{"title":"Coupling [Synthetic Reagents]","description":"\u003cp\u003e\u003cstrong\u003eCoupling [Synthetic Reagents]\u003c\/strong\u003e — mencakup reagen pembentuk ikatan amida, ester, dan turunan lain dalam sintesis organik, meliputi karbodiimida, garam fosfonium\/uronium\/formamidinium, turunan fosgen, ester aktif dan aditif, serta reagen pembentuk triflat. Kelompok ini berperan mengaktifkan gugus asam karboksilat atau alkohol agar bereaksi efisien dengan nukleofil pasangannya.\u003c\/p\u003e\u003cp\u003eCoupling reagents banyak dipakai pada sintesis peptida fase padat maupun larutan, pembentukan ikatan amida pada molekul kandidat riset, serta konversi alkohol atau fenol menjadi triflat untuk reaksi kopling logam transisi seperti Suzuki dan Negishi. Kimiawan sintesis di laboratorium akademik dan riset farmasi memanfaatkannya untuk mempercepat pembentukan ikatan dengan rasemisasi atau efek samping yang minimal.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t359255245\"\u003eTCI T3592 15458-53-4 Trifluoromethanesulfonyl Bromide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c011914064\"\u003eTCI C0119 530-62-1 1,1'-Carbonyldiimidazole [Coupling Agent for Peptides Synthesis]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t356955219\"\u003eTCI T3569 255825-38-8 N,N,N',N'-Tetramethyl-S-(1-oxido-2-pyridyl)thiouronium Tetrafluoroborate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c017814153\"\u003eTCI C0178 543-27-1 Isobutyl Chloroformate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t317754742\"\u003eTCI T3177 29540-81-6 1-(Trifluoromethanesulfonyl)imidazole\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c059714801\"\u003eTCI C0597 1079-66-9 Chlorodiphenylphosphine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t316754727\"\u003eTCI T3167 117632-84-5 1-(Trifluoromethanesulfonyl)-1H-benzotriazole\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c079315057\"\u003eTCI C0793 2491-17-0 1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide Metho-p-toluenesulfonate [for Peptide Synthesis]\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePilih jenis reagen sesuai gugus fungsi yang diaktifkan (asam karboksilat, alkohol, atau amina), pertimbangkan efisiensi reaksi dan kemudahan pemisahan hasil samping, serta stabilitas penyimpanan reagen yang umumnya sensitif kelembapan. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Reagen Sintesis Organik, sering dipakai bersamaan dalam satu alur kerja laboratorium:\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\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 7 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-peptide-coupling-agents\"\u003ePeptide Coupling Agents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-active-esters-additives-coupling-reagents\"\u003eActive Esters, Additives [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phosphonium-salts-uronium-salts-formamidinium-salts-coupling-reagents\"\u003ePhosphonium Salts, Uronium Salts, Formamidinium Salts [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-coupling-reagents-other\"\u003eCoupling Reagents (Other)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-triflate-formation-coupling-reagents\"\u003eTriflate Formation [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carbodiimides-coupling-reagents\"\u003eCarbodiimides [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phosgene-derivatives-coupling-reagents\"\u003ePhosgene Derivatives [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/reagen-sintesis-organik\"\u003eReagen Sintesis Organik\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"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":555000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085971697882,"sku":"TCI2510C011914066","price":555000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0119.jpg?v=1767094704"},{"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085975466202,"sku":"TCI2510C017814155","price":505000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0178.jpg?v=1767094828"},{"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":5982000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0793.jpg?v=1767095766"},{"product_id":"tci2510c107715483","title":"TCI C1077 4457-32-3 4-Nitrobenzyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Nitrobenzyl Chloroformate (TCI C1077, CAS 4457-32-3) is a widely used reagent for installing the p-nitrobenzyloxycarbonyl (pNZ) protecting group on amines in peptide chemistry. Because the pNZ group is removed under reductive conditions, it provides valuable orthogonality against acid- and base-labile protecting groups. AMI Scientific supplies this TCI reagent in a 25 g pack size suited to research and development laboratories. As a moisture-sensitive and corrosive chloroformate, it should be handled in a fume hood following the official TCI Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086047588570,"sku":"TCI2510C107715483","price":3634000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1077.jpg?v=1768204581"},{"product_id":"tci2510c124215716","title":"TCI C1242 2942-58-7 Diethyl Cyanophosphonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1242 Diethyl Cyanophosphonate (DEPC) is a well-established coupling reagent for activating carboxylic acids toward amide and ester bond formation. It is frequently applied in peptide synthesis, where it offers effective coupling under comparatively mild conditions. The reagent is highly toxic and moisture-sensitive, and hydrolysis can release extremely hazardous gas, so it must be handled only by trained personnel in a fume hood. Available in 5 g and 25 g packs, it must be stored, used, and disposed of strictly in accordance with the official TCI safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGUZMAN et al. (1997). ChemInform Abstract: A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199747196\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199747196\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGuzmán et al. (1997). A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919708005008\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919708005008\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDemir et al. (2009). Cyanide Ion Promoted Addition of Acylphosphonates to Diethyl Cyanophosphonate: Synthesis of Phosphonocyanohydrin O-Phosphates. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1216634\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1216634\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":48086058598618,"sku":"TCI2510C124215716","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086058631386,"sku":"TCI2510C124215717","price":1666000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1242.jpg?v=1768204586"},{"product_id":"tci2510c137915903","title":"TCI C1379 135540-11-3 1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(Chloro-1-pyrrolidinylmethylene)pyrrolidinium Hexafluorophosphate is a coupling reagent of the chloroformamidinium salt type, widely recognised in peptide chemistry. Its role in the laboratory is to activate carboxylic acid groups so that they can react with amines to form amide bonds — the core step in assembling a peptide chain. The reagent converts a relatively unreactive carboxylic acid into a highly reactive intermediate species, allowing the amidation reaction to proceed at mild temperatures and in a far shorter time than conventional methods require.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this reagent a preferred choice are its high activation efficiency combined with a low tendency toward racemisation — two factors that are decisive for the success of peptide synthesis whenever a stereogenic centre must be preserved. The two pyrrolidine rings flanking the central carbon give the molecule a distinctive electronic and steric character, different from that of other uronium or phosphonium reagents. For this reason it is frequently selected when a coupling is difficult to achieve, for example with amino acids bearing bulky side chains or with sterically hindered amines. The hexafluorophosphate anion contributes to the handling character of the salt.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in research groups and institutional facilities engaged in peptide synthesis, medicinal chemistry, and chemical biology, whether in universities, government research institutes, or industrial R\u0026amp;D units. It is normally used at bench scale for the stepwise construction of peptide sequences and for amide bond formation in general synthetic work, in settings where reaction efficiency and stereochemical integrity are both required outcomes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolid-phase peptide synthesis — the reagent activates the incoming protected amino acid efficiently, allowing each coupling cycle on the resin to reach completion quickly under mild conditions.\u003c\/li\u003e\n\u003cli\u003eSolution-phase peptide coupling — its rapid activation of carboxylic acids enables amide bond formation between fragments in solution without the extended reaction times associated with conventional activation methods.\u003c\/li\u003e\n\u003cli\u003eSterically hindered couplings — the distinctive steric and electronic character imparted by the two pyrrolidine rings makes it a useful option when bulky side chains obstruct standard uronium or phosphonium reagents.\u003c\/li\u003e\n\u003cli\u003eStereochemically sensitive amidation — the low racemisation tendency of this reagent supports reactions in which an existing stereogenic centre must be retained throughout the coupling step.\u003c\/li\u003e\n\u003cli\u003eGeneral amide bond formation in medicinal chemistry — routine conversion of carboxylic acids to amides during analogue preparation benefits from the reagent's high activation efficiency at mild temperature.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 135540-11-3\u003c\/li\u003e\n\u003cli\u003eProduct code: C1379\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard laboratory pack sizes; please confirm the currently offered packaging when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a cool, dry place in a tightly closed container, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in a cool, dry location inside a tightly closed original container, kept away from moisture, direct sunlight, and sources of heat or ignition. Keep the container sealed when not in use, as coupling reagents of this class are generally sensitive to atmospheric humidity. Weigh and transfer the material in a fume hood, wearing safety glasses, chemical-resistant gloves, and a laboratory coat. Avoid inhalation of dust and contact with skin or eyes. Do not store together with strong bases, strong oxidising agents, or amines. Always consult the manufacturer's Safety Data Sheet before use, and dispose of residues and contaminated materials in accordance with applicable chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086066561242,"sku":"TCI2510C137915903","price":2802000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086066594010,"sku":"TCI2510C137915904","price":2802000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1379.jpg?v=1768204593"},{"product_id":"tci2510c140015931","title":"TCI C1400 7693-46-1 4-Nitrophenyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1400 4-Nitrophenyl Chloroformate (CAS 7693-46-1) is a widely used activating reagent in peptide chemistry and bioconjugation. It converts alcohols and amines into activated 4-nitrophenyl carbonates or carbamates, in which 4-nitrophenolate serves as an excellent leaving group for subsequent nucleophilic attack. This two-step approach provides controlled access to unsymmetrical carbamates, prodrug linkers, activated PEG derivatives, and immobilised ligands without handling phosgene directly. AMI Scientific offers 25 g and 250 g packs; the reagent is moisture-sensitive and performs best when stored and handled under dry conditions.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSammet (2009). 4-Nitrophenyl Chloroformate: A Versatile Coupling Reagent. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1218291\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1218291\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eEl Seoud et al. (2006). Kinetics of the pH‐independent hydrolyses of 4‐nitrophenyl chloroformate and 4‐nitrophenyl heptafluorobutyrate in water‐acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity. \u003cem\u003eJournal of Physical Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/poc.1081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/poc.1081\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMikulec et al. (1996). Use ofp-nitrophenyl chloroformate chemistry to immobilize protein on orthopedic biomaterials. \u003cem\u003eJournal of Biomedical Materials Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/(sici)1097-4636(199610)32:2\u0026lt;203::aid-jbm8\u0026gt;3.0.co;2-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/(sici)1097-4636(199610)32:2\u0026lt;203::aid-jbm8\u0026gt;3.0.co;2-x\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":48086067675354,"sku":"TCI2510C140015931","price":2752000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086067708122,"sku":"TCI2510C140015932","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1400.jpg?v=1768204595"},{"product_id":"tci2510c140815947","title":"TCI C1408 37091-73-9 2-Chloro-1,3-dimethylimidazolinium Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1408 2-Chloro-1,3-dimethylimidazolinium chloride (DMC, CAS 37091-73-9) is a versatile imidazolinium-based activating agent for peptide and organic synthesis. It converts carboxylic acids into activated species for amide bond formation and serves as an efficient dehydrating agent. DMC is also valued for activating hydroxyl groups, including in carbohydrate chemistry under aqueous conditions. Because the reagent is strongly moisture sensitive, handle it under inert gas and keep containers tightly sealed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086068265178,"sku":"TCI2510C140815947","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086068297946,"sku":"TCI2510C140815948","price":1389000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1408.jpg?v=1767096891"},{"product_id":"tci2510c163916288","title":"TCI C1639 37091-73-9 2-Chloro-1,3-dimethylimidazolinium Chloride (ca. 25% in Dichloromethane)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-1,3-dimethylimidazolinium Chloride (ca. 25% in Dichloromethane) is a chemical compound widely used in laboratory settings, particularly in organic chemistry and peptide synthesis. This compound is known for its reactivity and is commonly employed in substitution reactions and molecular modification processes. Its solubility in dichloromethane makes it suitable for various chemical experiments. In Indonesian laboratories, it is frequently used for research in chemical biology and organic synthesis. The compound is preferred due to its stability and effectiveness in controlled environments, making it a reliable choice for scientific studies and academic research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086082289882,"sku":"TCI2510C163916288","price":1868000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1639.jpg?v=1767097255"},{"product_id":"tci2510c165116306","title":"TCI C1651 101385-69-7 2-Chloro-1,3-dimethylimidazolinium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-1,3-dimethylimidazolinium Hexafluorophosphate is a chemical compound widely used in peptide chemistry and organic synthesis. Its unique structure allows it to participate in various chemical reactions, making it a valuable reagent in laboratory settings. This compound is particularly useful in biological and pharmaceutical research due to its reactivity and stability under controlled conditions. It is commonly applied in the synthesis of peptides, modification of organic molecules, and catalytic processes. Its availability in different packaging options makes it accessible for researchers in Indonesia, supporting scientific advancements in chemistry and biotechnology.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086082846938,"sku":"TCI2510C165116306","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086082879706,"sku":"TCI2510C165116307","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1651.jpg?v=1768204615"},{"product_id":"tci2510c167616342","title":"TCI C1676 3140-73-6 2-Chloro-4,6-dimethoxy-1,3,5-triazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-4,6-dimethoxy-1,3,5-triazine is a heterocyclic compound widely used in organic chemistry for the synthesis of complex molecules. Its structure allows it to participate in various chemical reactions, making it a valuable building block for researchers. The presence of chlorine and methoxy groups enhances its reactivity, enabling targeted chemical modifications. This compound is commonly applied in pharmaceutical research, chemical synthesis, and academic studies. Its stability and versatility make it an essential material in Indonesian laboratories for scientific innovation and discovery.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086084255962,"sku":"TCI2510C167616342","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086084288730,"sku":"TCI2510C167616343","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086084321498,"sku":"TCI2510C167616344","price":783000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1676.jpg?v=1768816678"},{"product_id":"tci2510c192616549","title":"TCI C1926 330641-16-2 O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1926 O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium Tetrafluoroborate, commonly known as TCTU, is a uronium\/aminium-class coupling reagent designed specifically for amide bond formation in peptide synthesis. The reagent works by activating a carboxylic acid group into an active ester derived from 6-chloro-1-hydroxybenzotriazole, which is then attacked by a free amine group to form the peptide bond. In peptide chemistry and medicinal chemistry laboratories, reagents of this type serve as the backbone of the residue assembly process because they determine the efficiency, speed, and stereochemical purity of the final product.\u003c\/p\u003e\n\u003cp\u003eThe property that makes TCTU a widely preferred choice is the presence of the chloro group on the benzotriazole ring. This electron-withdrawing substituent makes the resulting active ester more reactive than its non-chlorinated counterparts, so coupling proceeds faster and reaches completion more thoroughly, including on peptide sequences that are sterically difficult to assemble. This high reactivity also helps suppress racemization, because the activated residue reacts with the amine promptly before it has the opportunity to form an oxazolone intermediate. As a tetrafluoroborate salt, the reagent offers handling characteristics suited to routine synthetic work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCTU is typically used in university research groups, pharmaceutical research and development units, and peptide chemistry facilities that carry out manual or automated solid-phase synthesis. It is generally selected when a coupling step has failed with a milder reagent, when a difficult sequence requires more aggressive activation, or when stereochemical integrity must be preserved across a long assembly. Analysts commonly pair it with a tertiary amine base in a polar aprotic solvent according to the established protocol for the target sequence.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolid-phase peptide synthesis (SPPS): the reagent activates the incoming protected amino acid rapidly, allowing each coupling cycle to reach completion before the next deprotection step begins on resin.\u003c\/li\u003e\n\u003cli\u003eDifficult and sterically hindered sequence coupling: the chlorinated benzotriazole active ester provides the elevated reactivity needed to drive acylation of aggregated or hindered chains to completion.\u003c\/li\u003e\n\u003cli\u003eSolution-phase amide bond formation: chemists apply the reagent to join carboxylic acid and amine fragments in medicinal chemistry work where a clean, fast condensation is required.\u003c\/li\u003e\n\u003cli\u003ePeptide fragment condensation: the low racemization tendency makes the reagent suitable for joining pre-assembled segments where stereochemical integrity at the junction residue is critical.\u003c\/li\u003e\n\u003cli\u003eMethod development and coupling optimization studies: researchers use the reagent as a high-reactivity benchmark when comparing activation strategies, reaction times, and epimerization levels across protocols.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS Number: 330641-16-2\u003c\/li\u003e\n\u003cli\u003eProduct Code: TCI C1926\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: available in standard catalogue pack sizes; please confirm the currently listed packaging option\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in a tightly closed container, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in a cool, dry area inside a tightly closed original container, protected from moisture and away from incompatible materials. Uronium-type coupling reagents are sensitive to humidity, so the container should be kept sealed and returned to storage promptly after weighing; handling inside a desiccator or a dry environment is recommended for frequently opened stock. Weigh and dispense the material in a fume hood, and use gloves, safety goggles, and a laboratory coat. Avoid inhalation of dust and contact with skin or eyes. Follow the manufacturer's safety data sheet and institutional chemical waste procedures for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086092120282,"sku":"TCI2510C192616549","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086092153050,"sku":"TCI2510C192616550","price":505000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1926.jpg?v=1768204629"},{"product_id":"tci2510c198816607","title":"TCI C1988 330645-87-9 O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1988, also known as O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium Hexafluorophosphate, is a chemical compound widely used in peptide chemistry. It functions as an activating reagent in peptide bond formation reactions, facilitating efficient amidation processes. This compound plays a crucial role in the synthesis of peptides, which is essential for various biochemical and pharmaceutical research applications. Its effectiveness in promoting peptide coupling makes it a vital component in modern laboratory workflows.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes of TCI C1988 is its high reactivity and stability under controlled laboratory conditions. These properties allow for consistent and reliable results in peptide synthesis experiments. The compound is also non-toxic at low concentrations, making it a safer option for laboratory use compared to other reagents. Its solid form and ease of handling further enhance its appeal among researchers, contributing to its widespread adoption in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI C1988 is frequently utilized in molecular biology, pharmacology, and organic chemistry research. Its role in drug development and protein studies underscores its importance in advancing scientific knowledge. The compound’s reliability and performance in peptide synthesis make it a preferred choice for researchers aiming to produce high-quality peptides for various applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: TCI C1988 is ideal for peptide synthesis due to its ability to activate amide bonds, enabling efficient coupling reactions in solid-phase peptide synthesis.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Research: The compound supports the production of peptides used in studying protein structures and functions, aiding in genetic and biochemical investigations.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It is commonly used in the development of therapeutic peptides, contributing to the creation of new drugs and treatments.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: Its reactivity and stability make it a valuable reagent in organic synthesis, particularly in the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: TCI C1988 facilitates the synthesis of peptides for use in biochemical assays, supporting research into enzyme activity and molecular interactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 330645-87-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTCI C1988 should be stored in a cool, dry environment to maintain its chemical stability and reactivity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which could affect its performance. Due to its solid form, it is typically stored in glass or plastic containers that are resistant to chemical degradation. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. While it is non-toxic at low concentrations, proper handling and storage are essential to ensure consistent results and safety in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48276170834138,"sku":"TCI2510C198816607","price":531000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1988.jpg?v=1768204632"},{"product_id":"tci2510c232517070","title":"TCI C2325 41864-22-6 1,1'-Carbonyldi(1,2,4-triazole)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,1'-Carbonyldi(1,2,4-triazole) is a chemical compound widely used in research laboratories, particularly in the fields of peptide chemistry and biochemical applications. This compound plays a crucial role in the synthesis of bioactive molecules and serves as a reagent in various chemical reactions. Its unique chemical structure allows for specific interactions with biological molecules, making it an essential tool for researchers working on molecular modifications and functional group transformations. Due to its versatility, it is frequently utilized in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties, including its stability under certain conditions and reactivity towards environmental factors, make it a preferred choice for laboratory applications. The presence of triazole rings in its molecular structure enhances its stability and provides a wide range of reactivity in chemical reactions. This characteristic is particularly valuable in covalent reactions and molecular modifications, where precise control over chemical interactions is required. Its solubility in organic solvents further simplifies its use in synthesis and processing procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,1'-Carbonyldi(1,2,4-triazole) is commonly used in biological chemistry, pharmaceutical research, and biotechnology applications. Its role in developing new drug compounds and studying molecular interactions makes it an important component in the research toolkit of scientists in these fields. The compound's reliability and effectiveness have made it a standard material in many research projects conducted in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Chemistry Research: This compound is ideal for peptide synthesis due to its ability to form stable intermediates and facilitate coupling reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical Reactions: Its reactivity allows it to participate in various biochemical processes, making it useful in enzyme studies and molecular interactions.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It is used in the synthesis of bioactive compounds, aiding in the creation of new pharmaceutical agents.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: The compound’s structural versatility supports its use in modifying molecular structures for research purposes.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: Its solubility in organic solvents makes it suitable for a wide range of synthetic reactions in laboratory settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 41864-22-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled with appropriate laboratory safety measures, including the use of personal protective equipment. Storage conditions should avoid direct sunlight and high humidity to ensure long-term stability. It is important to ensure that the compound is kept away from incompatible materials to prevent any potential chemical reactions. Proper labeling and storage practices help maintain the integrity of the compound during laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086120595674,"sku":"TCI2510C232517070","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086120628442,"sku":"TCI2510C232517071","price":1666000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2325.jpg?v=1768204649"},{"product_id":"tci2510c255117345","title":"TCI C2551 133894-48-1 Chlorotripyrrolidinophosphonium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2551 Chlorotripyrrolidinophosphonium Hexafluorophosphate is a phosphonium-based coupling reagent used in peptide chemistry and amide synthesis. It works by activating a carboxylic acid group so that it becomes ready to react with an amino group, forming the amide bond that serves as the backbone of every peptide chain. Its cationic structure consists of a phosphorus atom bound to three pyrrolidine rings and one chlorine atom, with hexafluorophosphate acting as the counter-anion. This anion is inert and does not interfere with the progress of the coupling reaction, whether the work is carried out in a flask or on solid-phase synthesis.\u003c\/p\u003e\n\u003cp\u003eThis reagent is chosen primarily when the coupling to be performed is classified as difficult. Such conditions arise with sterically hindered amino acids, with residues whose nitrogen is methylated, or in the joining of long peptide fragments, where ordinary coupling reagents frequently give low yields. The distinctive activation pathway of this chlorophosphonium class of reagent makes it effective on those problematic substrates. Because it does not carry a tertiary amino group capable of terminating the chain, the reagent is also safe to use in the presence of an excess of free amine. The hexafluorophosphate anion contributes to this well-behaved reaction profile.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in research groups and institutional facilities engaged in peptide synthesis and organic synthesis work. It is generally reached for in the specific situations described above, rather than as the default reagent for routine, unhindered couplings. Analysts and synthetic chemists working on fragment condensation, N-methylated sequences, or hindered residues keep a reagent of this class on hand precisely because the standard options tend to underperform on those steps.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolid-phase peptide synthesis: the reagent activates the carboxylic acid component for amide bond formation on resin, and the inert hexafluorophosphate anion does not interfere with the coupling step.\u003c\/li\u003e\n\u003cli\u003eCoupling of sterically hindered amino acids: its distinctive activation pathway makes this chlorophosphonium class effective on bulky residues where ordinary coupling reagents frequently return low yields.\u003c\/li\u003e\n\u003cli\u003eN-methylated residue coupling: residues whose nitrogen is methylated are a classic difficult case for standard reagents, and this phosphonium reagent is selected specifically for such demanding substrates.\u003c\/li\u003e\n\u003cli\u003ePeptide fragment condensation: the joining of long peptide fragments is one of the difficult coupling situations for which this reagent is chosen over conventional alternatives.\u003c\/li\u003e\n\u003cli\u003eGeneral amide synthesis in solution: the reagent activates carboxylic acids toward amino groups in flask chemistry, and carries no chain-terminating tertiary amino group when free amine is present in excess.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 133894-48-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003eProduct code: C2551\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the catalogue pack sizes offered for this product code\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's stated conditions on the product label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container in a cool, dry place, tightly closed and protected from moisture, following the storage conditions stated by the manufacturer on the product label. Keep the material in its original supplier container with an intact closure; transfer only into clean, dry, chemically compatible vessels that are clearly labelled. Handle in a well-ventilated area or a fume hood, wearing a laboratory coat, safety glasses, and suitable gloves. Avoid contact with skin and eyes and avoid breathing any dust. Weigh out and reseal promptly to limit exposure to atmospheric moisture. Consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086132130010,"sku":"TCI2510C255117345","price":2020000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2551.jpg?v=1768204669"},{"product_id":"tci2510c273317589","title":"TCI C2733 1075198-30-9 (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylaminomorpholinocarbenium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis complex chemical compound, TCI C2733 (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylaminomorpholinocarbenium Hexafluorophosphate, is a specialized reagent used in chemical biology and peptide chemistry. It serves as a key component in the synthesis of organic compounds and bioactive molecules, playing a crucial role in laboratory research that demands high reactivity and molecular specificity. Its unique structure enables it to participate in reactions that produce highly structured products, making it indispensable in advanced chemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's complex molecular architecture and high reactivity make it a preferred choice for researchers seeking precision in synthetic reactions. It is known for its stability under controlled conditions, although it is sensitive to moisture and air exposure. These properties make it ideal for applications where exact control over reaction conditions is essential. Its ability to facilitate the formation of specific molecular structures enhances its utility in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used by researchers in chemical biology, pharmaceutical development, and materials science. Its application spans various experimental protocols, including the synthesis of complex organic molecules and the development of bioactive compounds. Due to its unique properties, it is a valuable tool for scientists aiming to achieve precise and reproducible results in their work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide chemistry due to its ability to facilitate the formation of specific molecular structures, enhancing the efficiency of synthetic processes.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: Its high reactivity and molecular specificity make it a preferred reagent in the creation of bioactive molecules for pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: The compound's complex structure supports its use in the synthesis of complex organic compounds, enabling precise chemical transformations.\u003c\/li\u003e\n\u003cli\u003eMolecular Specificity Studies: Its unique reactivity allows researchers to study molecular interactions with high accuracy, supporting advanced chemical investigations.\u003c\/li\u003e\n\u003cli\u003eAdvanced Synthetic Pathways: It is used in multi-step synthetic routes where controlled reactivity and structural precision are critical for successful outcomes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1075198-30-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires protection from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment away from moisture and air exposure to maintain its stability and reactivity. It is recommended to use airtight containers made of inert materials such as glass or high-density polyethylene to prevent contamination and degradation. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures in place. Researchers should avoid prolonged exposure to air and moisture to ensure the compound remains effective for its intended applications. Proper storage conditions are essential to preserve its chemical integrity and ensure consistent performance in experimental protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086194323674,"sku":"TCI2510C273317589","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086194356442,"sku":"TCI2510C273317590","price":1541000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2733.jpg?v=1769144359"},{"product_id":"tci2510c344418484","title":"TCI C3444 153433-26-2 2-Chloro-1,3-dimethylimidazolinium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-1,3-dimethylimidazolinium Tetrafluoroborate is a chemical compound widely used as a catalyst in various chemical reactions within laboratory settings. This material belongs to the category of carbon-donor ligands and is known for its ability to facilitate both substitution and electrophilic reactions. Its ionic structure enhances its reactivity in reactive environments, making it a valuable tool for chemists working on complex organic synthesis. The compound is particularly effective in accelerating chemical processes without undergoing significant degradation, which is essential for maintaining the integrity of experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make this compound a preferred choice is its versatility in functioning as either a homogeneous or heterogeneous catalyst, depending on the reaction conditions. The presence of the tetrafluoroborate ion contributes to its stability and reactivity across a range of conditions. Additionally, its solubility in organic solvents simplifies handling and processing, making it a practical option for laboratory use. These characteristics ensure that it remains a reliable and efficient catalyst in diverse chemical applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in organic chemistry research, especially in the synthesis of heterocyclic compounds and substitution reactions. Its stability and reactivity make it highly relevant for a variety of chemical processes. Due to its effectiveness and ease of use, it is a popular choice among researchers and chemists in the region. Its role in advancing chemical synthesis and reaction mechanisms underscores its importance in modern laboratory practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound's ability to act as a versatile catalyst, enhancing reaction efficiency and yield in complex molecule formation.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound synthesis relies on its catalytic properties, enabling the formation of ring structures with high specificity and selectivity.\u003c\/li\u003e\n\u003cli\u003eElectrophilic substitution reactions are effectively catalyzed by this material, promoting the formation of desired products with minimal side reactions.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes utilize its stability and reactivity to improve reaction rates and reduce energy consumption in large-scale applications.\u003c\/li\u003e\n\u003cli\u003eResearch laboratories use it for studying catalytic mechanisms, providing insights into reaction pathways and improving synthetic methodologies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 153433-26-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Carbon-Donor Ligands [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this material. Avoid contact with incompatible substances, and always follow standard laboratory safety protocols to minimize risks. Regular inspection of storage conditions is advised to ensure the material remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086247702746,"sku":"TCI2510C344418484","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086247735514,"sku":"TCI2510C344418485","price":783000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3444.jpg?v=1767099593"},{"product_id":"tci2510c346118505","title":"TCI C3461 893413-42-8 (6-Chloro-1H-benzotriazol-1-yloxy)tripyrrolidinophosphonium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(6-Chloro-1H-benzotriazol-1-yloxy)tripyrrolidinophosphonium Hexafluorophosphate is a synthetic reagent widely used in chemical synthesis, particularly in coupling reactions. This compound plays a crucial role in facilitating the formation of chemical bonds, especially in reactions such as Ugi, HATU, and carbon activation. It is a key catalyst in organic chemistry, enabling efficient and controlled synthesis of complex molecules. Its unique molecular structure contributes to its effectiveness in promoting chemical reactions under mild conditions.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons this reagent is preferred is its stability and reactivity. The presence of chlorine in its molecular structure enhances its reactivity, allowing it to participate in a variety of synthetic pathways. Additionally, it is effective in low-temperature reactions, reducing the need for extreme conditions that can be costly or damaging. Its reliability and consistent performance make it a trusted choice for researchers and laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is highly relevant for organic chemistry research. It is commonly used in academic institutions, research centers, and pharmaceutical industries. Its availability and proven effectiveness make it a preferred option for scientists aiming to achieve high-quality results in synthetic processes. Its role in enabling complex molecular structures is vital for advancing chemical research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where this reagent is used to activate carbon atoms and facilitate coupling reactions, enabling the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from this compound's ability to support efficient and selective chemical transformations, crucial for drug development and compound synthesis.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry laboratories relies on this reagent for its reliability and effectiveness in a wide range of synthetic reactions, supporting educational and exploratory studies.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes utilize this compound for its stability and reactivity, ensuring consistent results in large-scale production environments.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications leverage this reagent's controlled reactivity for precise and reproducible chemical reactions in experimental setups.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 893413-42-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible materials and ensure proper ventilation in the workspace. The compound should not be stored near heat sources or in areas with high humidity. Regular inspection of storage conditions is advised to ensure optimal preservation and safety in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086249013466,"sku":"TCI2510C346118505","price":505000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3461.jpg?v=1769144283"},{"product_id":"tci2510d025419609","title":"TCI D0254 693-13-0 N,N'-Diisopropylcarbodiimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N’-Diisopropylcarbodiimide (DIC), also known as TCI D0254, is a widely used chemical compound in organic synthesis, particularly in the activation of carboxylic acid groups. This reagent plays a crucial role in the formation of amide and ester bonds, making it an essential tool in peptide chemistry and complex molecule synthesis. Its ability to efficiently activate carboxylic acid groups enables researchers to achieve high yields and purity in their reactions, which is vital in both academic and industrial laboratory settings.\u003c\/p\u003e\n\u003cp\u003eDIC is favored for its high reactivity and effectiveness in catalytic reactions. It is known for its ability to form highly efficient carbodiimide activators, which significantly enhance the rate of amide bond formation. Its stability under controlled conditions makes it a reliable choice for synthetic processes. However, it is highly sensitive to moisture and air, requiring careful handling and storage. These properties make it a preferred reagent in applications where precision and efficiency are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N,N’-Diisopropylcarbodiimide is commonly used in organic chemistry research, especially in the synthesis of bioactive compounds and peptides. It is a key reagent in pharmaceutical and biochemical research, supporting the development of new drugs and materials. Its versatility and effectiveness make it a valuable tool for scientists working in various fields of chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis for Pharmacological Research: DIC is ideal for peptide synthesis due to its ability to efficiently activate carboxylic acid groups, enabling the formation of stable amide bonds necessary for drug development.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It is widely used in the synthesis of bioactive compounds, where high reactivity and selectivity are required for complex molecule formation.\u003c\/li\u003e\n\u003cli\u003eBiochemical Studies: DIC supports the creation of complex molecules used in biochemical experiments, enhancing the accuracy and efficiency of reaction processes.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Applications: Its role in activating functional groups makes it useful in the development of advanced materials with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: DIC is employed in reactions requiring precise control over bond formation, ensuring high purity and reproducibility in analytical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 693-13-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry, cool, and well-ventilated conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN,N’-Diisopropylcarbodiimide should be stored in a dry, cool, and well-ventilated area away from moisture and air. It is typically kept in a sealed container to prevent exposure to humidity, which can degrade its effectiveness. Due to its reactivity, it should be handled in a fume hood to minimize inhalation risk. Appropriate personal protective equipment, such as gloves and safety goggles, should be worn during handling. The compound is sensitive to moisture, so it is important to ensure that all containers are tightly sealed and stored in a controlled environment to maintain its stability and efficacy.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086362390746,"sku":"TCI2510D025419609","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086362423514,"sku":"TCI2510D025419610","price":1363000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0254.jpg?v=1767101058"},{"product_id":"tci2510d043619870","title":"TCI D0436 538-75-0 N,N'-Dicyclohexylcarbodiimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N’-Dicyclohexylcarbodiimide (DCC) is a chemical compound widely used in peptide synthesis and organic molecule coupling reactions. It functions as a catalyst in the activation of carboxylic acids, enabling the efficient formation of amide bonds. This compound is essential in laboratory settings where complex molecules such as peptides, proteins, or pharmacological agents are being synthesized. Its stability and reactivity make it a reliable choice for various organic chemistry applications. DCC is particularly favored for its ability to facilitate high-yield reactions without requiring additional reagents, thus streamlining the synthesis process.\u003c\/p\u003e\n\u003cp\u003eThe unique molecular structure of DCC, featuring two cyclohexyl groups surrounding the carbodiimide core, contributes to its stability and reactivity. This structure enhances the efficiency of chemical reactions by providing a robust platform for bond formation. Additionally, DCC is not prone to unwanted side reactions in laboratory environments, minimizing the risk of degradation or contamination. Its inertness in the presence of other compounds ensures that it remains a safe and effective reagent for a wide range of chemical processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DCC is commonly used in research across chemistry, pharmacy, and biotechnology fields. It plays a crucial role in the synthesis of peptides and the modification of organic molecules, supporting both academic and industrial research. Its availability in the local market ensures that researchers have access to this essential compound for their experimental needs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: DCC is ideal for peptide synthesis due to its ability to activate carboxylic acid groups, enabling the formation of stable amide bonds with amino acids.\u003c\/li\u003e\n\u003cli\u003eOrganic Molecule Coupling: It facilitates efficient coupling reactions between organic molecules, making it a preferred choice for chemical modifications.\u003c\/li\u003e\n\u003cli\u003eProtein Modification: DCC is used in the chemical modification of proteins, allowing for the introduction of specific functional groups without disrupting the protein structure.\u003c\/li\u003e\n\u003cli\u003ePharmacological Research: It supports the synthesis of pharmacological compounds, aiding in the development of new drugs and therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eBiotransformation Studies: DCC is useful in studies involving the transformation of organic compounds, providing a reliable method for bond formation in complex molecules.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 538-75-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDCC should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture, which can affect its performance. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. While it is generally inert, it is advisable to avoid contact with incompatible substances to ensure safety. Proper storage conditions help preserve its effectiveness for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086384410842,"sku":"TCI2510D043619870","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"400g","offer_id":48086384443610,"sku":"TCI2510D043619871","price":531000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0436.jpg?v=1767101296"},{"product_id":"tci2510d043719872","title":"TCI D0437 538-75-0 N,N'-Dicyclohexylcarbodiimide (25% in Pyridine, ca. 1.2mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N’-Dicyclohexylcarbodiimide (DCC) is a widely used chemical compound in peptide synthesis and molecular coupling reactions. It is a liquid solution dissolved in pyridine with a concentration of approximately 1.2 mol\/L. This reagent plays a crucial role in activating carboxyl groups, enabling the formation of peptide bonds between two molecules. Its effectiveness and stability make it a key component in various synthetic processes. DCC is particularly valuable in laboratories where the production of complex molecules with specific structures is required.\u003c\/p\u003e\n\u003cp\u003eThe unique properties of N,N’-Dicyclohexylcarbodiimide make it a preferred choice for chemical synthesis. It is chemically stable under certain reaction conditions and exhibits high reactivity, allowing reactions to proceed efficiently. Its resistance to moisture and moderate temperatures enhances its usability in diverse laboratory settings. Additionally, its ability to function as a reliable activating agent ensures consistent results in peptide chemistry applications. These characteristics contribute to its popularity among researchers and scientists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N,N’-Dicyclohexylcarbodiimide is commonly used in organic and biochemical research. It is particularly relevant for academic institutions and research organizations focused on the synthesis of bioactive compounds. Its reliability and effectiveness make it a go-to reagent for those working on complex molecular structures and peptide-based experiments. Its consistent performance supports a wide range of scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: DCC is ideal for peptide synthesis due to its ability to activate carboxyl groups, enabling efficient coupling reactions.\u003c\/li\u003e\n\u003cli\u003eMolecular Coupling Reactions: Its chemical stability and reactivity make it suitable for various molecular coupling processes in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: DCC supports the synthesis of bioactive compounds, making it a valuable tool in biochemical studies.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: Its high efficiency and reliability make it a preferred reagent in synthetic organic chemistry applications.\u003c\/li\u003e\n\u003cli\u003eStructural Chemistry Studies: DCC is used to produce complex molecules with specific structural requirements, aiding in structural chemistry research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 538-75-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: 250 mL, 500 mL\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN,N’-Dicyclohexylcarbodiimide should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture, which can affect its stability. Due to its chemical reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with skin and eyes, and use appropriate personal protective equipment when handling. Ensure that the storage area is secure and inaccessible to unauthorized personnel. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mL","offer_id":48086384476378,"sku":"TCI2510D043719872","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0437.jpg?v=1768204841"},{"product_id":"tci2510d139321131","title":"TCI D1393 5439-14-5 3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. It plays a crucial role in organic and pharmaceutical research, where the formation of complex molecular structures is essential. This compound is a key component in the development of bioactive molecules, making it indispensable in modern laboratory settings. Its unique chemical structure allows for versatile functionalization, enabling researchers to design and synthesize a wide range of compounds with specific biological activities.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability under controlled conditions, which simplifies synthesis and molecular manipulation. Its ability to react with various reagents enhances its utility in diverse chemical transformations. The solid form of this compound facilitates easy handling and storage, making it a preferred choice for laboratory applications. Additionally, its high reactivity ensures efficient synthesis of new compounds, contributing to its widespread use in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one is extensively used in chemical, pharmaceutical, and biochemical research. It is commonly found in academic institutions and research centers, where it supports the development of new drugs and advanced chemical materials. Its versatility and reliability make it a fundamental tool in the pursuit of scientific innovation and discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: This compound is ideal for creating complex heterocyclic structures due to its versatile reactivity and stability.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research: It is used in the development of bioactive molecules, contributing to drug discovery and design.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies: Its role in molecular manipulation supports investigations into biological processes and molecular interactions.\u003c\/li\u003e\n\u003cli\u003eAcademic research: Widely utilized in universities and research institutions for teaching and experimental purposes.\u003c\/li\u003e\n\u003cli\u003eIndustrial applications: It is employed in the production of specialty chemicals and pharmaceutical intermediates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 5439-14-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and contaminants. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances to ensure safe laboratory practices. Proper storage and handling are essential to preserve the compound’s integrity and ensure safe usage in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086438871258,"sku":"TCI2510D139321131","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086438904026,"sku":"TCI2510D139321132","price":1339000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1393.jpg?v=1767103018"},{"product_id":"tci2510d160121410","title":"TCI D1601 25952-53-8 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride [Coupling Agent for Peptides Synthesis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride (EDC.HCl) is a chemical compound widely used as a coupling agent in peptide synthesis. It plays a crucial role in activating carboxyl groups, enabling the formation of stable ester bonds between amino acid molecules. This compound is essential in laboratory settings where the synthesis of peptides is required, particularly in biochemical and pharmaceutical research. Its ability to facilitate efficient and reliable peptide bond formation makes it a fundamental reagent in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eEDC.HCl is known for its high reactivity and effectiveness in promoting esterification reactions. Its chemical properties allow it to activate carboxylic acid groups, making them more susceptible to nucleophilic attack by amino groups. This makes it a preferred choice for researchers working on peptide synthesis, as it ensures consistent and reproducible results. The compound's stability under certain conditions further enhances its usability in various experimental setups, contributing to its widespread adoption in both academic and industrial laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, EDC.HCl is commonly used in biochemical and pharmacological research. It is a key reagent in the development of vaccines, drugs, and bioactive compounds. Its availability and reliability make it an essential tool for scientists engaged in peptide-based research. The compound’s role in enabling the synthesis of complex peptide structures supports its importance in both basic and applied research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: EDC.HCl is ideal for peptide synthesis due to its ability to activate carboxyl groups, enabling efficient coupling of amino acids.\u003c\/li\u003e\n\u003cli\u003eBiomedical Research: It supports the development of therapeutic peptides and bioactive compounds, making it essential for biomedical studies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: EDC.HCl is used in drug discovery to create peptide-based therapeutics with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its role in forming stable ester bonds makes it useful in biochemical assays requiring precise molecular interactions.\u003c\/li\u003e\n\u003cli\u003eDrug Target Validation: It aids in the synthesis of peptides used to study protein interactions and validate drug targets in pharmacological research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 25952-53-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEDC.HCl should be stored in a cool, dry environment, away from moisture and direct light to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to avoid any potential fumes. Avoid contact with incompatible substances, and always follow standard laboratory safety protocols when working with this compound. Proper storage and handling will help preserve its effectiveness and ensure safe usage in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086449914074,"sku":"TCI2510D160121410","price":1413000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086449946842,"sku":"TCI2510D160121411","price":1413000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086449979610,"sku":"TCI2510D160121412","price":1413000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086450012378,"sku":"TCI2510D160121413","price":1413000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1601.jpg?v=1767103323"},{"product_id":"tci2510d166221508","title":"TCI D1662 74124-79-1 Di(N-succinimidyl) Carbonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDi(N-succinimidyl) Carbonate (DSC) is a chemical reagent widely used in organic chemistry reactions, particularly in the synthesis of organic compounds and the modification of biological molecules. This compound is known for its ability to react with amino groups, making it a valuable tool in peptide and protein synthesis. Its role in activating amide bonds is critical in various biochemical processes, supporting research in chemical biology and molecular engineering. DSC is commonly employed in laboratories where efficient activation of amino groups is required, especially in the development of complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe reactivity and specificity of DSC make it a preferred choice for researchers working in chemical biology and peptide chemistry. Its high reactivity ensures effective activation of amino groups, which is essential for the formation of stable amide bonds. Additionally, DSC is known for its stability under controlled conditions, although it is sensitive to moisture and air exposure. These properties make it a reliable and efficient reagent for a wide range of laboratory applications. Its versatility and effectiveness in activating functional groups have made it a standard in many research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DSC is frequently used in biological chemistry, pharmaceutical research, and biotechnology. It plays a key role in the modification of biological molecules and the synthesis of compounds with specific structural requirements. Its relevance in these fields is due to its ability to facilitate precise chemical reactions, supporting the development of new drugs and advanced biochemical techniques. DSC is an essential component in the toolkit of researchers working on molecular-level innovations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide and protein synthesis due to its ability to activate amino groups efficiently in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic compound modification where amide bond formation is required for structural stability.\u003c\/li\u003e\n\u003cli\u003eBiochemical research applications that rely on amide bond activation for molecular interactions.\u003c\/li\u003e\n\u003cli\u003eDrug development processes that involve the synthesis of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eBiotransformation studies requiring precise chemical activation of functional groups.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 74124-79-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a dry, cool place away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDi(N-succinimidyl) Carbonate should be stored in a dry, cool environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can degrade its reactivity. Due to its sensitivity, it is best stored in a desiccator or a container with a drying agent. Always handle the compound in a well-ventilated area and avoid direct contact with skin or eyes. Proper personal protective equipment, such as gloves and safety goggles, should be used when handling this reagent. It is important to ensure that the storage area is free from potential contaminants and that the compound is kept in a secure location to prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086454272218,"sku":"TCI2510D166221508","price":1842000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086454304986,"sku":"TCI2510D166221509","price":1842000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1662.jpg?v=1767103435"},{"product_id":"tci2510d203822071","title":"TCI D2038 111160-56-6 Diphenyl (2,3-Dihydro-2-thioxo-3-benzoxazolyl)phosphonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiphenyl (2,3-Dihydro-2-thioxo-3-benzoxazolyl)phosphonate is a synthetic reagent widely used in laboratory settings for its unique chemical properties. This compound plays a crucial role in organic chemistry, particularly in coupling reactions where it facilitates the formation of complex molecular structures. Its ability to participate in various synthetic pathways makes it an essential tool for researchers aiming to develop new compounds with pharmaceutical or industrial applications. The compound is especially valuable in the synthesis of heterocyclic and phosphonate derivatives, which are key components in drug development and chemical innovation.\u003c\/p\u003e\n\u003cp\u003eThe chemical stability of Diphenyl (2,3-Dihydro-2-thioxo-3-benzoxazolyl)phosphonate under controlled conditions, combined with its reactivity in targeted reactions, makes it a preferred choice for synthetic chemists. Its complex molecular structure allows for versatile interactions with other reagents, enabling the synthesis of a wide range of compounds. The compound’s reactivity is carefully balanced to ensure it can be used effectively without compromising the integrity of the reaction. This combination of stability and reactivity ensures that it remains a reliable and efficient reagent in laboratory processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the development of new compounds with medical or industrial applications. Its availability and effectiveness in facilitating complex syntheses make it a popular choice among researchers. The compound is often utilized in academic and industrial settings to support the creation of novel chemical structures and to advance scientific understanding in the field of synthetic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this reagent's ability to participate in coupling reactions, enabling the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eDrug development projects often incorporate this compound due to its role in synthesizing heterocyclic and phosphonate derivatives, which are essential in pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes utilize this material for the production of specialty chemicals, leveraging its reactivity in controlled synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eResearch laboratories use it to explore new synthetic methodologies, particularly in the creation of novel compounds with potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eAcademic institutions employ this reagent in teaching and experimental studies to demonstrate advanced synthetic techniques and chemical reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 111160-56-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation and supplier specifications\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled with care using appropriate personal protective equipment such as gloves and safety goggles. Storage conditions should be maintained to ensure stability and prevent degradation. It is important to store it in a well-ventilated area to minimize any potential risks associated with its chemical properties. Proper labeling and safe handling procedures are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48275720962266,"sku":"TCI2510D203822071","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2038.jpg?v=1769180552"},{"product_id":"tci2510d223422345","title":"TCI D2234 527-61-7 2,6-Dimethyl-1,4-benzoquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Dimethyl-1,4-benzoquinone is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. As a building block in chemical reactions, it plays a crucial role in the development of complex organic molecules. Its aromatic structure, featuring two methyl groups at positions 2 and 6, along with two keto groups at positions 1 and 4, makes it a valuable intermediate in various synthetic pathways. This compound is particularly useful in oxidation and reduction reactions due to its stable yet reactive nature. It is commonly found in both academic and industrial research environments, where its chemical properties support a wide range of experimental applications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice for laboratory use. It is non-colored, solid in form, and soluble in organic solvents, which simplifies its handling and integration into chemical processes. Its relatively high melting and boiling points allow for efficient thermal processing in laboratory settings. These physical characteristics contribute to its reliability in synthetic procedures, enabling consistent results. The compound’s stability under controlled conditions ensures that it remains effective for multiple applications without degrading prematurely.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Dimethyl-1,4-benzoquinone is frequently used in organic chemistry research and pharmaceutical development. Its role in synthesizing compounds with pharmaceutical and industrial applications makes it an essential material for researchers. Many institutions and laboratories in Indonesia rely on this compound for its predictable performance and compatibility with various chemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 2,6-Dimethyl-1,4-benzoquinone is used for its ability to participate in oxidation and reduction reactions, making it ideal for creating complex organic molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from this compound due to its role in the synthesis of various drug compounds, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes often incorporate this material because of its stability and reactivity, allowing it to be used in the production of specialty chemicals and intermediates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories use it as a reference standard for identifying and quantifying compounds in various samples through spectroscopic and chromatographic methods.\u003c\/li\u003e\n\u003cli\u003ePolymer science research employs this compound in the development of new materials, leveraging its chemical structure to create polymers with specific functional properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 527-61-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its stability. Due to its chemical nature, it should be kept away from strong oxidizing or reducing agents to avoid unwanted reactions. Proper labeling of storage containers is essential for safety and identification. In laboratory settings, personal protective equipment such as gloves and goggles should be worn when handling this material to ensure safe usage. Regular inspection of storage conditions is advised to ensure optimal preservation of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086505881818,"sku":"TCI2510D223422345","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086505914586,"sku":"TCI2510D223422346","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086505947354,"sku":"TCI2510D223422347","price":1162000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2234.jpg?v=1767104449"},{"product_id":"tci2510d225622386","title":"TCI D2256 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Di-tert-butyl-1,4-benzoquinone is a chemical compound widely used in laboratory settings for various organic synthesis reactions. As a building block in chemistry, it plays a crucial role in the development of complex molecules, including dyes, pharmaceuticals, and industrial chemicals. Its aromatic structure, combined with two tert-butyl groups at positions 2 and 6, provides stability and controlled reactivity, making it a valuable tool for synthetic chemists. This compound is particularly useful in oxidation and reduction reactions due to its ability to participate in redox processes.\u003c\/p\u003e\n\u003cp\u003eThe compound’s non-heterocyclic nature and structural features make it a preferred choice for organic chemists. The tert-butyl groups reduce excessive reactivity, allowing for better control during synthesis. Its chemical stability ensures consistent performance in laboratory experiments, while its reactivity enables participation in a wide range of chemical transformations. These properties make it a reliable and versatile reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Di-tert-butyl-1,4-benzoquinone is commonly used by researchers and students in organic chemistry. It supports the development of new compounds and the modification of existing ones, contributing to advancements in chemical research. Its availability in the local market ensures easy access for those conducting experiments requiring high-quality reagents. This compound is essential for maintaining the efficiency and accuracy of chemical synthesis processes in Indonesian laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where this compound serves as a versatile building block for creating complex molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its role in the synthesis of active pharmaceutical ingredients and drug intermediates.\u003c\/li\u003e\n\u003cli\u003eDye and pigment development utilizes its structural properties to produce stable and color-fast compounds.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on its reactivity and stability for the creation of specialty chemicals.\u003c\/li\u003e\n\u003cli\u003eTeaching and research in academic institutions use it for demonstrating redox reactions and synthetic techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 719-22-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: 250g, 500g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or polyethylene to prevent moisture absorption and contamination. Due to its chemical nature, it should be kept separate from strong oxidizing or reducing agents to avoid unwanted reactions. In a laboratory setting, proper ventilation is essential when handling this material to ensure safe working conditions. Always use appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure. Regular inspection of storage containers is advised to maintain the integrity and safety of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086507323610,"sku":"TCI2510D225622386","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086507356378,"sku":"TCI2510D225622387","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2256.jpg?v=1767104490"},{"product_id":"tci2510d291923284","title":"TCI D2919 3945-69-5 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium Chloride is a chemical compound widely used in chemical and biochemical applications within laboratory settings. It belongs to the category of peptide chemistry and is commonly employed as a reagent or modifier in the synthesis of complex compounds. This compound plays a crucial role in molecular structure formation by acting as a linker or binder, facilitating the creation of specific molecular architectures. Its presence in various synthetic processes highlights its importance in both organic and biochemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and moderate reactivity, making it suitable for reactions under specific conditions. The presence of the dimethoxytriazine group in its molecular structure contributes to its unique chemical properties and stability, enabling it to participate effectively in a wide range of synthetic reactions. These characteristics make it a reliable choice for researchers looking to achieve consistent and reproducible results in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in organic chemistry and biochemical research. Its reliability in chemical reactions has made it an essential material for the development of new compounds, particularly in the fields of pharmacology and biotechnology. Its versatility and effectiveness have solidified its position as a valuable resource in both academic and industrial research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide synthesis due to its ability to act as a linker, enabling the formation of complex molecular structures with high specificity.\u003c\/li\u003e\n\u003cli\u003eBioconjugation Reactions: Its chemical stability and reactivity make it suitable for bioconjugation, where it helps attach biomolecules to other compounds for functional studies.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in organic synthesis to modify and create new compounds, offering versatility in reaction conditions and outcomes.\u003c\/li\u003e\n\u003cli\u003eDrug Development: The compound's role in creating stable molecular structures supports its use in drug development, particularly in the design of novel pharmaceutical agents.\u003c\/li\u003e\n\u003cli\u003eStructural Chemistry Studies: Its unique molecular structure allows for detailed investigations into chemical reactivity and molecular interactions in various experimental setups.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 3945-69-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various pack sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental use. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this material. It is important to follow standard safety protocols to minimize risks associated with chemical exposure. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086596845786,"sku":"TCI2510D291923284","price":1565000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086596878554,"sku":"TCI2510D291923285","price":1565000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2919.jpg?v=1767105562"},{"product_id":"tci2510d326223513","title":"TCI D3262 165534-43-0 3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one is a synthetic reagent widely used in laboratory settings for its unique chemical properties. This compound plays a crucial role in coupling reactions, where it facilitates the formation of specific chemical bonds between molecules. Its complex structure allows for high reactivity and specificity, making it an essential component in organic synthesis. Due to its ability to interact with various molecular structures, it is highly valued in chemical research and development.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high reactivity and structural versatility make it a preferred choice for researchers seeking precision in their synthetic processes. Its stability under controlled conditions ensures reliable performance during experiments, reducing the risk of unwanted side reactions. Additionally, its compatibility with a range of solvents and reaction conditions enhances its utility across different laboratory applications. These characteristics contribute to its popularity among scientists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research and the development of new compounds. Its role in synthetic reactions is vital for advancing chemical studies and innovation. Due to its effectiveness and reliability, it is a sought-after material for researchers and practitioners in educational institutions and research facilities across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this reagent due to its ability to facilitate specific bond formations and its high reactivity in coupling processes.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for developing new chemical compounds as it enables controlled and efficient synthetic pathways in research settings.\u003c\/li\u003e\n\u003cli\u003eIn pharmaceutical research, it supports the creation of complex molecular structures necessary for drug development and testing.\u003c\/li\u003e\n\u003cli\u003eIt is used in analytical chemistry for its role in modifying and stabilizing compounds during various experimental procedures.\u003c\/li\u003e\n\u003cli\u003eIts stability under controlled conditions makes it suitable for long-term storage and use in multiple laboratory protocols.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 165534-43-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis reagent should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its chemical integrity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and goggles. It is advisable to store it away from incompatible substances to avoid any potential chemical interactions. Proper labeling of storage containers is essential for safety and easy identification. Regular inspection of storage conditions ensures that the reagent remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086605856986,"sku":"TCI2510D326223513","price":2045000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3262.jpg?v=1768204964"},{"product_id":"tci2510d326323514","title":"TCI D3263 125700-69-8 O-(3,4-Dihydro-4-oxo-1,2,3-benzotriazin-3-yl)-N,N,N',N'-tetramethyluronium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3263, with CAS number 125700-69-8, is a synthetic reagent used in chemical reactions, particularly in coupling reactions. It is a complex compound containing a 1,2,3-benzotriazine group and a tetramethyluronium tetrafluoroborate moiety. This structure gives it high reactivity, making it a valuable tool in organic synthesis. Its unique chemical composition allows it to participate in a variety of synthetic processes, contributing to the development of new compounds in both research and industrial settings.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stability under specific conditions, yet it remains highly reactive towards various organic substrates. This dual nature makes it an ideal choice for reactions that require a catalyst or an active reagent. Its solubility in organic solvents further enhances its versatility, enabling its use in a wide range of experimental conditions. These properties ensure that TCI D3263 is a reliable and efficient reagent in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI D3263 is widely used in organic chemistry research, especially in pharmaceutical and material science applications. Its ability to provide precise and reliable results makes it a preferred choice for scientists working on complex chemical syntheses. The compound’s effectiveness and consistency contribute to the success of various research projects in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from TCI D3263 due to its high reactivity and ability to facilitate coupling reactions in complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this reagent for the synthesis of active pharmaceutical ingredients, leveraging its stability and reactivity in controlled environments.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments often incorporate TCI D3263 to develop new polymers and functional materials through efficient chemical bonding processes.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry labs use TCI D3263 in preparative reactions to isolate and purify compounds with high specificity and yield.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes rely on TCI D3263 for scalable synthesis of organic compounds, ensuring consistency and efficiency in production settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 125700-69-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTCI D3263 should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the reagent in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and goggles. The substance should be stored away from incompatible materials to avoid any potential chemical interactions. In laboratory settings, it is essential to follow standard safety protocols to ensure safe handling and proper disposal. Always ensure that the storage area is well-ventilated to minimize any risk associated with its use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086605889754,"sku":"TCI2510D326323514","price":1287000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086605922522,"sku":"TCI2510D326323515","price":1287000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3263.jpg?v=1769180602"},{"product_id":"tci2510d402924497","title":"TCI D4029 1892-57-5 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4029, 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide, is known in most laboratories simply by the abbreviation EDC or EDAC. It is a carbodiimide-class coupling reagent that forms the backbone of modern peptide chemistry. Its primary function is to activate carboxylic acid groups, converting them into a highly reactive O-acylisourea intermediate that can then be attacked directly by an amine to form an amide bond or a peptide bond. Because it joins two molecular fragments together under mild conditions, this reagent is used widely across peptide synthesis, biomolecule conjugation, and the immobilization of proteins onto solid surfaces in biochemistry laboratories.\u003c\/p\u003e\n\u003cp\u003eThe property that has made EDC so popular is its water solubility, together with the fact that its by-product is a urea derivative that is also water soluble. The dimethylaminopropyl group in its structure is weakly basic and can be protonated, which means that both excess reagent and reaction by-products can be removed simply by washing with water or dilute acid, without the time-consuming chromatography required when working with dicyclohexylcarbodiimide. The reagent performs well over a weakly acidic to neutral pH range and is commonly paired with additives to improve coupling efficiency and suppress side reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI D4029 is a routine choice wherever amide bond formation is carried out under mild aqueous or mixed-solvent conditions. University research groups, biochemistry and biotechnology laboratories, and analytical development groups rely on it for peptide synthesis work, for preparing bioconjugates, and for attaching biomolecules to solid supports. Its straightforward aqueous work-up makes it particularly convenient for laboratories that prefer to avoid extended purification steps for every coupling reaction.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide synthesis — EDC activates the carboxyl terminus of an amino acid or peptide fragment so that it couples cleanly with a free amine to form the peptide bond under mild conditions.\u003c\/li\u003e\n\u003cli\u003eAmide bond formation in organic synthesis — the reagent converts carboxylic acids into reactive O-acylisourea intermediates, allowing amines to be coupled without the harsh conditions normally needed for direct amidation.\u003c\/li\u003e\n\u003cli\u003eBiomolecule conjugation — because it works in weakly acidic to neutral aqueous media, EDC is well suited to joining proteins, peptides, and other sensitive biomolecules that would not survive aggressive coupling chemistry.\u003c\/li\u003e\n\u003cli\u003eProtein immobilization on solid surfaces — carboxyl-functionalized supports can be activated with EDC and then coupled to amine groups on proteins, a standard route for preparing functionalized surfaces in biochemistry work.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions requiring simple work-up — the water-soluble urea by-product and protonatable dimethylaminopropyl group allow removal by water or dilute acid washing, making EDC ideal where chromatographic purification is impractical.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 1892-57-5\u003c\/li\u003e\n\u003cli\u003eChemical name: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide (EDC \/ EDAC)\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in a cool, dry place in its original tightly closed container, following the storage conditions specified on the manufacturer's label and Safety Data Sheet. Carbodiimide reagents are moisture sensitive, so keep the container well sealed and allow it to reach room temperature before opening to limit condensation on the contents. Handle in a fume hood or a well-ventilated area, wearing gloves, safety glasses, and a laboratory coat, and avoid contact with skin and eyes as well as inhalation of any dust or vapour. Keep away from incompatible materials, weigh out only the quantity needed for the reaction, and dispose of residues and contaminated materials in accordance with your institution's chemical waste procedures. Always consult the Safety Data Sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086651896026,"sku":"TCI2510D402924497","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086651928794,"sku":"TCI2510D402924498","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086651961562,"sku":"TCI2510D402924499","price":1363000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4029.jpg?v=1767106964"},{"product_id":"tci2510d534726230","title":"TCI D5347 691-24-7 N,N'-Di-tert-butylcarbodiimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N'-Di-tert-butylcarbodiimide (DTB-CI), also known as TCI D5347, is a widely used chemical compound in laboratory settings for activating carboxyl groups during organic synthesis. It functions as a coupling agent that facilitates the formation of esters and amides from carboxylic acids through efficient activation mechanisms. This reagent is essential in chemical laboratories for its ability to enhance reaction rates without undergoing chemical changes itself, making it a reliable catalyst in various synthetic processes. Its role is critical in the development of complex organic molecules, particularly in the field of medicinal chemistry and polymer science.\u003c\/p\u003e\n\u003cp\u003eDTB-CI is valued for its chemical stability under controlled conditions, although it is highly sensitive to moisture and air. Its molecular structure, featuring two tert-butyl groups, contributes to its overall stability and reactivity. These properties make it a preferred choice for researchers needing a consistent and effective reagent for activating carboxylic acid groups. The compound’s versatility allows it to be used in a wide range of reaction conditions, making it a staple in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DTB-CI is commonly used in organic chemistry research, especially in the synthesis of compounds requiring carboxyl group activation. It is frequently found in academic and industrial research settings, particularly in fields such as pharmaceutical development and materials science. Its reliability and effectiveness make it a go-to reagent for chemists working on complex molecular structures.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for ester and amide formation due to its efficient carboxyl activation properties\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry research to develop pharmaceutical compounds requiring functional group modification\u003c\/li\u003e\n\u003cli\u003ePolymer science applications for cross-linking and modifying polymer chains through carboxyl group reactions\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production for large-scale synthesis of organic compounds with high purity\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry departments for teaching and experimental studies on coupling reactions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 691-24-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a dry, cool, and well-ventilated area away from moisture and air\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDTB-CI should be stored in a dry, cool, and well-ventilated area to prevent moisture absorption, which can degrade its effectiveness. It is recommended to use airtight containers made of glass or high-density polyethylene to minimize exposure to air and humidity. Due to its sensitivity, it should be handled in a fume hood to avoid inhalation of vapors. Always ensure proper personal protective equipment is worn when handling this compound. Avoid contact with water or moisture during storage and use to maintain its chemical integrity. Regular inspection of storage conditions is advised to ensure optimal performance in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086755475674,"sku":"TCI2510D534726230","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086755508442,"sku":"TCI2510D534726231","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5347.jpg?v=1767108642"},{"product_id":"tci2510d628927348","title":"TCI D6289 293311-03-2 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6289, with the CAS number 293311-03-2, is a chemical compound widely used in laboratory settings for its unique structural and functional properties. This compound, known as 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium Tetrafluoroborate, plays a key role in chemical and biochemical applications, particularly in peptide chemistry. Its complex structure, combining morpholine and triazine rings, makes it a versatile reagent in organic synthesis. It is especially valuable in the development of new compounds and the study of molecular interactions.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its excellent solubility in organic solvents and its ability to participate in substitution and coupling reactions. These characteristics make it ideal for use in controlled chemical environments where stability and reactivity are essential. Its molecular structure also allows it to be a key component in the synthesis of complex organic molecules. The compound’s stability under controlled laboratory conditions further enhances its reliability in research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers and academic institutions for the development of new chemical compounds and the advancement of biochemical studies. Its availability in the local market supports scientific research and experimentation, making it a valuable resource for both educational and industrial applications. Its role in accelerating peptide synthesis and other chemical processes underscores its importance in modern laboratory practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide synthesis due to its ability to facilitate efficient coupling reactions and its stability in organic solvents.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its unique molecular structure makes it suitable for studying molecular interactions and biological processes in biochemical experiments.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: The compound’s reactivity and solubility properties make it a preferred choice for various organic synthesis reactions.\u003c\/li\u003e\n\u003cli\u003eDrug Development: It is often used in the development of new pharmaceutical compounds due to its role in creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: Its stability and reactivity make it a useful reagent in analytical methods requiring precise chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 293311-03-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity and stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that it is stored away from incompatible substances to avoid any potential chemical reactions. Proper labeling of storage containers is essential for safety and easy identification. Regular monitoring of storage conditions ensures that the compound remains effective for its intended laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086801744090,"sku":"TCI2510D628927348","price":2550000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6289.jpg?v=1767110039"},{"product_id":"tci2510e036328108","title":"TCI E0363 16357-59-8 1-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline is a chemical compound widely used in laboratory settings for its unique molecular structure and reactivity. This compound plays a crucial role in chemical and biochemical experiments, particularly in the synthesis of organic compounds and the development of peptide chemistry. Its complex structure allows it to participate in various chemical reactions, making it an essential reagent for researchers working in advanced synthetic pathways. Due to its versatility, it is frequently utilized in both academic and industrial research environments where precise chemical manipulation is required.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under controlled conditions and its solubility in organic solvents, which facilitates efficient chemical reactions and purification processes. Its reactivity and specificity make it a preferred choice for applications requiring high precision and controlled outcomes. The compound’s sensitivity to moisture and light necessitates careful handling and storage, but these properties also contribute to its effectiveness in targeted chemical synthesis. These characteristics ensure that it remains a reliable and consistent material for laboratory use.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in chemical and biochemical research, particularly in academic institutions and research centers. Its application spans various fields, including organic synthesis and molecular interaction studies. Researchers rely on its predictable behavior and chemical properties to achieve accurate and reproducible results in their experiments. Its presence in Indonesian laboratories underscores its importance in advancing scientific research and development in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This compound is ideal for creating complex organic molecules due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry: It is used in the development of peptide-based compounds, offering a stable platform for molecular modifications.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: Its unique structure allows it to be used in studying molecular interactions and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic Compound Research: It plays a key role in the synthesis of heterocyclic compounds, which are essential in pharmaceutical and biochemical applications.\u003c\/li\u003e\n\u003cli\u003eControlled Reaction Environments: Its stability under specific conditions makes it suitable for experiments requiring precise chemical control.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 16357-59-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent exposure to humidity and contaminants. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures in place. Always ensure that the storage area is well-ventilated and free from potential sources of contamination. Proper labeling and secure storage are essential to prevent accidental exposure and ensure safe usage in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086840312026,"sku":"TCI2510E036328108","price":1918000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0363.jpg?v=1771058792"},{"product_id":"tci2510e084728644","title":"TCI E0847 3849-21-6 Ethyl Cyano(hydroxyimino)acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyano(hydroxyimino)acetate is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block for the creation of complex molecular structures, offering versatility in chemical reactions due to its unique functional groups. This compound is particularly valued for its ability to participate in specific chemical transformations, making it a preferred choice for researchers aiming to develop new compounds and materials. Its role in synthetic chemistry is crucial, especially in the design of pharmaceuticals and specialty chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits chemical stability under controlled conditions, yet it remains highly reactive to changes in pH, temperature, and catalysts. This reactivity allows for precise control in synthetic processes, ensuring the desired outcomes in laboratory experiments. Its ability to form various chemical bonds further enhances its utility in diverse applications. The compound’s reactivity and selectivity make it an essential tool in synthetic chemistry, enabling the development of new compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl Cyano(hydroxyimino)acetate is commonly used by chemists in organic synthesis research and the development of new materials. It plays a vital role in academic and industrial research settings, supporting both educational and innovative projects. Its relevance in chemical education and research makes it a valuable resource for universities and research institutions focused on advancing chemical knowledge and applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research where precise chemical transformations are required due to its reactivity and selectivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceutical compounds as a building block for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eChemical education in academic institutions for teaching synthetic chemistry techniques and molecular design.\u003c\/li\u003e\n\u003cli\u003eIndustrial research applications in the creation of specialty chemicals and advanced materials.\u003c\/li\u003e\n\u003cli\u003eCustom compound synthesis projects requiring versatile and adaptable chemical intermediates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3849-21-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyano(hydroxyimino)acetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound should be stored away from incompatible substances to avoid potential chemical interactions. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications. Proper labeling and secure storage are essential to maintain safety and prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086900506842,"sku":"TCI2510E084728644","price":1692000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086900539610,"sku":"TCI2510E084728645","price":1692000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0847.jpg?v=1767111863"},{"product_id":"tci2510e090128722","title":"TCI E0901 137156-41-3 Ethyl 1-Hydroxy-1H-1,2,3-triazole-4-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 1-Hydroxy-1H-1,2,3-triazole-4-carboxylate is a synthetic chemical compound widely used in laboratory settings for its reactivity and versatility. As a coupling reagent, it plays a crucial role in the synthesis of heterocyclic compounds and triazole derivatives. This compound is particularly valuable in organic chemistry due to its ability to participate in a variety of chemical reactions, making it an essential tool for researchers. Its unique molecular structure, combining a triazole ring with an ethyl ester group, contributes to its effectiveness in forming complex molecular bonds.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and stability make it a preferred choice for synthetic chemists. Its molecular structure allows it to interact with various ligands and reagents, facilitating the formation of new chemical bonds. This property is especially important in applications requiring precise control over reaction conditions. Additionally, its chemical stability ensures that it remains effective even under a range of experimental conditions, making it reliable for use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the synthesis of heterocyclic compounds and the development of new chemical materials. It is also found in pharmaceutical and food chemistry research, where its reactivity and stability make it a valuable component in the formulation of new compounds and the study of chemical interactions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and ability to form complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical materials in industrial and academic research settings.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the synthesis of triazole derivatives and related compounds.\u003c\/li\u003e\n\u003cli\u003eFood chemistry studies involving the creation of new compounds and chemical interactions.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions in synthetic chemistry where precise bond formation is required.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 137156-41-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation is essential when working with this material to ensure safe laboratory conditions. Avoid exposure to incompatible substances to maintain its stability and effectiveness in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086906339546,"sku":"TCI2510E090128722","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086906372314,"sku":"TCI2510E090128723","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0901.jpg?v=1768205246"},{"product_id":"tci2510e091628744","title":"TCI E0916 136849-72-4 O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eO-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium Tetrafluoroborate is a specialized chemical compound commonly referred to as TCI E0916. This compound is widely used in laboratory settings for its unique reactivity and specificity in peptide chemistry. It plays a crucial role in the synthesis of complex peptides, particularly in peptide coupling reactions. Due to its chemical structure, it is highly effective in forming amide bonds under controlled conditions, making it an essential tool for researchers in chemical biology.\u003c\/p\u003e\n\u003cp\u003eThis compound is known for its high reactivity and stability under specific conditions, which makes it a preferred choice for various synthetic applications. Its ability to function as an efficient coupling agent is due to its molecular structure, which allows it to react selectively with organic substrates. The compound’s stability in anhydrous environments and at low temperatures further enhances its utility in laboratory processes. These properties ensure reliable results in peptide synthesis and related chemical reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in biochemical research and peptide synthesis projects. It is particularly favored by academic institutions and research centers that focus on chemical biology and medicinal chemistry. Its application in these settings supports the development of new pharmaceutical compounds and bioactive molecules. The compound’s versatility and effectiveness make it a valuable resource for scientists working in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing complex peptides due to its high reactivity and specificity in forming amide bonds.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: It supports research in chemical biology by enabling the creation of custom peptide sequences for various studies.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Reactions: Its ability to react with a wide range of organic substrates makes it suitable for amide coupling reactions.\u003c\/li\u003e\n\u003cli\u003eAnhydrous Reaction Conditions: The compound remains stable in anhydrous environments, making it suitable for reactions requiring dry conditions.\u003c\/li\u003e\n\u003cli\u003eLow-Temperature Reactions: It functions effectively at low temperatures, making it a preferred choice for controlled synthesis processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 136849-72-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. The compound is stable under anhydrous conditions and at low temperatures, making it suitable for storage in a refrigerator if required. It is important to avoid contact with water or other reactive substances to ensure its effectiveness and safety in laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086907814106,"sku":"TCI2510E091628744","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086907846874,"sku":"TCI2510E091628745","price":657000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0916.jpg?v=1768205247"},{"product_id":"tci2510e130629271","title":"TCI E1306 333717-40-1 O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E1306, also known as O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium Hexafluorophosphate, is a synthetic reagent widely used in chemical synthesis, particularly in coupling reactions. This compound plays a crucial role in facilitating the formation of chemical bonds between molecules, making it an essential tool in organic chemistry research. Its unique molecular structure allows for highly specific and efficient reactions, which are vital in the development of new compounds and materials.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make TCI E1306 a preferred choice is its high reactivity and ability to form stable bonds with various substrates. The compound’s controlled reactivity and molecular stability ensure consistent results in chemical processes, making it reliable for laboratory applications. Its effectiveness as a coupling reagent is further enhanced by its ability to maintain reaction specificity, which is critical in complex synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI E1306 is commonly used in scientific research and chemical product development. It is particularly relevant for researchers in organic chemistry, pharmacy, and biochemistry due to its versatility and efficiency. Its availability and performance make it a valuable resource for both academic and industrial applications in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research: TCI E1306 is ideal for creating complex organic molecules due to its high reactivity and specificity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development: This reagent is used to synthesize new drug compounds by facilitating efficient bond formation between functional groups.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies: Its ability to form stable bonds makes it suitable for modifying biomolecules in biochemical experiments.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production: TCI E1306 supports the creation of industrial chemicals by enabling precise and controlled chemical reactions.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications: It is used in analytical processes to ensure accurate and reproducible results in chemical analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 333717-40-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in powder or crystalline form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTCI E1306 should be stored in a cool, dry environment to maintain its chemical stability and reactivity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which can affect its performance. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. The reagent should not be stored near incompatible substances to avoid any potential chemical interactions. Proper labeling and storage conditions are essential to ensure the safety of laboratory personnel and the integrity of the compound. Regular monitoring of storage conditions will help maintain the quality and effectiveness of TCI E1306 in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086946644186,"sku":"TCI2510E130629271","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086946676954,"sku":"TCI2510E130629272","price":758000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1306.jpg?v=1769180775"},{"product_id":"tci2510f072630681","title":"TCI F0726 164298-23-1 Fluoro-N,N,N',N'-tetramethylformamidinium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI F0726 is Fluoro-N,N,N',N'-tetramethylformamidinium Hexafluorophosphate, a coupling reagent widely known by the abbreviation TFFH. Unlike uronium- or phosphonium-based coupling reagents that operate through active esters, this reagent converts a carboxylic acid group into an acyl fluoride in situ. The acyl fluoride is an activated species reactive enough to form an amide bond, yet far more resistant to hydrolysis than the corresponding acyl chloride. This makes handling at the bench considerably more forgiving and results easier to reproduce across runs.\u003c\/p\u003e\n\u003cp\u003eThe advantage that makes this reagent a preferred choice lies in its ability to overcome difficult couplings. The acyl fluoride is small in size, so steric hindrance is reduced, which makes it especially useful for amino acids bearing bulky side chains such as valine and isoleucine derivatives and quaternary amino acids. The reagent also does not generate guanidinylation side products on free amines, a problem that occasionally arises with uronium reagents. In addition, TFFH performs well with amino acids containing sensitive functional groups, including arginine, because activation proceeds rapidly and minimizes lactam formation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in peptide chemistry and chemical biology settings where amide bond formation is the central transformation. It suits academic research groups, pharmaceutical development laboratories, and synthesis facilities that prepare peptide sequences or small-molecule amides. Workers reach for it particularly when standard coupling conditions have already been attempted and a sterically demanding or side-reaction-prone residue requires a more robust activation route.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolid-phase peptide synthesis: the in situ acyl fluoride route drives couplings to completion on resin-bound sequences where conventional active ester chemistry stalls or gives incomplete conversion.\u003c\/li\u003e\n\u003cli\u003eCoupling of sterically hindered amino acids: the compact acyl fluoride intermediate reduces steric congestion, making it effective for valine, isoleucine, and quaternary amino acid derivatives that resist standard reagents.\u003c\/li\u003e\n\u003cli\u003eArginine-containing sequence assembly: rapid activation limits the residence time of the activated species and thereby minimizes lactam formation, a common side reaction with this residue.\u003c\/li\u003e\n\u003cli\u003eSynthesis involving free amine substrates: because the reagent produces no guanidinylation by-products on free amines, it avoids a side reaction that complicates purification when uronium reagents are used.\u003c\/li\u003e\n\u003cli\u003eGeneral amide bond formation in chemical biology: the greater hydrolytic stability of acyl fluorides compared with acyl chlorides gives more forgiving handling and more reproducible yields between batches.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 164298-23-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003eChemical name: Fluoro-N,N,N',N'-tetramethylformamidinium Hexafluorophosphate (TFFH)\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required quantity when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container under the conditions stated on the manufacturer label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry place, away from moisture and from sources of heat or ignition, following the conditions given on the manufacturer label and safety data sheet. Because the reagent generates a moisture-sensitive activated species during use, keep the container sealed when not in use and weigh out portions promptly to limit exposure to humid air. Use the original manufacturer container or a compatible tightly sealed glass vessel, clearly labelled. Handle inside a fume hood with appropriate personal protective equipment, including safety glasses, gloves, and a laboratory coat, and avoid contact with skin, eyes, and inhalation of any dust. Keep it separate from incompatible materials and dispose of residues in accordance with local chemical waste regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087028105434,"sku":"TCI2510F072630681","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087028138202,"sku":"TCI2510F072630682","price":1541000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0726.jpg?v=1769056097"},{"product_id":"tci2510f118431289","title":"TCI F1184 2118332-08-2 2-Fluoro-6-(trifluoromethyl)benzoic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Fluoro-6-(trifluoromethyl)benzoic Anhydride is a fluorinated organic compound widely used in chemical laboratories for the synthesis of complex organic molecules. This compound serves as a key building block in various chemical reactions, particularly those involving electrophilic substitution and functional group transformations. Its unique molecular structure, featuring both fluorine and trifluoromethyl groups, makes it an essential reagent in the development of new pharmaceuticals and bioactive compounds. Due to its chemical stability and reactivity, it is a valuable tool for researchers aiming to explore novel synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s fluorinated structure contributes to its high reactivity and selectivity in chemical reactions. The presence of fluorine atoms enhances the molecule’s stability while also influencing its reactivity in different reaction conditions. This combination of properties makes it a preferred choice for chemists working on advanced synthetic strategies. Its ability to participate in a wide range of reactions, including acylation and esterification, further solidifies its role in modern chemical research. The compound is especially useful in applications requiring precise control over molecular functionality.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Fluoro-6-(trifluoromethyl)benzoic Anhydride is commonly used in pharmaceutical and industrial chemistry research. It plays a crucial role in the development of new drugs and chemical materials. Researchers in Indonesia rely on this compound for its versatility and effectiveness in complex synthetic processes. Its application is widespread in both academic and industrial settings, supporting innovation in chemical synthesis and drug discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical synthesis for the development of bioactive compounds due to its fluorinated structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for electrophilic substitution reactions and functional group modifications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production for the creation of specialized materials and intermediates.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects requiring precise molecular modifications and synthetic flexibility.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical analysis in laboratories focusing on fluorinated compound behavior and reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2118332-08-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture exposure, which can affect its stability. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong bases or reducing agents. Keep the material away from heat sources and ensure proper labeling for safe handling and disposal. Regular monitoring of storage conditions is essential to ensure optimal performance and safety in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087065329882,"sku":"TCI2510F118431289","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1184.jpg?v=1768360372"},{"product_id":"tci2510h039532937","title":"TCI H0395 524-38-9 N-Hydroxyphthalimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxyphthalimide (NHP) is a chemical compound widely used in various laboratory applications, particularly in peptide chemistry and chemical biology. It serves as a key reagent in the synthesis of peptides and their derivatives, playing a crucial role in molecular conjugation and modification processes. Its reactivity allows it to participate in reactions with amines, amino acids, and other substrates, making it indispensable in biochemical research. Due to its stability and controlled reactivity, NHP is a preferred choice for experiments requiring precise chemical interactions.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons NHP is favored in laboratories is its ability to undergo nucleophilic reactions while maintaining structural integrity. This property ensures consistent results in complex synthetic procedures. Additionally, NHP exhibits good solubility in organic solvents, which simplifies mixing and separation during experiments. These characteristics make it highly suitable for use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, NHP is commonly utilized in peptide synthesis, biomedical compound development, and pharmaceutical research. Its reliability and effectiveness in chemical reactions make it a valuable tool for scientists working in the fields of chemistry and biology. The compound's versatility supports a wide range of experimental needs, contributing to the advancement of scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: NHP is used to facilitate peptide bond formation through nucleophilic reactions, enhancing the efficiency of peptide synthesis processes.\u003c\/li\u003e\n\u003cli\u003eBiomedical Compound Development: Its reactivity and solubility make it ideal for synthesizing complex biologically active compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: NHP supports the development of pharmaceuticals by enabling controlled chemical modifications of molecular structures.\u003c\/li\u003e\n\u003cli\u003eMolecular Conjugation Studies: The compound's ability to react with various substrates aids in the study of molecular interactions and conjugation mechanisms.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: NHP is a preferred reagent in reactions requiring stable and reactive intermediates, supporting a broad range of chemical investigations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 524-38-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxyphthalimide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Due to its solid form, it is best stored in a sealed container made of inert material such as glass or polyethylene to avoid chemical interactions. Laboratory personnel should handle NHP with care, using appropriate personal protective equipment when necessary. Proper storage ensures the compound remains effective for use in various biochemical and chemical applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087200891098,"sku":"TCI2510H039532937","price":683000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087200923866,"sku":"TCI2510H039532938","price":683000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087200956634,"sku":"TCI2510H039532939","price":683000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0395.jpg?v=1768205514"},{"product_id":"tci2510h046833022","title":"TCI H0468 80029-43-2 1-Hydroxybenzotriazole Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Hydroxybenzotriazole Monohydrate is a chemical compound widely utilized in various chemical reactions and biosynthetic processes. It plays a crucial role in laboratory settings as a reagent for the formation of ester and amide bonds. This compound is particularly valued for its ability to activate carboxyl groups in organic compounds, thereby accelerating chemical reactions. Its unique molecular structure makes it an essential component in many synthetic pathways, especially in the field of glycoscience. Due to its stability and reactivity, it is frequently employed in biochemical and pharmacological research.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability under normal conditions, combined with its high reactivity in specific environments, makes it a preferred choice for researchers. The presence of a water molecule in its monohydrate form enhances its reactivity, allowing for more efficient reactions. This property is particularly beneficial in applications requiring precise functional group activation. Additionally, its solubility in organic solvents simplifies its use in a wide range of experimental procedures. These characteristics contribute to its popularity among scientists working in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Hydroxybenzotriazole Monohydrate is commonly used in chemical and biological research. It is a key reagent in the synthesis of glycosides and other complex organic molecules. Many research institutions in Indonesia rely on this compound for its reliability and effectiveness in various experimental setups. Its consistent performance and availability make it a go-to material for researchers in the field of chemical biology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGlycoside Synthesis: This compound is ideal for activating carboxyl groups in sugar derivatives, enabling efficient glycosidic bond formation.\u003c\/li\u003e\n\u003cli\u003ePeptide Coupling Reactions: Its ability to activate carboxylic acid groups makes it suitable for peptide synthesis and modification processes.\u003c\/li\u003e\n\u003cli\u003eBioconjugation Studies: The compound facilitates the coupling of biomolecules, making it useful in bioconjugation and molecular labeling techniques.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the preparation of esters and amides, supporting a variety of organic reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eEnzymatic Reaction Optimization: Its reactivity and stability help in studying enzyme mechanisms and substrate interactions in biochemical experiments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 80029-43-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities, including 5g, 25g, and 100g\u003c\/li\u003e\n\u003cli\u003ePhysical form: White crystalline powder\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is not flammable but may react with strong acids or bases. Proper ventilation is advised during handling to ensure a safe laboratory environment. Always follow standard chemical safety protocols to minimize any potential risks associated with its use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087212294362,"sku":"TCI2510H046833022","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"200g","offer_id":48087212327130,"sku":"TCI2510H046833023","price":1591000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0468.jpg?v=1767116459"},{"product_id":"tci2510h052833110","title":"TCI H0528 21715-90-2 N-Hydroxy-5-norbornene-2,3-dicarboximide [for Peptide Synthesis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxy-5-norbornene-2,3-dicarboximide, frequently abbreviated in the literature as HONB, is a coupling additive reagent prepared specifically for peptide synthesis work. Structurally it is a cyclic imide fused to a norbornene framework, with the N-hydroxy group serving as its reactive centre. In a laboratory workflow, this reagent is used together with a carbodiimide or another activating reagent to convert a carboxylic acid into an active ester, which then reacts with an amine group to form the amide bond. Its role is to make the coupling reaction proceed more cleanly and under better control.\u003c\/p\u003e\n\u003cp\u003eThe principal reason chemists select this reagent is its ability to suppress racemisation at the alpha carbon of an amino acid during activation — a classic problem that can compromise the chiral purity of a peptide product. The active esters it forms are reactive enough to complete the coupling at a reasonable rate, yet stable enough to be isolated and stored when a workflow calls for it. The hydrophobic norbornene framework offers a practical advantage during purification, because reagent by-products are generally easier to separate than those of comparable additives.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories the reagent is typically found in university research groups, pharmaceutical and biotechnology development units, and contract synthesis facilities engaged in peptide chemistry. It is normally handled at the bench scale alongside standard carbodiimide activators, and is ordered as a supporting reagent within a wider peptide synthesis programme rather than as a bulk consumable. Its packaging and grade designation for peptide synthesis make it suitable for work where chiral integrity of the product must be preserved.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolution-phase peptide coupling — added with a carbodiimide to generate the active ester in situ, giving cleaner amide bond formation and reduced side reactions.\u003c\/li\u003e\n\u003cli\u003eRacemisation-sensitive fragment condensation — chosen where two peptide fragments are joined and the alpha carbon of the C-terminal residue is most vulnerable to epimerisation.\u003c\/li\u003e\n\u003cli\u003ePreparation of isolable active esters — the esters formed are stable enough to be purified and stored, allowing coupling steps to be staged across separate working sessions.\u003c\/li\u003e\n\u003cli\u003eAmide bond formation in general organic synthesis — applicable wherever a carboxylic acid must be activated toward an amine under mild and controllable conditions.\u003c\/li\u003e\n\u003cli\u003eMethod development and reagent comparison studies — used as a reference additive when evaluating coupling efficiency, chiral purity, and by-product removal against alternative additives.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI, catalogue number H0528\u003c\/li\u003e\n\u003cli\u003eCAS number: 21715-90-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eGrade designation: for Peptide Synthesis\u003c\/li\u003e\n\u003cli\u003ePack sizes: supplied in the manufacturer's standard catalogue pack sizes; please refer to the current product listing\u003c\/li\u003e\n\u003cli\u003ePhysical form and storage class: refer to the manufacturer's specification sheet and safety data sheet supplied with the product\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry place, away from direct sunlight, heat sources, moisture, and incompatible materials such as strong bases and strong oxidising agents. Keep the container sealed when not in use to limit moisture uptake, and allow refrigerated stock to reach room temperature before opening so that condensation does not enter the bottle. Handle in a well-ventilated area or fume hood using a laboratory coat, chemical-resistant gloves, and eye protection. Use clean, dry spatulas and glassware when weighing to avoid contaminating the bulk material. Follow the manufacturer's safety data sheet for detailed exposure controls, spill response, and waste disposal, and observe institutional procedures for chemical waste handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087219372250,"sku":"TCI2510H052833110","price":1263000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48087219405018,"sku":"TCI2510H052833111","price":1263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0528.jpg?v=1771058577"},{"product_id":"tci2510h062333251","title":"TCI H0623 6066-82-6 N-Hydroxysuccinimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0623 N-Hydroxysuccinimide, commonly abbreviated as NHS, is a carboxyl-activating reagent that forms the backbone of modern peptide chemistry and bioconjugation. When paired with a carbodiimide such as EDC or DCC, NHS converts carboxylic acids into NHS esters that are considerably more reactive toward primary amines. These active esters then form amide bonds efficiently with the amino groups of lysine residues on proteins, with amine groups on linkers, or with the next amino acid in a peptide synthesis sequence, which is why this reagent is almost always kept on hand in biochemistry laboratories.\u003c\/p\u003e\n\u003cp\u003eThe property that makes NHS so dependable is its ability to suppress side reactions while simultaneously improving coupling yields. Without NHS, the O-acylisourea intermediate generated from a carbodiimide readily rearranges into unreactive N-acylurea or is wastefully hydrolysed; the presence of NHS traps that intermediate as an active ester that is far more stable and remains selective toward amines. NHS also helps suppress racemisation during peptide synthesis, an important advantage whenever stereochemical purity is a requirement. It takes the form of a white crystalline solid that dissolves in water and in polar organic solvents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, NHS is a routine item in university biochemistry groups, research institutes, and industrial R\u0026amp;D units engaged in peptide synthesis, protein labelling, and the preparation of conjugated reagents. Because it is used in small portions across many separate couplings, a single container typically supports an extended series of experiments. Its stability as a crystalline solid also makes it practical for facilities where reagents are ordered periodically rather than continuously, provided humidity is properly controlled.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide bond formation in solution-phase and solid-phase synthesis, where NHS esters couple amino acid building blocks efficiently while suppressing the racemisation that would compromise stereochemical purity of the final peptide.\u003c\/li\u003e\n\u003cli\u003eProtein bioconjugation via lysine residues, where NHS activation of carboxyl-bearing labels allows stable amide linkage to primary amine groups on the protein surface under mild aqueous conditions.\u003c\/li\u003e\n\u003cli\u003eCarbodiimide-mediated coupling with EDC or DCC, in which NHS intercepts the unstable O-acylisourea intermediate and converts it into a longer-lived active ester, markedly raising coupling efficiency.\u003c\/li\u003e\n\u003cli\u003ePreparation of crosslinkers and linker reagents, where NHS-activated termini are introduced onto spacer molecules so that the resulting reagent reacts selectively with amine functionalities during later assembly steps.\u003c\/li\u003e\n\u003cli\u003eSurface functionalisation of amine-bearing supports and resins, where NHS ester chemistry immobilises carboxyl-containing molecules through covalent amide bonds that resist hydrolysis better than physically adsorbed alternatives.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6066-82-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePhysical form: white crystalline solid\u003c\/li\u003e\n\u003cli\u003eSolubility: soluble in water and polar organic solvents\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed on this product page\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore N-Hydroxysuccinimide in a tightly closed original container in a cool, dry place away from moisture, since the solid is hygroscopic in practice and water uptake degrades activation performance. Keep the container closed when not in use and allow it to reach room temperature before opening if it has been stored cold, so that condensation does not form on the crystals. Handle the material in a fume hood or a well-ventilated area, wearing gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust during weighing. Prepare activated ester solutions fresh where the protocol calls for it, as NHS esters hydrolyse in aqueous media over time. Consult the manufacturer's safety data sheet before first use and follow local institutional rules for chemical waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087224975578,"sku":"TCI2510H062333251","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087225008346,"sku":"TCI2510H062333252","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087225041114,"sku":"TCI2510H062333253","price":1162000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0623.jpg?v=1767116767"},{"product_id":"tci2510h130434102","title":"TCI H1304 106627-54-7 N-Hydroxysulfosuccinimide Sodium Salt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H1304 N-Hydroxysulfosuccinimide Sodium Salt, commonly abbreviated as Sulfo-NHS, is a carboxyl-activating reagent of central importance in bioconjugation chemistry. It is used together with a water-soluble carbodiimide such as EDC to convert carboxylate groups into a far more stable active ester intermediate, so that the subsequent reaction with primary amine groups on proteins, peptides, or material surfaces proceeds with higher and more reproducible yields. Its role in the laboratory is that of a supporting reagent that transforms an otherwise inefficient aqueous amidation reaction into a reliable routine procedure.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent the preferred choice is the sulfonate group in its structure, which confers excellent solubility in water and in buffer solutions. Because of this, activation can be carried out directly in aqueous systems without the addition of organic solvents such as dimethylformamide, which can potentially damage protein structure or reduce biological activity. The negative charge of the sulfonate group also prevents the reagent and its active ester from crossing cell membranes, making it well suited to the selective labelling of cell-surface proteins. The Sulfo-NHS active ester also remains sufficiently long-lived at near-neutral pH for practical handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university research groups, biotechnology laboratories, and diagnostic development units that prepare protein conjugates in-house. It is commonly ordered alongside EDC as a working pair for coupling antibodies, enzymes, or peptides to carriers, particles, or plate surfaces. Because the entire procedure can be performed in aqueous buffer, it fits laboratories that work with biological samples and prefer to avoid organic solvent handling at the bench.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProtein and peptide conjugation, where the stabilised active ester allows amide bond formation with primary amines in aqueous buffer at higher and more reproducible yields.\u003c\/li\u003e\n\u003cli\u003eAntibody labelling and immunoassay development, since the reagent supports controlled coupling of antibodies to enzymes, reporters, or carrier proteins without organic solvent exposure.\u003c\/li\u003e\n\u003cli\u003eCell-surface protein labelling, because the negatively charged sulfonate group prevents membrane penetration so only proteins exposed on the outer surface are modified.\u003c\/li\u003e\n\u003cli\u003eSurface functionalisation of particles and materials, where carboxyl-bearing surfaces are activated in water and then coupled to amine-containing ligands or biomolecules.\u003c\/li\u003e\n\u003cli\u003eImmobilisation of biomolecules onto plates, resins, or sensor supports, providing a stable activated intermediate that makes routine aqueous amidation procedures more predictable.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 106627-54-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Bioconjugation\u003c\/li\u003e\n\u003cli\u003eProduct code: H1304\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research pack sizes; please confirm the current options when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's recommendation stated on the product label.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in its original tightly closed container, kept dry and protected from moisture, since activating reagents of this type are sensitive to water uptake during storage. Keep the container in a cool place away from heat, direct sunlight, and incompatible chemicals, and allow it to reach room temperature before opening to reduce condensation inside the bottle. Handle in a well-ventilated area or fume hood, wearing a laboratory coat, safety goggles, and suitable gloves. Prepare working solutions fresh immediately before use, and follow the manufacturer's safety data sheet and your institutional chemical waste procedures for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087270359258,"sku":"TCI2510H130434102","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087270392026,"sku":"TCI2510H130434103","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1304.jpg?v=1767117758"},{"product_id":"tci2510h145434311","title":"TCI H1454 26198-21-0 1-Hydroxy-6-(trifluoromethyl)benzotriazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Hydroxy-6-(trifluoromethyl)benzotriazole is a chemical compound widely used in organic synthesis as a building block for the development of complex molecular structures. This compound plays a crucial role in laboratory settings, particularly in the creation of pharmaceuticals and specialty chemicals. Its unique molecular structure, which includes a trifluoromethyl group, makes it a versatile reagent for various chemical transformations. Due to its stability and reactivity, it is frequently employed in synthetic pathways that require controlled chemical reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's fluorinated structure provides it with distinctive electronic properties, making it highly desirable in both organic and pharmaceutical research. The presence of fluorine atoms enhances the molecule's stability and reactivity, allowing it to participate effectively in substitution and condensation reactions. These properties make it a preferred choice for chemists aiming to design molecules with specific functional groups and desired biological activities. Its compatibility with a wide range of reaction conditions further contributes to its popularity in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Hydroxy-6-(trifluoromethyl)benzotriazole is commonly used in scientific research and drug development projects. Its ability to facilitate the synthesis of active pharmaceutical ingredients makes it a valuable tool for researchers working on new drug formulations. The compound's role in creating stable molecular structures also supports its application in the development of advanced chemical products. Its reliability and effectiveness in laboratory settings have made it a standard component in many research programs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requiring fluorine substitution due to its stable and reactive fluorinated structure.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds where controlled reactivity and molecular stability are essential for drug design.\u003c\/li\u003e\n\u003cli\u003eCondensation reactions in the creation of functionalized aromatic compounds for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry to produce active pharmaceutical ingredients with enhanced bioavailability and stability.\u003c\/li\u003e\n\u003cli\u003eSynthesis of specialty chemicals that require precise molecular modifications and controlled chemical reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 26198-21-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its fluorinated nature, it is important to handle it with care, using appropriate personal protective equipment. The compound is generally stable under normal laboratory conditions but should be stored away from incompatible substances. Proper ventilation should be maintained in the laboratory to ensure safe handling. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087291855066,"sku":"TCI2510H145434311","price":1136000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087291887834,"sku":"TCI2510H145434312","price":1136000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1454.jpg?v=1768819076"},{"product_id":"tci2510h176534694","title":"TCI H1765 85342-65-0 N-Hydroxytetrachlorophthalimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxytetrachlorophthalimide is a chemical compound widely used in laboratory settings for its versatile reactivity in organic and catalytic reactions. As a key reagent in synthetic chemistry, it plays a crucial role in the development of complex organic molecules and catalytic processes. Its unique chemical structure allows it to participate in various reaction mechanisms, making it a valuable tool for chemists seeking to manipulate molecular structures with precision. This compound is particularly useful in applications where high reactivity and specificity are required.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties, including its ability to undergo substitution, redox, and bond-forming reactions, make it a preferred choice for researchers. Its stability under controlled conditions enhances its reliability in laboratory experiments, while its reactivity ensures that it can be effectively utilized in a wide range of chemical transformations. These characteristics make it an essential component in both organic and inorganic chemistry research. Its compatibility with various reaction conditions further broadens its applicability in synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N-Hydroxytetrachlorophthalimide is commonly used in academic and research institutions. It is particularly favored in organic chemistry departments for its role in catalytic and synthetic processes. Its presence in laboratory workflows supports the advancement of chemical research, contributing to the development of new compounds and methodologies. Its use is widespread in both teaching and experimental settings, making it a standard reagent in many chemical laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from its reactivity in forming new chemical bonds and modifying molecular structures.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes utilize its ability to act as a catalyst in various reaction mechanisms, enhancing reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eRedox reactions take advantage of its electron transfer properties, making it suitable for oxidation and reduction pathways.\u003c\/li\u003e\n\u003cli\u003eSubstitution reactions rely on its capacity to replace functional groups in organic molecules with high specificity.\u003c\/li\u003e\n\u003cli\u003eResearch in inorganic chemistry uses its unique chemical properties to explore new reaction pathways and molecular interactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 85342-65-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxytetrachlorophthalimide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the workspace to minimize inhalation risks. Avoid contact with incompatible materials to prevent potential chemical reactions. Proper storage and handling practices help maintain the integrity and effectiveness of the compound in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087320723674,"sku":"TCI2510H176534694","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087320756442,"sku":"TCI2510H176534695","price":1086000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1765.jpg?v=1767118468"},{"product_id":"tci2510i086536158","title":"TCI I0865 2902-68-3 Iodosodilactone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIodosodilactone is a chemical compound widely used in synthetic chemistry applications within laboratory settings. As a coupling reagent, it plays a crucial role in forming carbon-carbon bonds, making it essential for various organic synthesis processes. Its unique molecular structure allows it to participate in multiple reaction types, including nucleophilic substitution and cross-coupling reactions. This versatility makes it a valuable tool for researchers aiming to create new compounds or modify existing molecular structures with precision.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Iodosodilactone make it a preferred choice for synthetic chemists. It exhibits stability under specific conditions, which is vital for maintaining reaction efficiency and product purity. However, it is highly sensitive to moisture and air exposure, requiring careful handling to prevent degradation. Its reactivity with other chemical substances also necessitates controlled storage and usage protocols to ensure safety and effectiveness in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Iodosodilactone is commonly used in both fundamental and applied chemical research. It is frequently found in academic and industrial research settings where organic synthesis is required. Its application spans across various scientific disciplines, supporting advancements in pharmaceutical, materials science, and chemical engineering. Researchers rely on its performance to achieve reliable and reproducible results in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for creating complex molecular structures due to its coupling capabilities.\u003c\/li\u003e\n\u003cli\u003eCross-coupling reactions where stable and reactive intermediates are required.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions benefiting from its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical development for compound modification and drug synthesis.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications for the synthesis of polymers and functional materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2902-68-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry, cool, and well-ventilated conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eIodosodilactone should be stored in a dry, cool, and well-ventilated area away from moisture and direct sunlight. It is recommended to use airtight containers made of inert materials such as glass or polyethylene to prevent exposure to air and humidity. Due to its sensitivity, it should be handled with care, using appropriate personal protective equipment. Laboratory personnel should ensure that the compound is kept in a secure location to avoid accidental exposure. Proper labeling and storage practices are essential to maintain its chemical integrity and ensure safe usage in research environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087421944026,"sku":"TCI2510I086536158","price":3811000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0865.jpg?v=1767120460"},{"product_id":"tci2510m067038437","title":"TCI M0670 61751-44-8 9-Methyl-3,4-dihydro-2H-pyrido[1,2-a]pyrimidin-2-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9-Methyl-3,4-dihydro-2H-pyrido[1,2-a]pyrimidin-2-one is a chemical compound widely used in laboratory settings as a building block for the synthesis of complex heterocyclic compounds. This versatile compound plays a crucial role in organic chemistry research, particularly in the development of pharmaceuticals and industrial chemicals. Its structural framework allows for further modification, making it an essential tool for chemists aiming to create molecules with specific functional properties. In the laboratory, it is frequently employed in reactions that require precise molecular manipulation and structural innovation.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and reactivity make it a preferred choice for chemists. Its heterocyclic structure provides a solid foundation for chemical transformations, enabling participation in substitution, reduction, and cyclization reactions. Additionally, its solubility in organic solvents facilitates ease of handling and processing in laboratory environments. These properties ensure that it remains a reliable and efficient component in various synthetic pathways, supporting both academic and industrial research efforts.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9-Methyl-3,4-dihydro-2H-pyrido[1,2-a]pyrimidin-2-one is commonly used in organic chemistry research, especially in educational institutions and research centers. Its role in the synthesis of complex molecules makes it a valuable resource for students and researchers alike. Its availability and chemical properties make it a staple in the chemical laboratories of Indonesia, contributing to the advancement of scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex heterocyclic compounds due to its stable and modifiable structure.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drugs and therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production as a key intermediate in the synthesis of various compounds.\u003c\/li\u003e\n\u003cli\u003eEducational purposes in chemistry courses to teach synthetic methods and molecular design.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the creation of bioactive molecules with specific functions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 61751-44-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its stability. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during manipulation. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Regular monitoring of storage conditions is advised to ensure optimal preservation and usability of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087554064602,"sku":"TCI2510M067038437","price":2323000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0670.jpg?v=1767123458"},{"product_id":"tci2510m118639166","title":"TCI M1186 68985-08-0 2,4-Mesitylenedisulfonyl Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,4-Mesitylenedisulfonyl Dichloride is a chemical compound widely used as a building block in the synthesis of complex organic compounds. Its unique molecular structure features two disulfonyl groups attached to carbon atoms at positions 2 and 4 of mesitylene, making it a valuable reagent in organic chemistry. In laboratory settings, this compound plays a crucial role in various synthetic reactions, particularly those involving substitution and coupling mechanisms. Its versatility allows chemists to create molecules with specific functional groups, enhancing its importance in research and development.\u003c\/p\u003e\n\u003cp\u003eThe compound's highly reactive nature makes it suitable for a range of chemical reactions, including nucleophilic, electrophilic, and redox processes. Its reactivity is complemented by its stability under certain conditions, which facilitates long-term storage and use. This combination of reactivity and stability ensures that it remains a reliable choice for researchers working on complex organic syntheses. Additionally, its chemical properties make it an essential tool for those exploring new synthetic pathways and molecular designs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,4-Mesitylenedisulfonyl Dichloride is commonly used in organic chemistry research, especially in the study of heterocyclic compound synthesis and the development of complex molecular structures. Many research institutions and universities rely on this compound as a key component in advanced chemical experiments. Its presence in these laboratories underscores its significance in both academic and industrial chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for the development of new pharmaceuticals due to its ability to form complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions in organic synthesis where it acts as a versatile reagent for bond formation between different molecular entities.\u003c\/li\u003e\n\u003cli\u003eRedox reactions where its reactive nature facilitates electron transfer processes in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions due to its electrophilic characteristics that allow for efficient reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eStructural modification of organic molecules to create compounds with desired functional groups and properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 68985-08-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and potential degradation. Due to its reactivity, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid contact with incompatible materials such as strong bases or reducing agents. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087591190746,"sku":"TCI2510M118639166","price":3155000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087591223514,"sku":"TCI2510M118639167","price":3155000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1186.jpg?v=1767124493"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-coupling-synthetic-reagents.oembed?page=7","provider":"AMI Scientific","version":"1.0","type":"link"}