{"title":"Asymmetric Hydrogenation Catalysts","description":"\u003cp\u003e\u003cstrong\u003eAsymmetric Hydrogenation Catalysts\u003c\/strong\u003e — menghimpun kompleks logam transisi kiral berbasis ligan fosfin atau salen, seperti turunan DENEB, BINAP-rutenium, dan kompleks kobalt salen kiral, yang berfungsi sebagai katalis dalam reaksi hidrogenasi asimetris. Kekiralan pada ligan pendukung menentukan selektivitas enansiomer produk yang dihasilkan.\u003c\/p\u003e\u003cp\u003eKatalis-katalis ini dipakai kimiawan sintesis organik dalam reaksi hidrogenasi asimetris terhadap keton, imina, atau olefin tersubstitusi untuk menghasilkan senyawa kiral dengan selektivitas enansiomer tinggi. Kompleks berbasis rutenium-BINAP umum digunakan pada hidrogenasi keton beta-fungsional, sementara katalis kobalt salen kiral dimanfaatkan dalam reaksi hidrogenasi asimetris substrat olefin tertentu dalam riset metodologi sintesis.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t307854609\"\u003eTCI T3078 1333981-84-2 (R,R)-Ts-DENEB(regR)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d213022189\"\u003eTCI D2130 112022-83-0 (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t307754607\"\u003eTCI T3077 1384974-37-1 (S,S)-Ts-DENEB(regR)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d213122191\"\u003eTCI D2131 112022-81-8 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b30678806\"\u003eTCI B3067 132071-87-5 [(R)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Dichloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d591126899\"\u003eTCI D5911 112022-83-0 (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine (ca. 1mol\/L in Toluene)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b23158030\"\u003eTCI B2315 259259-80-8 (1S,2S)-N,N'-Bis(2-acetyl-3-oxo-2-butenylidene)-1,2-dimesitylethylenediaminato Cobalt(II)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d591226901\"\u003eTCI D5912 112022-81-8 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine (ca. 1mol\/L in Toluene)\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan konfigurasi kiral (R atau S) katalis yang sesuai dengan enansiomer produk yang ditargetkan, serta kestabilan kompleks logam terhadap udara dan pelarut yang dipakai dalam prosedur reaksi. 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 Hydrogenation [Catalysis], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-hydrogenation-catalysts\"\u003eHydrogenation Catalysts\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-transition-elements-catalysis-and-inorganic-chemistry\"\u003eTransition Elements [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-metallic-salts-catalysis-and-inorganic-chemistry\"\u003eMetallic Salts [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-nitrogen-donor-ligands-catalysis\"\u003eNitrogen-Donor Ligands [Catalysis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-main-group-elements-catalysis-and-inorganic-chemistry\"\u003eMain-group Elements [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-cross-coupling-reaction-using-transition-metal-catalysts-c-c-bond-form\"\u003eCross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-hydrogenation-catalysis\"\u003eHydrogenation [Catalysis]\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510d213022189","title":"TCI D2130 112022-83-0 (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2130, (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine, is a chiral catalyst belonging to the oxazaborolidine family, widely known among synthetic chemists as the CBS catalyst. The compound is used together with a hydride source such as borane to carry out enantioselective reduction of prochiral ketones, delivering secondary alcohols in which one configuration predominates. Its role in the laboratory is strategically important because many bioactive molecules and active pharmaceutical ingredients display the desired activity in only one enantiomeric form, making control of chirality a fundamental requirement in modern synthesis.\u003c\/p\u003e\n\u003cp\u003eThe properties that lead chemists to select this catalyst are its ability to provide high selectivity under relatively mild reaction conditions, its effectiveness in substoichiometric amounts, which conserves material, and the fact that the products it generates are straightforward to separate during post-reaction work-up. The bicyclic framework, bearing two bulky phenyl groups at the 5-position, creates a well-defined steric environment around the boron atom, and it is precisely this environment that directs the approach of hydride to one face of the ketone. Because the catalyst is available both as the (R) form and as its enantiomeric counterpart, the chemist can choose which configuration of the alcohol product to obtain.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this catalyst is typically used in organic synthesis and medicinal chemistry research groups at universities, in research institutes, and in pharmaceutical development laboratories where a defined stereochemical outcome is required. It is generally applied on a small preparative scale, in method development and route-scouting work, and in the preparation of chiral intermediates and reference standards, where reagent quantities are modest and consistent enantioselectivity matters more than throughput.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnantioselective reduction of prochiral ketones — the defined steric environment around boron directs hydride delivery to a single ketone face, giving secondary alcohols with one dominant configuration.\u003c\/li\u003e\n\u003cli\u003eSynthesis of chiral pharmaceutical intermediates — many active pharmaceutical ingredients are active in only one enantiomeric form, so a catalyst that controls configuration is essential to the route.\u003c\/li\u003e\n\u003cli\u003ePreparation of chiral secondary alcohol building blocks — the alcohol products serve as stereochemically defined starting points for further transformations in multi-step synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eAsymmetric synthesis method development — the catalyst works under relatively mild conditions and in substoichiometric amounts, making it economical for screening and optimising reduction protocols.\u003c\/li\u003e\n\u003cli\u003eAccess to a chosen product configuration — because both the (R) form and its enantiomer are available, chemists can select which enantiomeric alcohol a given synthetic route produces.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 112022-83-0\u003c\/li\u003e\n\u003cli\u003eChemical name: (R)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the tightly closed original container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from moisture, heat, and sources of ignition, and follow the storage conditions printed on the manufacturer's label and safety data sheet. Keep the material in its original container or in a clean, dry, well-sealed vessel that is compatible with boron-containing reagents; transfer under an inert atmosphere where the laboratory protocol calls for it. Handle only in a functioning fume hood, wearing safety glasses, chemically resistant gloves, and a laboratory coat. Because the compound is used together with borane-type hydride sources, keep it separate from water, alcohols, oxidising agents, and other incompatible chemicals. Label all working containers clearly, minimise exposure of the material to air and humidity during weighing, and dispose of residues and contaminated consumables in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086496968922,"sku":"TCI2510D213022189","price":1799000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086497001690,"sku":"TCI2510D213022190","price":5988000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2130.jpg?v=1767104260"},{"product_id":"tci2510d213122191","title":"TCI D2131 112022-81-8 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2131 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine is a chiral oxazaborolidine catalyst and the enantiomeric counterpart of the (R) variant. As a member of the CBS class of catalysts, it is used together with borane as the hydride source to reduce prochiral ketones into chiral secondary alcohols, delivering the opposite product configuration compared with its paired catalyst. The availability of both enantiomers is precisely what makes this catalyst system so useful in synthesis laboratories, because researchers can select the desired direction of chiral induction simply by switching catalysts, without having to redesign the entire synthetic route.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that lead researchers to choose this catalyst are its high level of enantioselectivity across a wide range of ketone types, the small catalyst loading required because it operates catalytically rather than stoichiometrically, and reaction conditions that are relatively mild, so other functional groups on the substrate molecule generally remain intact. The rigid bicyclic framework, bearing two bulky phenyl groups, forms a well-defined steric pocket around the boron atom, and it is this pocket that controls the orientation of the ketone as it coordinates. The generally straightforward post-reaction workup is a further practical advantage.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this catalyst is typically used in academic and industrial research settings where a single enantiomer of a secondary alcohol is required, such as asymmetric synthesis studies, the preparation of chiral intermediates, and method development work. Because both enantiomeric forms of the catalyst are available, laboratories can run comparative experiments on the same substrate and obtain either product configuration, which supports teaching, publication-oriented research, and process development on a laboratory scale.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric reduction of prochiral ketones — used with borane as hydride source to deliver chiral secondary alcohols with high enantioselectivity across many ketone classes.\u003c\/li\u003e\n\u003cli\u003ePreparation of chiral intermediates — provides access to a defined alcohol configuration for downstream synthetic steps without redesigning the overall route.\u003c\/li\u003e\n\u003cli\u003eEnantiomer-selection studies — pairing this (S) catalyst with the (R) variant allows either product configuration to be obtained on the same substrate.\u003c\/li\u003e\n\u003cli\u003eMethodology and route development — the small catalytic loading and mild conditions make it practical for screening reduction conditions on sensitive, multifunctional substrates.\u003c\/li\u003e\n\u003cli\u003eTeaching and demonstration of stereocontrol — the rigid bicyclic structure with two bulky phenyl groups clearly illustrates how a steric pocket around boron governs ketone orientation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D2131\u003c\/li\u003e\n\u003cli\u003eCAS number: 112022-81-8\u003c\/li\u003e\n\u003cli\u003eChemical name: (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes and storage: available in the pack sizes offered by the manufacturer; store according to the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this catalyst in its original tightly closed container, in a cool, dry, and well-ventilated area away from moisture, direct sunlight, and heat sources, and follow the specific storage conditions printed on the manufacturer's label and safety data sheet. Oxazaborolidine catalysts are generally moisture-sensitive, so handling under dry, inert conditions and minimising exposure to air during weighing is advisable. Use appropriate personal protective equipment, including gloves, safety glasses, and a laboratory coat, and carry out transfers in a fume hood. Keep the material separate from incompatible substances, and consult the safety data sheet before use and for disposal guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086497067226,"sku":"TCI2510D213122191","price":1885000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086497099994,"sku":"TCI2510D213122192","price":6241000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2131.jpg?v=1767104264"},{"product_id":"tci2510d591226901","title":"TCI D5912 112022-81-8 (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine (ca. 1mol\/L in Toluene)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical material, (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine, is a chiral catalyst dissolved in toluene at a concentration of approximately 1 mol\/L. It plays a critical role in asymmetric synthesis by enabling precise control over the stereochemistry of chemical reactions. As a key component in chiral catalysis, it is widely used in the production of complex organic compounds where stereochemical purity is essential. Its application extends to various synthetic pathways that require enantioselective outcomes, making it an essential tool for researchers in organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe material is highly valued for its purity and efficiency in catalytic processes. It maintains stability under various reaction conditions, ensuring consistent performance in laboratory settings. Its molecular structure is designed to facilitate selective interactions in asymmetric reactions, enhancing the yield and selectivity of desired products. This reliability and effectiveness make it a preferred choice for both academic and industrial research. Additionally, its controlled chemical properties contribute to safe and efficient experimental procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is particularly relevant for organic chemistry research, especially in asymmetric synthesis. It supports the development of new compounds with specific stereochemical configurations, which are crucial for pharmaceutical and materials science applications. Its availability through AMI Scientific ensures that researchers in Indonesia have access to high-quality chiral catalysts for advanced chemical studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in organic chemistry laboratories for producing enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions requiring precise stereochemical control in pharmaceutical research and development.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex organic molecules where chiral catalysts are essential for achieving desired product configurations.\u003c\/li\u003e\n\u003cli\u003eResearch applications in academic institutions focused on advanced chemical transformations and stereochemistry.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes that demand high selectivity and efficiency in catalytic systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 112022-81-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid (dissolved in toluene)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from moisture and incompatible substances.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis material should be stored in a cool, dark location, away from moisture and incompatible substances. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound. Avoid contact with skin and eyes, and follow standard laboratory safety protocols to minimize risk. Regular inspection of storage conditions is advised to maintain the integrity of the product.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086783197402,"sku":"TCI2510D591226901","price":2503000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086783230170,"sku":"TCI2510D591226902","price":6184000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5912.jpg?v=1767109422"},{"product_id":"tci2510n101643891","title":"TCI N1016 199541-17-8 [NH2Me2][(RuCl((S)-binap))2(mu-Cl)3]","description":"\u003cp\u003e\u003cstrong\u003e[NH2Me2][(RuCl((S)-binap))2(mu-Cl)3]\u003c\/strong\u003e (CAS 199541-17-8) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a phosphine ligand in transition-metal catalysis.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C90H72Cl5NP4Ru2\u003c\/li\u003e\n\u003cli\u003eCAS number: 199541-17-8\u003c\/li\u003e\n\u003cli\u003eTCI product code: N1016\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e Dimethylammonium Dichlorotri(mu-chloro)bis[(S)-(-)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]diruthenate(II)\u003c\/p\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087855726810,"sku":"TCI2510N101643892","price":4161000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N1016.jpg?v=1767130677"},{"product_id":"tci2510n101943897","title":"TCI N1019 944451-08-5 [NH2Me2][(RuCl((R)-xylbinap))2(mu-Cl)3]","description":"\u003cp\u003e\u003cstrong\u003e[NH2Me2][(RuCl((R)-xylbinap))2(mu-Cl)3]\u003c\/strong\u003e (CAS 944451-08-5) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a phosphine ligand in transition-metal catalysis.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C106H104Cl5NP4Ru2\u003c\/li\u003e\n\u003cli\u003eCAS number: 944451-08-5\u003c\/li\u003e\n\u003cli\u003eTCI product code: N1019\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e Dimethylammonium Dichlorotri(mu-chloro)bis[(R)-(+)-2,2'-bis[di(3,5-xylyl)phosphino]-1,1'-binaphthyl]diruthenate(II)\u003c\/p\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087855825114,"sku":"TCI2510N101943897","price":1575000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N1019.jpg?v=1767130681"},{"product_id":"tci2510n102043898","title":"TCI N1020 944451-10-9 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