{"title":"Proline-Based Organocatalysts [Asymmetric Synthesis]","description":"\u003cp\u003e\u003cstrong\u003eProline-Based Organocatalysts [Asymmetric Synthesis]\u003c\/strong\u003e — mencakup turunan prolina yang difungsikan sebagai organokatalis kiral, mulai dari amida, anilida, hingga prolina bergugus pelindung silil. Struktur cincin pirolidin dengan pusat kiralnya menjadi dasar kemampuan katalitik kelompok ini.\u003c\/p\u003e\u003cp\u003eProline-Based Organocatalysts ini dipakai dalam sintesis asimetris seperti reaksi aldol dan Michael untuk membangun pusat kiral baru secara selektif, oleh kimiawan sintesis organik di bidang kimia farmasi dan material kiral. Turunannya juga dipelajari sebagai katalis dalam reaksi organokatalitik lain.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t308054612\"\u003eTCI T3080 1089663-51-3 N-(2-Thiophenesulfonyl)-L-prolinamide\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\/tci2510b34409343\"\u003eTCI B3440 259212-61-8 trans-4-(tert-Butyldiphenylsilyloxy)-L-proline\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\/tci2510a09451255\"\u003eTCI A0945 64030-44-0 (S)-(+)-2-(Anilinomethyl)pyrrolidine\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\/tci2510t021950983\"\u003eTCI T0219 34592-47-7 L-Thioproline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b692713811\"\u003eTCI B6927 131180-57-9 (S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan konfigurasi stereokimia (L atau D), kemurnian enansiomer, serta jenis gugus pelindung atau substituen yang memengaruhi selektivitas katalitik. 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 Asymmetric Synthesis, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-building-blocks\"\u003eChiral Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-catalysts-chiral-ligands-chiral-reagents\"\u003eChiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-resolution-reagents\"\u003eChiral Resolution Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-resolving-reagents\"\u003eChiral Resolving Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-auxiliaries\"\u003eChiral Auxiliaries\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-epoxidation-asymmetric-synthesis\"\u003eEpoxidation [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l2-asymmetric-synthesis\"\u003eAsymmetric Synthesis\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":"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":"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":"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":"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":"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":"tci2510m116139129","title":"TCI M1161 63126-47-6 (S)-2-(Methoxymethyl)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M1161, also known as (S)-2-(Methoxymethyl)pyrrolidine with CAS number 63126-47-6, is a chiral reagent widely used in asymmetric synthesis. This compound plays a crucial role in laboratories by enabling the selective formation of chiral molecules, which are essential in pharmaceutical and biochemical research. Its application allows scientists to produce compounds with specific stereochemistry, which is vital for drug development and other advanced chemical processes. Due to its unique molecular structure, it is a key component in the synthesis of bioactive molecules with high specificity and efficiency.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chiral nature and reactivity make it a preferred choice for researchers aiming to achieve high enantioselectivity in their reactions. Its ability to interact selectively with substrates enhances the effectiveness of synthetic pathways, reducing the need for additional purification steps. This reagent is particularly valuable in complex syntheses where precise control over molecular structure is required. Its stability and compatibility with various reaction conditions further contribute to its reliability in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in chemical, pharmaceutical, and biotechnology research. Local scientists rely on it to develop new synthetic methods that produce active compounds efficiently and cost-effectively. Its role in advancing research in these fields is significant, supporting innovation in drug discovery and other scientific applications.\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 nature, enabling the selective formation of enantiomers with high efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is widely used in drug development to create chiral compounds with specific biological activities and improved therapeutic effects.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Researchers use it to explore new synthetic pathways and reaction mechanisms in organic chemistry, enhancing the understanding of stereochemical control.\u003c\/li\u003e\n\u003cli\u003eBiotransformation Studies: Its reactivity makes it suitable for studying how chiral compounds interact with biological systems and undergo metabolic transformations.\u003c\/li\u003e\n\u003cli\u003eGreen Chemistry Initiatives: It supports sustainable chemical processes by enabling efficient and selective reactions that minimize waste and byproducts.\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: 63126-47-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; 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: Liquid\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 glass or polyethylene to prevent contamination and degradation. Due to its chiral nature, it is important to handle it with care to avoid any unintended racemization or loss of enantiomeric purity. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling this material. It is also advisable to keep it in a well-ventilated area to ensure safe working conditions. 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":48087589617882,"sku":"TCI2510M116139129","price":3079000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087589650650,"sku":"TCI2510M116139130","price":10575000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1161.jpg?v=1767124440"},{"product_id":"tci2510m116939139","title":"TCI M1169 84025-81-0 (R)-2-(Methoxymethyl)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-2-(Methoxymethyl)pyrrolidine is the enantiomeric counterpart of SMP and is widely known by the abbreviation RMP. The compound is a chiral cyclic amine bearing a stereogenic centre of (R) configuration at position 2 of the pyrrolidine ring. In the laboratory its role is identical to that of its partner enantiomer, namely to install chiral information into a chemical transformation, but with the opposite direction of induction. Its availability allows researchers to access both configurations of a target product simply by switching the chiral reagent, without having to redesign an entire synthetic route that has already been optimised.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound valuable is the conformational rigidity of the pyrrolidine ring combined with the methoxymethyl group, which acts simultaneously as a steric director and an electron donor. This combination generates a tightly defined chiral environment around the nitrogen atom, so that discrimination between the two prochiral faces of a substrate proceeds effectively. The secondary amine nitrogen nevertheless remains reactive enough to form enamines, hydrazones, carbamates and amides, giving the chemist a broad choice of derivatisation chemistry from a single starting reagent.\u003c\/p\u003e\n\u003cp\u003eBecause the material is generally liquid at room temperature, addition to a reaction mixture can be carried out volumetrically with a micropipette or a syringe. This suits the working practice of Indonesian laboratories, where asymmetric synthesis is typically performed on small to moderate scale in university research groups, graduate research projects and pharmaceutical or fine-chemical development units that need both enantiomeric series of a product for comparative evaluation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric enamine chemistry — the secondary amine condenses readily with carbonyl substrates, and the rigid chiral pocket around nitrogen directs the approaching electrophile to one prochiral face.\u003c\/li\u003e\n\u003cli\u003eChiral auxiliary attachment — the nitrogen forms stable amides and carbamates with substrates, carrying stereochemical information through subsequent steps before being removed again.\u003c\/li\u003e\n\u003cli\u003eChiral hydrazone formation — conversion to the corresponding hydrazone derivative provides a stereodirecting handle for alkylation work that requires reliable facial discrimination at the carbonyl carbon.\u003c\/li\u003e\n\u003cli\u003eEnantiodivergent route development — using RMP in place of SMP reverses the sense of induction, letting a laboratory obtain the opposite product configuration without redesigning an optimised synthesis.\u003c\/li\u003e\n\u003cli\u003eChiral ligand preparation — the amine serves as a building block for ligands whose methoxymethyl oxygen can participate as an additional donor site in a coordinated metal centre.\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: 84025-81-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003eCatalogue reference: M1169\u003c\/li\u003e\n\u003cli\u003ePhysical form: generally liquid at room temperature, suitable for volumetric transfer by micropipette or syringe\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI research pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in the 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 and well-ventilated area, away from heat sources, direct sunlight and incompatible materials, following the conditions stated on the manufacturer's label and safety data sheet. Keep the material in its original supplier container, or in a chemically compatible sealed glass vessel if transfer is necessary, and reseal immediately after each withdrawal because amines readily absorb atmospheric moisture and carbon dioxide. Handle only in a functioning fume hood while wearing safety goggles, a laboratory coat and chemically resistant gloves. Use clean, dry syringes or pipettes for each transfer to avoid contamination, and label all secondary containers clearly. Consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087590011098,"sku":"TCI2510M116939139","price":3358000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087590043866,"sku":"TCI2510M116939140","price":11433000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1169.jpg?v=1767124452"},{"product_id":"tci2510m118339162","title":"TCI M1183 84466-85-3 (S)-(-)-1-Methyl-2-(1-piperidinomethyl)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(-)-1-Methyl-2-(1-piperidinomethyl)pyrrolidine is a chiral diamine that combines an N-methylated pyrrolidine ring with a piperidinylmethyl group at the 2-position. This arrangement places two tertiary nitrogen atoms at precisely the right distance to function as a bidentate ligand — a molecule that binds a single metal center through two coordination points at once. In asymmetric synthesis laboratories, compounds of this type are used to bind and orient organometallic reagents so that attack on a prochiral substrate occurs predominantly on one face of the molecule, yielding a product enriched in a single enantiomer.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this compound attractive are the combination of strong Lewis basicity from its two tertiary nitrogens with a rigid chiral framework. The pyrrolidine ring restricts conformational freedom, while the larger piperidine ring provides directed steric hindrance around the coordination center. Because both nitrogen atoms are tertiary, the compound carries no N–H protons that could interfere with organolithium or Grignard reagents, making it suitable for use under strongly basic conditions. The (S) configuration with negative optical rotation gives the material a clear stereochemical identity for reproducible work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this chiral building block is typically encountered in university and institutional research groups working on enantioselective methodology, in pharmaceutical development laboratories exploring routes to single-enantiomer intermediates, and in synthetic chemistry teaching programmes at the graduate level. It is normally handled in small quantities under inert atmosphere on a Schlenk line or in a glovebox, alongside anhydrous solvents and the organometallic reagents whose selectivity it is intended to control.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnantioselective organolithium additions — the two tertiary nitrogens chelate the lithium center and create a chiral environment that biases addition to one face of a prochiral carbonyl substrate.\u003c\/li\u003e\n\u003cli\u003eAsymmetric Grignard reactions — the ligand coordinates the magnesium center without any N–H protons to quench the reagent, allowing facial selectivity to be imposed under strongly basic conditions.\u003c\/li\u003e\n\u003cli\u003eChiral ligand screening studies — its rigid pyrrolidine backbone and defined (S) configuration make it a useful reference entry when comparing bidentate diamine ligands for a new transformation.\u003c\/li\u003e\n\u003cli\u003eEnantioselective deprotonation methodology — the compound can direct strong bases toward one of two enantiotopic protons, generating configurationally defined carbanion intermediates for further functionalisation.\u003c\/li\u003e\n\u003cli\u003eChiral auxiliary and intermediate synthesis — as a building block bearing a defined stereocenter, it serves as a starting point for preparing more elaborate ligands and auxiliaries in research-scale routes.\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: 84466-85-3\u003c\/li\u003e\n\u003cli\u003eCatalogue number: M1183\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: research-scale packs; available sizes confirmed at time of order\u003c\/li\u003e\n\u003cli\u003eStorage: store in a cool, dark place under inert gas, in a tightly sealed container\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, dark place, preferably under an inert gas atmosphere such as nitrogen or argon, since tertiary amines of this type are sensitive to air and moisture. Keep the material in its original glass container with a chemically resistant closure, and avoid transferring it to containers whose seals have not been verified. Handle in a working fume hood using nitrile gloves, safety goggles, and a laboratory coat. Amines are corrosive and have a strong odour, so avoid inhalation and skin contact. Withdraw aliquots using dry syringes or cannula technique to limit atmospheric exposure, and keep the compound away from strong acids and oxidising agents. Consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":50506731290842,"sku":"TCI2510M118339162","price":3534000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1183.jpg?v=1767124489"},{"product_id":"tci2510o037044730","title":"TCI O0370 80875-98-5 (2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic Acid","description":"\u003cp\u003e\u003cstrong\u003e(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic Acid\u003c\/strong\u003e (CAS 80875-98-5) adalah produk kimia berkualitas tinggi dari TCI dengan grade \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eAplikasi:\u003c\/strong\u003e Senyawa heterosiklik beranggota lima yang digunakan sebagai building block dalam sintesis farmasi, agrokimia, dan material 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