{"title":"Chiral Heterocyclic Building Blocks","description":"\u003cp\u003e\u003cstrong\u003eChiral Heterocyclic Building Blocks\u003c\/strong\u003e — menghimpun senyawa heterosiklik dengan pusat stereogenik tunggal atau ganda, mencakup turunan tetrahidrofuran, oksazolidin, azetidin, dan bisiklik beroksigen-nitrogen dalam konfigurasi (R) atau (S) yang terdefinisi. Kelompok ini menyediakan kerangka kiral siap pakai untuk sintesis asimetris yang mempertahankan integritas stereokimia.\u003c\/p\u003e\u003cp\u003eChiral Heterocyclic Building Blocks dipakai kimiawan sintetik dan peneliti kimia farmasi dalam sintesis asimetris untuk membangun molekul target dengan stereokimia terkontrol, termasuk zat antara pada pembuatan senyawa kompleks bertingkat tinggi. Turunan Boc-terlindungi dan oksazolidin dikarboksilat umum digunakan sebagai auksiliari kiral atau substrat reaksi diastereoselektif, sementara amina tetrahidrofuran kiral berperan sebagai blok bangun pada pembentukan pusat stereogenik baru melalui reaksi substitusi atau reduksi.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t438556147\"\u003eTCI T4385 111769-26-7 (R)-Tetrahydrofuran-3-amine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b553812198\"\u003eTCI B5538 1013028-26-6 3-tert-Butyl 4-Methyl (4R,5S)-2,2,5-Trimethyloxazolidine-3,4-dicarboxylate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t290254380\"\u003eTCI T2902 97538-67-5 (2R,5S)-2-Trichloromethyl-3-oxa-1-azabicyclo[3.3.0]octan-4-one\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b565712353\"\u003eTCI B5657 108149-65-1 tert-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t255253912\"\u003eTCI T2552 7175-81-7 (S)-(+)-Tetrahydrofurfurylamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b568212385\"\u003eTCI B5682 877399-00-3 (R)-5-Bromo-3-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]pyridin-2-amine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t255153909\"\u003eTCI T2551 7202-43-9 (R)-(-)-Tetrahydrofurfurylamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b634313200\"\u003eTCI B6343 51077-14-6 (S)-1-(tert-Butoxycarbonyl)azetidine-2-carboxylic Acid\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan konfigurasi stereokimia (R atau S) serta kemurnian optik (ee) yang sesuai kebutuhan sintesis, dan status gugus pelindung (seperti Boc) yang menentukan kompatibilitas dengan tahap reaksi berikutnya. 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 Chiral Building Blocks, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-non-heterocyclic-building-blocks\"\u003eChiral Non-Heterocyclic Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-privileged-ligands-and-complexes-asymmetric-synthesis\"\u003ePrivileged Ligands and Complexes [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-hydrogenation-asymmetric-synthesis\"\u003eHydrogenation [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-chiral-building-blocks\"\u003eChiral Building Blocks\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":"tci2510b553812198","title":"TCI B5538 1013028-26-6 3-tert-Butyl 4-Methyl (4R,5S)-2,2,5-Trimethyloxazolidine-3,4-dicarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5538 3-tert-Butyl 4-Methyl (4R,5S)-2,2,5-Trimethyloxazolidine-3,4-dicarboxylate is a chiral building block designed for asymmetric synthesis applications. This oxazolidine derivative features defined (4R,5S) stereochemistry, making it a valuable intermediate for constructing enantiomerically pure compounds. It is commonly employed in medicinal chemistry research and drug development workflows that require precise stereochemical control.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085886107866,"sku":"TCI2510B553812198","price":2828000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5538.jpg?v=1767092486"},{"product_id":"tci2510b565712353","title":"TCI B5657 108149-65-1 tert-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5657 *tert*-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate (CAS 108149-65-1) is a high-purity chiral building block for asymmetric synthesis applications. This (S)-configured oxazolidine derivative serves as a versatile chiral auxiliary and protecting group in the stereoselective construction of complex organic molecules. It is particularly valuable in pharmaceutical research and academic laboratories for the synthesis of enantiomerically pure bioactive compounds, modified peptides, and chiral catalyst development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894332634,"sku":"TCI2510B565712353","price":3105000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085894365402,"sku":"TCI2510B565712354","price":10777000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5657_22d79aea-51d9-4815-adce-173c88eb6d08.jpg?v=1767862809"},{"product_id":"tci2510b634313200","title":"TCI B6343 51077-14-6 (S)-1-(tert-Butoxycarbonyl)azetidine-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6343, also known as (S)-1-(tert-butoxycarbonyl)azetidine-2-carboxylic Acid, is a chiral building block essential in asymmetric synthesis. This compound is widely used in laboratories to create complex molecules with specific stereochemistry. Its azetidine ring structure, modified with a tert-butoxycarbonyl group, makes it a versatile tool for chemists aiming to control the spatial arrangement of atoms in organic molecules. This material plays a crucial role in the development of pharmaceuticals and bioactive compounds, where precise stereochemistry is required for biological activity.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its chemical stability under controlled conditions and its solubility in various organic solvents. These properties make it an ideal candidate for use in a wide range of synthetic reactions. Its ability to act as a precursor in asymmetric reactions allows for the selective formation of stereoisomers, which is essential in drug development and fine chemical synthesis. The compound's reliability and reproducibility in laboratory settings make it a preferred choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to pharmacology, organic chemistry, and biochemistry. It is particularly valuable in the development of new drugs and in the study of molecular mechanisms. Many research institutions and universities in Indonesia rely on this material to advance their scientific work and contribute to the field of medicinal chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound enables the selective formation of stereoisomers, crucial for drug development and bioactive compound creation.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its role as a chiral building block, allowing for the synthesis of complex molecules with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drugs, as its stereochemistry can influence biological activity and pharmacological properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies often incorporate this material to investigate molecular interactions and structural requirements for biological function.\u003c\/li\u003e\n\u003cli\u003eIt is also used in the synthesis of fine chemicals, where precise stereochemical control is essential for industrial and research 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: 51077-14-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 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. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its organic nature, it is best stored in airtight glass or plastic containers that are resistant to chemical degradation. Proper labeling and storage conditions are essential to ensure the integrity of the material. In laboratory settings, it should be handled with care, using appropriate personal protective equipment. Regular monitoring of storage conditions is advised to maintain the quality and effectiveness of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085931851994,"sku":"TCI2510B634313200","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6343.jpg?v=1767093516"},{"product_id":"tci2510b640013283","title":"TCI B6400 170033-47-3 tert-Butyl (R)-2-Methylpiperazine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6400, tert-butyl (R)-2-methylpiperazine-1-carboxylate (CAS 170033-47-3), is a mono-Boc-protected chiral piperazine building block with defined (R) configuration at C-2. The selective protection leaves the N-4 nitrogen free for alkylation, acylation, sulfonylation, reductive amination, or Buchwald–Hartwig coupling. Subsequent acid-mediated Boc removal unmasks the second nitrogen for further elaboration, making the reagent well suited to multi-step medicinal chemistry routes. AMI Scientific supplies it in 1 g and 5 g packs; refer to the lot Certificate of Analysis for stereochemical and purity data.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSTUDER et al. (1995). ChemInform Abstract: Synthesis and First Applications of a New Chiral Auxiliary (tert‐Butyl 2‐(tert‐Butyl)‐5,5‐dimethyl‐4‐oxoimidazolidine‐1‐carboxylate) (V).. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199547157\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199547157\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMamat et al. (2012). Synthesis and Molecular Structure of tert-Butyl 4-(2-tert-butoxy-2-oxoethyl)piperazine-1-carboxylate. \u003cem\u003eCrystals\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/cryst2010090\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/cryst2010090\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGrauer et al. (2009). Synthesis of rac-tert-butyl 3-(benzyloxycarbonylamino)-2-(4-bromophenyl)-tetrahydrofuran-3-carboxylate. \u003cem\u003eMolbank\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m596\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m596\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":"1g","offer_id":48085938208986,"sku":"TCI2510B640013283","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085938241754,"sku":"TCI2510B640013284","price":3484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6400_d10dda81-1f79-4d4e-b518-b61c3a510bbe.jpg?v=1767865644"},{"product_id":"tci2510c132515820","title":"TCI C1325 94594-90-8 (-)-10,2-Camphorsultam","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1325 (-)-10,2-Camphorsultam, widely known as Oppolzer's sultam, is a classic chiral auxiliary built on the rigid camphor framework. Substrates are attached to the sultam nitrogen, transformed with high facial selectivity, and then released once the new stereocentre is set. It performs reliably in enolate alkylation, aldol reactions, Diels-Alder cycloadditions, and conjugate additions, and its crystalline derivatives often allow diastereomer purification. AMI Scientific supplies this TCI product in 1 g and 5 g packs, best stored cool, dry, and tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBaciocchi et al. (1994). Stereoselective Heteroaromatic Homolytic Substitution with Carbon Radicals Derived from Oppolzer's Camphorsultam. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-1994-23016\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-1994-23016\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1990). (\u0026amp;#8722;)-D-2,10-CAMPHORSULTAM. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.069.0154\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.069.0154\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhang et al. (2019). Asymmetric Difluoromethylthiolation of Carbon Nucleophiles with Optically Pure Difluoromethylthiolating Reagents Derived from Camphorsultam. \u003cem\u003eChinese Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/cjoc.201900298\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/cjoc.201900298\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":"1g","offer_id":48086063186138,"sku":"TCI2510C132515820","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086063218906,"sku":"TCI2510C132515821","price":986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1325.jpg?v=1769180338"},{"product_id":"tci2510c136315883","title":"TCI C1363 88056-92-2 (-)-2-Cyano-6-phenyloxazolopiperidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1363 (-)-2-Cyano-6-phenyloxazolopiperidine (CAS 88056-92-2) is a bicyclic chiral synthon designed for the asymmetric synthesis of piperidine alkaloids. Its alpha-aminonitrile function is remarkably versatile: deprotonation generates a stabilised carbanion for reaction with electrophiles, while loss of cyanide delivers an iminium ion that reacts with nucleophiles. The chiral oxazolidine framework controls the facial approach of incoming reagents, giving substituted piperidines with high diastereoselectivity before the auxiliary is removed. AMI Scientific supplies this TCI chiral building block in a 1 g pack size for asymmetric synthesis research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086065807578,"sku":"TCI2510C136315883","price":5781000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1363.jpg?v=1767096849"},{"product_id":"tci2510c139115919","title":"TCI C1391 107869-45-4 (+)-10-Camphorsulfonimine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1391 (+)-10-Camphorsulfonimine (CAS 107869-45-4) is a chiral building block derived from the rigid camphor framework and used in asymmetric synthesis. Its sulfonimine group is most commonly oxidised to the corresponding camphor-derived oxaziridine, a well-established reagent for enantioselective oxygen transfer. Typical applications include asymmetric hydroxylation of enolates and the preparation of chiral sulfoxides from sulfides. AMI Scientific supplies the (+)-enantiomer in a 5 g pack, complementing the (-)-form for researchers who need access to both product configurations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086067216602,"sku":"TCI2510C139115919","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1391.jpg?v=1769180345"},{"product_id":"tci2510c139315920","title":"TCI C1393 60886-80-8 (-)-10-Camphorsulfonimine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1393 (-)-10-Camphorsulfonimine (CAS 60886-80-8) is the opposite enantiomer of the camphor-derived sulfonimine used in asymmetric synthesis. Oxidation of its imine group affords a camphor-based oxaziridine that transfers oxygen with defined stereochemical preference. It is applied in enantioselective α-hydroxylation of carbonyl compounds and in the asymmetric oxidation of sulfides to chiral sulfoxides. Available from AMI Scientific in a 5 g pack, it lets researchers select the product configuration required by their synthetic route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086067282138,"sku":"TCI2510C139315920","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1393.jpg?v=1769144480"},{"product_id":"tci2510c258517394","title":"TCI C2585 100858-33-1 (R)-1-Carbobenzoxy-3-pyrrolidinol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-1-Carbobenzoxy-3-pyrrolidinol is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemistry. This compound plays a crucial role in the development of pharmaceuticals and bioactive molecules by providing a chiral building block that enables precise control over the stereochemical outcome of reactions. Its application in chemical laboratories is essential for the synthesis of complex structures with defined optical properties, making it a key component in advanced organic chemistry research.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique structure and chemical stability make it a preferred choice for synthetic chemists. It exhibits high reactivity in various chemical transformations, including hydrolysis, reduction, and substitution reactions. Its ability to participate in multiple reaction pathways without significant degradation ensures its reliability in laboratory settings. Additionally, its chiral nature allows for the selective formation of enantiomers, which is vital in drug development and biochemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry and pharmacology research. It is a fundamental tool for scientists working on the synthesis of bioactive compounds, particularly in academic and research institutions. Its presence in laboratory workflows highlights its importance in advancing chemical and pharmaceutical innovation 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 creating chiral molecules with precise stereochemistry, which is essential in drug development and bioactive compound synthesis.\u003c\/li\u003e\n\u003cli\u003eChiral Building Block Research: It serves as a foundational element in constructing complex molecules with specific optical properties, supporting advanced organic chemistry studies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Its role in synthesizing active pharmaceutical ingredients makes it a valuable resource for medicinal chemistry and pharmacology research.\u003c\/li\u003e\n\u003cli\u003eBiochemical Studies: The compound's ability to interact with enzymes and reactive species makes it useful in biochemical investigations and enzyme kinetics.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Education: It is frequently used in teaching and research settings to demonstrate chiral synthesis techniques and molecular structure manipulation.\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: 100858-33-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 sunlight and moisture. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it should be kept in a well-ventilated area to minimize exposure. Proper labeling and storage are essential to ensure safe handling and prevent accidental use in incompatible reactions. Always follow standard safety protocols when working with chiral compounds to maintain a safe and efficient laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086133997786,"sku":"TCI2510C258517394","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086134030554,"sku":"TCI2510C258517395","price":3005000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2585.jpg?v=1767098526"},{"product_id":"tci2510c283217706","title":"TCI C2832 160982-16-1 (S)-6-Chloro-4-hydroxy-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine 1,1-Dioxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-6-Chloro-4-hydroxy-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine 1,1-Dioxide is a chiral building block used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in laboratories where precise control over stereochemistry is required. Its unique heterocyclic structure enables it to participate in various chemical reactions, making it a valuable tool for researchers. It is widely used in the development of pharmaceutical compounds and is essential for creating molecules with specific stereochemical configurations.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its chemical stability under certain conditions and its solubility in organic solvents. These properties make it suitable for a range of synthetic processes. Its ability to act as a chiral building block allows for the synthesis of compounds with high stereochemical purity. This makes it an ideal choice for applications requiring precise stereochemical control. Its reliability and effectiveness have made it a staple in many research laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical and organic chemistry research. It is a key component in the development of new therapeutic agents. Many research institutions and universities rely on it for advancing drug discovery and chemical synthesis. Its versatility and reliability make it a preferred material for scientific investigations in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules with specific stereochemical configurations, essential for pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eDrug Development: Its role in synthesizing complex organic compounds makes it valuable in the creation of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is used in the synthesis of heterocyclic compounds, contributing to the advancement of chemical knowledge.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: Its chiral properties enable the study of stereochemical effects on biological activity.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is widely used in educational and research settings to teach and explore asymmetric 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: 160982-16-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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\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 chemical stability. It is recommended to use airtight containers 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 important to ensure proper ventilation in the workspace to avoid inhalation of vapors. The compound should not be exposed to incompatible materials, and storage conditions should be regularly monitored to ensure its integrity. Always follow standard laboratory safety protocols when working with this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086198780122,"sku":"TCI2510C283217706","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086198812890,"sku":"TCI2510C283217707","price":3610000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2832.jpg?v=1767098859"},{"product_id":"tci2510c320218184","title":"TCI C3202 207557-35-5 (S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in laboratories where precise control over stereochemistry is essential. Its chiral nature allows for the synthesis of molecules with specific biological activities, making it a valuable tool in both academic and industrial research. As a key component in organic chemistry, it supports the development of new compounds with potential applications in medicine and chemical industries.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral structure and reactivity make it a preferred choice for researchers aiming to achieve enantioselective reactions. Its ability to participate in various synthetic pathways ensures versatility in laboratory applications. The availability of this compound in its chiral form enables scientists to design and produce molecules with desired stereochemistry, which is critical for pharmaceutical and specialty chemical development. This feature enhances its utility in advanced chemical synthesis processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-1-(Chloroacetyl)-2-pyrrolidinecarbonitrile is commonly used in organic chemistry research, particularly in the development of new compounds with medical or industrial potential. Local researchers rely on this compound to create molecules with specific properties, aligning with the needs of their studies. Its application in asymmetric synthesis supports innovation in chemical research and drug discovery efforts.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for producing compounds with specific biological activities due to its chiral structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for constructing complex molecular frameworks requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development to create enantiomerically pure compounds with targeted pharmacological effects.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis for the production of specialty chemicals with defined stereochemistry.\u003c\/li\u003e\n\u003cli\u003eAcademic studies in stereochemistry and chiral molecule design for educational and research purposes.\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: 207557-35-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its chiral nature, it is important to handle the compound with care to avoid contamination or unintended stereochemical changes. General laboratory precautions include wearing appropriate personal protective equipment, such as gloves and safety goggles, when handling the material. Proper labeling of containers is essential to ensure safe storage and use in the laboratory. Always follow standard chemical safety protocols to minimize risks associated with handling chiral compounds.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086218932442,"sku":"TCI2510C320218184","price":2474000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086218965210,"sku":"TCI2510C320218185","price":8582000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3202.jpg?v=1767099340"},{"product_id":"tci2510c325518251","title":"TCI C3255 95687-41-5 N-Carbobenzoxy-trans-4-hydroxy-L-prolinol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Carbobenzoxy-trans-4-hydroxy-L-prolinol is a chiral building block used in asymmetric synthesis to construct complex molecular structures. This compound plays a vital role in organic chemistry laboratories, where it serves as a key intermediate in the development of bioactive compounds. Its chiral nature allows for precise control over stereochemistry in synthetic reactions, which is essential for creating molecules with specific biological activities. This compound is widely utilized in research settings to explore new synthetic pathways and to enhance the efficiency of chemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique structural features and solubility in organic solvents make it a preferred choice for chemists working in asymmetric synthesis. Its stability under controlled conditions ensures consistent performance during chemical reactions, reducing the risk of degradation. Additionally, its ability to act as a substrate or intermediate in various synthetic processes increases its versatility in laboratory applications. These properties make it an essential tool for researchers aiming to develop new pharmaceuticals and advanced chemical materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N-Carbobenzoxy-trans-4-hydroxy-L-prolinol is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new compounds. Its application spans across academic and industrial research, supporting advancements in pharmaceutical and chemical industries. The compound's reliability and effectiveness have made it a standard component in many laboratory workflows in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis: This compound is ideal for creating chiral molecules with specific stereochemical configurations, essential for drug development and bioactive compound synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research: It is frequently used in studies involving complex molecule construction and functional group manipulation.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development: Its chiral structure supports the synthesis of compounds with targeted biological activities, aiding in the creation of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eSynthetic intermediate applications: It serves as a versatile building block in multi-step organic syntheses, enabling the formation of diverse molecular architectures.\u003c\/li\u003e\n\u003cli\u003eAcademic and industrial research: Widely used in both academic and industrial settings to explore new chemical pathways and improve synthetic efficiency.\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: 95687-41-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\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 sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its chiral nature, it is important to maintain strict handling protocols to avoid contamination or unintended stereochemical changes. In laboratory settings, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper labeling of containers is essential to ensure safe storage and easy identification. The compound is generally stable under normal laboratory conditions when stored correctly.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086222930138,"sku":"TCI2510C325518251","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3255.jpg?v=1767099360"},{"product_id":"tci2510c333218366","title":"TCI C3332 6216-63-3 N-Carbobenzoxy-L-prolinol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Carbobenzoxy-L-prolinol (TCI C3332, CAS 6216-63-3) is a chiral building block widely used in asymmetric synthesis within laboratory settings. It serves as a key intermediate in the development of chiral molecules, which are essential in pharmaceutical and organic chemistry research. This compound is particularly valuable for its ability to maintain stereochemical integrity during complex synthetic processes. Its role in the laboratory is critical for creating molecules with specific spatial configurations, which are often required in drug development and advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its chemical stability and controlled reactivity under specific conditions. The presence of a protected carboxyl group allows for selective chemical modifications without compromising the core structure of the molecule. This feature makes it highly versatile for various synthetic transformations. Additionally, its good solubility in organic solvents enhances its usability in a wide range of chemical reactions. These properties make it a reliable and efficient choice for researchers working in asymmetric synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N-Carbobenzoxy-L-prolinol is commonly used in organic chemistry research, especially in the fields of asymmetric synthesis and drug development. Its availability supports local scientific efforts in creating chiral compounds with specific biological activities. Researchers rely on this compound to advance their work in synthesizing complex molecules with precise stereochemistry, contributing to the growth of scientific innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis of chiral compounds due to its stereochemical stability and controlled reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals requiring precise molecular configurations for drug efficacy.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research involving selective functional group modifications in complex molecules.\u003c\/li\u003e\n\u003cli\u003eCreation of chiral intermediates for use in advanced synthetic pathways and catalytic reactions.\u003c\/li\u003e\n\u003cli\u003eSupport for academic and industrial research in the production of bioactive molecules with specific spatial arrangements.\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: 6216-63-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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\u003eN-Carbobenzoxy-L-prolinol 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 could affect its stability. General laboratory precautions include handling with care to avoid contamination and ensuring proper ventilation when working with the compound. Due to its chemical nature, it should be stored separately from incompatible substances. Proper labeling and storage conditions are essential to ensure safety and maintain the quality of the compound for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086234169562,"sku":"TCI2510C333218366","price":1339000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3332.jpg?v=1767099480"},{"product_id":"tci2510d214922220","title":"TCI D2149 132958-72-6 (3R)-(+)-3-(Dimethylamino)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(3R)-(+)-3-(Dimethylamino)pyrrolidine is a chiral compound widely used in asymmetric synthesis to produce molecules with defined stereochemistry. This material plays a crucial role in laboratories where precise control over molecular structure is essential. It is particularly valuable in pharmaceutical and organic chemistry research, where the stereochemistry of a compound can significantly impact its biological activity. As a chiral building block, it serves as a foundational element in the development of complex molecules with specific functional properties.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique structure, featuring a dimethylamino group, provides reactivity and versatility in chemical reactions. This makes it an ideal choice for chemists aiming to synthesize enantiomerically pure compounds. Its stability under various reaction conditions further enhances its utility in both academic and industrial settings. The ability to selectively interact with other reagents allows for the creation of a wide range of derivatives, expanding its applicability in synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently utilized in research focused on drug development and organic synthesis. It is a key reagent in studies related to pharmacology, where the stereochemistry of a molecule can determine its efficacy and safety. Its availability and reliability make it a preferred choice for researchers working on complex chemical transformations and molecular design.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound enables the creation of enantiomerically pure compounds, essential for pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its reactivity and ability to form diverse derivatives, supporting the synthesis of complex molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research relies on its chiral properties to design drugs with specific biological activities and reduced side effects.\u003c\/li\u003e\n\u003cli\u003eAcademic institutions use it in teaching and research to demonstrate stereochemistry and asymmetric synthesis techniques.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it to produce high-purity compounds for specialized applications in medicine and materials science.\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: 132958-72-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or crystalline, depending on the supplier\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 use airtight containers to prevent moisture absorption and maintain its chemical integrity. Proper labeling of containers is essential for safe handling and identification. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and goggles, to ensure safety. Due to its reactivity, it should be stored separately from strong oxidizing agents. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086498541786,"sku":"TCI2510D214922220","price":3155000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086498574554,"sku":"TCI2510D214922221","price":10524000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2149.jpg?v=1767104294"},{"product_id":"tci2510d219322288","title":"TCI D2193 132883-44-4 (3S)-(-)-3-(Dimethylamino)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(3S)-(-)-3-(Dimethylamino)pyrrolidine is a chiral building block essential in asymmetric synthesis, playing a critical role in the creation of molecules with specific stereochemistry. This compound is widely used in chemical research to produce compounds with defined biological activities. Its importance lies in its ability to influence the stereochemical outcome of reactions, making it a valuable tool in the development of pharmaceuticals and organic compounds. In laboratory settings, it serves as a key reagent for synthesizing complex molecules with precise structural features.\u003c\/p\u003e\n\u003cp\u003eThe compound's optical activity and high purity make it a preferred choice for researchers aiming to achieve enantiomeric control in chemical reactions. Its chiral nature allows for the selective formation of specific isomers, which is crucial in drug development and other specialized chemical applications. The compound's reactivity and compatibility with various reagents further enhance its utility in synthetic processes. These properties ensure its reliability and effectiveness in producing compounds with desired biological properties.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (3S)-(-)-3-(Dimethylamino)pyrrolidine is commonly used in organic chemistry research, particularly in pharmaceutical and asymmetric synthesis projects. It is a fundamental component in the development of new therapeutic agents and is utilized by academic institutions and research centers to advance chemical innovation. Its role in creating compounds with specific stereochemistry makes it an essential material for scientific exploration and drug discovery efforts.\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 specific enantiomers with desired biological activities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It is widely used in drug development to create compounds with precise stereochemistry, enhancing the efficacy and safety of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its role as a chiral building block makes it a key reagent in the synthesis of complex organic molecules, supporting advanced chemical research.\u003c\/li\u003e\n\u003cli\u003eIsomer Selectivity Studies: The compound's optical activity allows researchers to study and control isomer selectivity, which is critical in understanding molecular behavior and reactivity.\u003c\/li\u003e\n\u003cli\u003eAcademic and Industrial Research: It is frequently used in both academic and industrial settings to develop new chemical compounds and improve existing synthetic methods.\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: 132883-44-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, 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 light and moisture to maintain its stability and purity. 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 important to handle the compound with care to avoid any unintended racemization or loss of optical activity. In laboratory settings, proper personal protective equipment should be worn when handling the material. Regular monitoring of storage conditions ensures the compound remains suitable for use in chemical synthesis and research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086503162074,"sku":"TCI2510D219322288","price":3155000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086503194842,"sku":"TCI2510D219322289","price":10524000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2193.jpg?v=1767104384"},{"product_id":"tci2510d265822969","title":"TCI D2658 132747-20-7 (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane Dihydrobromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2658, (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane Dihydrobromide (CAS 132747-20-7), is a chiral bicyclic diamine supplied as its dihydrobromide salt. The bicyclo[2.2.1]heptane framework, carrying two nitrogen atoms at positions 2 and 5, produces a rigid bridged structure with a clearly defined (1S,4S) stereochemical configuration. In the laboratory it is regarded as a high-value chiral building block, because it provides a ready-to-use chiral nitrogen scaffold that is difficult to prepare in-house through conventional synthesis. Having it on the shelf saves considerable time on routes toward active molecules and asymmetric ligands.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound a preferred choice are its conformational rigidity and its stereochemical purity. Because the bicyclic framework is almost incapable of free rotation, the two nitrogen atoms are held in fixed spatial orientations relative to one another. This produces a consistent chiral environment, which is extremely useful for controlling the direction from which a reagent approaches a substrate in asymmetric reactions. The dihydrobromide salt form adds practical advantages: it is a more stable solid, it does not readily absorb carbon dioxide, and it is easier to weigh accurately than the free diamine, which is strongly basic and hygroscopic.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material typically appears in synthetic and medicinal chemistry groups at universities and research institutes, and in R\u0026amp;D units developing fine chemicals or pharmaceutical intermediates. It is normally purchased in small quantities for method development and route scouting rather than for bulk production. Because the salt form tolerates ambient handling better than the free base, it suits laboratories where reagents are weighed on an open bench and where a genuinely inert-atmosphere workflow is not always practical.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChiral ligand synthesis — the fixed geometry of the two nitrogen donors makes it a direct precursor to bidentate nitrogen ligands with a predictable, reproducible chiral pocket around the metal centre.\u003c\/li\u003e\n\u003cli\u003eAsymmetric catalysis studies — the rigid, stereochemically defined framework helps steer the approach of reagents to one face of a substrate, supporting systematic screening of enantioselective transformations.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical intermediate routes — supplies a pre-formed chiral diazabicyclic core to medicinal chemistry programmes, removing several difficult stereoselective steps from the overall synthetic sequence.\u003c\/li\u003e\n\u003cli\u003eChiral building block library work — used as a stock scaffold for diversification at either nitrogen, letting chemists build analogue series while retaining the same defined (1S,4S) configuration throughout.\u003c\/li\u003e\n\u003cli\u003eMethod development and route scouting — the stable, easily weighed dihydrobromide salt is convenient for small-scale trial reactions where accurate charging of a chiral amine matters more than bulk quantity.\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\u003eProduct code: D2658\u003c\/li\u003e\n\u003cli\u003eCAS number: 132747-20-7\u003c\/li\u003e\n\u003cli\u003eChemical name: (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane Dihydrobromide\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid (dihydrobromide salt); pack sizes available on request\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container, 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 place, away from moisture and from direct sunlight. Amine salts of this type are best kept in their original tightly sealed glass or chemically compatible plastic container, with the cap replaced immediately after each use to limit exposure to atmospheric humidity. Weigh the solid in a fume hood or well-ventilated area using clean, dry spatulas, and avoid creating dust. Wear safety glasses, gloves, and a laboratory coat, and avoid contact with skin, eyes, and clothing. Because the free amine liberated from this salt is strongly basic, handle any neutralisation step with care and add base slowly with cooling. Keep the material segregated from strong oxidising agents, label all secondary containers clearly, and consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086571122906,"sku":"TCI2510D265822969","price":4089000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2658.jpg?v=1767105155"},{"product_id":"tci2510d366124007","title":"TCI D3661 42399-49-5 (2S,3S)-(+)-2,3-Dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3661, (2S,3S)-(+)-2,3-Dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, is a chiral building block belonging to the asymmetric synthesis group. The molecule is built on a seven-membered benzothiazepinone framework carrying two defined stereogenic centres at positions 2 and 3, together with a 4-methoxyphenyl substituent and a secondary hydroxyl group. This skeleton is the core framework of the benzothiazepine class, a structure widely recognised in medicinal chemistry, while the hydroxyl group and the free amide nitrogen provide two clear points of functionalisation. In the laboratory the material serves as an enantiomerically pure starting material for constructing benzothiazepine derivatives and as a reference compound in analytical work.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound the preferred choice is its established stereochemical purity, defined as the (2S,3S) configuration. In asymmetric synthesis, beginning from a material whose stereochemistry is already correct is far more efficient than constructing the chiral centres from scratch, because it removes the need for racemate resolution, for expensive chiral catalysts, and for the complicated chiral chromatographic purification that such routes normally demand. The positive optical rotation confirms the identity of the enantiomer, and the rigid bicyclic framework gives predictable geometry that carries through to subsequent transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this type of chiral building block is typically used in university and institutional research groups working on asymmetric synthesis and medicinal chemistry, as well as in analytical and quality-control laboratories that need a defined stereochemical standard. Because the stereocentres are already set, the compound suits work programmes where chiral resolution capability is limited, allowing a synthetic route to proceed on a single-enantiomer basis from the first step onwards.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBenzothiazepine derivative synthesis — the seven-membered benzothiazepinone core is supplied intact, so researchers can proceed directly to derivatisation rather than assembling the ring system themselves.\u003c\/li\u003e\n\u003cli\u003eAsymmetric synthesis route development — the defined (2S,3S) configuration allows single-enantiomer routes to be planned without racemate resolution steps or expensive chiral catalyst screening at the outset.\u003c\/li\u003e\n\u003cli\u003eSelective functionalisation studies — the secondary hydroxyl group and the free amide nitrogen provide two clearly distinguishable reactive positions for controlled, stepwise chemical modification work.\u003c\/li\u003e\n\u003cli\u003eAnalytical reference material — the compound serves as a reference standard in analytical work where a stereochemically defined benzothiazepine structure is required for identification or method verification.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry structural exploration — the benzothiazepine skeleton is widely recognised in medicinal chemistry, making this building block suitable for structure-oriented exploratory synthesis around that framework.\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: 42399-49-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical name: (2S,3S)-(+)-2,3-Dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one\u003c\/li\u003e\n\u003cli\u003eStereochemistry: (2S,3S) configuration, positive optical rotation\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale pack sizes; please confirm the required quantity when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store as indicated on the manufacturer's label and accompanying documentation\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 direct sunlight, moisture, and incompatible chemicals, following the storage conditions stated on the manufacturer's label and safety data sheet. Keep the material in its original supplier container, or in a clean, chemically compatible and clearly labelled vessel if it must be transferred. Handle in a fume hood using standard laboratory protective equipment, including a lab coat, safety glasses, and suitable gloves. Avoid generating dust, avoid contact with skin and eyes, weigh out only the amount required, and reseal the container promptly to limit exposure to air and humidity. Dispose of residues and contaminated materials in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086631842010,"sku":"TCI2510D366124007","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086631874778,"sku":"TCI2510D366124008","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3661.jpg?v=1767106366"},{"product_id":"tci2510d421024741","title":"TCI D4210 151213-40-0 (1S,6S)-2,8-Diazabicyclo[430]nonane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1S,6S)-2,8-Diazabicyclo[430]nonane is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in chemical laboratories, especially in research focused on optically active compounds and pharmaceutical products. Its unique stereochemistry allows chemists to create molecules with specific asymmetric configurations, which is essential in drug development and advanced organic synthesis. As a key component in chiral synthesis, it enables the production of enantiomerically pure compounds, which are vital in various scientific applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stable chemical properties and controlled reactivity, making it a preferred choice for synthetic chemists. Its high optical activity ensures precise control over the stereochemistry of the final product, which is critical in pharmaceutical and fine chemical industries. The complex cyclic structure of this compound provides a versatile platform for further functionalization, allowing for the synthesis of a wide range of derivatives with diverse chemical properties. These characteristics make it an essential tool for researchers aiming to achieve high selectivity in their synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in projects requiring asymmetric synthesis. It is frequently employed in academic and industrial settings where the development of optically active compounds is necessary. Its reliability and performance in various chemical reactions make it a go-to material for scientists working on advanced synthetic methodologies. Its application is widespread across different research domains, contributing to the advancement of chemical science in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis projects benefit from this compound's ability to control stereochemistry, enabling the production of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this material for the synthesis of optically active drugs, ensuring high selectivity and efficacy in drug development.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry studies rely on its complex structure to create diverse molecular derivatives, supporting advanced synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eAcademic research institutions use it to explore new synthetic routes and develop novel compounds with specific stereochemical properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it for the production of specialty chemicals requiring precise stereochemical control.\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: 151213-40-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\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 chemical integrity. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and degradation. Handling should be done with appropriate personal protective equipment, including gloves and safety goggles, to ensure safety in the laboratory. Due to its optical activity and chemical stability, it is important to avoid exposure to strong oxidizing or reducing agents. Regular monitoring of storage conditions is advised to ensure the compound remains suitable for use in synthetic processes. Proper labeling of containers is essential for safe handling and to prevent accidental misuse in the laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086678929626,"sku":"TCI2510D421024741","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086678962394,"sku":"TCI2510D421024742","price":2953000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4210.jpg?v=1767107230"},{"product_id":"tci2510d433724908","title":"TCI D4337 106092-09-5 (S)-(-)-2,6-Diamino-4,5,6,7-tetrahydrobenzothiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4337 (S)-(-)-2,6-Diamino-4,5,6,7-tetrahydrobenzothiazole, CAS 106092-09-5, is a chiral building block supplied by TCI under catalog code D4337 and belongs to the asymmetric synthesis category. Its molecule combines an aromatic thiazole ring fused to a hydrogenated cyclohexane ring, and it carries two amino groups that sit in distinctly different chemical environments. One amino group is attached to the thiazole ring, while the other resides on a saturated carbon that constitutes a stereogenic centre with the S configuration. In the laboratory, this compound serves as an enantiomerically pure scaffold for constructing target molecules that require defined stereochemical specificity.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material highly valued is that chirality is already defined and available from the very beginning of the synthesis. Researchers do not need to carry out racemate resolution or design a separate asymmetric catalyst, because the stereochemical information is already carried within the starting material and is transferred through to the final product. In addition, the two amino groups of differing character permit selective functionalisation: the aliphatic amine at position six is generally more nucleophilic and more readily alkylated or acylated, whereas the amine on the thiazole ring exhibits different reactivity, allowing chemists to address each nitrogen in a controlled sequence.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this chiral building block is typically used in university research groups, pharmaceutical chemistry laboratories, and contract synthesis facilities working on stereochemically defined targets. It is normally handled at bench scale for multi-step synthetic routes, method development, and reference-standard preparation, where obtaining a single enantiomer reliably matters more than reaction scale. Because it removes the need for in-house resolution or bespoke catalyst development, it is a practical choice for groups with limited chiral separation infrastructure.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis of stereochemically defined targets: the S configuration at the saturated carbon is fixed in the starting material, so the required stereochemistry is carried through the route without a separate resolution step.\u003c\/li\u003e\n\u003cli\u003eChiral building block assembly in multi-step routes: the fused thiazole and hydrogenated cyclohexane framework provides a rigid, pre-formed core onto which further substituents can be elaborated by the synthetic chemist.\u003c\/li\u003e\n\u003cli\u003eSelective mono-functionalisation studies: the aliphatic amine at position six is generally more nucleophilic and more readily alkylated or acylated than the thiazole-bound amine, enabling controlled, sequential derivatisation.\u003c\/li\u003e\n\u003cli\u003ePreparation of enantiomerically pure intermediates for pharmaceutical chemistry research: the compound supplies stereochemical information directly, which is essential where biological activity depends on a single enantiomer.\u003c\/li\u003e\n\u003cli\u003eMethodology and route-development work in academic research groups: the two amino groups of differing reactivity make this molecule a useful substrate for exploring chemoselective amine protection, coupling, and derivatisation strategies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (catalog code D4337)\u003c\/li\u003e\n\u003cli\u003eCAS Number: 106092-09-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical name: (S)-(-)-2,6-Diamino-4,5,6,7-tetrahydrobenzothiazole\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the required pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions stated on the product label and safety data sheet\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 heat, direct sunlight, and incompatible materials, and follow the storage conditions specified by the manufacturer on the label and safety data sheet. Keep the material in its original supplier container, or transfer it only to a clean, chemically compatible and clearly labelled container. As an amine-containing compound, it should be protected from moisture and air where practicable. Handle in a fume hood using appropriate personal protective equipment, including safety goggles, gloves, and a laboratory coat. Avoid inhalation of dust and contact with skin and eyes, wash hands thoroughly after handling, and dispose of residues and contaminated materials in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086687678682,"sku":"TCI2510D433724908","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086687711450,"sku":"TCI2510D433724909","price":5805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4337.jpg?v=1767107426"},{"product_id":"tci2510d523426093","title":"TCI D5234 36923-21-4 Diphenylmethyl 7beta-Amino-3-cephem-4-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiphenylmethyl 7beta-Amino-3-cephem-4-carboxylate is a chemical compound used in asymmetric synthesis to produce bioactive compounds. This material plays a crucial role in laboratory settings where precise control over stereochemistry is required. It is widely utilized in the development of pharmaceuticals and pharmacological agents due to its unique structural features. Its ability to participate in asymmetric reactions makes it a valuable tool for chemists working on complex molecular transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound's properties make it a preferred choice for researchers in organic chemistry and pharmacology. Its stable chemical nature allows for easy manipulation under various reaction conditions. The chiral building block nature of this compound enables the synthesis of molecules with high biological activity. Its specificity in chemical reactions ensures that it can be reliably used in a wide range of synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers and scientists in the fields of organic chemistry and pharmacology. It is an essential component in the development of new compounds with specific therapeutic effects. Its availability in the local market supports research and development efforts in various academic and industrial institutions. The compound is frequently used in laboratory synthesis applications, contributing to the advancement of drug discovery and chemical innovation.\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 creation of enantiomerically pure compounds essential for pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its use in the synthesis of bioactive compounds makes it a key material for drug discovery and development in pharmaceutical laboratories.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Researchers in organic chemistry benefit from its ability to participate in complex synthetic reactions, supporting the creation of novel molecular structures.\u003c\/li\u003e\n\u003cli\u003eChiral Compound Development: The compound's role as a chiral building block is crucial in the design of new chiral compounds with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eBioactive Molecule Synthesis: It is widely used in the synthesis of molecules with high biological activity, contributing to the advancement of medicinal chemistry.\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: 36923-21-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various pack sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard chemical specifications)\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 chemical stability. It is recommended to keep it in a tightly sealed container to prevent moisture absorption. Suitable storage containers include glass or high-density polyethylene vessels. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid exposure to heat and direct light to preserve its integrity. Proper ventilation is essential when working with this material in a laboratory setting. Always follow standard safety protocols to ensure safe handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086750363866,"sku":"TCI2510D523426093","price":6058000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5234.jpg?v=1767108533"},{"product_id":"tci2510d601027020","title":"TCI D6010 147081-29-6 (S)-1-Boc-3-methylpiperazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-1-Boc-3-methylpiperazine is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in the development of pharmaceuticals and organic chemicals, enabling the creation of enantiomerically pure substances. Its importance lies in its ability to influence the stereochemistry of target molecules, which is essential for achieving desired pharmacological effects. As a key component in synthetic pathways, it supports the design of compounds with high specificity and efficacy in various therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and controlled reactivity, making it a reliable choice for complex synthetic processes. Its Boc (tert-butoxycarbonyl) group provides additional functionality, allowing for versatile chemical modifications. The chiral nature of (S)-1-Boc-3-methylpiperazine ensures that it can be used to generate enantiomerically pure products, which are critical in drug development. This property makes it a preferred material for researchers aiming to produce molecules with specific stereochemical configurations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-1-Boc-3-methylpiperazine is commonly used in pharmacology, organic chemistry, and biochemistry research. It supports the development of new drugs and the modification of existing chemical compounds for medical and industrial applications. Its availability from reliable suppliers ensures that researchers can access this essential material for their experimental needs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, which are essential for drug development and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It supports the synthesis of active pharmaceutical ingredients with specific stereochemical configurations, enhancing drug efficacy and selectivity.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its reactivity and stability make it a valuable tool for exploring new synthetic pathways and chemical transformations.\u003c\/li\u003e\n\u003cli\u003eBiochemical Investigations: It is used in the development of bioactive molecules that interact with specific biological targets, aiding in the study of molecular mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug Modification Projects: Its Boc group allows for controlled chemical modifications, facilitating the design of new therapeutic agents with improved properties.\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: 147081-29-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. Proper labeling of storage containers is essential to ensure safe handling and prevent cross-contamination. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure. Regular monitoring of storage conditions is advised to ensure the material remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086787588314,"sku":"TCI2510D601027020","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086787621082,"sku":"TCI2510D601027021","price":4216000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6010.jpg?v=1767109571"},{"product_id":"tci2510d615227199","title":"TCI D6152 113451-59-5 tert-Butyl (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane-2-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6152 113451-59-5 tert-Butyl (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane-2-carboxylate is a chiral building block essential in asymmetric synthesis. This compound is widely used in laboratories for creating complex molecular structures with specific stereochemistry. Its role is critical in the development of pharmaceuticals and organic compounds where precise control over molecular configuration is necessary. Due to its chiral nature, it serves as a key intermediate in the synthesis of enantiomerically pure compounds, which are vital in drug development and other advanced chemical applications.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique chiral structure allows it to participate in reactions that yield products with distinct biological activities. Its stability under standard laboratory conditions ensures consistent performance and ease of handling. Additionally, its compatibility with various synthetic methodologies makes it a versatile tool in both academic and industrial research settings. This reliability and effectiveness make it a preferred choice for chemists working on complex synthesis projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in pharmaceutical and synthetic chemistry applications. It is valued for its ability to produce compounds with specific stereochemical properties, which are crucial for developing new drugs and specialized chemical products. Its widespread use in local research institutions highlights its importance in advancing chemical innovation 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 synthesis due to its chiral structure, enabling the creation of enantiomerically pure products essential in pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is widely used in organic chemistry studies for constructing complex molecular frameworks with precise stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Its role in producing compounds with specific biological activities makes it a key component in drug discovery and formulation processes.\u003c\/li\u003e\n\u003cli\u003eChiral Compound Synthesis: The compound serves as a chiral building block, allowing for the synthesis of various chiral compounds with tailored properties.\u003c\/li\u003e\n\u003cli\u003eAdvanced Chemical Applications: It is applied in advanced chemical research where precise control over molecular configuration is required for specialized 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: 113451-59-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 humidity, which could affect its chemical integrity. In laboratory settings, proper ventilation should be ensured when handling the compound to minimize any potential risks associated with its chemical properties. Always follow standard safety protocols when working with chiral compounds, as they can have specific handling requirements. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086793847002,"sku":"TCI2510D615227199","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6152.jpg?v=1767109823"},{"product_id":"tci2510e043428195","title":"TCI E0434 381670-31-1 (3S)-(-)-3-(Ethylamino)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E0434 (3S)-(-)-3-(Ethylamino)pyrrolidine is a chiral building block that carries two nitrogen atoms of distinctly different character: the ring nitrogen of the pyrrolidine core, and an ethylamino group attached at the third carbon whose configuration is defined as S. Cyclic diamines of this type are important starting materials in asymmetric synthesis, because the rigid pyrrolidine framework helps direct the geometry of a reaction, while the two amine groups provide attachment points for acylation, alkylation, sulfonylation, and the formation of ureas and amides during later stages of building a target molecule.\u003c\/p\u003e\n\u003cp\u003eThe advantage that makes this compound a preferred choice lies in its stereochemical purity being defined from the outset. Beginning a synthesis from material that is already chiral is far more efficient than working through the resolution of a racemic mixture partway along the reaction route, since resolution always sacrifices half of the material and adds further purification steps. In addition, the difference in steric hindrance and nucleophilicity between the secondary ring amine and the ethylamino group allows one nitrogen to be reacted selectively before the other, so that chemists can assemble substitutions in stages without losing control over the regiochemistry of the product.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, material of this kind is typically used in synthetic and medicinal chemistry laboratories at universities and research institutes, where enantiomerically defined intermediates are required for work on chiral molecules. It suits research groups developing multi-step synthetic routes, method development studies in asymmetric synthesis, and laboratories preparing small quantities of structurally defined intermediates for further transformation rather than bulk production work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis route development: the defined S configuration is carried through subsequent steps, so the stereochemistry of the final target is established by the starting material rather than by a later resolution stage.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry intermediate preparation: the two differentiated nitrogen atoms allow systematic structural variation around a rigid pyrrolidine core when building small sets of related analogues for study.\u003c\/li\u003e\n\u003cli\u003eSelective mono-functionalisation studies: the differing steric hindrance and nucleophilicity of the ring amine and the ethylamino group let chemists acylate or alkylate one nitrogen first under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eAmide and urea formation chemistry: both amine centres react readily with acylating and isocyanate-type partners, making this compound a convenient anchor point for constructing nitrogen-linked molecular fragments.\u003c\/li\u003e\n\u003cli\u003eChiral ligand and auxiliary investigations: the rigid cyclic diamine framework with a fixed stereocentre is a useful scaffold for preparing and evaluating nitrogen-donor structures in stereoselective reaction studies.\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: 381670-31-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: E0434\u003c\/li\u003e\n\u003cli\u003ePack sizes: research-scale packs as listed in the TCI catalogue for this item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer 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 place away from heat sources, direct sunlight, and incompatible materials such as strong acids and oxidising agents. Amines of this type are best kept in their original supplier packaging, which is selected for compatibility with the contents; where transfer is necessary, use a clean, dry, chemically compatible container with a secure closure and a clear label. Handle the compound in a fume hood using safety glasses, gloves, and a laboratory coat, avoiding contact with skin and eyes and inhalation of vapour. Minimise exposure to air and moisture by closing the container promptly after dispensing. Consult the manufacturer's safety data sheet before use, and follow local institutional rules for chemical waste collection and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086847684826,"sku":"TCI2510E043428195","price":6511000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0434.jpg?v=1768818691"},{"product_id":"tci2510e099328850","title":"TCI E0993 63422-71-9 (R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis compound, known as (R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid, is a chiral building block widely used in asymmetric synthesis. It plays a crucial role in laboratories where precise control over stereochemistry is required. Its complex structure, combining a piperazine chain with a benzeneacetic acid group, makes it an essential component in the development of bioactive compounds. Due to its chiral nature, it enables the synthesis of enantiomerically pure molecules, which is vital in pharmaceutical research and organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique chemical structure allows for highly specific and efficient chemical reactions. Its chiral properties are particularly valuable in the separation of isomers, a process essential for creating compounds with desired biological activities. Additionally, its chemical stability under standard laboratory conditions ensures ease of handling and storage, making it a reliable choice for researchers. The compound's versatility and effectiveness in asymmetric synthesis have made it a preferred material in various scientific applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers in pharmaceutical and organic chemistry fields. It supports the development of new drugs and specialized chemical compounds. Its role in enabling precise stereoselective reactions makes it a key component in advanced research projects. The compound's availability and reliability contribute to its widespread use in academic and industrial research settings across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, which is critical in drug development and organic chemistry research.\u003c\/li\u003e\n\u003cli\u003eChiral Building Block Applications: Its complex structure makes it a preferred choice for constructing molecules with specific stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: The compound's chiral properties are essential for developing bioactive compounds with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: It supports the synthesis of complex molecules, enabling researchers to explore new chemical reactions and pathways.\u003c\/li\u003e\n\u003cli\u003eIsomer Separation Processes: Its chiral nature allows for the efficient separation of isomers, which is vital in advanced synthetic chemistry 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: 63422-71-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline appearance\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 to prevent exposure to humidity and air. Due to its chiral nature, it is important to handle it with care to avoid contamination or degradation. Standard laboratory safety practices should be followed, including the use of personal protective equipment when handling. The compound is generally stable under normal laboratory conditions, making it suitable for long-term storage and routine use in research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086915743962,"sku":"TCI2510E099328850","price":784000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086915776730,"sku":"TCI2510E099328851","price":2550000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0993.jpg?v=1767112124"},{"product_id":"tci2510e099428852","title":"TCI E0994 62893-24-7 (R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]-4-hydroxybenzeneacetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis compound, known as (R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]-4-hydroxybenzeneacetic Acid, is a chiral building block used in asymmetric synthesis to construct complex molecular structures. It plays a critical role in organic chemistry and pharmaceutical research by enabling the synthesis of molecules with specific biological activities. Due to its chiral nature, it allows for the selective production of enantiomers, which is essential in drug development and bioactive compound creation. Its structural complexity, featuring both piperazine and benzoate groups, makes it a versatile tool for chemists seeking to design molecules with precise stereochemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high purity and solid form make it ideal for laboratory use, as it ensures consistent results and simplifies handling during chemical reactions. Its stability under controlled conditions further enhances its reliability in research settings. The presence of functional groups such as hydroxyl and amide allows for a wide range of chemical modifications, making it a preferred choice for synthetic chemists working on complex molecule synthesis. Its compatibility with various reaction conditions also contributes to its popularity in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in pharmaceutical and organic chemistry research. It is particularly valuable for studies involving drug development, bioactive compound synthesis, and molecular modeling. Its ability to provide precise stereochemical control is especially important in the creation of compounds with specific pharmacological effects. Researchers in Indonesia rely on this compound for experiments requiring high accuracy and reproducibility in molecular structure manipulation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDrug development research benefits from this compound’s ability to produce enantiomers with specific biological activities, enabling the creation of more effective and targeted pharmaceuticals.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis projects utilize its chiral structure to build complex molecules with precise stereochemistry, enhancing the efficiency of synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eBioactive compound research leverages its functional groups to design molecules with specific interactions in biological systems, supporting advancements in medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eMolecular modeling studies use its structural complexity to simulate and predict the behavior of chiral compounds in various chemical environments.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications take advantage of its stability and purity for accurate spectroscopic and chromatographic analysis in laboratory 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: 62893-24-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 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 contamination and degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is also essential when working with this compound to minimize exposure to vapors. Care should be taken to avoid contact with incompatible substances, and all handling should follow standard laboratory safety protocols. Its solid form makes it relatively easy to manage, but care must be taken to prevent physical damage during storage and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086915875034,"sku":"TCI2510E099428852","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086915907802,"sku":"TCI2510E099428853","price":1237000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0994.jpg?v=1767112128"},{"product_id":"tci2510e142329444","title":"TCI E1423 84793-24-8 N-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-[1-(S)-Ethoxycarbonyl-3-phenylpropyl]-L-alanine-N-carboxyanhydride is a chiral building block used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in laboratories where precise control over molecular chirality is essential. It is widely used in organic chemistry and pharmaceutical research to develop compounds with specific biological activities. Its ability to introduce chirality into molecular frameworks makes it a valuable tool for creating enantiomerically pure substances, which are critical in drug development and other advanced chemical applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its chemical stability and its ability to act as a precursor in specific chemical reactions. Its chiral nature allows for the synthesis of compounds with defined stereochemistry, which is vital in the pharmaceutical industry. The compound’s structural characteristics enable it to participate in various synthetic pathways, making it a versatile reagent for researchers aiming to achieve high levels of molecular precision. Its reliability and consistency in performance make it a trusted choice in both academic and industrial laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in pharmaceutical and active compound synthesis. Researchers at universities and research institutions rely on it for experiments requiring high molecular precision. Its application is especially relevant in the development of new drugs and bioactive molecules, where controlling stereochemistry is essential for achieving desired biological effects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules with specific stereochemistry, essential in drug development and bioactive compound synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It supports the synthesis of complex organic structures, aiding in the exploration of new chemical reactions and molecular designs.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: Its ability to produce enantiomerically pure compounds makes it a key reagent in the creation of pharmaceuticals with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: Used in university laboratories for teaching and research, it helps students and scientists understand the principles of chirality and asymmetric synthesis.\u003c\/li\u003e\n\u003cli\u003eActive Compound Synthesis: It is frequently employed in the synthesis of active pharmaceutical ingredients, where precise molecular structure is critical for efficacy and safety.\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: 84793-24-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 chemical properties)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and 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 moisture and direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. In laboratory settings, it should be handled with care using appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. Proper labeling of storage containers is essential for easy identification and safe handling. The compound should not be exposed to incompatible substances or high temperatures, as this may lead to degradation or unintended chemical reactions. Regular monitoring of storage conditions is advised to ensure optimal preservation of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086959456474,"sku":"TCI2510E142329444","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086959489242,"sku":"TCI2510E142329445","price":633000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1423.jpg?v=1767112839"},{"product_id":"tci2510f134431494","title":"TCI F1344 136725-53-6 (S)-3-Fluoropyrrolidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-3-Fluoropyrrolidine Hydrochloride is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in laboratories where precise control over molecular structure is essential. It serves as a key building block in the development of pharmaceuticals and organic chemicals, enabling the synthesis of compounds with desired stereochemical properties. Its importance lies in its ability to influence the final product's pharmacological profile, making it a fundamental tool in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound's optical activity and chiral nature make it a preferred choice for researchers aiming to produce enantiomerically pure substances. Its molecular structure allows for selective interactions in chemical reactions, which is vital for creating bioactive compounds with high specificity. This property ensures that the resulting products are not only more effective but also safer for therapeutic applications. As a result, it is highly valued in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-3-Fluoropyrrolidine Hydrochloride is commonly used in applied research, particularly in drug development and the synthesis of bioactive compounds. Researchers across various institutions rely on this compound to conduct experiments that require strict control over molecular structure. Its versatility and reliability make it an essential component in the toolkit of chemists working on complex synthetic pathways.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating enantiomerically pure molecules, which is critical in pharmaceutical research where stereochemistry significantly affects drug efficacy.\u003c\/li\u003e\n\u003cli\u003eChiral Compound Development: Its chiral nature makes it a preferred choice for synthesizing compounds with specific stereochemical configurations, enhancing the effectiveness of bioactive agents.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It supports the development of new organic compounds by providing a reliable chiral building block for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery Programs: Researchers use it to explore new therapeutic agents, as its stereochemistry can influence the biological activity of the final product.\u003c\/li\u003e\n\u003cli\u003eBioactive Molecule Synthesis: It is essential in the creation of molecules with specific biological functions, enabling the design of compounds with targeted pharmacological 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: 136725-53-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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\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 keep it in a tightly sealed container to prevent exposure to air and humidity. Due to its chiral nature, it should be handled with care to avoid contamination or degradation. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper ventilation is also advised to ensure safe working conditions. The compound is not classified as hazardous under standard laboratory safety guidelines but should still be treated with the usual precautions for chemical handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087078437082,"sku":"TCI2510F134431494","price":2650000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1344.jpg?v=1767114358"},{"product_id":"tci2510f134631497","title":"TCI F1346 136725-55-8 (R)-3-Fluoropyrrolidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-3-Fluoropyrrolidine Hydrochloride is a chiral compound widely used in asymmetric synthesis to construct molecules with optical activity. This material plays a crucial role in chemical laboratories, particularly in the development of pharmaceuticals and organic compounds. Its chiral structure allows for the formation of enantiomers, which are essential in creating drugs with specific biological activities. As a chiral building block, it is integral to the synthesis of complex molecules that require precise stereochemical control.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under standard laboratory conditions and its availability in various packaging formats, making it accessible for both research and industrial applications. Its ability to form specific molecular structures with high efficiency makes it a preferred choice for chemists working on advanced synthesis projects. The compound’s chemical properties ensure consistency and reliability in experimental outcomes, supporting reproducibility and accuracy in scientific research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (R)-3-Fluoropyrrolidine Hydrochloride is commonly used in pharmaceutical and chemical research. It is a key component in experiments requiring controlled molecular structures, especially in drug development and organic synthesis. Its availability in the local market facilitates its use by researchers and institutions, contributing to the advancement of scientific studies in chemistry and pharmacology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, essential in pharmaceutical research for developing effective and safe drugs.\u003c\/li\u003e\n\u003cli\u003eChiral Compound Development: Its chiral structure supports the synthesis of complex molecules with specific stereochemistry, enhancing the precision of chemical reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is frequently used in experiments that require controlled molecular structures, aiding in the study of reaction mechanisms and stereochemical outcomes.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery: The compound’s ability to form specific molecular configurations makes it valuable in the early stages of drug development.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is widely utilized in universities and research institutions for teaching and experimental purposes in organic chemistry and pharmacology.\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: 136725-55-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory requirements\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\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity. Since it is a solid, it should be kept in a well-ventilated area to avoid any potential chemical interactions. Laboratory personnel should handle it with care, using appropriate personal protective equipment when necessary. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in experiments. Proper labeling and storage practices help maintain the integrity of the material and ensure safe handling in a laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087078633690,"sku":"TCI2510F134631497","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087078666458,"sku":"TCI2510F134631498","price":7874000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1346.jpg?v=1767114361"},{"product_id":"tci2510h086733575","title":"TCI H0867 17342-08-4 (S)-5-(Hydroxymethyl)-2-pyrrolidinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0867 (S)-5-(Hydroxymethyl)-2-pyrrolidinone is a five-membered lactam carrying a hydroxymethyl group at the five position with a defined (S) configuration. The compound belongs to the chiral building block family, meaning it is an intermediate that already carries stereochemical information, so researchers do not need to construct the chiral centre from scratch. In organic synthesis laboratories, this material serves as the basic framework for assembling target molecules that require a pyrrolidinone ring, for example alkaloid derivatives, cyclic amino acid analogues, and the various chiral auxiliaries used in stereoselective reactions.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound a frequent choice is the combination of two orthogonal functional groups within one small molecule, namely a cyclic amide and a primary alcohol. Its primary hydroxyl group is readily activated through tosylation, oxidation, or protection with a silyl group, while the lactam nitrogen can be alkylated or acylated to extend the chain. The preserved enantiomeric purity allows the compound to be used as a single source of chirality, so the configuration of the final product can be planned from the very beginning of the synthetic route without expensive and wasteful resolution steps.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically requested by university research groups and institutional laboratories working on asymmetric synthesis, natural product chemistry, and medicinal chemistry programmes. It is generally ordered in small research quantities for multi-step route development, method optimisation, and postgraduate thesis work, where a reliable stereochemical starting point shortens the overall sequence and reduces the number of purification stages needed before the target molecule is reached.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlkaloid derivative synthesis: the intact pyrrolidinone ring provides the nitrogen heterocycle core directly, so the route can begin from an already assembled chiral scaffold rather than building one.\u003c\/li\u003e\n\u003cli\u003eCyclic amino acid analogue preparation: the lactam and pendant hydroxymethyl arm map cleanly onto the backbone of constrained amino acid targets used in peptide modification studies.\u003c\/li\u003e\n\u003cli\u003eChiral auxiliary preparation: the defined (S) centre transfers stereochemical information to subsequent bond-forming steps, making it suitable for auxiliaries applied in stereoselective reaction development.\u003c\/li\u003e\n\u003cli\u003eSelective functional group transformation studies: the orthogonal cyclic amide and primary alcohol allow tosylation, oxidation, or silyl protection to be examined independently on one small substrate.\u003c\/li\u003e\n\u003cli\u003eMulti-step asymmetric route development: single-source chirality lets the final configuration be planned from the outset, removing costly resolution steps from the overall synthetic sequence.\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: 17342-08-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eCatalogue code: H0867\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research pack sizes; please confirm the specific size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: store according to the conditions stated on the manufacturer label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container in a cool, dry, and well-ventilated area, tightly closed and protected from moisture and direct sunlight, following the conditions printed on the manufacturer label and safety data sheet. Keep the material in its original supplier container or in a compatible, clearly labelled chemical bottle with a secure closure. Handle in a fume hood using standard personal protective equipment, including safety glasses, a laboratory coat, and suitable chemical-resistant gloves. Avoid contact with skin and eyes and avoid inhaling dust or vapour. Because the compound is used as a source of chirality, minimise prolonged exposure to air and humidity, close the container promptly after weighing, and consult the safety data sheet before handling, waste disposal, or any spill response.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087240507610,"sku":"TCI2510H086733575","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087240540378,"sku":"TCI2510H086733576","price":3610000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0867.jpg?v=1767117139"},{"product_id":"tci2510h093333682","title":"TCI H0933 48172-10-7 (S)-(+)-2-Hydroxy-4-phthalimidobutyric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(+)-2-Hydroxy-4-phthalimidobutyric Acid is a chiral building block that carries a defined stereogenic centre at the carbon bearing the hydroxyl group, together with a terminal amino group already masked as a phthalimide. The structure combines three elements that asymmetric synthesis chemists need at once: stereochemical purity established from the outset, a carboxylic acid function ready for coupling, and an amine group kept safely hidden until the moment it is to be revealed. Its primary role in the laboratory is to deliver a chiral side chain into a target molecule without the chemist having to perform the asymmetric induction step independently.\u003c\/p\u003e\n\u003cp\u003eThe property that most often drives its selection is the reliability of the phthalimide protection. This group is robust towards a wide range of reaction conditions, including acidic media, so the amine does not interfere during activation and coupling of the carboxylic acid, yet it can be removed cleanly at a late stage using hydrazine or an equivalent method. The S configuration at the hydroxyl-bearing carbon survives ordinary transformations because that centre is not prone to epimerisation. The compound is a crystalline solid and dissolves in polar organic solvents such as dimethylformamide, which suits it to standard solution-phase coupling chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this material is typically found in university and institutional research groups working on asymmetric synthesis, medicinal chemistry, and peptide-related chemistry, as well as in pharmaceutical development laboratories building chiral intermediates. It is usually handled in small quantities on the milligram to gram scale within multi-step synthetic sequences, where a stereochemically defined starting material shortens the route and removes the need to develop and validate an in-house asymmetric induction step.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChiral side-chain introduction: the defined S centre is installed directly into the target molecule, sparing the chemist from designing, optimising, and validating a separate asymmetric induction step in the route.\u003c\/li\u003e\n\u003cli\u003ePeptide and peptidomimetic assembly: the free carboxylic acid is ready for standard activation and coupling while the phthalimide keeps the terminal amine from competing during amide bond formation.\u003c\/li\u003e\n\u003cli\u003eMulti-step medicinal chemistry sequences: the phthalimide withstands acidic and many other reaction conditions, allowing several synthetic operations to be carried out before the amine is finally unmasked.\u003c\/li\u003e\n\u003cli\u003eOrthogonal protecting-group strategies: the amine is liberated cleanly with hydrazine or an equivalent method at a late stage, giving a deprotection step that is independent of acid-labile protecting groups.\u003c\/li\u003e\n\u003cli\u003eStereochemically demanding intermediate preparation: the hydroxyl-bearing centre resists epimerisation through routine transformations, so enantiomeric integrity is carried through the sequence to the final product.\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: 48172-10-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the manufacturer's standard research-scale pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: crystalline solid, soluble in polar organic solvents such as dimethylformamide\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place as directed on the manufacturer's label\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 incompatible reagents, following the storage conditions stated on the manufacturer's label and safety data sheet. Amber glass or the supplier's original packaging is suitable; ensure the container is resealed promptly after each use to limit moisture uptake by the crystalline solid. Weigh and transfer the compound in a fume hood using clean, dry spatulas, and wear a laboratory coat, safety glasses, and chemical-resistant gloves. Avoid generating dust during handling, keep solutions labelled and dated, and dispose of residues and contaminated consumables through the laboratory's established chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087244636378,"sku":"TCI2510H093333682","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0933.jpg?v=1767117254"},{"product_id":"tci2510h120033964","title":"TCI H1200 253129-03-2 (3R,4R)-1-Benzyl-4-hydroxy-3-pyrrolidinemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(3R,4R)-1-Benzyl-4-hydroxy-3-pyrrolidinemethanol is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in the development of bioactive compounds, particularly in pharmaceutical and organic chemistry research. Its chiral nature allows for the formation of enantiomers, which is essential in processes requiring precise stereochimical control. As a key component in synthetic pathways, it supports the creation of molecules with specific biological activities.\u003c\/p\u003e\n\u003cp\u003eThe compound's ability to interact with various functional groups makes it highly versatile in chemical synthesis. Its structural characteristics enable it to participate in a wide range of reactions, making it a preferred choice for researchers aiming at high precision in their experiments. The compound's stability under controlled conditions further enhances its usability in laboratory settings. Its adaptability and reliability in synthetic applications contribute to its popularity among scientists working in advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in academic institutions and research centers focused on drug development and bioactive compound synthesis. Its availability supports the needs of experimental work, enabling researchers to conduct studies with a high degree of accuracy and reproducibility. The compound's role in advancing chemical innovation makes it an essential tool for scientific inquiry 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 selective formation of enantiomers in complex molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: Its use in creating bioactive molecules makes it a key component in pharmaceutical research, supporting the design of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is widely used in organic chemistry experiments, particularly in the development of new chemical structures and functional group transformations.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery Programs: The compound's ability to participate in diverse reactions supports drug discovery efforts, aiding in the synthesis of potential drug candidates.\u003c\/li\u003e\n\u003cli\u003eStereoselective Reactions: Its chiral nature makes it suitable for stereoselective reactions, allowing for precise control over the stereochemistry of the final product.\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: 253129-03-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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\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 to prevent exposure to air and humidity, which could affect its stability. In laboratory settings, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize inhalation risks. It is important to ensure that the storage area is secure and accessible only to authorized personnel. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087260233946,"sku":"TCI2510H120033964","price":5729000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1200.jpg?v=1767117606"},{"product_id":"tci2510h124134006","title":"TCI H1241 66673-40-3 (R)-5-(Hydroxymethyl)-2-pyrrolidinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H1241, CAS 66673-40-3, is (R)-5-(Hydroxymethyl)-2-pyrrolidinone, a chiral organic compound that serves as a fundamental building block in asymmetric synthesis. Its structure combines a five-membered lactam ring (2-pyrrolidinone) with a hydroxymethyl group at the 5-position, presenting two distinct reactive sites within a single compact molecule. In organic chemistry research laboratories, a compound of this type becomes a starting point for researchers who want to construct complex molecules with controlled stereochemical configuration, particularly in drug discovery programmes and chiral catalyst development work.\u003c\/p\u003e\n\u003cp\u003eThe principal characteristic that makes this material a preferred choice is its stereochemical purity. The clearly defined (R) configuration allows researchers to carry chirality information from the starting material through to the final product without requiring expensive and material-wasteful racemic resolution steps. The primary hydroxyl group on the side chain is readily derivatised through esterification, etherification, tosylation, or oxidation, while the lactam nitrogen can be alkylated or protected according to the requirements of the synthetic route. This combination of two orthogonal reactive points is precisely what gives the compound its high degree of flexibility in multi-step synthetic planning.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, materials of this type are generally used within university research groups, chemistry postgraduate programmes, and pharmaceutical research and development divisions working on stereoselective synthesis. The compound is typically ordered in research-scale quantities for route exploration, method development, and the preparation of intermediates that will be carried forward into subsequent reaction steps. Its role is as a chiral starting material whose configuration is retained throughout the synthetic sequence being developed.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis route development — the defined (R) configuration lets researchers establish stereochemistry at the outset rather than relying on downstream resolution of racemic mixtures.\u003c\/li\u003e\n\u003cli\u003eChiral building block for drug discovery — the pyrrolidinone core appears widely in bioactive scaffolds, making this a practical entry point for constructing stereochemically defined candidate molecules.\u003c\/li\u003e\n\u003cli\u003eChiral catalyst and ligand preparation — both the hydroxyl group and the lactam nitrogen can be modified to build ligand frameworks that transfer chirality in catalytic transformations.\u003c\/li\u003e\n\u003cli\u003eSelective derivatisation studies — the primary hydroxyl undergoes esterification, etherification, tosylation, or oxidation, allowing systematic comparison of reaction conditions on a single well-defined substrate.\u003c\/li\u003e\n\u003cli\u003eProtecting group strategy work — the lactam nitrogen can be alkylated or protected independently of the side chain, supporting orthogonal protection schemes in multi-step synthetic sequences.\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: 66673-40-3\u003c\/li\u003e\n\u003cli\u003eChemical name: (R)-5-(Hydroxymethyl)-2-pyrrolidinone\u003c\/li\u003e\n\u003cli\u003eCatalogue code: H1241\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale packaging; please confirm the currently available sizes when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: 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 the container tightly closed in a cool, dry, well-ventilated area away from direct sunlight and sources of heat or ignition, 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, clearly labelled closed container if transfer is necessary, and minimise exposure to atmospheric moisture during weighing. Handle in a fume hood using appropriate personal protective equipment, including gloves, safety goggles, and a laboratory coat. Avoid contact with skin and eyes and avoid inhalation of dust. Review the safety data sheet before first use, and dispose of residues and contaminated materials through the laboratory's chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087262396634,"sku":"TCI2510H124134006","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087262429402,"sku":"TCI2510H124134007","price":5427000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1241.jpg?v=1767117647"},{"product_id":"tci2510h136834202","title":"TCI H1368 68108-18-9 (S)-(-)-4-Hydroxy-2-pyrrolidone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(-)-4-Hydroxy-2-pyrrolidone is a five-membered lactam bearing a hydroxyl group at the four position with a defined, pre-established stereochemical configuration. As a chiral building block, this compound occupies an important position in asymmetric synthesis laboratories because it supplies a stereogenic centre that is already formed from the outset. Researchers do not need to undertake racemic resolution steps or costly and time-consuming asymmetric catalysis; instead, they can build the target molecule directly onto a framework whose optical purity has been preserved from the moment the starting material arrives in the laboratory.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material especially valuable is the presence of two complementary reactive sites within a small molecule: a secondary hydroxyl group that can be esterified, oxidised, or converted into a leaving group, and a lactam nitrogen that can be alkylated or acylated. Its compact molecular size keeps the contribution to the mass of the target molecule efficient, while the pyrrolidinone framework is widely recognised as a core that appears frequently in bioactive molecules. The preserved enantiomeric purity makes it a dependable reference point when the final synthetic product must meet stereochemical requirements.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on asymmetric synthesis, medicinal chemistry, and the preparation of enantiomerically defined intermediates. It suits work where a reliable chiral starting material shortens a synthetic route and where the stereochemical integrity of the final product must be demonstrable. Supplied by AMI Scientific under the TCI brand, it serves both teaching-linked research activities and dedicated synthetic chemistry programmes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis route development: the pre-set stereogenic centre removes the need for racemic resolution or expensive asymmetric catalysis steps, shortening the overall route to the target molecule.\u003c\/li\u003e\n\u003cli\u003eChiral intermediate preparation: the secondary hydroxyl group can be esterified, oxidised, or converted into a leaving group, giving chemists several complementary directions from a single starting material.\u003c\/li\u003e\n\u003cli\u003eLactam nitrogen functionalisation studies: the nitrogen can be alkylated or acylated independently of the hydroxyl group, allowing selective derivatisation strategies to be explored on one compact framework.\u003c\/li\u003e\n\u003cli\u003eBioactive scaffold construction: the pyrrolidinone core appears frequently in biologically active molecules, making this compound a practical entry point for building such frameworks with defined stereochemistry.\u003c\/li\u003e\n\u003cli\u003eEnantiomeric purity reference work: preserved optical purity makes the material a dependable point of comparison when the stereochemical requirements of a final synthetic product must be verified.\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: H1368\u003c\/li\u003e\n\u003cli\u003eCAS number: 68108-18-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale pack sizes listed by the manufacturer; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: 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 the container tightly closed in a cool, dry place away from direct sunlight, moisture, and incompatible materials, following the storage conditions stated on the manufacturer's label and safety data sheet. Keep the material in its original supplied container, or transfer it only into clean, chemically compatible and clearly labelled containers. Handle in a well-ventilated area or fume hood, wearing a laboratory coat, safety glasses, and suitable gloves. Because the compound is hygroscopic-sensitive chemistry of this type depends on dry conditions, minimise the time the container stays open and close it promptly after weighing. Consult the safety data sheet before first use and dispose of residues through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087281008858,"sku":"TCI2510H136834202","price":1566000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1368.jpg?v=1767117903"},{"product_id":"tci2510h165634568","title":"TCI H1656 132127-34-5 (3R,4S)-3-Hydroxy-4-phenyl-2-azetidinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(3R,4S)-3-Hydroxy-4-phenyl-2-azetidinone is a chiral building block widely used in asymmetric synthesis to create compounds with specific stereochemistry. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of bioactive molecules. Its unique molecular structure, featuring both hydroxyl and phenyl groups, allows for versatile chemical reactions and functional group modifications. As a key intermediate, it supports the synthesis of complex molecules requiring precise stereocontrol, making it an essential tool for researchers in medicinal chemistry and pharmaceutical development.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and reactivity make it a preferred choice for synthetic chemists. Its ability to participate in various reaction mechanisms, such as nucleophilic substitution and ring-opening reactions, enhances its utility in the laboratory. The 3R,4S configuration ensures that the resulting products maintain the desired stereochemistry, which is vital for pharmaceutical applications where biological activity depends on molecular structure. This makes it a reliable and efficient reagent for advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmacological studies and the synthesis of bioactive compounds. Its application is widespread in academic and industrial settings focused on developing new drugs and therapeutic agents. The compound’s versatility and specificity make it a valuable resource for researchers aiming to achieve precise stereochemical control in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research due to its chiral configuration and reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise stereocontrol for drug molecule development.\u003c\/li\u003e\n\u003cli\u003eSynthesis of bioactive compounds in medicinal chemistry laboratories.\u003c\/li\u003e\n\u003cli\u003eResearch into novel drug candidates with specific stereochemical requirements.\u003c\/li\u003e\n\u003cli\u003eDevelopment of complex organic molecules in academic and industrial 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: 132127-34-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (exact form may vary based on supplier)\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 may affect its stability. In laboratory settings, proper personal protective equipment (PPE) such as gloves and safety goggles should be worn when handling this material to ensure safety. It should be kept in a well-ventilated area to minimize inhalation risks. Avoid contact with incompatible substances to prevent any potential chemical reactions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48087311941850,"sku":"TCI2510H165634568","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087311974618,"sku":"TCI2510H165634569","price":2702000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1656.jpg?v=1767118331"},{"product_id":"tci2510i039035507","title":"TCI I0390 5306-85-4 Isosorbide Dimethyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIsosorbide Dimethyl Ether (IDME), with the CAS number 5306-85-4, is a chemical compound widely used in organic reactions, particularly in asymmetric synthesis. This compound plays a crucial role in laboratory settings where the creation of chiral molecules is essential. IDME serves as a valuable chiral building block, enabling the synthesis of complex organic structures with high stereochemical control. Its importance is especially evident in pharmaceutical research, where the development of new drugs often requires precise molecular configurations.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of IDME make it a preferred choice for researchers. It exhibits both stability and reactivity, allowing it to participate in a variety of chemical reactions under different conditions. The molecular structure of IDME supports the formation of new bonds with various reagents, enhancing its versatility in synthetic pathways. These characteristics make it a reliable and efficient material for laboratories aiming to achieve high yields and specificity in their chemical processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, IDME is extensively used in chemical and pharmaceutical research. It is a key component in the synthesis of new compounds with potential medical or industrial applications. Due to its reliable performance in chemical reactions, IDME is a sought-after material among researchers and scientists working in the field of asymmetric synthesis and drug development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: IDME is ideal for creating chiral molecules due to its structural properties and reactivity, enabling precise stereochemical control in complex organic reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its role in synthesizing new compounds with medical potential makes it a vital material for drug development and chemical innovation.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: IDME supports the formation of new bonds with various reagents, making it suitable for a wide range of synthetic pathways in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Production: The compound's stability and reactivity make it a preferred choice for producing specialized chemicals used in various industrial applications.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: IDME is frequently used in academic institutions for teaching and research, providing students and scientists with a reliable tool for exploring chemical reactions and molecular 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: 5306-85-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\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\u003eIDME should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Always ensure proper ventilation when working with this compound to minimize exposure. Regularly check the container for any signs of leakage or degradation to maintain the integrity of the material. Proper storage and handling practices are essential to ensure the safety of laboratory personnel and the effectiveness of the compound in chemical processes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087375741146,"sku":"TCI2510I039035507","price":1515000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0390.jpg?v=1767119556"},{"product_id":"tci2510i058035796","title":"TCI I0580 240408-78-0 (R,R,R)-Triglycidyl Isocyanurate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R,R,R)-Triglycidyl Isocyanurate is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. It plays a crucial role in chemical laboratories where precise control over stereochemistry is essential. This material is particularly valuable in organic chemistry research, enabling the synthesis of chiral compounds with high enantiomeric purity. Its unique molecular structure allows for specific reactivity under various reaction conditions, making it an indispensable tool for researchers working on stereoselective reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and predictable reactivity, which simplifies the synthesis process in laboratory settings. Its chiral nature ensures that it can be used effectively in applications requiring stereochiral control, such as pharmaceutical development and the creation of complex organic molecules. This makes it a preferred choice for chemists aiming to achieve high selectivity and efficiency in their synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (R,R,R)-Triglycidyl Isocyanurate is commonly used in organic chemistry research, especially in asymmetric synthesis and the development of new compounds. It is frequently employed by research institutions and universities to meet the demands of chemical and pharmaceutical studies. Its availability in solid form facilitates easy handling and integration into various chemical reactions, enhancing its practicality in laboratory environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis for the creation of complex organic compounds due to its chiral structure and stereoselective reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development where precise stereochemical control is necessary for drug molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research for building molecular frameworks with high enantiomeric purity.\u003c\/li\u003e\n\u003cli\u003eChiral Compound Synthesis to produce enantiomerically pure substances used in various scientific applications.\u003c\/li\u003e\n\u003cli\u003eAcademic Research in Indonesian universities for teaching and experimental purposes in synthetic chemistry.\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: 240408-78-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\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\u003eThis compound 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 chiral nature, it is important to handle it with care to avoid any unintended stereochemical changes during synthesis. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard laboratory safety protocols when handling this material to ensure safe and efficient use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087396155610,"sku":"TCI2510I058035796","price":1768000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0580.jpg?v=1768819117"},{"product_id":"tci2510i058135797","title":"TCI I0581 240408-81-5 (S,S,S)-Triglycidyl Isocyanurate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S,S,S)-Triglycidyl Isocyanurate is a chiral building block widely used in asymmetric synthesis and organic chemistry research. This compound plays a crucial role in the development of optically active molecules, which are essential in pharmaceutical and materials science applications. Its complex molecular structure enables the formation of compounds with high optical activity, making it a valuable tool for chemists seeking to control stereochemistry in synthetic pathways. In the laboratory, it serves as a versatile reagent that supports the creation of complex molecular architectures with precise stereochemical control.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and reactivity under various reaction conditions. Its unique molecular structure, consisting of three glycidyl units and one isocyanate group, allows it to participate in a range of reactions, including Michael additions and asymmetric couplings. These properties make it an ideal choice for researchers aiming to achieve specific stereochemical outcomes in their synthetic processes. Its ability to maintain structural integrity while being reactive under controlled conditions ensures reliable performance in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S,S,S)-Triglycidyl Isocyanurate is commonly used in organic chemistry research, particularly in the field of asymmetric synthesis. It is a preferred material for studies involving chiral molecule construction and the development of optically active compounds. Its application is widespread in academic and industrial research settings where precise control over molecular structure is required.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating optically active molecules due to its chiral structure and reactivity in asymmetric reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is widely used in the synthesis of complex organic molecules, supporting the development of new chemical compounds with specific stereochemistry.\u003c\/li\u003e\n\u003cli\u003eChiral Building Block Applications: Its molecular framework allows for the construction of diverse chiral compounds, making it a key reagent in synthetic chemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: The compound's ability to form optically active products makes it useful in drug synthesis and related research.\u003c\/li\u003e\n\u003cli\u003eMolecular Structure Studies: It is employed in investigations requiring precise control over molecular configuration and stereochemistry.\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: 240408-81-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\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 chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances to ensure safe laboratory practices. Proper storage conditions help preserve its structural integrity and reactivity for extended use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087396188378,"sku":"TCI2510I058135797","price":1363000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0581.jpg?v=1767119968"},{"product_id":"tci2510l015037056","title":"TCI L0150 37112-31-5 Levoglucosenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eLevoglucosenone (LGVN), with the CAS number 37112-31-5, is an organic compound known for its complex structure and significant role in asymmetric synthesis. As a chiral building block, it is widely used in chemical reactions to produce compounds with specific asymmetric structures. Its importance spans across various fields, including pharmaceutical development, industrial chemistry, and material research. In the laboratory, LGVN serves as a foundational reagent for reactions requiring precise stereochimical control, making it indispensable in advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eThe chemical stability and reactivity of LGVN make it a preferred choice for researchers. It exhibits favorable properties that allow for effective substitution and reduction reactions under controlled conditions. Its ability to withstand specific reaction environments minimizes side reactions, ensuring higher yields and purity in the final products. These characteristics make LGVN a reliable and efficient reagent for complex molecular synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, LGVN is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new compounds. Its application is prevalent in studies requiring high precision in structural control. Researchers rely on LGVN for its consistent performance and adaptability in various synthetic pathways, supporting innovation in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis applications benefit from LGVN’s chiral properties, enabling the creation of enantiomerically pure compounds with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research utilizes LGVN for its stability and reactivity, supporting the synthesis of complex molecular structures with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development relies on LGVN to produce chiral intermediates, which are essential for drug molecule design and optimization.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate LGVN for its versatility in synthetic pathways, contributing to the production of specialty chemicals and materials.\u003c\/li\u003e\n\u003cli\u003eMaterial science research uses LGVN as a building block for creating advanced polymers and functional materials with specific stereochemical properties.\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: 37112-31-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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\u003eLevoglucosenone 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 could affect its reactivity. For optimal preservation, it should be stored away from heat sources and direct sunlight to avoid any potential decomposition. In laboratory settings, it is important to handle LGVN with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Proper labeling of containers is also essential to prevent accidental misuse. Regular monitoring of storage conditions ensures the integrity of the compound remains intact for use in chemical synthesis processes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087484235994,"sku":"TCI2510L015037056","price":4468000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087484268762,"sku":"TCI2510L015037057","price":15370000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510L0150.jpg?v=1769142805"},{"product_id":"tci2510l020737118","title":"TCI L0207 1200-22-2 (R)-alpha-Lipoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI L0207 (R)-alpha-Lipoic Acid is the single-enantiomer form of lipoic acid, a cyclic sulfur compound that occurs naturally as an essential cofactor in the enzyme complexes of energy metabolism, including pyruvate dehydrogenase. Unlike a racemic mixture, this preparation presents the R configuration, which is the biologically active form of the molecule. In the laboratory, the compound is used both as a chiral building block for asymmetric synthesis and as a test substance in biochemical research examining redox processes inside the cell, where defined stereochemistry is a requirement rather than a convenience.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of this material lies in its dithiolane group, a five-membered ring containing two sulfur atoms, which can convert reversibly between its oxidised and reduced forms. This reversible redox behaviour is precisely what has made lipoic acid known as an antioxidant capable of acting in both aqueous and lipid environments. In addition, the molecule carries a carboxylic acid group at the end of its chain, so it is readily conjugated into esters or amides for further synthetic work. High enantiomeric purity matters here because the R and S forms do not display identical biological behaviour.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically encountered in university and institutional research groups working on asymmetric synthesis, natural product chemistry, and cellular biochemistry. Because the compound is sensitive to light and heat, it is normally handled in facilities that can provide controlled storage and protected working conditions. It is usually weighed out in small portions for synthesis or assay work rather than kept in open bulk containers on the bench.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChiral building block in asymmetric synthesis, where the defined R configuration and the reactive carboxylic acid terminus allow controlled elaboration into stereochemically pure target molecules.\u003c\/li\u003e\n\u003cli\u003eRedox biochemistry research, since the dithiolane ring converts reversibly between oxidised and reduced states and therefore serves as a well-characterised probe of cellular redox processes.\u003c\/li\u003e\n\u003cli\u003eAntioxidant studies in mixed media, because lipoic acid is active in both aqueous and lipid environments and suits experiments that span the two phases.\u003c\/li\u003e\n\u003cli\u003eEnzyme cofactor investigations relating to energy metabolism, including work on pyruvate dehydrogenase and the other complexes in which lipoic acid naturally participates.\u003c\/li\u003e\n\u003cli\u003ePreparation of esters and amides for downstream synthesis, using the terminal carboxylic acid group as a straightforward handle for conjugation to other molecular fragments.\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: 1200-22-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: L0207\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed by TCI for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: sensitive to light and heat; keep protected from both\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container protected from light and away from sources of heat, in a cool location consistent with the supplier's stated conditions for this item. Amber glass or an opaque secondary container is appropriate, and the vessel should be kept tightly closed to limit exposure to air and moisture. Handle the material in a well-ventilated area or fume hood, wearing gloves, safety glasses, and a laboratory coat. Use clean, dry spatulas when weighing, return the container to storage promptly after use, and consult the manufacturer's safety data sheet before first handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087488135386,"sku":"TCI2510L020737118","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087488168154,"sku":"TCI2510L020737119","price":6361000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087488200922,"sku":"TCI2510L020737120","price":15875000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510L0207.jpg?v=1767121541"},{"product_id":"tci2510l023837164","title":"TCI L0238 100986-89-8 Levofloxacin Q-Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eLevofloxacin Q-Acid (TCI L0238), with CAS number 100986-89-8, is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This material plays a crucial role in the laboratory by enabling the synthesis of complex organic compounds with precise stereochemistry. Its chiral nature allows for the creation of enantiomerically pure substances, which are essential in pharmaceutical and medicinal chemistry research. As a key building block, it supports the development of new therapeutic agents and advanced chemical structures.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chiral structure and high purity make it a preferred choice for researchers seeking precise control over molecular configuration. Its stability and availability in pure form ensure reliable results in synthetic processes. These properties are particularly valuable in applications requiring high accuracy and reproducibility. The compound’s ability to participate in asymmetric reactions makes it an essential tool for scientists working on drug development and organic synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Levofloxacin Q-Acid is commonly used in pharmaceutical and organic chemistry research. It is a fundamental component in the development of new medicinal compounds and is utilized by academic institutions and research centers. Its role in creating bioactive molecules supports advancements in medical science and chemical innovation within the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: Levofloxacin Q-Acid is ideal for asymmetric synthesis due to its chiral structure, enabling the creation of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its use in drug development supports the synthesis of bioactive molecules with specific therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: The compound is widely used in organic synthesis to build complex molecular frameworks with precise stereochemistry.\u003c\/li\u003e\n\u003cli\u003eMedicinal Chemistry Applications: It facilitates the design of new drugs by allowing controlled stereochemical outcomes in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: Indonesian universities and research institutions rely on this compound for teaching and experimental studies in advanced chemistry.\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: 100986-89-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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\u003eLevofloxacin Q-Acid should be stored in a cool, dry environment to maintain its stability and purity. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Proper disposal methods should be followed to ensure compliance with safety regulations. The compound is not inherently hazardous under normal storage conditions but requires careful handling to maintain its integrity and effectiveness in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087490232538,"sku":"TCI2510L023837164","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087490265306,"sku":"TCI2510L023837165","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510L0238.jpg?v=1767121605"},{"product_id":"tci2510m110739059","title":"TCI M1107 139015-33-1 (3R)-(+)-3-(Methylamino)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M1107 (3R)-(+)-3-(Methylamino)pyrrolidine is a chiral building block consisting of a pyrrolidine ring bearing a methylamino group at the 3-position in a defined R configuration. The compound belongs to the family of cyclic diamines that are highly sought after in medicinal chemistry, because it provides two nitrogen centres of differing reactivity together with a stereogenic centre that determines the three-dimensional shape of the final molecule. In the synthesis of bioactive compounds, the absolute configuration at this position is frequently the factor that decides whether a molecule binds optimally to its biological target.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a preferred choice is its defined chiral purity from the very beginning of the synthetic route. By starting from a single-enantiomer material, researchers avoid the complexity of resolving a racemate at a late stage, a process that normally consumes time and cost while sacrificing half of the material. The ring nitrogen, a secondary amine, is strongly nucleophilic and is commonly used in nucleophilic aromatic substitution as well as metal-catalysed cross-coupling, while the methylamino group on the side chain offers a second point of functionalisation. The strong basicity of both nitrogen atoms also facilitates salt formation and purification handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in academic and industrial research groups working on asymmetric synthesis, medicinal chemistry, and the preparation of pharmaceutical intermediates. It is generally ordered in small quantities appropriate to exploratory route development, where a stereochemically defined starting material shortens the path to a target scaffold. University research laboratories, pharmaceutical R\u0026amp;D units, and contract synthesis facilities are the usual settings in which this reagent is applied.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis route development — the defined R configuration is fixed at the outset, so the stereochemical outcome of the target molecule is controlled without any later resolution step.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry scaffold construction — the cyclic diamine framework gives two nitrogen handles with different reactivity, allowing sequential and selective elaboration of a drug-like core structure.\u003c\/li\u003e\n\u003cli\u003eNucleophilic aromatic substitution reactions — the strongly nucleophilic secondary ring nitrogen readily displaces suitable leaving groups on activated aromatic systems to build nitrogen-linked architectures.\u003c\/li\u003e\n\u003cli\u003eMetal-catalysed cross-coupling chemistry — the ring nitrogen serves as a coupling partner in catalytic amination chemistry, introducing the chiral pyrrolidine unit directly onto an aryl framework.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical intermediate preparation — starting from a single-enantiomer building block avoids racemate separation at the final stage, saving time and cost and preserving material that would otherwise be discarded.\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: 139015-33-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical class: cyclic diamine \/ chiral pyrrolidine building block\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale pack sizes supplied by TCI; please confirm the available option when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: 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 the container tightly closed in a cool, dry, well-ventilated place, following the storage conditions stated on the manufacturer's label and safety data sheet. Amine compounds of this type are generally kept in their original tightly sealed container, protected from moisture and from prolonged exposure to air, and away from acids and other incompatible materials. Handle inside a fume hood using appropriate personal protective equipment, including safety glasses, chemical-resistant gloves, and a laboratory coat. Both nitrogen centres are strongly basic, so avoid contact with skin and eyes and prevent the generation of vapours. Return the container promptly to its designated storage location after use, and consult the safety data sheet before any handling, transfer, or disposal operation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087586078938,"sku":"TCI2510M110739059","price":3736000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087586111706,"sku":"TCI2510M110739060","price":11912000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1107.jpg?v=1767124330"},{"product_id":"tci2510m110839061","title":"TCI M1108 139015-32-0 (3S)-(-)-3-(Methylamino)pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(3S)-(-)-3-(Methylamino)pyrrolidine is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activity. This compound plays a crucial role in the development of pharmaceuticals and bioactive chemicals, where precise molecular structure is essential. Its chiral nature allows for the formation of enantiomers, which can have distinct biological effects, making it a key component in drug discovery and chemical research. In laboratories, it is valued for its versatility and ability to participate in various synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral properties and functional group compatibility make it a preferred choice for chemists working on complex molecule synthesis. Its ability to interact with a range of functional groups enables the creation of diverse chemical structures, enhancing its utility in both academic and industrial settings. The compound's stability and solubility characteristics further contribute to its reliability in laboratory applications. These features ensure that it remains a valuable tool for researchers aiming to develop new compounds with targeted biological activity.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (3S)-(-)-3-(Methylamino)pyrrolidine is commonly used by pharmacists and chemists for the development of new compounds, testing biological activity, and studying chemical reaction mechanisms. Its availability supports complex experiments and research projects, making it an essential material for scientific innovation 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 creating enantiomerically pure compounds, which are essential in pharmaceutical development due to their specific biological activity.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery: Its chiral structure allows for the synthesis of bioactive molecules, supporting research into new therapeutic agents with targeted effects.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: The compound's ability to form various isomers makes it useful in studying molecular interactions and reaction mechanisms in biological systems.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: It serves as a versatile starting material for constructing complex organic molecules, enhancing the scope of synthetic chemistry projects.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is frequently used in university and research institutions for teaching and exploring advanced synthetic methodologies in chemistry.\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: 139015-32-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on the specific product variant\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 made of glass or high-density polyethylene to prevent contamination and maintain stability. Due to its chiral nature, it is important to handle the compound with care to avoid any unintended isomer formation during synthesis. Always ensure proper ventilation when working with this material, and wear appropriate personal protective equipment such as gloves and safety goggles. The compound is generally stable under standard laboratory conditions, but it is advisable to follow the supplier’s guidelines for optimal storage and handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087586144474,"sku":"TCI2510M110839061","price":4342000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087586177242,"sku":"TCI2510M110839062","price":14235000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1108.jpg?v=1767124334"},{"product_id":"tci2510m117039141","title":"TCI M1170 121817-71-8 (R)-(+)-2-(Methoxymethyl)-1-pyrrolidinecarboxaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(+)-2-(Methoxymethyl)-1-pyrrolidinecarboxaldehyde is the N-formyl derivative of a chiral pyrrolidine bearing a methoxymethyl group. Adding the formyl group to the nitrogen atom converts the free amine into a protected amide, so this compound functions as a chiral building block whose nitrogen is already capped and no longer nucleophilic. In asymmetric synthesis laboratories, a protected form of this kind matters because it allows transformations to be carried out on other parts of the molecule without interference from side reactions of the amine, while preserving the integrity of the stereogenic centre throughout a sequence of steps.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes it a preferred choice is its better chemical stability compared with the parent free amine. The formyl group lowers the basicity of the nitrogen, so the compound is more resistant to air oxidation and to absorption of carbon dioxide. At the same time, the formyl amide belongs to the class of protecting groups that are relatively easy to remove again by hydrolysis under controlled conditions, so the chiral pyrrolidine can be recovered when required. The amide bond, with its hindered rotation, also produces a rigid conformation, which is in fact an advantage in directing stereochemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, the (R) configuration matters because the material is used where a defined single enantiomer is the whole point of the purchase. It is typically handled in university and institutional research groups working on asymmetric synthesis, and in method development work where a protected chiral pyrrolidine is carried through a multi-step route. Quantities are usually modest, consistent with research-scale rather than production-scale use.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis route development: the compound supplies a defined single-enantiomer pyrrolidine framework whose stereogenic centre survives multi-step sequences, giving reproducible stereochemical outcomes in route scouting.\u003c\/li\u003e\n\u003cli\u003eChiral building block incorporation: the methoxymethyl-substituted pyrrolidine core can be carried into larger target molecules while the capped nitrogen prevents unwanted nucleophilic participation during intermediate steps.\u003c\/li\u003e\n\u003cli\u003eProtected-amine chemistry: because the nitrogen is already present as a formyl amide, chemists can run transformations elsewhere on the molecule without a separate protection step at the start of the sequence.\u003c\/li\u003e\n\u003cli\u003eStereochemical direction studies: the hindered rotation of the amide bond produces a rigid conformation that is useful when investigating how a conformationally constrained scaffold directs the stereochemistry of a reaction.\u003c\/li\u003e\n\u003cli\u003eDeprotection and amine recovery work: the formyl group can be removed again by hydrolysis under controlled conditions, allowing the free chiral pyrrolidine to be regenerated when a route requires it.\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\u003eCatalogue reference: M1170\u003c\/li\u003e\n\u003cli\u003eCAS number: 121817-71-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: research-scale laboratory packs; please confirm the available pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in a tightly closed container, 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 and well-ventilated area, away from moisture and from sources of heat or ignition. Keep the material in its original supplier container, or in a chemically compatible sealed glass container that is clearly labelled with the compound name and CAS number. Handle in a fume hood using standard laboratory personal protective equipment, including safety glasses, gloves and a laboratory coat. Because the formyl amide is susceptible to hydrolysis, minimise exposure to atmospheric moisture by closing the container promptly after use. Consult the manufacturer's safety data sheet before first use, and dispose of residues through the laboratory's established chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087590076634,"sku":"TCI2510M117039141","price":1389000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1170.jpg?v=1767124456"},{"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":"tci2510m142439499","title":"TCI M1424 74879-18-8 (S)-(+)-2-Methylpiperazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(+)-2-Methylpiperazine is a chiral building block widely used in asymmetric synthesis, playing a crucial role in the development of complex organic molecules. This compound is essential for researchers working in pharmaceutical and organic chemistry, as it enables the creation of enantiomerically pure compounds. Its application spans various areas, including drug discovery and the synthesis of bioactive molecules. Due to its stereochemical properties, it is particularly valuable in the preparation of chiral intermediates that are critical for the synthesis of pharmaceuticals. The compound's unique structure allows for selective reactions, making it a preferred choice in modern synthetic strategies.\u003c\/p\u003e\n\u003cp\u003eOne of the key characteristics that make (S)-(+)-2-Methylpiperazine a preferred choice is its high chiral purity, which ensures consistent results in synthetic processes. Its stability under standard laboratory conditions also contributes to its reliability in various chemical reactions. The compound is known for its solubility in common organic solvents, which facilitates its use in a wide range of synthetic protocols. Additionally, its well-defined stereochemistry allows for precise control over the stereochemical outcome of reactions, making it an indispensable tool for chemists aiming to produce enantiomerically pure compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-(+)-2-Methylpiperazine is commonly used in academic and industrial research settings. It is particularly relevant in pharmaceutical research, where the development of new drugs requires the synthesis of chiral compounds. Its application supports both basic and applied research, contributing to advancements in organic chemistry and medicinal chemistry. As a key reagent in asymmetric synthesis, it is widely utilized in laboratories across Indonesia for its reliability and effectiveness in producing complex molecules.\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, essential for pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eChiral intermediate preparation benefits from its stereochemical properties, allowing for the synthesis of complex molecules with high enantiomeric purity.\u003c\/li\u003e\n\u003cli\u003eDrug discovery processes rely on this compound to create chiral compounds that are critical in the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research utilizes it for the synthesis of bioactive molecules, supporting studies on molecular structure and biological activity.\u003c\/li\u003e\n\u003cli\u003eBioactive compound testing involves using this material to evaluate the biological activity of complex organic molecules in various assays.\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: 74879-18-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 variant\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 sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Proper labeling of containers is essential to ensure safe handling and prevent cross-contamination. In laboratory settings, it is important to follow standard safety protocols, including the use of personal protective equipment when handling. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Regular monitoring of storage conditions helps maintain the integrity and effectiveness of the compound during its use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087609376986,"sku":"TCI2510M142439499","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087609409754,"sku":"TCI2510M142439500","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1424.jpg?v=1767124951"},{"product_id":"tci2510m193740021","title":"TCI M1937 104641-60-3 (R)-1-Methyl-3-pyrrolidinol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-1-Methyl-3-pyrrolidinol is a chiral compound widely used in asymmetric synthesis to construct molecules with optical activity. This material plays a crucial role in laboratories where precise stereochimical control is required, particularly in the development of pharmaceuticals and bioactive compounds. Its unique structure allows for the creation of enantiomers, making it an essential tool in the field of chiral building blocks. As a key component in asymmetric synthesis, it supports the production of complex molecules with specific spatial configurations, which are vital in drug discovery and advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and ease of handling make it a preferred choice for researchers working in organic chemistry and pharmaceutical development. Its ability to participate in various synthetic reactions without significant degradation ensures reliable results in laboratory settings. Additionally, its well-defined stereochemistry allows for reproducible outcomes, which is critical in scientific research. These properties contribute to its widespread use in both academic and industrial laboratories, where accuracy and consistency are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (R)-1-Methyl-3-pyrrolidinol is commonly used by researchers in pharmaceutical, organic chemistry, and biochemical fields. It is a fundamental reagent in the synthesis of bioactive compounds and is often incorporated into drug development projects. Its role in creating chiral molecules with specific biological activities makes it an indispensable tool for scientists working on new drug formulations and molecular modifications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for the production of optically active compounds, due to its chiral structure and stereoselective properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research and development, as it is used to create molecules with high biological activity and specific stereochemistry.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise control over molecular configuration and stereochemistry.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies involving the synthesis of chiral intermediates for drug discovery and modification.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis projects where the creation of enantiomers is essential for pharmaceutical 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: 104641-60-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, 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 sunlight and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. Due to its chiral nature, it is essential to handle the compound with care to avoid any unintended stereochemical changes. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the material. Proper ventilation should be maintained in the workspace to ensure safe handling and minimize exposure. The compound is generally non-hazardous under standard laboratory conditions but should be treated with the same caution as other chemical reagents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087637688538,"sku":"TCI2510M193740021","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087637721306,"sku":"TCI2510M193740022","price":4973000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1937.jpg?v=1768819189"},{"product_id":"tci2510m193840023","title":"TCI M1938 104641-59-0 (S)-1-Methyl-3-pyrrolidinol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-1-Methyl-3-pyrrolidinol, bearing CAS number 104641-59-0, is the enantiomeric counterpart of the R form: a cyclic amino alcohol built on a pyrrolidine ring with a methyl group on the nitrogen and a hydroxyl group at the three position, locked in the S configuration. As a chiral building block, this compound supplies a stereocentre that is already established, allowing researchers to assemble target molecules directly with controlled stereochemistry. This approach saves a significant amount of laboratory time because it avoids the resolution step required for racemic mixtures, a step that typically returns no more than half of the starting material as usable product.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound attractive is its combination of compact size and rich functionality. The tertiary amine is nucleophilic and basic, so it is readily quaternised or used as a metal coordination site, while the secondary alcohol at the three position serves as a connection point for esterification, etherification, or conversion into a leaving group. The S configuration presents a spatial orientation different from that of the R form, and it is precisely this difference in orientation that often determines whether a molecule binds strongly to its biological target. Both enantiomers are therefore frequently kept on hand for comparison.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically found in academic and industrial research groups working on asymmetric synthesis, medicinal chemistry, and the preparation of pharmaceutical intermediates. It is commonly ordered alongside the R enantiomer so that a research team can evaluate both spatial orientations within the same synthetic route and determine which one delivers the desired activity profile before committing to a larger preparation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis of target molecules, where the pre-formed S stereocentre lets chemists build stereochemically controlled products without running a separate resolution of a racemic mixture.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry and structure-activity studies, because the S spatial orientation frequently determines whether a candidate molecule binds strongly to its intended biological target compared with the R form.\u003c\/li\u003e\n\u003cli\u003ePreparation of pharmaceutical intermediates, where the compact pyrrolidine scaffold introduces a basic nitrogen and a functionalisable hydroxyl into a drug-like framework in a single step.\u003c\/li\u003e\n\u003cli\u003eDerivatisation chemistry through the secondary alcohol at position three, which serves as a handle for esterification, etherification, or conversion into a leaving group for subsequent substitution.\u003c\/li\u003e\n\u003cli\u003eLigand and metal-complex work, since the tertiary amine is both basic and nucleophilic and can act as a coordination site or be quaternised to alter the electronic character of the molecule.\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: 104641-59-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical class: cyclic amino alcohol, pyrrolidine ring with N-methyl group and hydroxyl at position three, S configuration\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the packaging options listed on this product page\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry place away from light; see handling notes below\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, protected from light and kept away from strong oxidising agents and acids. Amino alcohols are hygroscopic in character, so the original supplier bottle with an intact seal remains the most suitable container; transfer only the quantity required for immediate use and reseal the stock bottle promptly to limit exposure to atmospheric moisture. Handle in a fume hood while wearing nitrile gloves, safety glasses, and a laboratory coat, and avoid contact with skin and eyes. Consult the manufacturer's safety data sheet before first use and follow the disposal procedures set by your institution.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087637786842,"sku":"TCI2510M193840023","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087637819610,"sku":"TCI2510M193840024","price":4973000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1938.jpg?v=1767125801"},{"product_id":"tci2510m205840177","title":"TCI M2058 34381-71-0 (S)-(1-Methylpyrrolidin-2-yl)methanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-(1-Methylpyrrolidin-2-yl)methanol is a chiral building block widely used in asymmetric synthesis to construct molecules with optical activity. This compound plays a crucial role in the development of pharmaceuticals and other bioactive substances by enabling precise control over stereochemistry. Its unique structure allows it to be a key component in the synthesis of complex molecules that require strict stereochemical control. In laboratory settings, it is essential for creating compounds with specific spatial configurations, which are vital in drug discovery and development.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and high purity, making it a preferred choice for researchers working in chiral synthesis. Its ability to interact selectively with other molecules ensures that the final products maintain the desired stereochemistry. Additionally, its compatibility with various synthetic methodologies enhances its versatility in different experimental setups. These properties make it a reliable and efficient reagent for both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical, biochemical, and material science research. Local scientists and researchers frequently employ it to develop new drugs and bioactive compounds. Its role in creating molecules with specific optical properties is critical for advancing research in these fields. The compound’s reliability and effectiveness make it a standard tool in modern chemical synthesis practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules with precise stereochemical control, essential in pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It is used to synthesize bioactive compounds with specific optical properties, supporting drug discovery efforts.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its chiral nature makes it suitable for studying molecular interactions and enzyme mechanisms in biological systems.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: It serves as a key building block in the synthesis of complex organic molecules requiring stereochemical precision.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Applications: It is employed in the development of chiral materials with unique optical and chemical properties.\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: 34381-71-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\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 protocols to avoid any unintended stereochemical changes. Proper labeling and storage conditions ensure the compound remains stable and effective for extended use. Laboratory personnel should wear appropriate personal protective equipment when handling this material to ensure safety and compliance with standard operating procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087644635354,"sku":"TCI2510M205840177","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087644668122,"sku":"TCI2510M205840178","price":2853000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2058.jpg?v=1767125972"},{"product_id":"tci2510m209140227","title":"TCI M2091 75336-86-6 (R)-(-)-2-Methylpiperazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(-)-2-Methylpiperazine is a chiral compound widely used in asymmetric synthesis to construct complex molecular structures. This chemical plays a crucial role in laboratories where precise control over stereochemistry is essential. Its unique chiral configuration allows it to act as a building block in the development of pharmaceuticals and organic chemicals. As a key reagent in synthetic pathways, it supports the creation of enantiomerically pure compounds, which are vital in drug development and advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability under specific conditions and its ability to participate in nucleophilic and substitution reactions make it a preferred choice for chemists. Its chiral nature ensures that it can selectively influence reaction outcomes, enhancing the efficiency of synthetic processes. Additionally, its solid form and compatibility with various reagents make it versatile for use in a range of experimental setups. These properties contribute to its widespread application in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (R)-(-)-2-Methylpiperazine is commonly used in organic chemistry, pharmacology, and the synthesis of bioactive compounds. Its role in controlling stereochimical outcomes is particularly important in research focused on drug development and advanced chemical synthesis. The compound’s availability and reliability make it a valuable asset in scientific investigations requiring precise stereochemical control.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic chemistry research benefits from this compound's role in constructing complex molecular frameworks with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development utilizes its chiral properties to synthesize enantiomerically pure compounds essential for drug efficacy.\u003c\/li\u003e\n\u003cli\u003eBioactive compound synthesis relies on its ability to participate in nucleophilic and substitution reactions, enhancing synthetic versatility.\u003c\/li\u003e\n\u003cli\u003eAcademic research in asymmetric synthesis leverages its unique chiral configuration for precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production incorporates it as a key reagent in the creation of specialized organic compounds with specific stereochemical profiles.\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: 75336-86-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\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 place away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chiral nature, it is important to handle it with care to avoid any unintended stereochemical changes. Proper labeling of containers is essential for safe handling and to prevent mix-ups in the laboratory. Always ensure that the workspace is clean and free from potential reactive substances. When working with this material, it is advisable to use appropriate personal protective equipment to ensure safety during handling and experimentation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087647486170,"sku":"TCI2510M209140227","price":1086000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2091.jpg?v=1767126040"},{"product_id":"tci2510m215740320","title":"TCI M2157 116539-55-0 (S)-3-(Methylamino)-1-(2-thienyl)-1-propanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThe TCI M2157 116539-55-0 (S)-3-(Methylamino)-1-(2-thienyl)-1-propanol is a chiral building block used in asymmetric synthesis to produce compounds with defined stereochemistry. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of bioactive molecules. Its chiral structure allows for the creation of enantiomerically pure compounds, which are essential in pharmaceutical and medicinal research. Due to its unique molecular framework, it is a valuable tool for chemists aiming to control the stereochemical outcome of complex reactions.\u003c\/p\u003e\n\u003cp\u003eThis compound is preferred for its stability and compatibility with a wide range of reagents. Its ability to participate in various chemical reactions without undergoing unwanted side reactions makes it a reliable choice for synthetic chemists. Additionally, its solubility in organic solvents simplifies its use in laboratory settings, enabling efficient handling and reaction conditions. These properties make it a versatile and effective component in the synthesis of optically active compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the study of bioactive compound synthesis. It is widely utilized by research institutions and universities to develop new drugs or compounds with specific biological activities. Its role in creating chiral molecules is fundamental to advancing pharmaceutical and biochemical research 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 creating enantiomerically pure compounds, which are essential in drug development and pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its chiral structure makes it a key reagent for studying molecular stereochemistry and reaction mechanisms in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: It is frequently used in the synthesis of compounds with specific biological activities, supporting research into new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Studies: Its inherent chirality allows it to be used as a chiral auxiliary in catalytic reactions, enhancing the selectivity of complex transformations.\u003c\/li\u003e\n\u003cli\u003eStructural Elucidation: It is used in NMR and other analytical techniques to study the stereochemistry of complex molecules in synthetic 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: 116539-55-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\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 variant\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 exposure to moisture and air. For optimal stability, it should be stored in a controlled temperature environment, ideally between 15°C and 25°C. When handling, it is important to use appropriate personal protective equipment, such as gloves and safety goggles, to avoid skin contact or inhalation. Due to its chemical nature, it should be handled in a well-ventilated area or fume hood to ensure laboratory safety. Always follow standard chemical safety protocols when working with this compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087654400218,"sku":"TCI2510M215740320","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087654432986,"sku":"TCI2510M215740321","price":5427000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2157.jpg?v=1768819196"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-chiral-heterocyclic-building-blocks.oembed?page=8","provider":"AMI Scientific","version":"1.0","type":"link"}