce enantiomerically pure compounds, which are essential in pharmaceutical and biochemical research. Its ability to control stereochemistry makes it a valuable tool for researchers aiming to develop new drugs and bioactive compounds.\u003c\/p\u003e\n\u003cp\u003eThis reagent is preferred due to its high chiral purity and structural complexity, which enhance its reactivity in various synthetic conditions. The presence of the trimethylsilyl group contributes to its stability and solubility, making it suitable for a wide range of reaction environments. Additionally, its well-defined stereochemistry ensures consistent results in asymmetric reactions, which is vital for reproducibility in scientific research. These properties make it an ideal choice for applications requiring precise control over the stereochemical outcome of chemical reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists, pharmacologists, and biochemists working in academic and research institutions. It supports the development of new pharmaceuticals and bioactive compounds by enabling the synthesis of molecules with specific stereochemical configurations. Its application is particularly relevant in drug discovery and the creation of compounds with targeted biological activities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for producing enantiomerically pure compounds due to its chiral structure and catalytic properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research to develop drugs with specific stereochemistry for enhanced biological activity and reduced side effects.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies to synthesize chiral molecules with potential therapeutic applications in medicine and biotechnology.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise control over reaction stereochemistry for academic and industrial research.\u003c\/li\u003e\n\u003cli\u003eLigand development in asymmetric catalysis to improve reaction efficiency and selectivity in complex chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 848821-58-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on formulation and supplier specifications\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. In laboratory settings, proper personal protective equipment, such as gloves and safety goggles, should be worn when handling this material. Due to its chiral nature and potential reactivity, it should be kept in a secure location to prevent accidental exposure. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications in chemical synthesis and research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086640754906,"sku":"TCI2510D384324231","price":3761000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086640787674,"sku":"TCI2510D384324232","price":12038000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3843.jpg?v=1767106652"},{"product_id":"tci2510d386724272","title":"TCI D3867 943757-71-9 (R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether is a chiral reagent widely used in asymmetric synthesis to produce compounds with specific optical configurations. This compound plays a crucial role in chemical reactions where stereochemical control is essential. It functions as a chiral catalyst or ligand, enabling the selective formation of enantiomers. Its unique molecular structure allows for precise interactions with other reactants, making it a valuable tool in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s optically active nature and molecular complexity make it a preferred choice for researchers aiming at high stereocontrol. Its ability to influence reaction pathways and yield desired stereoisomers is critical in the development of pharmaceuticals and organic compounds. The trimethylsilyl ether group enhances its solubility and reactivity, contributing to its effectiveness in various synthetic protocols. These properties ensure its reliability in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new chemical materials. Researchers in educational and research institutions rely on it for experiments requiring precise molecular structure control. Its availability in small packaging makes it accessible for laboratory-scale applications, supporting innovation in chemical synthesis and drug discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for producing chiral compounds with specific optical activity, due to its ability to control stereochemistry in reaction pathways.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research where precise molecular structure control is required, as it enables selective formation of enantiomers.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and bioactive compounds, as its chiral nature is essential for creating molecules with desired biological activity.\u003c\/li\u003e\n\u003cli\u003eLigand-based catalytic reactions, where its chiral properties enhance reaction selectivity and efficiency in complex chemical transformations.\u003c\/li\u003e\n\u003cli\u003eSynthetic chemistry experiments requiring high stereocontrol, as it provides a reliable and consistent reagent for achieving desired stereochemical outcomes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 943757-71-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in small laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chiral nature, it is important to maintain the integrity of the compound during handling to avoid contamination or degradation. Proper labeling and safe storage practices are essential to ensure its effectiveness in laboratory applications. Always use appropriate personal protective equipment when handling this material to ensure safety in the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086642360538,"sku":"TCI2510D386724272","price":3257000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086642393306,"sku":"TCI2510D386724273","price":12593000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3867.jpg?v=1767106701"},{"product_id":"tci2510d398324431","title":"TCI D3983 903571-02-8 (+)-(5aR,10bS)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium Chloride Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3983 (+)-(5aR,10bS)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium Chloride Monohydrate is a chiral triazolium salt that serves as an N-heterocyclic carbene organocatalyst precursor. The compound belongs to the organocatalyst category within the field of catalysis, and it is used in asymmetric synthesis laboratories to deliver products with high enantiomeric purity. When treated with a suitable base, this triazolium salt loses a proton at the key position and forms the active carbene species, which is able to invert the polarity of a carbonyl group and direct the formation of new bonds to a single face of the molecule.\u003c\/p\u003e\n\u003cp\u003eThe feature that makes this catalyst a preferred choice is its rigid fused indanol framework combined with a mesityl group — 2,4,6-trimethylphenyl — on the triazolium nitrogen atom. The rigidity of the bicyclic structure produces a clearly defined chiral environment around the catalytic centre, while the bulky mesityl group provides directed steric hindrance so that a substrate can only approach from one particular orientation. The firmly assigned (5aR,10bS) configuration ensures that the catalyst consistently generates the intended product enantiomer, which is what allows results to be reproduced from one batch to the next.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically used in university and institutional research groups working on asymmetric methodology, in synthetic organic chemistry programmes, and in laboratories developing routes toward chiral building blocks. It is generally handled on a small scale in glassware under controlled conditions, where a defined chiral catalyst is required rather than a resolution step, and where the enantiomeric outcome of each reaction has to be verified analytically.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric organocatalysis — the defined (5aR,10bS) configuration and rigid framework give a single reliable chiral environment, so reactions favour one product enantiomer.\u003c\/li\u003e\n\u003cli\u003eN-heterocyclic carbene generation — deprotonation of the triazolium salt with a suitable base releases the active carbene species needed as the working catalyst in situ.\u003c\/li\u003e\n\u003cli\u003eUmpolung (polarity reversal) chemistry — the carbene formed from this salt inverts the normal polarity of carbonyl groups, opening bond constructions unavailable under classical conditions.\u003c\/li\u003e\n\u003cli\u003eEnantioselective bond-forming reactions — the bulky mesityl substituent blocks one approach path, restricting substrate orientation and directing new bonds to a single molecular face.\u003c\/li\u003e\n\u003cli\u003eMethod development and catalyst screening — as a well-defined single-enantiomer precursor it serves as a reference organocatalyst when comparing conditions, bases, and substrate scope.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 903571-02-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: supplied in standard TCI research-scale catalogue packs; please confirm the available size when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline triazolium chloride salt, isolated as the monohydrate\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry place, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated place away from moisture, since the material is a hygroscopic-type salt isolated as a monohydrate and its handling properties depend on controlled water content. Original tightly sealed glass or amber bottles are suitable; keep the closure intact and consider a desiccator or secondary sealed container for opened bottles. Weigh and transfer in a fume hood using dry spatulas and dry glassware, wearing safety glasses, a laboratory coat, and chemically resistant gloves. Avoid dust formation, inhalation, and contact with skin and eyes. Keep away from strong bases and incompatible reagents in storage, label all working solutions clearly, and consult the manufacturer's safety data sheet before use and for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086649372890,"sku":"TCI2510D398324431","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3983.jpg?v=1767106890"},{"product_id":"tci2510d398424432","title":"TCI D3984 919102-70-8 (-)-(5aS,10bR)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium Chloride Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3984 (-)-(5aS,10bR)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium Chloride Monohydrate is a chiral triazolium salt that represents the enantiomeric counterpart of the (+) variant. The compound functions as a precursor for N-heterocyclic carbene organocatalysts and is used in the laboratory to run asymmetric reactions that deliver product configurations opposite to those obtained with its paired enantiomer. Once activated with a suitable base, the salt generates a carbene species capable of reversing the normal reactivity pattern of carbonyl groups and controlling the direction of nucleophilic and electrophilic attack during the bond-forming step.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this catalyst valuable are its rigid indanol-derived bicyclic framework combined with the mesityl group installed on the triazolium nitrogen atom. The rigid structure locks the geometry of the catalytic centre, so the surrounding chiral environment stays consistent from one catalytic cycle to the next, while the bulky mesityl group shields one face of substrate approach. The (5aS,10bR) configuration ensures that the products formed carry stereochemistry opposite to the outcome obtained from the enantiomeric catalyst, which makes the pair useful for accessing either antipode of a target molecule.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this triazolium salt is typically handled in university and institutional research groups working on asymmetric synthesis and methodology development, as well as in industrial R\u0026amp;D settings preparing enantioenriched intermediates. It is normally weighed out in small catalytic quantities, activated in situ with base, and used alongside the (+) enantiomer when a study requires both product configurations for comparison, assignment of absolute stereochemistry, or verification of catalyst-controlled selectivity.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric NHC catalysis — the salt is deprotonated in situ to form the active carbene, and its fixed chiral pocket transfers stereochemical information directly to the newly formed bonds.\u003c\/li\u003e\n\u003cli\u003eCarbonyl umpolung chemistry — after activation the carbene reverses the conventional polarity of carbonyl groups, opening bond constructions that are not accessible through standard nucleophilic addition chemistry.\u003c\/li\u003e\n\u003cli\u003eEnantiodivergent synthesis — used deliberately in place of the (+) enantiomer when a laboratory needs the mirror-image product configuration from an otherwise identical reaction protocol and setup.\u003c\/li\u003e\n\u003cli\u003eStereochemical assignment studies — running a transformation with both enantiomers of this catalyst produces opposite antipodes, giving researchers a reliable internal reference for confirming absolute configuration.\u003c\/li\u003e\n\u003cli\u003eMethodology and catalyst screening — the rigid indanol-derived scaffold with its mesityl substituent serves as a well-defined benchmark structure when comparing chiral triazolium precursors in reaction development.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 919102-70-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003eChemical class: chiral triazolium salt, N-heterocyclic carbene (NHC) organocatalyst precursor\u003c\/li\u003e\n\u003cli\u003eHydration state: chloride monohydrate\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in laboratory research quantities as listed by the manufacturer; storage note — keep in a tightly closed original container, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry, well-ventilated area, away from moisture, strong bases, and incompatible chemicals, since triazolium salts are hygroscopic and can be deactivated by uncontrolled exposure to atmospheric water. Weigh and transfer the solid using clean, dry spatulas and glassware, and reseal the container promptly after use. Handle in a fume hood with a laboratory coat, nitrile gloves, and safety glasses, and consult the manufacturer's safety data sheet before use, disposal, or transport. Keep containers clearly labelled and segregated from bulk reagents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086649471194,"sku":"TCI2510D398424432","price":5200000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3984.jpg?v=1767106894"},{"product_id":"tci2510d441825007","title":"TCI D4418 65355-08-0 (R)-(+)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(+)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. This material plays a crucial role in laboratories where precise control over molecular structure is essential. It is commonly employed as a reagent or catalyst in reactions that require stereoselectivity, enabling the synthesis of complex organic compounds with defined chirality. Its importance extends across various research fields, including pharmaceuticals and materials science, where stereochemistry significantly influences the properties and biological activity of the final product.\u003c\/p\u003e\n\u003cp\u003eThe compound’s well-defined chiral properties make it a preferred choice for researchers aiming to achieve high enantiomeric purity. Its molecular structure allows for selective interactions in chemical reactions, making it ideal for applications where stereochemical control is paramount. Additionally, its stability under controlled laboratory conditions ensures consistent performance, which is vital for reproducible results. The compound’s specificity in reaction mechanisms also enhances its utility in developing new synthetic methodologies and optimizing existing ones.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used by researchers in academic and research institutions. It supports studies focused on asymmetric synthesis and the development of new compounds with specific pharmacological activities. Its application is integral to advancing research in pharmaceutical chemistry and materials science, contributing to the expansion of scientific knowledge in these areas.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research for producing chiral compounds with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new ligands and catalysts for enantioselective reactions in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex molecules in materials science to create compounds with unique physical and chemical properties.\u003c\/li\u003e\n\u003cli\u003eInvestigation of stereochemical effects on drug efficacy and toxicity in medicinal chemistry studies.\u003c\/li\u003e\n\u003cli\u003eSupport for academic research in universities and research centers focusing on advanced organic synthesis techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 65355-08-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to maintain strict handling procedures to ensure the integrity of its stereochemical properties. Always use appropriate personal protective equipment when handling the material. It should be kept in a secure location to prevent accidental exposure. Proper labeling and storage conditions are essential to maintain its stability and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086691250394,"sku":"TCI2510D441825007","price":3105000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086691283162,"sku":"TCI2510D441825008","price":10448000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4418.jpg?v=1767107539"},{"product_id":"tci2510d444525040","title":"TCI D4445 1092934-19-4 Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4445 1092934-19-4 Dipotassium (R)-1,1'-Binaphthyl-2,2'-disulfonate is a specialized chemical compound used in catalytic reactions, particularly in the field of organocatalysis. This compound is a key reagent in asymmetric synthesis, where it facilitates the formation of chiral molecules with high enantioselectivity. Its unique molecular structure, featuring two sulfonate groups attached to the binaphthyl framework, makes it highly effective in promoting specific reaction pathways. Due to its ability to accelerate chemical reactions without being consumed, it plays a crucial role in advancing research in organic chemistry and catalytic processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and structural symmetry make it a preferred choice for researchers seeking efficient and selective catalytic systems. Its ability to maintain stability under various reaction conditions ensures consistent performance in laboratory settings. Additionally, its well-defined chemical properties allow for precise control over reaction outcomes, making it a reliable material for both academic and industrial applications. The compound's effectiveness in asymmetric reactions has made it a standard in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, especially in the synthesis of complex molecules and asymmetric reactions. Its availability and performance make it a valuable tool for chemists working on drug development, material science, and other advanced chemical applications. The compound's role in promoting sustainable and efficient synthetic methods aligns with the growing emphasis on green chemistry in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric reactions due to its chiral structure, enabling the selective formation of enantiomers with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganocatalytic Reactions: Its catalytic properties make it suitable for a wide range of organocatalytic processes, enhancing reaction rates and selectivity.\u003c\/li\u003e\n\u003cli\u003eComplex Molecule Synthesis: The compound's ability to facilitate complex transformations makes it a preferred choice in the synthesis of intricate organic structures.\u003c\/li\u003e\n\u003cli\u003eGreen Chemistry Initiatives: Its efficiency and reduced byproduct formation align with sustainable chemical practices, supporting eco-friendly laboratory protocols.\u003c\/li\u003e\n\u003cli\u003eResearch and Development: It is commonly used in R\u0026amp;D settings for exploring new catalytic mechanisms and optimizing reaction conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1092934-19-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard chemical supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in powder or crystalline form\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Avoid exposure to incompatible substances such as strong oxidizers or acids. Ensure proper labeling and storage in designated chemical storage cabinets to maintain safety and prevent accidental spills or reactions. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086692331738,"sku":"TCI2510D444525040","price":7926000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4445.jpg?v=1767107576"},{"product_id":"tci2510d510725943","title":"TCI D5107 765278-73-7 (S)-(-)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5107, also known as (S)-(-)-3,3'-Dibromo-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol, is a chiral compound widely used in asymmetric synthesis. It serves as a chiral reagent or ligand, playing a crucial role in catalyzing reactions that produce enantiomerically pure compounds. This material is essential in modern organic chemistry for achieving high stereoselectivity and enantioselectivity in complex molecular transformations. Its application spans various research fields, including pharmaceutical development, material science, and synthetic chemistry. Due to its unique stereochemical properties, it is a preferred choice for researchers aiming to control the stereochemistry of reaction products with precision.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chiral nature and stable molecular structure make it an ideal candidate for asymmetric catalytic processes. Its high chiral purity ensures consistent and reproducible results in synthetic reactions, reducing the need for additional purification steps. The compound’s ability to maintain its stereochemical integrity under a range of reaction conditions enhances its versatility in laboratory settings. Additionally, its availability in practical packaging formats facilitates easy handling and use in both small-scale and large-scale experiments. These characteristics contribute to its widespread adoption in academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI D5107 is commonly used in organic chemistry research, particularly in the development of synthetic drugs and specialty chemicals. Its role in producing chiral compounds is critical for pharmaceutical applications where stereochemistry significantly impacts the efficacy and safety of the final product. Researchers in Indonesia rely on this compound to meet the growing demand for high-quality, chiral materials in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where TCI D5107 is used to produce enantiomerically pure compounds, ensuring high stereocontrol in complex reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its chiral properties, enabling the synthesis of drug molecules with desired stereochemistry for therapeutic efficacy.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often utilize this compound to explore stereoselective reactions and develop new synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications leverage its chiral structure to create advanced materials with specific optical or functional properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis relies on TCI D5107 for the production of chiral intermediates and final products in large-scale manufacturing processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 765278-73-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities suitable for both small and large-scale laboratory use\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically provided in powder or crystalline form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTCI D5107 should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent moisture absorption and maintain its chemical integrity. Due to its chiral nature, it is important to handle the material with care to avoid contamination or degradation. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. In laboratory settings, it is advisable to use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Regular monitoring of storage conditions helps maintain the quality and effectiveness of the material for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086744924378,"sku":"TCI2510D510725943","price":2349000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5107.jpg?v=1767108394"},{"product_id":"tci2510d591226901","title":"TCI D5912 112022-81-8 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine (ca. 1mol\/L in Toluene)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical material, (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine, is a chiral catalyst dissolved in toluene at a concentration of approximately 1 mol\/L. It plays a critical role in asymmetric synthesis by enabling precise control over the stereochemistry of chemical reactions. As a key component in chiral catalysis, it is widely used in the production of complex organic compounds where stereochemical purity is essential. Its application extends to various synthetic pathways that require enantioselective outcomes, making it an essential tool for researchers in organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe material is highly valued for its purity and efficiency in catalytic processes. It maintains stability under various reaction conditions, ensuring consistent performance in laboratory settings. Its molecular structure is designed to facilitate selective interactions in asymmetric reactions, enhancing the yield and selectivity of desired products. This reliability and effectiveness make it a preferred choice for both academic and industrial research. Additionally, its controlled chemical properties contribute to safe and efficient experimental procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is particularly relevant for organic chemistry research, especially in asymmetric synthesis. It supports the development of new compounds with specific stereochemical configurations, which are crucial for pharmaceutical and materials science applications. Its availability through AMI Scientific ensures that researchers in Indonesia have access to high-quality chiral catalysts for advanced chemical studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in organic chemistry laboratories for producing enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions requiring precise stereochemical control in pharmaceutical research and development.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex organic molecules where chiral catalysts are essential for achieving desired product configurations.\u003c\/li\u003e\n\u003cli\u003eResearch applications in academic institutions focused on advanced chemical transformations and stereochemistry.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes that demand high selectivity and efficiency in catalytic systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 112022-81-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid (dissolved in toluene)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from moisture and incompatible substances.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis material should be stored in a cool, dark location, away from moisture and incompatible substances. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound. Avoid contact with skin and eyes, and follow standard laboratory safety protocols to minimize risk. Regular inspection of storage conditions is advised to maintain the integrity of the product.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086783197402,"sku":"TCI2510D591226901","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086783230170,"sku":"TCI2510D591226902","price":5553000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5912.jpg?v=1767109422"},{"product_id":"tci2510d611227153","title":"TCI D6112 522-66-7 (-)-Dihydroquinine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-Dihydroquinine is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. In the laboratory, it functions as a chiral reagent that directs chemical reactions toward the desired product by influencing the reaction pathway. This compound is particularly valuable in organic chemistry and pharmaceutical research, where precise control over molecular structure is essential. Its role as a chiral catalyst allows for the efficient synthesis of complex molecules with high enantioselectivity, making it a key component in modern synthetic strategies.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make (-)-Dihydroquinine a preferred choice is its ability to act as an effective chiral catalyst in asymmetric reactions. Its complex molecular structure enables specific interactions with substrates, enhancing both the efficiency and selectivity of the reaction. Additionally, its stability under various reaction conditions contributes to its reliability in laboratory settings. These characteristics make it a versatile tool for researchers aiming to develop new compounds with biological activity or industrial applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (-)-Dihydroquinine is commonly used in research focused on organic chemistry and asymmetric synthesis. It is particularly relevant for institutions engaged in drug discovery, pharmaceutical development, and chemical innovation. Its application supports the creation of compounds with specific stereochemistry, which is crucial for the development of new medicines and specialized chemical products.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where (-)-Dihydroquinine is used to produce chiral compounds with high enantioselectivity, making it ideal for pharmaceutical and organic chemistry research.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from (-)-Dihydroquinine’s ability to direct reactions toward specific stereoisomers, which is essential for drug development and compound optimization.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often utilize this compound to explore new synthetic pathways and improve reaction efficiency through chiral catalysis.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis relies on (-)-Dihydroquinine to create compounds with defined stereochemistry, supporting the production of specialty chemicals and materials.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesia uses (-)-Dihydroquinine to advance studies in synthetic chemistry, contributing to the development of new methodologies and compounds.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 522-66-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e(-)-Dihydroquinine should be stored in a cool, dry place away from direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended stereochemical changes. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard safety protocols when handling chiral compounds, including the use of appropriate personal protective equipment. The compound is generally stable under normal laboratory conditions but should be kept in a controlled environment to preserve its properties for extended use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086792241370,"sku":"TCI2510D611227153","price":1995000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086792274138,"sku":"TCI2510D611227154","price":6940000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6112.jpg?v=1767109740"},{"product_id":"tci2510e097428826","title":"TCI E0974 1476067-44-3 (1R,3S,5R,7R,8aS)-7-Ethylhexahydro-1-(6-hydroxy-4-quinolinyl)-3,7-methano-1H-pyrrolo[2,1-c][1,4]oxazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis complex compound, with a chiral structure, plays a vital role in asymmetric synthesis within laboratory settings. It is a chiral reagent designed to facilitate the creation of molecules with specific stereochemical configurations. Its unique molecular architecture allows it to selectively interact with other molecules, making it a powerful tool for synthesizing compounds with precise spatial arrangements. In chemical research, this material is essential for achieving high enantioselectivity, which is crucial in the development of pharmaceuticals and other advanced chemical products.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature and molecular complexity make it a preferred choice for researchers aiming to control stereoselectivity in chemical reactions. Its ability to selectively interact with specific isomers enhances the efficiency and accuracy of synthetic processes. This reagent is particularly valued for its stability under standard laboratory conditions, which ensures consistent performance and ease of handling. Its reliability and effectiveness have made it a staple in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used by researchers in higher education institutions and research organizations. It is particularly relevant in fields such as pharmacology, organic chemistry, and industrial chemistry. Its application supports the development of new drugs and advanced chemical materials, contributing to scientific innovation and technological progress in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research due to its ability to selectively produce enantiomers with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise control over stereochemistry for the synthesis of complex molecules.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where chiral compounds are needed for the creation of high-value products.\u003c\/li\u003e\n\u003cli\u003eDrug development projects that rely on stereoselective reactions to achieve desired pharmacological effects.\u003c\/li\u003e\n\u003cli\u003eResearch in catalytic processes where chiral reagents are essential for enhancing reaction specificity and yield.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1476067-44-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and potential degradation. In laboratory settings, proper ventilation should be ensured when handling the material to minimize any risk of inhalation. Always wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. The material should be kept in a secure location, away from incompatible substances to ensure safe storage and handling. Regular monitoring of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086914269402,"sku":"TCI2510E097428826","price":5579000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0974.jpg?v=1767112088"},{"product_id":"tci2510e157929636","title":"TCI E1579 18422-53-2 Shi Epoxidation Diketal Catalyst","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eShi Epoxidation Diketal Catalyst is a chiral ketone derived from fructose and protected as a diketal, and it is the best known organocatalyst for the asymmetric epoxidation reaction developed by Shi. The catalyst works by forming a dioxirane in situ when it is treated with an oxidant source such as Oxone; the resulting chiral dioxirane then transfers an oxygen atom to the double bond of an alkene. In the laboratory, this material is the primary choice for researchers who wish to produce optically active epoxides without using heavy metals.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this catalyst distinctive is its origin in a natural sugar, which means it is available in enantiomerically pure form with a well defined chiral environment. Being metal free, it avoids residual metal contamination in the product, an important advantage for the synthesis of compounds that will subsequently be tested biologically. The reaction proceeds in a mixture of water and organic solvent at low temperature with pH control, conditions that are relatively mild and that do not require specialised pressurised equipment. The best selectivity is generally obtained with trans-disubstituted and trisubstituted alkenes, so the substrate scope is highly useful in natural product synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this catalyst is typically used in university and institutional research groups working on asymmetric synthesis, where optically active epoxides are needed as intermediates. Because the reaction is run in aqueous and organic solvent mixtures at low temperature with pH control, it can be carried out with standard glassware, cooling baths and pH monitoring already present in most synthetic chemistry laboratories, without investment in dedicated high pressure or inert atmosphere systems.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric epoxidation of alkenes: the catalyst generates a chiral dioxirane in situ with Oxone, transferring oxygen to the double bond and giving optically active epoxides.\u003c\/li\u003e\n\u003cli\u003eMetal free synthesis of biologically tested compounds: because no heavy metal is involved, the product is not contaminated with residual metal that could interfere with biological evaluation.\u003c\/li\u003e\n\u003cli\u003eNatural product synthesis: the best selectivity on trans-disubstituted and trisubstituted alkenes makes the substrate scope particularly useful for building optically active fragments of natural products.\u003c\/li\u003e\n\u003cli\u003ePreparation of chiral epoxide intermediates: enantiomerically pure epoxides obtained with this catalyst serve as versatile intermediates that can be opened to give further optically active building blocks.\u003c\/li\u003e\n\u003cli\u003eTeaching and research in organocatalysis: as the best known catalyst for Shi asymmetric epoxidation, it is a clear demonstration of metal free asymmetric catalysis based on a sugar derived chiral ketone.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: E1579\u003c\/li\u003e\n\u003cli\u003eCAS number: 18422-53-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003eChemical class: fructose derived chiral ketone protected as a diketal; metal free organocatalyst\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research packaging; please confirm the available pack sizes when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a tightly closed container in a cool, dry place away from oxidants\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the catalyst in its original tightly closed container in a cool, dry place, protected from moisture and light, and keep it clearly separated from the oxidant used in the reaction, such as Oxone, since the two are only combined under controlled conditions in the reaction vessel. Use clean, dry glass or the supplied packaging for weighing and transfer, and avoid introducing moisture into the bulk material. Handle the powder in a fume hood using a laboratory coat, safety glasses and chemically resistant gloves, following the safety data sheet supplied with the product. Because the reaction itself is run at low temperature with pH control in an aqueous and organic solvent mixture, prepare cooling baths and pH monitoring before the catalyst is weighed out, and dispose of residues according to the chemical waste procedures of your laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086971056346,"sku":"TCI2510E157929636","price":2752000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086971089114,"sku":"TCI2510E157929637","price":9869000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1579.jpg?v=1767113099"},{"product_id":"tci2510f081830795","title":"TCI F0818 2507-61-1 trans-4-Fluoro-L-proline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTrans-4-Fluoro-L-proline is a chemical compound widely used in catalytic reactions and organic synthesis within laboratory settings. It plays a crucial role in facilitating the formation of complex molecules through its unique molecular structure. The presence of a fluorine group at the fourth position enhances its reactivity and specificity, making it a valuable tool for chemists and researchers. This compound is particularly useful in asymmetric reactions, where precise control over reaction outcomes is essential. Its ability to act as both a catalyst and a reactant contributes to its versatility in various synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and solubility in organic solvents are key properties that make it a preferred choice in laboratory applications. These characteristics ensure that it remains effective under a range of experimental conditions. The fluorine substituent not only influences its reactivity but also improves its affinity for different substrates, enhancing its utility in diverse chemical processes. Its compatibility with a variety of reaction conditions and its predictable behavior in synthetic reactions further solidify its position as a reliable reagent in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, trans-4-Fluoro-L-proline is commonly used by chemists and pharmacologists in the development of new compounds. Its availability in the local market supports research efforts requiring high precision and specific reactivity. The compound is a popular choice for studies involving asymmetric synthesis and pharmaceutical applications, where its unique properties are essential for achieving desired outcomes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis applications benefit from trans-4-Fluoro-L-proline due to its ability to control stereochemical outcomes in complex reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound for the synthesis of chiral compounds with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often incorporate it as a catalyst for efficient and selective reactions in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eBioorganic synthesis projects rely on its unique reactivity to create molecules with tailored properties for drug development.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in chemical synthesis benefit from its stability and reactivity, enabling the production of complex organic structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2507-61-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTrans-4-Fluoro-L-proline should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical degradation. General laboratory precautions include handling the compound in a well-ventilated area and wearing appropriate personal protective equipment. It is important to avoid direct contact with skin and eyes, and to ensure proper disposal of any unused material in accordance with local regulations. Proper storage and handling ensure the compound remains effective and safe for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48087034167514,"sku":"TCI2510F081830795","price":2600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0818.jpg?v=1767113876"},{"product_id":"tci2510f089930908","title":"TCI F0899 88050-17-3 Fmoc-Hyp-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eFmoc-Hyp-OH (N-Fmoc-Hyp-OH) is a chemical compound widely used in organic reactions, particularly in peptide synthesis and aspartic acid derivatives. This compound plays a crucial role in laboratories by enabling the selective coupling of amino acids, which is fundamental to the creation of synthetic proteins and biological molecules. Its ability to participate in high-reactivity and structure-specific chemical reactions makes it an essential tool for researchers working in organic and biochemical fields. In Indonesian laboratories, Fmoc-Hyp-OH is a key reagent in various chemical processes due to its functional versatility and reliability.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons Fmoc-Hyp-OH is preferred is its chemical stability under specific conditions, combined with its high reactivity towards amino acid coupling agents. This dual nature allows it to be used in complex reactions without interfering with other processes, making it ideal for precision-based chemical applications. Additionally, its ability to maintain structural integrity during reactions ensures consistent results, which is vital in research settings where accuracy is paramount. The compound's compatibility with a wide range of reagents further enhances its utility in diverse chemical environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Fmoc-Hyp-OH is commonly used in organic chemistry and biochemical research. It is a staple in projects involving the synthesis of complex molecules and the development of analytical techniques. Its widespread use in academic and research institutions highlights its importance in advancing scientific knowledge and innovation in the field of chemistry and biochemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: Fmoc-Hyp-OH is ideal for peptide synthesis due to its ability to selectively couple amino acids, ensuring precise molecular structures in protein and peptide production.\u003c\/li\u003e\n\u003cli\u003eAspartic Acid Derivatives: This compound is used in the synthesis of aspartic acid derivatives, which are essential in biochemical research and pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003eAmino Acid Coupling Reactions: Its high reactivity with amino acid coupling agents makes it suitable for selective amino acid binding in complex chemical reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Fmoc-Hyp-OH is frequently used in organic chemistry experiments requiring high reactivity and structural specificity.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: It plays a key role in biochemical analysis, supporting the development of analytical techniques for molecular structure studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 88050-17-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eFmoc-Hyp-OH should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. In a laboratory setting, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Since it is a reactive chemical, it should be stored separately from incompatible substances to avoid any potential chemical interactions. Proper labeling and storage conditions ensure the safety of laboratory personnel and the integrity of the compound during its use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087042785498,"sku":"TCI2510F089930908","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087042818266,"sku":"TCI2510F089930909","price":3863000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0899.jpg?v=1767113955"},{"product_id":"tci2510g066532300","title":"TCI G0665 9037-55-2 D-Galactan [for Plant-based Organic Molecular Catalyst]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eD-Galactan is an organic compound used as a plant-based molecular catalyst in various chemical reactions. It serves as a key reagent in catalytic processes, offering a sustainable and efficient alternative to traditional chemical catalysts. This material is particularly valuable in organic chemistry research, where it facilitates the synthesis of complex compounds through catalytic activation. Its natural origin and biodegradable properties make it an environmentally friendly option for modern laboratory applications. D-Galactan is widely utilized in both academic and industrial settings, supporting a broad range of chemical transformations.\u003c\/p\u003e\n\u003cp\u003eD-Galactan possesses a complex polysaccharide structure that enhances its reactivity under specific conditions. This high reactivity, combined with its ability to bind to various substrates, makes it a preferred choice for catalytic applications. It is stable in neutral or slightly basic environments, which simplifies its handling and storage. Additionally, its biocompatibility and low toxicity contribute to its appeal in both chemical and biochemical research. These properties ensure that D-Galactan remains a reliable and versatile tool for laboratory scientists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, D-Galactan is commonly used in organic chemistry research, especially in the synthesis of complex molecules. It is also employed in biochemical and bioinformatics studies to understand natural reaction mechanisms. Its eco-friendly nature aligns with the growing emphasis on sustainable practices in scientific research. As a result, D-Galactan is an essential component in many laboratory workflows across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from D-Galactan’s catalytic properties, enabling efficient activation of complex substrates.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies utilize D-Galactan to investigate natural reaction mechanisms in biological systems.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in green chemistry rely on D-Galactan for its sustainable and non-toxic characteristics.\u003c\/li\u003e\n\u003cli\u003eBiodegradable material applications in environmental research leverage D-Galactan’s eco-friendly properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial-scale chemical processes incorporate D-Galactan for its cost-effective and efficient catalytic performance.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 9037-55-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eD-Galactan should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and contaminants. Due to its natural origin, it is generally non-toxic but should be handled with standard laboratory precautions to avoid inhalation or skin contact. Proper labeling and storage conditions ensure its effectiveness and safety in laboratory settings. Regular monitoring of storage conditions helps maintain the integrity of the material for optimal performance in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087137878234,"sku":"TCI2510G066532300","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087137911002,"sku":"TCI2510G066532301","price":3458000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510h029632805","title":"TCI H0296 51-35-4 trans-4-Hydroxy-L-proline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTrans-4-Hydroxy-L-proline is a chemical compound with a complex structure widely used in various chemical reactions, particularly in the field of organic catalysis. It plays a crucial role in laboratory settings as a substrate or cofactor in catalytic reactions that require specific chemical activation. This compound is essential for researchers working on organic synthesis, offering versatility in its application across different experimental setups. Its presence in laboratory workflows supports the development of new chemical compounds, pharmaceuticals, and industrial materials.\u003c\/p\u003e\n\u003cp\u003eThe properties that make trans-4-Hydroxy-L-proline a preferred choice include its stable molecular structure, ability to bind with various reactants, and participation in redox and substitution reactions. Its polar nature allows it to dissolve easily in organic solvents such as ethanol and acetone, making it suitable for a wide range of chemical processes. These characteristics enhance its utility in both synthetic and analytical applications, ensuring reliability and consistency in experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, trans-4-Hydroxy-L-proline is commonly used in organic and biochemical research. It is particularly relevant for studies involving the synthesis of pharmaceutical compounds and other organic molecules. Its availability and performance make it a key component in chemical research, supporting both academic and industrial investigations in the field of chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from trans-4-Hydroxy-L-proline due to its ability to participate in catalytic reactions and enhance reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eBiochemical research utilizes this compound as a substrate or cofactor in enzyme-mediated reactions, aiding in the study of metabolic pathways.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development relies on trans-4-Hydroxy-L-proline for the synthesis of complex organic molecules, supporting drug discovery efforts.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate this compound to produce specialty chemicals and functional materials with specific properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use trans-4-Hydroxy-L-proline as a standard for qualitative and quantitative analysis in chromatographic and spectroscopic techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 51-35-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTrans-4-Hydroxy-L-proline should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its polar nature, it is advisable to store it in a desiccator or a container with a drying agent to minimize exposure to humidity. Proper labeling of storage containers is essential for safe handling and easy identification. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe usage and prevent accidental contact. Regular inspection of storage conditions is necessary to maintain the integrity of the compound and ensure its effectiveness in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087185391834,"sku":"TCI2510H029632805","price":557000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087185424602,"sku":"TCI2510H029632806","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087185457370,"sku":"TCI2510H029632807","price":4594000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0296.jpg?v=1767116135"},{"product_id":"tci2510h075233415","title":"TCI H0752 1476-98-8 Hydroquinidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydroquinidine Hydrochloride is a chemical compound widely used in organic synthesis, particularly in asymmetric reactions. It plays a crucial role in laboratories by enabling the creation of chiral compounds with high selectivity. This compound is commonly employed as a catalyst or reagent in the synthesis of molecules with asymmetric structures. Its unique chiral properties allow for precise control over the final product, making it indispensable in both academic research and industrial applications.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature and molecular structure make it a preferred choice for applications requiring high precision. Its ability to interact specifically with substrates in chemical reactions ensures efficient and selective outcomes. Additionally, Hydroquinidine Hydrochloride is chemically stable under certain conditions, which enhances its reliability in laboratory settings. These characteristics make it a valuable tool for researchers aiming to develop bioactive compounds and pharmaceutical materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydroquinidine Hydrochloride is used in various research and development projects. Its availability in solid form simplifies handling and measurement, making it practical for routine use. It is particularly favored in pharmaceutical and chemical research due to its role in creating complex molecular structures. The compound supports the advancement of drug development and other scientific studies in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: Hydroquinidine Hydrochloride is ideal for asymmetric reactions due to its chiral properties, enabling the synthesis of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: This compound is used in the development of bioactive molecules, supporting the creation of new drug candidates with specific stereochemistry.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: It serves as a key reagent in organic synthesis, facilitating the formation of complex molecular structures with high selectivity.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Development: Its role as a chiral catalyst allows for precise control over reaction pathways, enhancing the efficiency of synthetic processes.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry Applications: It is used in analytical procedures to study chiral compounds and their interactions in various chemical environments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 1476-98-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydroquinidine Hydrochloride should be stored in a cool, dry environment to maintain its chemical stability. It is sensitive to moisture and air, so it should be kept in airtight containers to prevent degradation. Suitable storage containers include glass or high-density polyethylene bottles with tight-fitting lids. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is stored away from incompatible materials and in a well-ventilated area to minimize exposure risks. Regular monitoring of storage conditions is recommended to maintain the integrity of the compound during long-term use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087234281690,"sku":"TCI2510H075233415","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0752.jpg?v=1767116935"},{"product_id":"tci2510h076833436","title":"TCI H0768 110529-22-1 (S)-(+)-2-[Hydroxy(diphenyl)methyl]-1-methylpyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0768 110529-22-1, also known as (S)-(+)-2-[Hydroxy(diphenyl)methyl]-1-methylpyrrolidine, is a chiral reagent used in asymmetric synthesis. This compound plays a crucial role in laboratories where precise control over stereochemistry is required. It is a key component in the production of enantiomerically pure compounds, which are essential in pharmaceutical and chemical industries. Its unique structure allows it to act as a chiral catalyst or ligand, enabling the selective formation of specific stereoisomers.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chiral nature and high catalytic activity make it a preferred choice for researchers aiming to achieve high enantioselectivity. Its molecular structure is complex, allowing it to interact effectively with various substrates in asymmetric reactions. The compound’s consistency and purity ensure reliable results, making it a trusted material in both academic and industrial settings. Its ability to produce specific stereochemical configurations is vital for the development of new drugs and complex organic molecules.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in asymmetric synthesis and the development of new compounds. It is a common reagent in pharmaceutical and chemical research institutions, where it supports the creation of enantiomerically pure products. Its application is also seen in academic research, where it is used to study stereoselective reactions and improve synthetic methodologies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric reactions due to its chiral structure and high catalytic activity, enabling the selective formation of specific stereoisomers.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is used in drug development to produce enantiomerically pure compounds, which are critical for the efficacy and safety of pharmaceutical products.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: It supports the synthesis of complex organic molecules with controlled stereochemistry, making it a valuable tool in chemical research.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Development: Its unique properties make it suitable for the design and testing of new chiral catalysts in industrial and academic settings.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is frequently used in universities and research institutions for studying stereoselective reactions and improving synthetic methodologies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 110529-22-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from direct light to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Due to its chiral nature, it should be handled with care to avoid cross-contamination. In laboratory settings, personal protective equipment such as gloves and safety goggles should be worn when handling this material. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48087235068122,"sku":"TCI2510H076833436","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087235100890,"sku":"TCI2510H076833437","price":4771000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087235133658,"sku":"TCI2510H076833438","price":16101000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0768.jpg?v=1767116955"},{"product_id":"tci2510h078433458","title":"TCI H0784 144119-12-0 (R)-(-)-2-[Hydroxy(diphenyl)methyl]-1-methylpyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(-)-2-[Hydroxy(diphenyl)methyl]-1-methylpyrrolidine is a chiral compound widely used in asymmetric synthesis to produce molecules with specific optical configurations. This reagent plays a crucial role in chemical laboratories, particularly in reactions requiring precise stereochiral control. Its chiral nature allows it to act as a catalyst or ligand, enabling the selective formation of desired enantiomers. This makes it an essential tool in the development of pharmaceuticals and complex organic compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's polar nature and solubility in organic solvents such as ethyl acetate and acetone make it highly versatile in synthetic processes. Its stability under various reaction conditions and availability in multiple packaging formats further enhance its appeal. These properties contribute to its reliability and ease of use in both research and industrial settings. Additionally, its ability to influence biological activity through stereochemistry makes it a valuable asset in drug discovery and development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and pharmacologists for the synthesis of new therapeutic agents. Its application is particularly relevant in the development of pharmaceutical compounds, especially in the context of local research initiatives. The compound's role in creating molecules with specific biological activities underscores its importance in both academic and applied research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis of pharmaceutical compounds due to its chiral structure and ability to control enantiomer formation.\u003c\/li\u003e\n\u003cli\u003eDevelopment of complex organic molecules requiring precise stereochiral control in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in organic reactions where stereochemistry is critical for product specificity.\u003c\/li\u003e\n\u003cli\u003eLigand-based reactions in transition metal catalysis for enhanced selectivity and efficiency.\u003c\/li\u003e\n\u003cli\u003eResearch in drug discovery for the synthesis of compounds with specific biological activities and therapeutic potential.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 144119-12-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its polar nature, it may require careful handling when working with organic solvents. Always ensure proper ventilation in the laboratory and wear appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to heat sources and keep the compound away from incompatible materials to ensure safe storage and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48087235854554,"sku":"TCI2510H078433458","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087235887322,"sku":"TCI2510H078433459","price":4645000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087235920090,"sku":"TCI2510H078433460","price":15748000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0784.jpg?v=1767116984"},{"product_id":"tci2510h111433892","title":"TCI H1114 140853-10-7 Hydroquinidine 1,4-Phthalazinediyl Diether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydroquinidine, with the CAS number 140853-10-7, is an organic compound widely used in various chemical reactions, particularly in the fields of catalysis and organic chemistry. As a key component in catalytic processes, it plays a vital role in accelerating and directing chemical reactions with precision. This compound is known for its unique chemical structure, which allows it to function as both a catalyst and a reagent in specific reactions. Its versatility makes it an essential material for researchers aiming to achieve controlled and efficient chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe properties of Hydroquinidine make it a preferred choice in laboratory settings. It exhibits good solubility in organic solvents, which facilitates its use in a wide range of chemical processes. Additionally, its chemical stability under controlled conditions ensures reliable performance in experimental applications. However, it is sensitive to uncontrolled environments, which necessitates careful handling and storage. These characteristics make it suitable for use in both academic and industrial research environments where precision and consistency are critical.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydroquinidine is commonly used in scientific research across multiple disciplines, including pharmaceuticals, organic chemistry, and catalysis. Its availability and reliable quality make it a popular choice among researchers. The compound is particularly valued for its ability to enhance reaction efficiency and support the development of new chemical methodologies. Its role in advancing scientific research is well-recognized in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes Hydroquinidine for the development of new drugs due to its ability to participate in complex chemical reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments benefit from Hydroquinidine's solubility and reactivity, enabling efficient synthesis of target compounds.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in chemical synthesis rely on Hydroquinidine's role as a catalyst, improving reaction rates and selectivity.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use Hydroquinidine as a standard for qualitative and quantitative analysis in various solvent systems.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies incorporate Hydroquinidine to investigate its behavior in different chemical environments and its impact on reaction pathways.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 140853-10-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydroquinidine should be stored in a cool, dry place, away from light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or inert plastic to prevent contamination and exposure to air. Due to its sensitivity to uncontrolled environments, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation and to follow standard safety protocols when working with this compound. Regular monitoring of storage conditions is essential to preserve its effectiveness and ensure safe usage in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087256826074,"sku":"TCI2510H111433892","price":3863000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1114.jpg?v=1767117518"},{"product_id":"tci2510h111533893","title":"TCI H1115 140924-50-1 Hydroquinine 1,4-Phthalazinediyl Diether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydroquinine 1,4-Phthalazinediyl Diether, also known as TCI H1115 with CAS number 140924-50-1, is a specialized chemical compound used in asymmetric synthesis. It functions as a chiral catalyst or reagent, playing a crucial role in enabling selective chemical reactions. This compound is particularly valuable in laboratories where precise control over stereochemistry is required. Its unique molecular structure allows it to interact specifically with substrates, facilitating the formation of complex organic molecules with high stereochemical fidelity.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability under controlled conditions and its ability to efficiently bind to target molecules make it a preferred choice for researchers. Its chiral nature allows it to influence reaction pathways, leading to the production of enantiomerically pure compounds. This property is essential in applications such as pharmaceutical development, where the stereochemistry of a compound can significantly impact its biological activity. Its versatility in various organic reactions further enhances its appeal in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydroquinine 1,4-Phthalazinediyl Diether is commonly used in organic chemistry research, especially in asymmetric synthesis projects. It is a key component in the development of new drugs, industrial chemicals, and advanced materials. Its availability in the local market supports researchers in accessing high-quality reagents without the need for international imports, making it an essential tool for chemical innovation in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the production of enantiomerically pure compounds with high selectivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Its ability to control stereochemistry makes it valuable in the synthesis of chiral pharmaceutical intermediates, ensuring the desired biological activity.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is widely used in organic laboratories for its versatility in catalyzing complex reactions with controlled stereochemical outcomes.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Production: Its application extends to the development of specialty chemicals, where precise stereochemical control is essential for product performance.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Innovation: It supports the synthesis of advanced materials with specific stereochemical properties, contributing to the development of new functional materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 140924-50-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled in a well-ventilated area, with appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances, and ensure proper disposal in accordance with local regulations. Regular inspection of storage conditions is advised to maintain the integrity of the compound. Always follow standard laboratory safety protocols when working with this material to ensure a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48087256858842,"sku":"TCI2510H111533893","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087256891610,"sku":"TCI2510H111533894","price":3358000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1115.jpg?v=1767117522"},{"product_id":"tci2510h170134621","title":"TCI H1701 485-65-4 Hydrocinchonine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydrocinchonine, with the CAS number 485-65-4, is a chemical compound classified under organocatalysts, playing a vital role in catalytic reactions within the laboratory setting. It is widely used in chemical synthesis to accelerate reaction processes without becoming part of the final product. This compound is particularly valuable in organic and inorganic chemistry due to its ability to interact with substrates and lower the activation energy required for reactions to occur. Its application spans various fields, including asymmetric catalysis and substitution reactions, making it an essential tool for researchers aiming to improve reaction efficiency and sustainability.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make Hydrocinchonine a preferred choice is its chemical stability and environmental friendliness. Unlike some traditional catalysts, it does not produce harmful byproducts or toxic waste, aligning with modern green chemistry principles. Additionally, its thermal stability allows it to function effectively under a wide range of reaction conditions, enhancing its versatility in laboratory settings. These characteristics make it a reliable and sustainable option for both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydrocinchonine is commonly used in research focused on organic and inorganic chemistry, especially in studies involving catalytic processes. Its role in promoting efficient and eco-friendly chemical reactions makes it a popular choice among scientists and researchers. The compound is also used in the development of new synthetic methods and in the optimization of existing chemical processes, contributing to the advancement of scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Catalysis: Hydrocinchonine is ideal for asymmetric reactions due to its ability to selectively influence reaction pathways, enabling the synthesis of chiral compounds with high enantiomeric purity.\u003c\/li\u003e\n\u003cli\u003eSubstitution Reactions: Its capacity to interact with substrates makes it effective in substitution reactions, where it facilitates the replacement of functional groups in organic molecules.\u003c\/li\u003e\n\u003cli\u003eGreen Chemistry Initiatives: The compound's non-toxic nature and lack of harmful byproducts make it a preferred choice for environmentally sustainable chemical processes.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Optimization: Hydrocinchonine helps reduce reaction times and improve yields, making it valuable in the development of efficient synthetic routes.\u003c\/li\u003e\n\u003cli\u003eInorganic Chemistry Research: It is used in studies involving inorganic reactions, where its stability and reactivity contribute to the exploration of new chemical mechanisms.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 485-65-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydrocinchonine should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to high temperatures and direct sunlight to ensure long-term usability. In laboratory settings, proper ventilation is essential when working with this compound to minimize any potential inhalation risks. Always follow standard safety protocols to ensure safe handling and storage practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087315022042,"sku":"TCI2510H170134621","price":3534000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087315054810,"sku":"TCI2510H170134622","price":11559000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1701.jpg?v=1767118392"},{"product_id":"tci2510h170234623","title":"TCI H1702 485-64-3 Hydrocinchonidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydrocinchonidine is a chemical compound classified under organocatalysts, widely used in laboratory settings to accelerate chemical reactions without directly participating in the chemical process. As an organocatalyst, it plays a crucial role in catalysis by lowering the activation energy required for reactions to proceed efficiently. This compound is particularly valuable in synthetic chemistry, where it helps achieve higher reaction yields and selectivity. Its application spans various fields, including organic synthesis and inorganic chemistry, making it a versatile tool for researchers.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make Hydrocinchonidine a preferred choice is its molecular structure, which allows for effective interaction with a wide range of substrates. This versatility enables it to be used in multiple reaction types, including asymmetric syntheses, where precise control over product stereochemistry is essential. Additionally, Hydrocinchonidine exhibits good stability under diverse chemical conditions, which enhances its reliability in laboratory experiments. Its relatively low toxicity also contributes to a safer working environment, reducing potential risks for laboratory personnel.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydrocinchonidine is commonly used in chemical research, especially in catalysis and organic synthesis. It is particularly relevant for academic institutions and industrial research centers that focus on developing new chemical processes and materials. Its effectiveness and safety profile make it a go-to choice for many researchers in the field of chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis: Hydrocinchonidine is ideal for asymmetric reactions due to its ability to control stereochemistry, making it suitable for complex organic molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic catalysis: It is widely used in organic chemistry for its catalytic efficiency and stability, enabling efficient reaction pathways in various synthetic processes.\u003c\/li\u003e\n\u003cli\u003eInorganic chemistry research: Hydrocinchonidine supports catalytic processes in inorganic reactions, offering a reliable alternative to traditional metal-based catalysts.\u003c\/li\u003e\n\u003cli\u003eGreen chemistry initiatives: Its low toxicity and environmental safety make it a preferred choice for sustainable and eco-friendly chemical processes.\u003c\/li\u003e\n\u003cli\u003eTeaching and research laboratories: It is commonly used in educational and research settings to demonstrate catalytic mechanisms and reaction optimization.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 485-64-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydrocinchonidine should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to avoid contamination and exposure to moisture. Due to its relatively low toxicity, handling precautions are generally less stringent than with other organic catalysts, but gloves and proper ventilation should still be used when working with the compound. It is important to keep the material away from incompatible substances such as strong oxidizers or acids. Regular inspection of storage conditions ensures the compound remains effective and safe for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087315087578,"sku":"TCI2510H170234623","price":2424000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087315120346,"sku":"TCI2510H170234624","price":8455000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1702.jpg?v=1767118396"},{"product_id":"tci2510h191834851","title":"TCI H1918 1435-55-8 Hydroquinidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydroquinidine, with the CAS number 1435-55-8, is a chemical compound widely utilized in laboratory settings for its catalytic properties. It belongs to the class of organocatalysts and is commonly found in the field of catalysis and inorganic chemistry. This compound plays a crucial role in accelerating chemical reactions without undergoing significant degradation, making it an essential tool for researchers. Its unique molecular structure allows it to interact effectively with various substrates, enabling the development of more efficient and precise chemical processes.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes that make Hydroquinidine a preferred choice is its chemical stability under specific conditions. This stability ensures consistent performance in laboratory experiments, reducing the risk of unpredictable outcomes. Additionally, Hydroquinidine exhibits strong binding capabilities with different substrates, enhancing its versatility in catalytic applications. These properties make it an ideal candidate for use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydroquinidine is frequently employed in scientific research, particularly in organic chemistry and catalysis. It is commonly found in university laboratories, research institutions, and other scientific facilities where chemical reactions require precision and efficiency. Its reliability and effectiveness have made it a standard component in many experimental setups, supporting the advancement of chemical research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from Hydroquinidine’s ability to catalyze complex transformations efficiently, enhancing reaction yields and reducing byproduct formation.\u003c\/li\u003e\n\u003cli\u003eCatalytic asymmetric synthesis relies on Hydroquinidine’s chiral properties, enabling the selective production of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use Hydroquinidine as a reagent for detecting and quantifying specific compounds in complex mixtures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research incorporates Hydroquinidine to develop new drug compounds by facilitating key chemical transformations in drug synthesis.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies utilize Hydroquinidine to analyze and monitor the presence of certain contaminants in water and soil samples.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1435-55-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydroquinidine should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its performance. Due to its potential reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store Hydroquinidine away from incompatible substances to ensure safety in the laboratory. Regular monitoring of storage conditions helps maintain the integrity of the compound for consistent experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087338516698,"sku":"TCI2510H191834851","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087338549466,"sku":"TCI2510H191834852","price":5503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1918.jpg?v=1767118703"},{"product_id":"tci2510i039535514","title":"TCI I0395 79815-20-6 (S)-(-)-Indoline-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(-)-Indoline-2-carboxylic Acid is a chiral compound widely used in asymmetric synthesis to produce molecules with specific optical configurations. This material plays a crucial role in laboratories where precise control over stereochemistry is required. Its application is particularly significant in pharmaceutical research and drug development, where the spatial arrangement of atoms can drastically affect biological activity. As a reagent or catalyst, it facilitates the formation of compounds with desired stereochemical properties, making it an essential tool in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its high purity and its ability to interact selectively with other reactants under controlled conditions. Its complex molecular structure allows for specific interactions with substrates, enabling the synthesis of enantiomerically pure products. These properties make it a preferred choice for applications requiring high precision and reproducibility. The chiral nature of this acid ensures that it can influence reaction pathways in a way that aligns with the desired outcome, enhancing the efficiency of asymmetric synthesis processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-(-)-Indoline-2-carboxylic Acid is commonly used in scientific research and drug development projects. It is a key component in studies focused on biological activity and the synthesis of new compounds. Its availability in the local market ensures that researchers and scientists have access to this essential material for their work. The compound supports both academic and industrial applications, contributing to advancements in chemical and pharmaceutical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for the production of enantiomerically pure compounds due to its chiral structure and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research to develop drugs with specific stereochemical configurations for enhanced biological activity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise control over stereocenter formation in complex molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical sciences for studying molecular interactions and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug development projects aiming to optimize the efficacy and safety of new therapeutic agents through stereocontrolled synthesis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 79815-20-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (exact form may vary based on supplier packaging)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its chemical integrity. As a chiral compound, it should be handled with care to avoid contamination or unintended stereochemical changes. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this material. Proper ventilation is essential to minimize inhalation risks. The compound is generally non-hazardous under normal storage conditions but should be treated as a chemical reagent requiring standard laboratory safety protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087376036058,"sku":"TCI2510I039535514","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087376068826,"sku":"TCI2510I039535515","price":1666000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0395.jpg?v=1767119564"},{"product_id":"tci2510i072835967","title":"TCI I0728 253430-48-7 beta-Isocupreidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBeta-Isocupreidine is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. It serves as a key reagent or catalyst in chemical reactions that require precise control over stereochemistry. In the laboratory, it plays a crucial role in various synthetic processes, enabling the creation of complex organic structures with high enantioselectivity. Its chiral nature makes it particularly valuable in the development of pharmaceuticals and specialty chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stability under controlled conditions and its ability to participate effectively in a range of chemical reactions. Its high purity and solid form make it ideal for use in laboratory settings where precision and reproducibility are essential. Beta-Isocupreidine is often selected for its reliability and consistent performance in synthetic protocols. Its chemical properties allow it to function as a ligand or catalyst, enhancing the efficiency of reactions such as Michael additions, aldol reactions, and enantioselective transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Beta-Isocupreidine is commonly used in organic chemistry research, especially in asymmetric synthesis and the development of new compounds. It is a preferred choice for researchers working on drug discovery, industrial chemical production, and academic studies. Its availability and performance make it a valuable tool for both academic and industrial applications in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis applications benefit from Beta-Isocupreidine’s chiral properties, enabling the selective formation of enantiomers in complex molecules.\u003c\/li\u003e\n\u003cli\u003eIn pharmaceutical research, it is used to synthesize chiral compounds with specific biological activities, supporting drug development efforts.\u003c\/li\u003e\n\u003cli\u003eFor enantioselective reactions, its ability to control stereochemistry ensures high yields of desired products in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eIn industrial chemical production, it contributes to the efficient synthesis of specialty chemicals with defined stereochemistry.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research relies on Beta-Isocupreidine for its consistent performance in catalytic and ligand-based reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 253430-48-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBeta-Isocupreidine should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air, which could affect its performance. The compound should be stored away from direct sunlight and sources of heat to ensure long-term integrity. In laboratory settings, it is important to handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is generally stable under normal storage conditions, it should be kept in a secure location to prevent accidental contamination or exposure. Proper storage ensures that Beta-Isocupreidine remains effective for use in synthetic processes requiring high precision and reliability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087412343002,"sku":"TCI2510I072835967","price":9035000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0728.jpg?v=1767120196"},{"product_id":"tci2510i080136066","title":"TCI I0801 850661-66-4 (S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine (ca. 6% in Toluene, ca. 0.1mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I0801, (S)-4-Isopropyl-3-(1-naphthylmethyl)-2,5,5-triphenyl-1,3,2-oxazaborolidine, CAS number 850661-66-4, is a chiral catalyst of the oxazaborolidine class supplied as a ready-to-use solution in toluene at approximately 6% concentration, corresponding to roughly 0.1 mol per litre. The molecule carries a boron centre embedded in an oxazaborolidine ring containing both nitrogen and oxygen, surrounded by phenyl groups and a bulky naphthylmethyl substituent. In the laboratory this class of catalyst acts as a chiral Lewis acid that activates carbonyl substrates or dienophiles while simultaneously steering the reaction towards a single enantiomer.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent a preferred choice is its presentation as a solution of defined concentration. Oxazaborolidine catalysts are highly sensitive to moisture and to air, so supplying the material dissolved in toluene removes the inconvenience of weighing a hygroscopic solid inside a glove box and allows catalytic doses to be withdrawn simply with a gas-tight syringe. The aromatic groups stacked around the boron centre create a tightly defined chiral pocket, so one face of the substrate is decisively blocked and the product is formed with enantiomeric excess.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories a reagent of this type belongs to research groups and analytical or synthetic units working on asymmetric synthesis, typically in university chemistry departments, pharmaceutical development laboratories and contract research settings where a single enantiomer of an intermediate must be prepared. The solution format suits laboratories that handle air-sensitive chemistry with Schlenk lines or inert-atmosphere manifolds rather than full glove-box infrastructure, and makes small-scale catalytic work practical.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnantioselective reduction of prochiral ketones: the chiral boron centre coordinates and activates the carbonyl group while the surrounding aryl framework blocks one face, so the resulting secondary alcohol is obtained with enantiomeric excess rather than as a racemate.\u003c\/li\u003e\n\u003cli\u003eAsymmetric Diels-Alder cycloadditions: acting as a chiral Lewis acid, the catalyst activates the dienophile and biases the approach of the diene, giving cycloadducts whose absolute configuration is controlled by the catalyst rather than by the substrate.\u003c\/li\u003e\n\u003cli\u003ePreparation of single-enantiomer pharmaceutical intermediates: research groups use catalytic quantities of this reagent to install a defined stereocentre early in a synthetic route, avoiding the material losses associated with resolving a racemic mixture later.\u003c\/li\u003e\n\u003cli\u003eMethodology and catalyst screening studies: because the reagent arrives at a known concentration of about 0.1 mol per litre, catalyst loadings can be varied accurately by syringe volume, which makes systematic optimisation experiments straightforward and reproducible.\u003c\/li\u003e\n\u003cli\u003eAir-sensitive small-scale synthesis under inert atmosphere: the toluene solution can be transferred by gas-tight syringe through a septum into a Schlenk flask, so the moisture-sensitive catalyst never has to be handled as an open solid.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 850661-66-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: supplied in TCI standard solution pack sizes; please confirm the available size when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: solution in toluene, approximately 6% (ca. 0.1 mol\/L)\u003c\/li\u003e\n\u003cli\u003eStorage note: moisture-sensitive and air-sensitive; keep the container tightly sealed under inert gas\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the sealed bottle in a cool, dry place away from direct sunlight, ignition sources and oxidising agents, and follow the storage temperature stated on the manufacturer's label and safety data sheet. Keep the container under an inert gas blanket and close it immediately after each withdrawal, since both the catalyst and the toluene solvent are sensitive to moisture and air. Withdraw aliquots with a dry, gas-tight syringe through the septum rather than pouring, and keep all glassware oven-dried. Handle the solution in a fume hood because toluene is a flammable and volatile solvent, and wear safety glasses, a laboratory coat and solvent-resistant gloves. Ground containers when transferring larger volumes, keep a suitable fire extinguisher accessible, and dispose of residues as halogen-free organic solvent waste in line with institutional procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mL","offer_id":48087417585882,"sku":"TCI2510I080136066","price":3610000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0801.jpg?v=1767120328"},{"product_id":"tci2510i080736073","title":"TCI I0807 1226896-38-3 (R,R)-2-Iodo-1,3-bis[1-(mesitylcarbamoyl)ethoxy]benzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I0807 (R,R)-2-Iodo-1,3-bis[1-(mesitylcarbamoyl)ethoxy]benzene, CAS number 1226896-38-3, is a chiral aryl iodide designed to serve as a pre-catalyst for oxidative transformations based on hypervalent iodine chemistry. Structurally, the molecule consists of a benzene ring bearing an iodine atom at the central position, flanked by two ether arms that each carry a mesityl amide group in the (R,R) configuration. In the laboratory, the compound is activated in situ by a suitable oxidant, raising the iodine atom to a higher oxidation state and generating a chiral hypervalent iodine species capable of transferring oxygen or functional groups to a substrate enantioselectively.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound a preferred choice begin with its symmetric and rigid scaffold design. The two identical flanking arms create a symmetric chiral environment on both sides of the iodine centre, so the orientation of an incoming substrate can be controlled decisively. The amide groups act both as hydrogen-bond donors and as stabilising elements through intramolecular coordination to the hypervalent iodine centre, which makes the active species more robust and raises the selectivity obtained. The bulky mesityl groups add further steric shielding around the reaction centre, reinforcing facial discrimination during the stereo-determining step.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically encountered in university and institutional research groups working on asymmetric synthesis, particularly those developing metal-free enantioselective oxidation methods. It is used on small research scales, where the catalyst is generated in situ and screened against a range of oxidants, solvents and substrates. Groups pursuing chiral building blocks for pharmaceutical or natural-product targets use it as part of methodology development and catalyst comparison studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnantioselective oxidative transformations — the compound is activated in situ to a chiral hypervalent iodine species that transfers oxygen or functional groups to substrates with facial control from the (R,R) scaffold.\u003c\/li\u003e\n\u003cli\u003eMetal-free asymmetric catalysis method development — researchers avoiding transition metals use this organocatalytic aryl iodide because the chiral information resides entirely in the organic backbone rather than a metal centre.\u003c\/li\u003e\n\u003cli\u003eChiral catalyst screening studies — the defined (R,R) configuration and symmetric two-armed design make it a useful benchmark entry when comparing catalyst scaffolds for enantioselectivity in oxidation reactions.\u003c\/li\u003e\n\u003cli\u003ePreparation of enantiomerically enriched building blocks — reactions catalysed by this reagent deliver stereodefined products suited to downstream elaboration toward pharmaceutical intermediates and natural-product fragments in research-scale work.\u003c\/li\u003e\n\u003cli\u003eMechanistic and structure-activity investigations — the amide hydrogen-bond donors and bulky mesityl groups provide clear structural handles for studying how coordination and steric bulk govern selectivity outcomes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 1226896-38-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eChemical name: (R,R)-2-Iodo-1,3-bis[1-(mesitylcarbamoyl)ethoxy]benzene; product code I0807\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale catalogue pack sizes; please refer to the current TCI listing for options\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in the original tightly closed container, protected from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry and well-ventilated place, away from light, moisture and oxidising agents. Amber glass or the supplier's original packaging is suitable; keep the container sealed when not in use to prevent moisture uptake and to preserve the integrity of the chiral scaffold. Handle the material in a fume hood using gloves, safety glasses and a laboratory coat, and avoid generating dust during weighing. Transfer with clean, dry spatulas and glassware, close the container promptly after use, and dispose of residues and contaminated consumables through the laboratory's chemical waste procedure. Always consult the supplier safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087418142938,"sku":"TCI2510I080736073","price":1591000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0807.jpg?v=1767120340"},{"product_id":"tci2510i112236487","title":"TCI I1122 1399008-27-5 N,N'-[(2S,2'S)-[(2-Iodo-1,3-phenylene)bis(oxy)]bis(propane-2,1-diyl)]bis(mesitylamide)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I1122 1399008-27-5 is a complex chemical compound used in asymmetric synthesis, playing a vital role in laboratories that require precise control over stereochemistry. This chiral catalyst or ligand is essential for producing compounds with specific asymmetric structures, which are critical in pharmaceutical and organic chemistry research. Its unique molecular structure allows it to direct reactions toward the desired product, making it a valuable tool for researchers aiming to achieve high-purity synthetic outcomes.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability under specific conditions and its ability to enhance reaction efficiency make it a preferred choice in modern chemical laboratories. Its complex molecular architecture enables it to interact effectively with various substrates, facilitating the synthesis of chiral compounds with high selectivity. This stability ensures that it remains effective across different experimental setups, providing consistent results. Its reliability and performance in controlled environments further solidify its position as a key reagent in asymmetric synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used by chemists engaged in asymmetric synthesis, particularly in research related to drug development, organic compounds, and complex molecules. Its availability and adherence to international quality standards make it a trusted choice for researchers seeking reliable and high-quality reagents. The compound's versatility and effectiveness in achieving specific stereochemical outcomes make it an essential component in many chemical research projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for the production of specific drug compounds requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research focused on the development of chiral molecules with high enantiomeric purity.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical reactions that demand controlled stereoselectivity and efficient catalytic activity.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex organic structures where chiral reagents are necessary for achieving desired product configurations.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research involving the creation of compounds with specific spatial arrangements for therapeutic applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1399008-27-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and effectiveness. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could potentially degrade its properties. Due to its complex molecular structure, it is important to handle it with care to avoid contamination. Laboratory personnel should ensure that the storage area is well-ventilated and free from sources of heat or direct light. Proper labeling of containers is essential to ensure safe handling and prevent accidental use. General laboratory precautions include wearing appropriate personal protective equipment when handling the compound to minimize any potential risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087441735898,"sku":"TCI2510I112236487","price":4645000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I1122.jpg?v=1767120807"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-asymmetric-organocatalysts.oembed?page=7","provider":"AMI Scientific","version":"1.0","type":"link"}