{"title":"Organic Synthesis Reagents","description":"\u003cp\u003e\u003cstrong\u003eOrganic Synthesis Reagents\u003c\/strong\u003e — a collection of functional reagents for synthetic transformations, ranging from acid-base, oxidation-reduction, and fluorination reagents to hypervalent iodine compounds and aryne or heteroaryne precursors. This category also includes phase transfer catalysts, dehydrating reagents, and reagents supporting radical reactions and carbon-carbon bond-forming coupling.\u003c\/p\u003e\u003cp\u003eThese organic synthesis reagents are used by chemists for various transformations such as oxidation of alcohols to aldehydes or ketones, carbon-carbon bond-forming coupling reactions, selective fluorination, and protection-deprotection of functional groups during stepwise synthesis. Polymer-based reagents and inorganic salts also support simplification of the purification step in laboratory-scale synthesis routes.\u003c\/p\u003e\u003cp\u003eExample products in this collection: \u003ca href=\"\/en\/products\/tci2510a20382592\"\u003eTCI A2038 1336-21-6 Ammonia Solution (28% in Water)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b554512201\"\u003eTCI B5545 131765-96-3 Dicyclohexylamine Borane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510p284948718\"\u003eTCI P2849 1310-58-3 Potassium Hydroxide (Pellets)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b555712215\"\u003eTCI B5557 1637638-66-4 2-(tert-Butyldimethylsilyl)-1,3-phenylene Bis(trifluoromethanesulfonate)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510p114546751\"\u003eTCI P1145 57-10-3 Palmitic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b555912217\"\u003eTCI B5559 613676-07-6 2,5-Bis(trimethylsilyl)-1,4-phenylene Bis(trifluoromethanesulfonate)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510p093046438\"\u003eTCI P0930 26299-14-9 Pyridinium Chlorochromate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b557312236\"\u003eTCI B5573 1868173-47-0 4-Biphenylyl(2,4,6-trimethoxyphenyl)iodonium Trifluoromethanesulfonate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePay attention to reagent purity and concentration, compatibility with particular solvents or reaction conditions, and physical form (solid, solution, or specialty gas), which affect how the reagent is handled in the laboratory. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on each item's page.\u003c\/p\u003e\u003cp\u003eOther parallel categories under Chemistry, often used together in one laboratory workflow:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/building-blocks-sintesis-organik\"\u003eBuilding Blocks for Organic Synthesis\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-chemical-biology\"\u003eChemical Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-pharmaceutical-development-and-drug-discovery-research-reagents\"\u003ePharmaceutical Development and Drug Discovery Research Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/katalis-dan-kimia-anorganik\"\u003eCatalysts \u0026amp; Inorganic Chemistry\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-catalysis-and-inorganic-chemistry\"\u003eCatalysis and Inorganic Chemistry\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-organometallic-reagents\"\u003eOrganometallic Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eThis collection is further divided into 12 more specific groups:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-c-c-bond-formation-synthetic-reagents\"\u003eC-C Bond Formation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-c-x-non-halogen-bond-formation-synthetic-reagents\"\u003eC-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-protection-deprotection-derivatization\"\u003eProtection, Deprotection, Derivatization\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-acids-bases-synthetic-reagents\"\u003eAcids, Bases [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chelation-complexation-compounds\"\u003eChelation\/Complexation Compounds\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-phase-transfer-catalysts\"\u003ePhase Transfer Catalysts\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-coupling-synthetic-reagents\"\u003eCoupling [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-aryne-precursors-heteroaryne-precursors\"\u003eAryne Precursors, Heteroaryne Precursors\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-fluorination-reagents-synthetic-reagents\"\u003eFluorination Reagents [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-oxidation-synthetic-reagents\"\u003eOxidation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-specialty-gases-synthetic-reagents\"\u003eSpecialty Gases [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-reduction-synthetic-reagents\"\u003eReduction [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eBack to \u003ca href=\"\/en\/collections\/tci-l1-chemistry\"\u003eChemistry\u003c\/a\u003e. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — the official TCI Japan distributor in Indonesia — to check availability and lead time directly from Japan.\u003c\/p\u003e","products":[{"product_id":"tci2510b554512201","title":"TCI B5545 131765-96-3 Dicyclohexylamine Borane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDicyclohexylamine Borane (DCAB) is a stable borane complex widely employed as a selective reducing agent in organic synthesis. It effectively reduces aldehydes, ketones, carboxylic acids, and amides to their corresponding alcohols and amines under mild conditions. This reagent is particularly valued in pharmaceutical and fine chemical research for its ease of handling and reliable performance in controlled reduction reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085886238938,"sku":"TCI2510B554512201","price":1060000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085886271706,"sku":"TCI2510B554512202","price":3307000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5545_9bee8e35-9990-4d74-9f7e-8a6575f770f5.jpg?v=1792630688"},{"product_id":"tci2510b560312281","title":"TCI B5603 917604-39-8 1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate (CAS 917604-39-8) is a masked N-Heterocyclic Carbene (NHC) precursor supplied by TCI, widely employed in organometallic catalyst synthesis. Upon thermal decarboxylation, it liberates the active NHC ligand in situ, offering a convenient and air-stable alternative to handling free carbenes. This compound is extensively applied in cross-coupling reactions, hydrogenation, and olefin metathesis catalyzed by transition metal complexes such as palladium, ruthenium, and iridium.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085890367706,"sku":"TCI2510B560312281","price":2550000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5603_c7036df6-9ddf-470c-87bb-ba03700669f2.jpg?v=1792630750"},{"product_id":"tci2510b572812453","title":"TCI B5728 192436-83-2 4-Bromo-N-methoxy-N-methylbenzamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5728 4-Bromo-N-methoxy-N-methylbenzamide (CAS 192436-83-2) is a Weinreb amide building block featuring a para-bromo substituent, widely utilized in organic synthesis for the controlled formation of aldehydes and ketones. The bromo group also enables further diversification through cross-coupling reactions such as Suzuki or Heck couplings. This compound is a valuable intermediate in medicinal chemistry research and natural product synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085899608282,"sku":"TCI2510B572812453","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085899641050,"sku":"TCI2510B572812454","price":5603000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5728.jpg?v=1792630840"},{"product_id":"tci2510b579812537","title":"TCI B5798 2650-51-3 Butyltrimethylammonium Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eButyltrimethylammonium Bromide (CAS 2650-51-3) is a quaternary ammonium salt widely used as a phase transfer catalyst in organic synthesis. It facilitates the migration of reactants between aqueous and organic phases, enhancing reaction rates in systems with poor mutual solubility. This compound is commonly applied in alkylation, oxidation, and nucleophilic substitution reactions, as well as in the synthesis of functional materials and porous catalysts.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085903802586,"sku":"TCI2510B579812537","price":1287000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085903835354,"sku":"TCI2510B579812538","price":4316000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5798_2899a205-5cab-4bb4-8168-5ea2f0b79861.jpg?v=1792630893"},{"product_id":"tci2510b597312754","title":"TCI B5973 51641-96-4 1,4-Bis(3-isocyanopropyl)piperazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,4-Bis(3-isocyanopropyl)piperazine is a diisocyanate heterocyclic building block employed in laboratory synthesis of polyureas and polyurethanes via step-growth polymerization. Its dual isocyanate functionality enables crosslinking and chain extension, making it suitable for designing advanced coatings, adhesives, and interpenetrating polymer networks. The piperazine core contributes enhanced rigidity and thermal stability to the resulting polymeric materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085912551642,"sku":"TCI2510B597312754","price":3634000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5973_7905f7a2-3f4c-4861-a81a-15f63c9a0f72.jpg?v=1792631055"},{"product_id":"tci2510b604512850","title":"TCI B6045 245679-18-9 1,3-Dimesityl-4,5-dihydro-1H-imidazol-3-ium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Dimesityl-4,5-dihydro-1H-imidazol-3-ium Tetrafluoroborate is a widely used imidazolium salt serving as an N-Heterocyclic Carbene (NHC) ligand precursor for transition metal catalysis. It is commonly employed to generate active catalytic species for cross-coupling reactions, olefin metathesis, and asymmetric hydrogenation. The mesityl substituents provide optimal steric bulk and electronic properties, making this compound a standard building block in organometallic and synthetic chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085916614874,"sku":"TCI2510B604512850","price":3584000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6045_a787c942-29ef-4644-8cc6-c64f8461ae9b.jpg?v=1792631128"},{"product_id":"tci2510b605112852","title":"TCI B6051 3779-42-8 (3-Bromopropyl)trimethylammonium Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(3-Bromopropyl)trimethylammonium Bromide is a quaternary ammonium salt widely utilized as a phase transfer catalyst in organic synthesis laboratories. It facilitates reactions between aqueous and organic phases by efficiently shuttling ions across phase boundaries, thereby accelerating reaction rates and improving product yields. Common applications include alkylation, oxidation, and nucleophilic substitution reactions, as well as its use as a precursor for surface modification and cationic surfactant synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085916811482,"sku":"TCI2510B605112852","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6051_cdad2e6b-b992-48d2-8730-5863b663b6f8.jpg?v=1792631136"},{"product_id":"tci2510b605212853","title":"TCI B6052 29166-72-1 2-tert-Butyl-1,1,3,3-tetramethylguanidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-tert-Butyl-1,1,3,3-tetramethylguanidine (CAS 29166-72-1), commonly known as Barton's base, is a sterically hindered, strong, non-nucleophilic guanidine base widely employed in organic synthesis. Its primary applications include selective deprotonation, elimination reactions, and serving as a base in coupling and condensation reactions where nucleophilic interference must be avoided. This TCI-grade reagent is available in 1 g and 5 g packaging, making it suitable for both small-scale exploratory research and routine synthetic workflows.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085916844250,"sku":"TCI2510B605212853","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085916877018,"sku":"TCI2510B605212854","price":4795000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6052.jpg?v=1792631139"},{"product_id":"tci2510b612012935","title":"TCI B6120 2794-60-7 Barium(II) Trifluoromethanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBarium(II) Trifluoromethanesulfonate (CAS 2794-60-7) is a high-purity Lewis acid catalyst widely utilized in organic synthesis for activating carbonyl groups and facilitating carbon-carbon bond formation under mild conditions. This compound serves as a key reagent in Friedel-Crafts acylation, aldol condensations, and various fluorinated building block syntheses. Its stability and ease of handling make it a reliable choice for research laboratories working with fluorinated intermediates and catalytic transformations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085920776410,"sku":"TCI2510B612012935","price":1920000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085920809178,"sku":"TCI2510B612012936","price":5755000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6120_f8c6cb4f-6f72-418a-be55-17c655f74a39.jpg?v=1792631215"},{"product_id":"tci2510b619913024","title":"TCI B6199 905459-27-0 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6199 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride is a palladium(II) NHC catalyst specifically developed for C–H bond activation reactions. This catalyst enables direct functionalization of carbon–hydrogen bonds, streamlining synthetic pathways in organic chemistry. It is widely employed in C–H arylation, alkylation, and alkenylation reactions for the synthesis of pharmaceuticals, agrochemicals, and advanced functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085924249818,"sku":"TCI2510B619913024","price":3736000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085924282586,"sku":"TCI2510B619913025","price":12669000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085924315354,"sku":"TCI2510B619913026","price":42952000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6199.jpg?v=1792631285"},{"product_id":"tci2510b625513090","title":"TCI B6255 887919-35-9 Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II) is a palladium(II) pre-catalyst featuring a bulky electron-rich phosphine ligand, designed for high-performance cross-coupling reactions. This compound is widely employed in Suzuki-Miyaura, Buchwald-Hartwig amination, and Heck coupling reactions to construct carbon-carbon and carbon-heteroatom bonds. It is an essential reagent for synthetic chemistry laboratories working on pharmaceutical intermediates, agrochemicals, and advanced organic materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085926707418,"sku":"TCI2510B625513090","price":4442000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6255_d0f61224-3ab9-4447-86e8-712730ce4b06.jpg?v=1792631327"},{"product_id":"tci2510b628113116","title":"TCI B6281 1062158-66-0 3-[2,6-Bis(1-methylethyl)phenyl]-5,6,7,8-tetrahydro-4H-cycloheptathiazolium Perchlorate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6281 is a thiazolium perchlorate compound featuring a sterically demanding 2,6-diisopropylphenyl substituent, designed as a carbon-donor ligand precursor for catalytic applications. This compound serves as a valuable building block in the development of N-heterocyclic carbene (NHC)-based transition metal catalysts, widely utilized in cross-coupling reactions, olefin metathesis, and other catalytic transformations. Its well-defined structure and reliable purity make it suitable for both academic research and industrial chemistry laboratories focused on catalyst design and mechanistic studies.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085928575194,"sku":"TCI2510B628113116","price":2726000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085928607962,"sku":"TCI2510B628113117","price":10877000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6281.jpg?v=1792631347"},{"product_id":"tci2510b643513320","title":"TCI B6435 2488525-05-7 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6435 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone (CAS 2488525-05-7) is a specialty synthetic reagent classified for non-halogen C–X bond formation. Reagents of this N-sulfinylamine type are used to introduce sulfur- and nitrogen-containing fragments into organic frameworks, typically through reactions with nucleophiles or organometallic partners. It is aimed at researchers exploring modern synthetic methodology and medicinal chemistry applications. Handle the reagent in a fume hood, protect it from moisture, and consult the manufacturer's technical documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939749082,"sku":"TCI2510B643513320","price":3913000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939781850,"sku":"TCI2510B643513321","price":17893000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6435_e9fb4a3b-01c3-4d53-8ed4-d4eec33ad2f2.jpg?v=1792631536"},{"product_id":"tci2510b653213452","title":"TCI B6532 106-99-0 1,3-Butadiene (ca. 6% in Dichloromethane, ca. 1.5 mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI 1,3-Butadiene (ca. 6% in Dichloromethane, ca. 1.5 mol\/L) is a solution of 1,3-butadiene in dichloromethane. 1,3-Butadiene is the simplest conjugated diene. At room temperature it is a gas, so it is hard to measure and handle directly in the laboratory. This solution solves that problem: researchers can measure butadiene by volume with a pipette or syringe. Butadiene can then be used as a reagent in organic synthesis without special gas-handling equipment.\u003c\/p\u003e\n\u003cp\u003eThe stated concentration of about 1.5 mol\/L makes stoichiometric calculations simple, because the moles of butadiene follow directly from the volume of solution taken. Dichloromethane was chosen as the solvent because it dissolves many organic compounds and is relatively inert across a wide range of reaction types. The conjugated diene system makes butadiene highly reactive in cycloaddition reactions, especially the Diels–Alder reaction, which forms six-membered rings efficiently. Butadiene is also an important monomer in polymer chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, not every facility has a system for handling compressed or liquefied gases. For university research groups, teaching laboratories and industrial R\u0026amp;D units, this ready-to-use solution offers a practical way to work with butadiene using standard glassware and volumetric tools. It suits organic synthesis projects, studies of cycloaddition chemistry, and small-scale polymer chemistry work where dosing butadiene accurately and repeatably matters as much as convenience and safe handling.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDiels–Alder reactions: the conjugated diene system of 1,3-butadiene reacts readily with dienophiles to form six-membered rings, and the solution form allows measured additions without a gas line.\u003c\/li\u003e\n\u003cli\u003eGeneral organic synthesis: butadiene can be added as a reagent by pipette or syringe, so researchers can run reactions with it in ordinary glassware without special gas-handling equipment.\u003c\/li\u003e\n\u003cli\u003eStoichiometry-controlled experiments: the stated concentration of about 1.5 mol\/L lets chemists work out the moles of butadiene directly from the volume dispensed, which makes reaction planning easier.\u003c\/li\u003e\n\u003cli\u003eSmall-scale polymer chemistry studies: butadiene is an important monomer in polymer chemistry, so this solution is useful for exploratory, small-scale studies in that field.\u003c\/li\u003e\n\u003cli\u003eTeaching and method development: handling a measured liquid solution instead of a gas makes it practical to demonstrate and develop conjugated diene chemistry in laboratories without gas infrastructure.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code B6532)\u003c\/li\u003e\n\u003cli\u003eCAS number: 106-99-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the available options on the product page\u003c\/li\u003e\n\u003cli\u003ePhysical form: solution of 1,3-butadiene in dichloromethane (ca. 6%, ca. 1.5 mol\/L)\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly sealed and follow the storage conditions on the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the container tightly closed in its original packaging. Store it in a cool, well-ventilated chemical storage area away from heat, sparks, open flames and direct sunlight. Both butadiene and dichloromethane are volatile, so open the container only when needed and reseal it promptly to keep the concentration stable. Dispense with a clean, dry pipette or syringe, and work in a fume hood. Wear chemical-resistant gloves, safety glasses and a laboratory coat. Do not breathe the vapors, and avoid contact with skin and eyes. Before use, read the TCI Safety Data Sheet for the exact storage temperature, compatibility and disposal requirements. Dispose of waste and empty containers according to local regulations for halogenated solvents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48085945483482,"sku":"TCI2510B653213452","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085945516250,"sku":"TCI2510B653213453","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6532_ea9009a0-c51d-4a73-9733-c35ca3347200.jpg?v=1792631635"},{"product_id":"tci2510b653313454","title":"TCI B6533 106-99-0 1,3-Butadiene (ca. 5% in N,N-Dimethylformamide, ca. 0.9 mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6533 supplies 1,3-butadiene (CAS 106-99-0) as a solution in N,N-dimethylformamide, at approximately 5% (about 0.9 mol\/L) as stated by the manufacturer. The polar aprotic solvent makes this version well suited to palladium-, nickel- and copper-catalysed transformations where inorganic bases and metal complexes must remain in solution, such as butadiene telomerisation. Dispensing the diene by volume removes the need for gas-handling apparatus and improves reproducibility between runs. Butadiene is highly flammable and carcinogenic and DMF poses reproductive hazards, so use in a fume hood with full reference to the official SDS; AMI Scientific offers 100 mL and 500 mL sizes in original TCI packaging.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48085945745626,"sku":"TCI2510B653313454","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085945778394,"sku":"TCI2510B653313455","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6533_e169a19f-21af-41d2-b423-94dd03c1aaa4.jpg?v=1792631638"},{"product_id":"tci2510b653413456","title":"TCI B6534 106-98-9 1-Butene (ca. 3% in Dichloromethane, ca. 0.7 mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6534 provides 1-butene (CAS 106-98-9) as a solution in dichloromethane at approximately 3% (about 0.7 mol\/L) according to the manufacturer. Supplying this gaseous terminal alkene in solution allows accurate volumetric dosing without cylinders, regulators or cold traps. It is convenient for cross metathesis, hydroformylation, hydrofunctionalisation and olefin polymerisation studies, particularly with catalysts that operate well in chlorinated solvents. The solution is highly flammable and may develop vapour pressure, so open it cold and inside a fume hood; AMI Scientific supplies 100 mL and 500 mL sizes in original TCI packaging.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48085945811162,"sku":"TCI2510B653413456","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085945843930,"sku":"TCI2510B653413457","price":3105000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6534_4a223c41-8879-4b11-b974-64c550109fa5.jpg?v=1792631641"},{"product_id":"tci2510b653513458","title":"TCI B6535 106-98-9 1-Butene (ca. 8% in Tetrahydrofuran, ca. 1.3 mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6535 delivers 1-butene (CAS 106-98-9) in tetrahydrofuran at approximately 8% (about 1.3 mol\/L) as specified by the manufacturer. The ethereal solvent suits reactions involving organometallic reagents, borane chemistry and many transition-metal-catalysed transformations, complementing the dichloromethane version. Its comparatively higher concentration means smaller volumes are needed, keeping the reaction mixture from being over-diluted. Both 1-butene and THF are highly flammable and THF can form peroxides on prolonged storage, so keep containers closed, open them cold in a fume hood, and consult the official SDS; AMI Scientific supplies 100 mL and 500 mL sizes in original TCI packaging.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48085945876698,"sku":"TCI2510B653513458","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085945909466,"sku":"TCI2510B653513459","price":3105000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6535_f5ec6197-a001-4218-af31-85bbbfcd4667.jpg?v=1792631644"},{"product_id":"tci2510b655213480","title":"TCI B6552 2763205-15-6 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 is a spiro-linked building block bearing two pinacol boronate groups at the 2' and 7' positions of a spiro[cyclopenta-dipyridine-fluorene] framework. Its difunctional boronate handles make it a convenient monomer for palladium-catalysed Suzuki–Miyaura cross-coupling and for the assembly of conjugated oligomers and polymers. The rigid, orthogonal spiro geometry combined with electron-poor pyridine nitrogens is of particular interest in organic optoelectronic material research and in nitrogen-donor ligand design. AMI Scientific supplies this TCI product in 100 mg and 500 mg pack sizes; always consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085946859738,"sku":"TCI2510B655213480","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":6890000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552_2f2f4c5c-80a2-4de2-8583-9ea22d2ceb26.jpg?v=1792631678"},{"product_id":"tci2510b667313632","title":"TCI B6673 12230-71-6 Barium Hydroxide Octahydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6673 is Barium Hydroxide Octahydrate (CAS 12230-71-6), a strong inorganic base supplied as the familiar white crystalline octahydrate. Its ability to precipitate carbonate as insoluble barium carbonate makes it valuable for preparing carbonate-free basic solutions and for qualitative carbon dioxide testing. It also serves as a strong base in acid–base titrations and in hydrolysis reactions at laboratory scale. AMI Scientific offers this TCI product in a 500 g pack size; because soluble barium compounds are toxic and the material is corrosive, careful personal protection and waste handling are essential.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYoung (2006). Barium Hydroxide Octahydrate. \u003cem\u003eJournal of Chemical Education\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ed083p539\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ed083p539\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhang et al. (2019). Experimental study on powdered expansion of barium hydroxide octahydrate crystal. \u003cem\u003eJournal of Molecular Liquids\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molliq.2019.111907\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molliq.2019.111907\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2019). Experimental investigation of barium hydroxide octahydrate as latent heat storage materials. \u003cem\u003eSolar Energy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.solener.2018.11.013\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.solener.2018.11.013\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":"500g","offer_id":48085953085658,"sku":"TCI2510B667313632","price":657000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6673_77110bd0-3f76-4fc8-b498-e8d83b761c0d.jpg?v=1792631811"},{"product_id":"tci2510b681413729","title":"TCI B6814 2439-83-0 1-Bromoazepan-2-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6814 1-Bromoazepan-2-one (CAS 2439-83-0), also known as N-bromocaprolactam, is an N-bromoamide reagent derived from a seven-membered lactam. Its weak nitrogen–bromine bond makes it a convenient source of electrophilic bromine or nitrogen-centred amidyl radicals under suitable conditions. Chemists apply such reagents for controlled brominations, radical C–H functionalisation studies, and the preparation of halogenated intermediates for further cyclisation. Supplied in a 1 g pack, it must be handled in a fume hood and stored cold, dry, and strictly protected from light, heat, and reducing agents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085957148890,"sku":"TCI2510B681413729","price":1363000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6814_3e4d6c71-ebba-4010-b405-2de9422b6a37.jpg?v=1792631872"},{"product_id":"tci2510b708113899","title":"TCI B7081 1071965-73-5 Bromo[4-(trifluoromethyl)phenyl][tris(1,1-dimethylethyl)phosphine]palladium","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7081 is a well-defined palladium oxidative addition complex bearing a 4-(trifluoromethyl)phenyl group, a bromide, and a tri-tert-butylphosphine ligand. It functions as a ready-to-use precatalyst that delivers the highly active Pd\/P(t-Bu)₃ system without in-situ ligand mixing. The bulky, electron-rich phosphine promotes oxidative addition to challenging substrates, including aryl chlorides and sterically hindered partners. Supplied in a 250 mg research pack, it is best handled under inert atmosphere and stored cool and dry.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085964947674,"sku":"TCI2510B708113899","price":6032000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7081.jpg?v=1767094525"},{"product_id":"tci2510b708213900","title":"TCI B7082 3075704-21-8 [1,2-Bis(ethoxycarbonyl)hydrazineyl]triphenylphosphonium Trifluoromethanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7082 is a preformed phosphonium salt derived from triphenylphosphine and a dialkyl azodicarboxylate, stabilized as its trifluoromethanesulfonate. It streamlines Mitsunobu-type dehydrative couplings by combining both reagent components in a single, easily weighed solid. This avoids handling heat- and shock-sensitive liquid azodicarboxylates while fixing the reagent stoichiometry. Offered in 1 g, 5 g, and 25 g sizes, it should be kept dry, cool, and away from heat sources and strong reducing agents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085964980442,"sku":"TCI2510B708213900","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085965013210,"sku":"TCI2510B708213901","price":1894000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965045978,"sku":"TCI2510B708213902","price":5805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7082_d1432c49-a384-4e26-9073-814d32f0614a.jpg?v=1792631961"},{"product_id":"tci2510c001613932","title":"TCI C0016 5872-08-2 (+\/-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-10-Camphorsulfonic Acid, commonly abbreviated as CSA, is an organic sulfonic acid derived from camphor and supplied in its racemic form. It is a strong acid, yet unlike many strong acids it is a solid and dissolves in a wide range of organic solvents. That combination makes it a practical acid catalyst for synthetic work. In glycoscience and carbohydrate chemistry, CSA is a well-known catalyst for acetal and ketal formation, including the installation of benzylidene and isopropylidene protecting groups on the hydroxyl groups of sugars.\u003c\/p\u003e\n\u003cp\u003eResearchers choose CSA because it pairs strong acidity with easy handling. Because it is a solid, it can be weighed more accurately than liquid mineral acids, which helps when catalyst loading has to be controlled closely. Its solubility in organic solvents lets it work as an effective homogeneous catalyst, so the reaction mixture stays uniform. Compared with some other sulfonic acids, CSA is often regarded as mild enough for sensitive substrates. It also forms salts with amines, so it is useful as a counterion, including as a dopant for polyaniline in conductive polymer research. Note that CSA is hygroscopic.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, CSA is useful to laboratories working in synthetic organic chemistry, carbohydrate chemistry, natural product chemistry, and materials science at universities and research institutions. Carbohydrate chemists use it for routine protecting group steps in multistep syntheses of sugar derivatives. Natural product groups use it as a convenient acid catalyst during the modification of isolated compounds. Materials science laboratories use it when preparing doped conductive polymers for electronic and sensing studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAcetal and ketal formation: CSA is a strong acid that dissolves in organic solvents, so it catalyzes acetal and ketal formation efficiently under homogeneous conditions.\u003c\/li\u003e\n\u003cli\u003eCarbohydrate protecting group chemistry: CSA is widely used to install benzylidene and isopropylidene protecting groups on sugar hydroxyl groups, which is a routine step in glycoscience synthesis.\u003c\/li\u003e\n\u003cli\u003eAcid catalysis for sensitive substrates: CSA is often considered milder than some other sulfonic acids, so it suits reactions where delicate functional groups must survive acidic conditions.\u003c\/li\u003e\n\u003cli\u003ePrecise catalyst dosing in synthesis: As a solid, CSA can be weighed more accurately than liquid mineral acids, which makes catalyst loading easier to control and reproduce between runs.\u003c\/li\u003e\n\u003cli\u003eConductive polymer research: CSA forms salts with amines and works as a counterion, which makes it useful as a dopant for polyaniline in conductive polymer studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0016)\u003c\/li\u003e\n\u003cli\u003eCAS number: 5872-08-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: refer to the available options on the product listing\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, racemic (+\/-) form\u003c\/li\u003e\n\u003cli\u003eStorage note: hygroscopic, so keep the container tightly closed and protect it from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore (+\/-)-10-Camphorsulfonic Acid in its original tightly sealed container in a cool, dry, well-ventilated area. Because the material is hygroscopic, keep it away from humid air and close the container promptly after each use. A desiccator is a good choice for opened containers. Use chemically resistant containers suitable for strong acids, and keep the material away from bases and incompatible substances. CSA is a strong acid, so handle it with gloves, safety glasses, and a lab coat, and avoid creating or breathing dust. Weigh and transfer it in a fume hood or another well-ventilated area. Always follow the supplier's Safety Data Sheet and your institution's chemical safety procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085966225626,"sku":"TCI2510C001613932","price":858000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966258394,"sku":"TCI2510C001613933","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966291162,"sku":"TCI2510C001613934","price":5502000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0016_09924803-2e8a-415e-bee9-048d8e744abb.jpg?v=1792631988"},{"product_id":"tci2510c007514006","title":"TCI C0075 304655-80-9 Chloramine B Hydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Chloramine B Hydrate (catalog C0075, CAS 304655-80-9) is an aromatic chloramine reagent that serves as a controlled source of active chlorine in aqueous systems. It is used as an oxidizing and mild chlorinating reagent in synthetic work, and its redox behaviour also supports volumetric determinations in analytical laboratories. Because it releases chlorine on contact with acids, it must be stored separately from acidic and flammable materials in a cool, dry, light-protected place. AMI Scientific offers this TCI product in 25g and 100g pack sizes for both analytical and synthetic use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085969404122,"sku":"TCI2510C007514006","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085969436890,"sku":"TCI2510C007514007","price":4165000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0075_5c6a920d-2b3e-44da-969a-dbd531a119c8.jpg?v=1792632042"},{"product_id":"tci2510c007614008","title":"TCI C0076 7080-50-4 Chloramine T Trihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Chloramine T Trihydrate (catalog C0076, CAS 7080-50-4) is one of the most widely used active-chlorine reagents in the laboratory, valued for its stable solid form and easy dissolution in water. It functions both as a general oxidant in synthetic chemistry and as an electrophilic nitrogen source in carbon–nitrogen bond forming methodologies. In biochemistry and analytical work it is well known as an oxidizing reagent for protein labelling procedures and for colorimetric and titrimetric determinations. AMI Scientific supplies this TCI product in 25g and 500g pack sizes; keep it cool, dry, light-protected, and well away from acids and reducing agents.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMekky et al. (2022). Chloramine Trihydrate‐Mediated Tandem Synthesis of New Pyrrole and\/or Arene‐Linked Mono‐ and Bis(1,3,4‐Oxadiazole) Hybrids as Potential Bacterial Biofilm and MRSA Inhibitors. \u003cem\u003eChemistry \u0026amp; Biodiversity\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/cbdv.202200338\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/cbdv.202200338\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085969502426,"sku":"TCI2510C007614008","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085969535194,"sku":"TCI2510C007614009","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0076_6257d122-57a9-4e2a-b6f7-3f2fa7c45ab4.jpg?v=1792632049"},{"product_id":"tci2510c011914064","title":"TCI C0119 530-62-1 1,1'-Carbonyldiimidazole [Coupling Agent for Peptides Synthesis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0119 1,1'-Carbonyldiimidazole (CAS 530-62-1) is a widely used carbonyl activating agent for peptide and general amide bond formation. It converts carboxylic acids into reactive acyl imidazolides that readily couple with amines, alcohols, and other nucleophiles under mild conditions. Its by-products, imidazole and carbon dioxide, are typically easy to remove, simplifying downstream purification. Supplied by TCI in 5 g, 25 g, and 250 g packs, the reagent is highly moisture sensitive and should be handled under dry, inert conditions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085971632346,"sku":"TCI2510C011914064","price":555000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085971665114,"sku":"TCI2510C011914065","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085971697882,"sku":"TCI2510C011914066","price":8101000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0119_53a01754-afde-4d0a-aaff-f177351c8445.jpg?v=1792632094"},{"product_id":"tci2510c017214144","title":"TCI C0172 999-81-5 Chlorocholine Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Chlorocholine Chloride (CAS 999-81-5), commonly known as chlormequat chloride or CCC, is a water-soluble quaternary ammonium salt widely studied as a plant growth regulator associated with gibberellin biosynthesis inhibition. It is used in plant physiology and agronomic research on stem strength and plant height control, and as a quaternary ammonium salt it is also relevant to phase-transfer catalysis studies. The product is available in 25 g and 500 g packages for pot trials through to research-scale field work. Since the material is hygroscopic, weigh it in a well-ventilated area with gloves and eye protection, and reseal the container promptly to keep it dry.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKarakaya et al. (2013). Quantum Chemical Computational Study on Chlorocholine Chloride and Bromocholine Bromide. \u003cem\u003eAsian Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.14233\/ajchem.2013.14130\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.14233\/ajchem.2013.14130\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShaukat et al. (2019). Hydration and ion association of aqueous choline chloride and chlorocholine chloride. \u003cem\u003ePhysical Chemistry Chemical Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c9cp01016e\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c9cp01016e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDey et al. (2013). Efficient micropropagation and chlorocholine chloride induced stevioside production of Stevia rebaudiana Bertoni. \u003cem\u003eComptes Rendus. Biologies\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.crvi.2012.11.007\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.crvi.2012.11.007\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085975007450,"sku":"TCI2510C017214144","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085975040218,"sku":"TCI2510C017214145","price":10625000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0172_def5c7ca-f529-45bb-8d17-347a89231a56.jpg?v=1792632198"},{"product_id":"tci2510c017614149","title":"TCI C0176 501-53-1 Benzyl Chloroformate (30-35% in Toluene)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0176 Benzyl Chloroformate (30–35% in Toluene), CAS 501-53-1, is a widely used acylating reagent for introducing the Cbz (benzyloxycarbonyl) protecting group onto amines. Supplied as a toluene solution in a 25 mL pack, it is convenient to measure and dispense for research-scale organic and peptide synthesis. The resulting carbamates are stable under many reaction conditions yet can be removed by hydrogenolysis, supporting orthogonal protection strategies. Handle it in a fume hood with appropriate protective equipment, keep the container tightly closed, and store it in a cool, dry, well-ventilated area away from ignition sources.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLezama et al. (2014). Kinetics of the Gas-Phase Elimination Reaction of Benzyl Chloroformate and Neopentyl Chloroformate. \u003cem\u003eInternational Journal of Chemical Kinetics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/kin.20896\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/kin.20896\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePati et al. (2004). Synthesis of N‐Benzylated Anilines from the Reaction of Anilines and Benzyl Chloroformate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200431064\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200431064\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMizuno et al. (2003). Non‐phosgene Synthesis of Benzyl Chloroformate (CbzCl).. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200301081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200301081\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":"25mL","offer_id":48276754235610,"sku":"TCI2510C017614149","price":531000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0176_57731670-845b-4867-9a00-8a609dd0eb60.jpg?v=1792632205"},{"product_id":"tci2510c017814153","title":"TCI C0178 543-27-1 Isobutyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0178 Isobutyl Chloroformate, CAS 543-27-1, is a versatile chloroformate reagent commonly used to activate carboxylic acids as mixed anhydrides. This classical approach supports amide and peptide bond formation at low temperature and is also applied to esters, carbamates, and analytical derivatization. AMI Scientific offers 25 g, 100 g, and 500 g packs so laboratories can match the quantity to their working scale. The reagent is corrosive, flammable, and moisture sensitive, so use a fume hood, dry glassware, and store it tightly closed in a cool, dry, well-ventilated place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNedev et al. (1993). A convenient method for synthesis of Fmoc-amino acid p-nitroanilides based on isobutyl chloroformate as condensation agent.. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(00)60527-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(00)60527-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAhmed Soomro (2014). Gas Chromatographic Determination of Amino Acids and Polyamines in Human Skin Samples using Trifluoroacetylacetone and Isobutyl Chloroformate as Derivatizing Reagents. \u003cem\u003eJournal of Chromatography \u0026amp; Separation Techniques\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4172\/2157-7064.1000248\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4172\/2157-7064.1000248\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNEDEV et al. (1993). ChemInform Abstract: A Convenient Method for Synthesis of Fmoc‐Amino Acid p‐Nitroanilides, e.g. (S)‐(III), Based on Isobutyl Chloroformate as Condensation Agent.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199338293\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199338293\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085975400666,"sku":"TCI2510C017814153","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085975433434,"sku":"TCI2510C017814154","price":707000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085975466202,"sku":"TCI2510C017814155","price":1944000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0178_56e50c3c-7ff8-4d5f-95c9-e95162c87684.jpg?v=1792632212"},{"product_id":"tci2510c018714171","title":"TCI C0187 130-26-7 5-Chloro-8-hydroxy-7-iodoquinoline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0187 5-Chloro-8-hydroxy-7-iodoquinoline, CAS 130-26-7, is a halogenated 8-hydroxyquinoline derivative also known in the literature as clioquinol. Its 8-hydroxyquinoline core readily forms chelate complexes with metal ions, making it useful in coordination chemistry, metal–biomolecule interaction studies, and as a heterocyclic building block. AMI Scientific offers 25 g and 250 g packs for laboratory research use only. Handle the solid with gloves, eye protection, and adequate ventilation, and store it tightly closed in a cool, dry place protected from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGil et al. (2002). ChemInform Abstract: Enediolates of Carboxylic Acids in Synthesis: Synthesis of γ‐Chloro‐β‐hydroxy Acids.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200226026\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200226026\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085976219866,"sku":"TCI2510C018714171","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085976252634,"sku":"TCI2510C018714172","price":5603000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0187_e14127db-5bba-45e3-b42c-822463dbebcc.jpg?v=1792632223"},{"product_id":"tci2510c022714232","title":"TCI C0227 619-08-9 2-Chloro-4-nitrophenol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0227 2-Chloro-4-nitrophenol (CAS 619-08-9) is a substituted phenol whose chloro and nitro groups markedly increase the acidity of the hydroxyl function. It serves as a versatile non-heterocyclic building block for aryl ethers, esters, and other derivatives prepared through O-functionalization. The nitrophenol core also provides useful chromophoric behaviour, making it relevant to chromogenic substrate design and analytical work. Available from TCI in 25 g and 500 g pack sizes for both exploratory and routine laboratory synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085980840154,"sku":"TCI2510C022714232","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085980872922,"sku":"TCI2510C022714233","price":9061000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0227_dbcb6c61-4fb6-4ff7-841b-2f782bdb5014.jpg?v=1792632260"},{"product_id":"tci2510c027414300","title":"TCI C0274 107-05-1 Allyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0274 Allyl Chloride (CAS 107-05-1) is a highly reactive allylic halide and one of the most widely used allylating agents in organic synthesis. It introduces the allyl group onto oxygen, nitrogen, sulfur, and carbon nucleophiles, and serves as a precursor to epichlorohydrin and allyl organometallic reagents. The resulting allyl group can be further elaborated through metathesis, epoxidation, hydroboration, or used as a removable protecting group. Supplied in 25 mL and 500 mL packs, it is a flammable, toxic, and strongly irritating liquid that must be handled in a fume hood.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZulfiqar et al. (1999). Effect of allyl chloride comonomer on the thermal degradation of poly(methyl methacrylate-co-allyl chloride). \u003cem\u003ePolymer Degradation and Stability\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0141-3910(99)00087-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0141-3910(99)00087-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYadav et al. (2004). Acetyl Chloride—Ethanol Brings About a Remarkably Efficient Conversion of Allyl Acetates into Allyl Chlorides.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200410041\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200410041\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYadav et al. (2003). Acetyl chloride–ethanol brings about a remarkably efficient conversion of allyl acetates into allyl chlorides. \u003cem\u003eTetrahedron\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tet.2003.09.063\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tet.2003.09.063\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":"25mL","offer_id":48085984313562,"sku":"TCI2510C027414300","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085984346330,"sku":"TCI2510C027414301","price":633000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0274_bd8084cd-4db9-41a4-9bf7-986260b844ed.jpg?v=1792632308"},{"product_id":"tci2510c028314320","title":"TCI C0283 612-57-7 6-Chloroquinoline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0283 6-Chloroquinoline (CAS 612-57-7) carries its chlorine substituent on the carbocyclic ring of the quinoline system. Because this position is not activated by the ring nitrogen, the compound is most often elaborated through palladium-catalysed cross-coupling rather than direct nucleophilic substitution. The retained ring nitrogen makes it useful as a precursor to ligands and metal complexes, while the rigid aromatic core suits medicinal chemistry and functional materials research. AMI Scientific supplies this TCI building block in convenient 1 g and 5 g research-scale packs.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eda Silva et al. (2006). Standard molar enthalpies of formation of 2-chloroquinoline, 4-chloroquinoline, 6-chloroquinoline and 4,7-dichloroquinoline by rotating-bomb calorimetry. \u003cem\u003eThe Journal of Chemical Thermodynamics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jct.2005.03.011\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jct.2005.03.011\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAsadollahi et al. (2017). Synthesis and investigation of crystal structure and optical properties of brookite TiO2 nanoparticles capped with (2-chloroquinoline-3-yl) methanol. \u003cem\u003eJournal of Molecular Structure\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molstruc.2016.09.032\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molstruc.2016.09.032\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShiri et al. (2016). Highly selective organocatalytic three-component reaction of 2-chloroquinoline-3-carbaldehydes, 6-aminouracils, and cyclic methylene active compounds. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2016.10.057\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetlet.2016.10.057\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":48085985165530,"sku":"TCI2510C028314320","price":2347000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085985198298,"sku":"TCI2510C028314321","price":7395000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0283_b81cb8be-b8ab-4def-a593-b573d462e901.jpg?v=1792632331"},{"product_id":"tci2510c029114335","title":"TCI C0291 128-09-6 N-Chlorosuccinimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0291 N-Chlorosuccinimide (NCS, CAS 128-09-6) is a classic solid source of electrophilic chlorine that is far easier to weigh and handle than chlorine gas. It is routinely used for allylic and benzylic chlorination, alpha-chlorination of carbonyl compounds, and selective chlorination of electron-rich aromatics. NCS also drives controlled oxidations of alcohols to aldehydes and ketones, most notably in the Corey–Kim protocol with dimethyl sulfide. AMI Scientific supplies this TCI reagent in 25 g, 100 g, and 500 g packs; as an oxidising and corrosive solid, it should be kept cool, dry, and well away from reducing agents and combustible materials.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChauhan (2010). N-Chlorosuccinimide (NCS). \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1219581\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1219581\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDim et al. (2024). Ka-Band Rotational Spectroscopy of Succinimide and N-Chlorosuccinimide. \u003cem\u003eThe Journal of Physical Chemistry A\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/acs.jpca.4c06004\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/acs.jpca.4c06004\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2006). N-Chlorosuccinimide. \u003cem\u003eCold Spring Harbor Protocols\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1101\/pdb.caut256\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1101\/pdb.caut256\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085985951962,"sku":"TCI2510C029114335","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085985984730,"sku":"TCI2510C029114336","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085986017498,"sku":"TCI2510C029114337","price":3055000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0291_b57d193a-14b7-48a9-8e36-beddd881e826.jpg?v=1792632352"},{"product_id":"tci2510c032614390","title":"TCI C0326 123-41-1 Choline (47-50% in Water) (stabilized with Hydrazine Monohydrate)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0326 Choline, 47-50% in water and stabilised with hydrazine monohydrate (CAS 123-41-1), is a metal-free strong organic base supplied by Tokyo Chemical Industry. It is used as a base in organic synthesis, as a cholinium cation source for ionic liquids and deep eutectic solvents, and in electronic materials research where alkali metal contamination must be avoided. The solution is corrosive and contains hydrazine monohydrate, so it must be handled in a fume hood with chemical-resistant gloves, goggles, and a lab coat. Available in 25 g, 100 g, and 500 g packs, it should be stored tightly closed in a cool, well-ventilated area away from acids and oxidising agents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085990506714,"sku":"TCI2510C032614390","price":581000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085990539482,"sku":"TCI2510C032614391","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990572250,"sku":"TCI2510C032614392","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0326_895ab4cb-722c-4ecf-a234-9fc4ee08fc85.jpg?v=1792632385"},{"product_id":"tci2510c032914395","title":"TCI C0329 67-48-1 Choline Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0329 Choline Chloride (CAS 67-48-1) is a highly water-soluble quaternary ammonium salt widely used as a phase transfer catalyst in two-phase organic reactions. It is best known as a key component of deep eutectic solvents, typically combined with hydrogen bond donors such as urea, and is central to many green chemistry and electrodeposition studies. The compound also serves as a choline source in nutrition and biochemistry research. Supplied by Tokyo Chemical Industry in 25 g and 500 g packs, it is strongly hygroscopic and must be stored tightly closed in a cool, dry, moisture-free environment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLin et al. (2014). Henry’s constant of carbon dioxide-aqueous deep eutectic solvent (choline chloride\/ethylene glycol, choline chloride\/glycerol, choline chloride\/malonic acid) systems. \u003cem\u003eThe Journal of Chemical Thermodynamics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jct.2013.08.029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jct.2013.08.029\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZHANG et al. (2014). Properties and applications of choline chloride\/urea and choline chloride\/glycerol. \u003cem\u003eSCIENTIA SINICA Chimica\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1360\/n032014-00001\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1360\/n032014-00001\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAbbas et al. (2011). Anodic Dissolution of Refractory Metals in Choline Chloride Based Binary Mixtures. \u003cem\u003eECS Transactions\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1149\/1.3566089\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1149\/1.3566089\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085990703322,"sku":"TCI2510C032914395","price":555000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085990736090,"sku":"TCI2510C032914396","price":1591000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0329_bca30671-fbe9-48e7-8a29-db9615534465.jpg?v=1792632392"},{"product_id":"tci2510c038414469","title":"TCI C0384 13395-16-9 Bis(2,4-pentanedionato)copper(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0384 Bis(2,4-pentanedionato)copper(II), CAS 13395-16-9, is the well-known copper(II) acetylacetonate chelate used as a versatile copper source in synthesis and materials science. Its stable β-diketonate framework makes the complex convenient to weigh and dissolve, while the ligands are readily displaced once the active catalytic species forms. It is commonly applied as a catalyst precursor in copper-mediated coupling and C–H functionalisation studies, and as a precursor for copper-based thin films and nanoparticles. AMI Scientific supplies it in 25 g and 250 g packs; store in a tightly closed container in a cool, dry place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085995159770,"sku":"TCI2510C038414469","price":607000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085995192538,"sku":"TCI2510C038414470","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0384_41752859-403b-4ada-a50a-a897263ae333.jpg?v=1792632473"},{"product_id":"tci2510c044114561","title":"TCI C0441 105-56-6 Ethyl Cyanoacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyanoacetate from TCI is an ester that contains an active methylene group. In this compound, the CH2 group sits between two electron-withdrawing groups: a nitrile and an ethyl ester. Because of this structure, the methylene protons are fairly acidic and readily form a stabilized carbanion. This makes Ethyl Cyanoacetate one of the oldest and most widely used building blocks in organic synthesis laboratories. Chemists use it to form carbon-carbon bonds and to build many kinds of heterocyclic rings, from small exploratory reactions to multi-step synthetic routes.\u003c\/p\u003e\n\u003cp\u003eResearchers choose Ethyl Cyanoacetate because one small molecule offers three reactive sites: the active methylene carbon, the nitrile group and the ester group. The active carbon takes part in Knoevenagel condensations, alkylations and Michael additions. The nitrile and ester groups can join cyclization reactions that form pyrimidines, pyridones, thiophenes (through the Gewald reaction) and other heterocyclic frameworks that matter in medicinal chemistry. These reactions usually need only simple, easy-to-obtain base catalysts, so the reagent is practical for both research and teaching.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, Ethyl Cyanoacetate is in steady demand at organic chemistry and pharmacy laboratories in universities. There it supports undergraduate practical courses, final-year projects and graduate research on synthetic methods and heterocyclic compounds. Research groups working on bioactive molecules use it as a dependable starting material for building compound libraries. Its well-documented reactivity also makes it a good choice for showing students the basic ideas of carbanion chemistry. AMI Scientific supplies this TCI reagent to help these laboratories run their synthesis work smoothly.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKnoevenagel condensation: the acidic active methylene group condenses easily with aldehydes and ketones under mild base catalysis, giving dependable access to substituted alkenes for further synthesis.\u003c\/li\u003e\n\u003cli\u003eAlkylation reactions: the stabilized carbanion formed at the methylene carbon reacts with suitable electrophiles, so chemists can add new carbon substituents in a controlled way.\u003c\/li\u003e\n\u003cli\u003eMichael addition: as a soft, stabilized nucleophile, the carbanion adds to activated alkenes and builds new carbon-carbon bonds that are useful in longer synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eHeterocycle synthesis: the nitrile and ester groups take part in cyclization reactions that form pyrimidines, pyridones and related frameworks that are important in medicinal chemistry research.\u003c\/li\u003e\n\u003cli\u003eGewald reaction and teaching laboratories: it is a classic component for making thiophenes, and its simple base-catalyzed chemistry makes it a strong choice for showing students how carbanion reactions work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0441)\u003c\/li\u003e\n\u003cli\u003eCAS number: 105-56-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: please confirm the available pack sizes with AMI Scientific when you order\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: keep the container tightly closed in a cool, dry, well-ventilated area and follow the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Ethyl Cyanoacetate in its original tightly closed container, such as the supplier's glass bottle, in a cool, dry and well-ventilated place. Keep it away from heat, ignition sources, direct sunlight, and strong acids, bases and oxidizing agents. Handle it in a fume hood and wear suitable personal protective equipment, including chemical-resistant gloves, safety glasses and a laboratory coat. Do not inhale vapors and avoid contact with skin and eyes. Before use, read the Safety Data Sheet supplied with the product for hazard details, first-aid measures and disposal guidance, and dispose of waste according to your institution's rules and local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085998829786,"sku":"TCI2510C044114561","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085998862554,"sku":"TCI2510C044114562","price":1036000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0441_38a0d21b-b644-4bce-93cb-ef314b97135b.jpg?v=1792632547"},{"product_id":"tci2510c046014593","title":"TCI C0460 108-77-0 Cyanuric Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0460 Cyanuric Chloride (CAS 108-77-0) is a highly versatile triazine building block whose three chlorine atoms can be displaced stepwise under temperature control. This graded reactivity allows chemists to install up to three different nucleophiles on a single triazine core, supporting dye, ligand, and dendrimer synthesis. It is also widely used as an activating agent for amide and ester bond formation. Because it is moisture sensitive and corrosive, it should be handled in a fume hood with dry glassware and stored tightly sealed in a cool, dry place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(1994). Degussa strengthens its position in cyanuric chloride. \u003cem\u003eSealing Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/1350-4789(94)90186-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/1350-4789(94)90186-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHaval (2006). Cyanuric Chloride: Trichloro-1,3,5-triazine. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2006-948185\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2006-948185\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eOhe et al. (2007). Chemical Introduction of Sugars onto PET Fabrics Using Diamine and Cyanuric Chloride. \u003cem\u003eTextile Research Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1177\/0040517507076325\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1177\/0040517507076325\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086001189082,"sku":"TCI2510C046014593","price":631000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086001221850,"sku":"TCI2510C046014594","price":1212000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0460_48dc2974-27fc-42b4-936d-b746c71f138d.jpg?v=1792632574"},{"product_id":"tci2510c077615030","title":"TCI C0776 10016-20-3 alpha-Cyclodextrin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0776 alpha-Cyclodextrin (CAS 10016-20-3) is a cyclic oligosaccharide built from six glucose units, forming a truncated-cone cavity. Its hydrophilic exterior and hydrophobic interior allow it to form inclusion complexes with suitably sized guest molecules. Common laboratory uses include solubility enhancement, stabilisation of sensitive compounds, chiral separation, and supramolecular assemblies such as rotaxanes. AMI Scientific offers this TCI product in 10 g, 25 g, and 100 g pack sizes for a wide range of research needs.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRontoyianni et al. (1999). Dimeric Complex of Alpha Cyclodextrin with 1,12-Diaminododecane. Comparison with other Alpha Cyclodextrin Dimeric Complexes. \u003cem\u003eSupramolecular Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/10610279908559287\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/10610279908559287\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRontoyianni et al. (1999). Dimeric Complex of Alpha Cyclodextrin with 1, 12-Diaminododecane. Comparison with other Alpha Cyclodextrin Dimeric Complexes. \u003cem\u003eSupramolecular Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/10610279908048708\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/10610279908048708\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGawande et al. (2001). Alpha-Cyclodextrin Production using Cyclodextrin Glycosyltransferase fromKlebsiella pneumoniae AS-22. \u003cem\u003eStarch - Stärke\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/1521-379x(200102)53:2\u0026lt;75::aid-star75\u0026gt;3.0.co;2-j\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/1521-379x(200102)53:2\u0026lt;75::aid-star75\u0026gt;3.0.co;2-j\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":"10g","offer_id":48086027567322,"sku":"TCI2510C077615030","price":707000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086027600090,"sku":"TCI2510C077615031","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086027632858,"sku":"TCI2510C077615032","price":3281000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0776_46d1887c-3113-4a3c-8e53-a39fc6300e49.jpg?v=1792633020"},{"product_id":"tci2510c077715033","title":"TCI C0777 7585-39-9 beta-Cyclodextrin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0777 beta-Cyclodextrin is a cyclic oligosaccharide made of seven glucose units joined together to form a ring. Its structure resembles a truncated cone or doughnut, with a hydrophilic outer surface and a relatively hydrophobic inner cavity. This shape lets beta-cyclodextrin hold guest molecules inside its cavity and form inclusion complexes. In the laboratory it has an important role in glycoscience, supramolecular chemistry, pharmaceutical research and analytical chemistry, especially in studies that aim to improve the solubility and stability of other compounds.\u003c\/p\u003e\n\u003cp\u003eResearchers choose beta-cyclodextrin because its cavity suits many medium-sized organic molecules, including aromatic rings and many active pharmaceutical ingredients. The inclusion complexes it forms can make poorly water-soluble compounds more soluble, protect them from oxidation or light, and mask unwanted tastes or odours. Its hydroxyl groups can be chemically modified, so it is a common starting material for synthesising cyclodextrin derivatives. Because the glucose units that make up the ring are chiral, the material is also useful for chiral recognition and for separating enantiomers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, beta-cyclodextrin is widely used in pharmaceutical laboratories, university research groups and analytical facilities. Formulation scientists use it to study how inclusion complexation affects drug solubility and stability. Academic chemists use it as a model host molecule in supramolecular and glycoscience research, and as a starting material for modified cyclodextrins. Analytical laboratories use it in work on chiral separation and molecular recognition. Because it comes from TCI, researchers get a consistent reagent from a well-known brand for both routine work and research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolubility enhancement studies: the hydrophobic cavity holds poorly water-soluble molecules while the hydrophilic exterior keeps the complex soluble, which helps researchers improve aqueous solubility.\u003c\/li\u003e\n\u003cli\u003eDrug stabilisation research: when an active compound sits inside the cyclodextrin cavity, it is partly shielded from oxidation and light, so the material suits stability and formulation studies.\u003c\/li\u003e\n\u003cli\u003eSupramolecular host–guest chemistry: the cone-shaped ring with a cavity sized for many medium-sized organic molecules makes beta-cyclodextrin a standard model host for studying inclusion complexes.\u003c\/li\u003e\n\u003cli\u003eSynthesis of cyclodextrin derivatives: the many hydroxyl groups on the glucose units can be chemically modified, so the material is a practical starting point for making functionalised cyclodextrins.\u003c\/li\u003e\n\u003cli\u003eChiral recognition and enantiomer separation: the chiral glucose units give the cavity a chiral environment, so the material is used in research on recognising and separating enantiomers.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0777)\u003c\/li\u003e\n\u003cli\u003eCAS number: 7585-39-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: several pack sizes are available; see the product page for current options\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid powder\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry place, away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore beta-Cyclodextrin in its original tightly sealed container in a cool, dry, well-ventilated place, away from moisture, direct sunlight and strong oxidising agents. Reseal the container promptly after each use so the powder does not absorb moisture from the air. Wear standard laboratory protective equipment when handling it, including gloves, safety glasses and a lab coat. Avoid creating or breathing in dust, and weigh the material in a clean, dry area. Label any secondary containers clearly. Always check the supplier's Safety Data Sheet for full handling, first aid and disposal guidance before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086027665626,"sku":"TCI2510C077715033","price":2045000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086027698394,"sku":"TCI2510C077715034","price":5326000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0777_6fd8acc4-19cf-43fb-b09b-a9341ef178ca.jpg?v=1792633024"},{"product_id":"tci2510c079315057","title":"TCI C0793 2491-17-0 1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide Metho-p-toluenesulfonate [for Peptide Synthesis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0793 CMC (CAS 2491-17-0) is a water-soluble carbodiimide reagent developed for peptide synthesis and bioconjugation. Its quaternary ammonium moiety allows carboxyl activation and amide bond formation to proceed in aqueous media, which is valuable when working with sensitive biomolecules. Typical uses include peptide coupling, enzyme and biomolecule immobilisation, hydrogel crosslinking, and carbodiimide-based chemical probing of nucleic acids. Supplied by TCI in 5 g and 25 g packs, the salt is hygroscopic and should be kept cold, dry, and tightly closed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086029172954,"sku":"TCI2510C079315057","price":5982000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086029205722,"sku":"TCI2510C079315058","price":22334000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0793_c28272d9-52d0-451c-b038-36ed28f6ff87.jpg?v=1792633044"},{"product_id":"tci2510c079515061","title":"TCI C0795 17341-93-4 2,2,2-Trichloroethyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0795 2,2,2-Trichloroethyl Chloroformate (CAS 17341-93-4) is the standard reagent for introducing the Troc protecting group onto amines and alcohols. Troc protection is valued for its orthogonality, since it can be removed reductively — typically with zinc — without disturbing acid- or base-labile protecting groups. The reagent is also used to prepare carbamates and carbonates in carbohydrate, peptide, and natural product synthesis. Supplied by TCI in 25 g and 250 g packs, it is moisture-sensitive and corrosive, and must be handled dry in a fume hood.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHE et al. (1991). ChemInform Abstract: Di‐(2,2,2‐Trichloroethyl) Carbonate: By‐Product in Reactions with 2,2, 2‐Trichloroethyl Chloroformate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199110106\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199110106\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHe et al. (1990). DI-(2,2,2-Trichloroethyl)-Carbonate: Byproduct in Reactions with 2,2,2-Trichloroethyl Chloroformate. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919008053155\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919008053155\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eOliveira dos Reis (2007). 2,2,2-Trichloroethyl Chloroformate (TrocCl). \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2007-980374\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2007-980374\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086029336794,"sku":"TCI2510C079515061","price":1716000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086029369562,"sku":"TCI2510C079515062","price":9943000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0795_1b8bde1c-c0fb-492c-97f8-04fedbe33d98.jpg?v=1792633051"},{"product_id":"tci2510c080215074","title":"TCI C0802 3481-09-2 N-Chlorophthalimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0802 N-Chlorophthalimide (CAS 3481-09-2) is a phthalimide-based N-chloro reagent supplied by AMI Scientific in 25 g and 500 g packs. Its readily activated N–Cl bond makes it useful both as an electrophilic chlorine source and as a nitrogen radical precursor. Modern synthetic groups apply it in photocatalytic transformations and C–H functionalisation strategies. Store it cool, dry, and protected from light, and review the official TCI Safety Data Sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWu et al. (2005). Copolymerization of bis(chlorophthalimide)s with 2,5-dichlorobenzophenone catalyzed by NiBr2\/PPh3\/Zn. \u003cem\u003ePolymer\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.polymer.2005.07.017\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.polymer.2005.07.017\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKIRSCH et al. (1998). ChemInform Abstract: Imidyl Radicals. Part 2. Radical Addition of N‐Chlorophthalimide and N‐Bromophthalimide to Alkenes.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199826151\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199826151\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKarthik et al. (2026). Comprehensive Experimental and Computational Characterization of N-Chlorophthalimide: Structural Insights, Cancer-Protein Docking, and Cytotoxicity. \u003cem\u003eChemistry Africa\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s42250-026-01616-w\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s42250-026-01616-w\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086029893850,"sku":"TCI2510C080215074","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086029926618,"sku":"TCI2510C080215075","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0802_4b4c84b3-597d-46b1-9f60-69a2ae5f1c94.jpg?v=1792633065"},{"product_id":"tci2510c085815153","title":"TCI C0858 294-93-9 12-Crown 4-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e12-Crown-4 Ether from TCI, product code C0858 (CAS 294-93-9), is a small cyclic crown ether. Its ring is made of four oxygen atoms linked by ethylene groups. In the laboratory it serves as a complexing agent, or macrocyclic ligand, that can enclose a metal cation within its central cavity. This ability makes it an important compound in supramolecular chemistry, organic synthesis, and electrochemical studies. Researchers use it to control the solubility and reactivity of metal salts in organic solvents that normally dissolve ionic compounds poorly.\u003c\/p\u003e\n\u003cp\u003eThe main reason to choose this compound is its relatively small cavity, which interacts best with small cations, particularly the lithium ion. Larger crown ethers such as 15-crown-5 or 18-crown-6 are better suited to sodium or potassium. This size-based selectivity is what makes 12-Crown-4 useful for separating lithium salts or for activating the counter-anion of a lithium salt. The compound is a liquid, so it can be measured easily by pipette or syringe. Purity and full technical data are given in the certificate of analysis supplied by TCI.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, growing interest in lithium battery research and energy storage materials makes a lithium-selective ligand like 12-Crown-4 relevant to many laboratories. University chemistry departments, research institutes, and industrial R\u0026amp;D groups use it in electrolyte studies, coordination chemistry research, and synthetic work that involves lithium reagents. It also suits teaching laboratories and graduate research projects that demonstrate host–guest chemistry and how ring size governs cation selectivity.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLithium ion complexation: its small cavity selectively binds lithium cations, so researchers can study or control lithium coordination in organic media without competing interference from larger alkali metals.\u003c\/li\u003e\n\u003cli\u003eElectrochemistry and battery research: it is used in studies of lithium-containing electrolytes, where complexing the lithium cation can change ion mobility, solvation behaviour, and the overall performance of the system.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis with lithium reagents: by enclosing the lithium cation, it frees the counter-anion and makes it more reactive, which helps chemists adjust reaction rates and selectivity in lithium-mediated transformations.\u003c\/li\u003e\n\u003cli\u003eSupramolecular and host–guest chemistry: as a classic macrocyclic ligand, it is a basic model compound for studying how ring size and donor atoms affect the binding and recognition of metal cations.\u003c\/li\u003e\n\u003cli\u003eSolubilising metal salts in organic solvents: it helps dissolve ionic lithium salts in organic solvents that normally dissolve them poorly, which opens up reaction media and analytical conditions that would otherwise be out of reach.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0858)\u003c\/li\u003e\n\u003cli\u003eCAS number: 294-93-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Chelation\/Complexation Compounds\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the product listing or contact AMI Scientific for available pack sizes\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid\u003c\/li\u003e\n\u003cli\u003eStorage: see the TCI certificate of analysis and Safety Data Sheet for recommended storage conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep 12-Crown-4 Ether in its original, tightly closed container in a cool, dry, well-ventilated area, away from heat sources, direct sunlight, and incompatible materials. Follow the storage conditions on the TCI label and Safety Data Sheet. Because the product is a liquid, use clean pipettes or syringes to transfer it and limit exposure to air and moisture. Handle it in a fume hood and wear suitable gloves, safety glasses, and a lab coat. Avoid skin contact and inhaling vapour. Read the Safety Data Sheet before first use, and dispose of residues and contaminated materials according to your institution's chemical waste procedures and local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1mL","offer_id":48086033498330,"sku":"TCI2510C085815153","price":1212000.0,"currency_code":"IDR","in_stock":true},{"title":"5mL","offer_id":48086033531098,"sku":"TCI2510C085815154","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0858_2a91efa7-ffc8-413d-b22b-f45707fb1f35.jpg?v=1792633137"},{"product_id":"tci2510c085915155","title":"TCI C0859 33100-27-5 15-Crown 5-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0859 15-Crown 5-Ether (CAS 33100-27-5) is a macrocyclic polyether whose five oxygen donor atoms coordinate alkali metal cations, with a cavity size commonly associated with sodium ion binding. It is widely used as a phase-transfer catalyst, solubilizing inorganic salts into organic media and enhancing the reactivity of the accompanying anion. Researchers also employ it as an ionophore in ion-selective membrane formulations and as a host molecule in supramolecular host–guest studies. Offered in 5mL and 25mL packs, the liquid reagent should be kept tightly closed, cool, and dry, and handled with suitable protective equipment in a fume hood.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKijima et al. (2003). Enzymatic Hydrolysis of 4′-(1-Chloro-2-Acetoxyethyl)-Benzo-15-Crown-5-Ether and 4′-Acetoxyethyl-Benzo-15-Crown-5-Ether; a Facile Synthesis of the Optically Active Chlorohydrin Analogue Incorporating Crown Ether. \u003cem\u003eJournal of Chemical Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3184\/030823403103174362\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3184\/030823403103174362\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGROMOV et al. (1996). ChemInform Abstract: Crown Ether Styryl Dyes. Part 14. Synthesis, Luminescence and Complex Formation of trans‐Isomers of Chromogenic 15‐Crown‐5‐ether.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199608202\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199608202\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShubert et al. (2009). Jet-Cooled Electronic and Vibrational Spectroscopy of Crown Ethers: Benzo-15-Crown-5 Ether and 4′-Amino-Benzo-15-Crown-5 Ether. \u003cem\u003eThe Journal of Physical Chemistry A\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jp904231d\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jp904231d\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":"5mL","offer_id":48086033563866,"sku":"TCI2510C085915155","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086033596634,"sku":"TCI2510C085915156","price":4115000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0859_cb197e80-6555-4fcf-8dd2-e750b2c5078a.jpg?v=1792633140"},{"product_id":"tci2510c086015157","title":"TCI C0860 17455-13-9 18-Crown 6-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0860 18-Crown 6-Ether (CAS 17455-13-9) is the most widely used member of the crown ether family, with six oxygen donors forming a cavity well matched to the potassium ion. By sequestering K⁺, it liberates the counter-anion and markedly enhances its nucleophilicity and basicity, a principle exploited in phase-transfer catalysis and anion activation. It also serves as a reference ligand in ion-recognition studies, as an ionophore in ion-selective membranes, and as a recognition unit in supramolecular architectures. Supplied in 5g, 25g, and 100g packs, this hygroscopic solid must be stored tightly sealed in a cool, dry place and handled with gloves and eye protection.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMaruyama et al. (2007). Probing cations recognized by a crown ether with the 3D-RISM theory. II. 18-crown-6 ether. \u003cem\u003eCondensed Matter Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5488\/cmp.10.3.315\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5488\/cmp.10.3.315\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWagner et al. (1995). [Cs+(15-Crown-5)(18-Crown-6)e-]6 · (18-Crown-6): Properties of the First Mixed Crown Ether Electride. \u003cem\u003eJournal of Solid State Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/jssc.1995.1278\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/jssc.1995.1278\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBotezatu et al. (2020). Thienyl-phenyl Ethylenes with Crown Ether Fragments and Their Photocyclization Products: UV-Vis, NMR, Redox Response for Complexation. A 18-Crown-6 Ether Restricted with a Tricyclic Aromatic Moiety. \u003cem\u003eMacroheterocycles\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.6060\/mhc200496f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.6060\/mhc200496f\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":"5g","offer_id":48086033629402,"sku":"TCI2510C086015157","price":707000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086033662170,"sku":"TCI2510C086015158","price":2045000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086033694938,"sku":"TCI2510C086015159","price":6058000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0860_e7ca259e-2a68-4c03-8abb-26fc540a0589.jpg?v=1792633144"},{"product_id":"tci2510c086915172","title":"TCI C0869 17465-86-0 gamma-Cyclodextrin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0869 gamma-Cyclodextrin (CAS 17465-86-0) is a cyclic oligosaccharide built from eight alpha-1,4-linked glucose units, forming a truncated-cone structure with a hydrophilic exterior and a hydrophobic inner cavity. Its cavity is the largest among the common native cyclodextrins, allowing it to host relatively bulky guest molecules in inclusion complexes. Researchers use it to improve the aqueous solubility and stability of hydrophobic compounds, to encapsulate sensitive actives, and as a chiral selector in chromatographic and capillary electrophoresis separations. Available in 5g, 25g, and 100g packs, this hygroscopic white powder should be kept tightly sealed in a cool, dry place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePapaioannou et al. (2020). Dielectric behavior of gamma-cyclodextrin polymer and carboxymethyl gamma-cyclodextrin polymer cross-linked both by epichlorohydrin. \u003cem\u003eJournal of Molecular Structure\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molstruc.2020.127831\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molstruc.2020.127831\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1990). 4904306 Separation and purification of gamma cyclodextrin. \u003cem\u003eBiotechnology Advances\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0734-9750(90)90790-i\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0734-9750(90)90790-i\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eÖRGÜL (2024). Comparison the solubility and dissolution rate effects of beta-cyclodextrin and gamma-cyclodextrin complexations of rosuvastatin calcium. \u003cem\u003eJournal of Research in Pharmacy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.29228\/jrp.740\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.29228\/jrp.740\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":"5g","offer_id":48086034776282,"sku":"TCI2510C086915172","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086034809050,"sku":"TCI2510C086915173","price":2752000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086034841818,"sku":"TCI2510C086915174","price":7395000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0869_66756e92-5132-4b46-8fd2-e69776259b4d.jpg?v=1792633156"},{"product_id":"tci2510c090015218","title":"TCI C0900 7585-39-9 beta-Cyclodextrin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0900 beta-Cyclodextrin (CAS 7585-39-9) is a cyclic oligosaccharide composed of seven glucopyranose units, featuring a hydrophobic inner cavity and a hydrophilic outer surface. This architecture allows it to form inclusion complexes with suitably sized guest molecules, a property widely exploited in solubility enhancement, stabilisation studies, and supramolecular chemistry. It also serves as a starting scaffold for modified cyclodextrin derivatives and as a basis for chiral separation media. AMI Scientific offers this TCI product in several pack sizes to suit both preliminary trials and ongoing research programmes.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYAMAMURA et al. (1991). Preparation of Heptakis(6-O-(p-tosyl))-.BETA.-cyclodextrin and Heptakis(6-O-(p-tosyl))-2-O-(p-tosyl)-.BETA.-cyclodextrin and Their Conversion to Heptakis(3,6-anhydro)-.BETA.-cyclodextrin.. \u003cem\u003eChemical and Pharmaceutical Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1248\/cpb.39.2505\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1248\/cpb.39.2505\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eM. (2011). Antibacterial Activity of \u0026amp;beta;-Cyclodextrin and 2-Hydroxypropyl-\u0026amp;beta;-Cyclodextrin Trimethoprim Complexes. \u003cem\u003eAmerican Journal of Microbiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3844\/ajmsp.2011.1.8\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3844\/ajmsp.2011.1.8\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMunir (2023). Beta-Cyclodextrin: A Cyclodextrin Derivative and its Various Applications. \u003cem\u003ePolymer Science: Peer Review Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.31031\/psprj.2023.04.000597\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.31031\/psprj.2023.04.000597\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086036709594,"sku":"TCI2510C090015218","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086036742362,"sku":"TCI2510C090015219","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086036775130,"sku":"TCI2510C090015220","price":3332000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0900_505ed369-1bb6-4b4a-b710-ddc3ed5913cf.jpg?v=1792633200"},{"product_id":"tci2510c092415250","title":"TCI C0924 3518-65-8 Chloromethylsulfonyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0924 Chloromethylsulfonyl Chloride (CAS 3518-65-8) is a highly reactive synthetic reagent used for protection, deprotection, and derivatisation chemistry. It reacts readily with amines and alcohols to form sulfonamides and sulfonate esters, while the chloromethyl group offers an additional site for further functionalisation. The reagent is supplied in a 5 g pack suited to reactive-reagent handling practice. Because it is corrosive and moisture sensitive, use dry glassware in a fume hood, keep the container tightly closed, and follow the official TCI safety data sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48276742078682,"sku":"TCI2510C092415250","price":1491000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0924.jpg?v=1768816371"}],"url":"https:\/\/amiscientific.com\/en\/collections\/reagen-sintesis-organik.oembed?page=74","provider":"AMI Scientific","version":"1.0","type":"link"}