{"title":"Reagents for Oligosaccharide Synthesis [Glycoscience]","description":"\u003cp\u003e\u003cstrong\u003eReagents for Oligosaccharide Synthesis [Glycoscience]\u003c\/strong\u003e — berisi reagen pendukung sintesis dan derivatisasi oligosakarida, mencakup pereaksi pelabelan gugus amina seperti hidrazin dan aminobenzamida, turunan biotin-PEG untuk konjugasi, serta katalis asam sulfonat. Kelompok ini menunjang tahapan pelabelan, purifikasi, dan konjugasi struktur karbohidrat kompleks dalam riset glikosains.\u003c\/p\u003e\u003cp\u003eReagents for Oligosaccharide Synthesis digunakan peneliti glikobiologi dan kimia karbohidrat untuk reaksi derivatisasi ujung pereduksi gula, pelabelan fluoresen maupun kromatografi, serta konjugasi biotin-streptavidin melalui linker PEG-azida. Reagen seperti 2-aminopiridin dan 2-aminobenzamida umum dipakai pada analisis glikan dengan HPLC atau spektrometri massa, sedangkan turunan biotin-PEG mendukung studi interaksi glikoprotein dan afinitas biomolekul.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510h017232585\"\u003eTCI H0172 7803-57-8 Hydrazine Monohydrate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b554612203\"\u003eTCI B5546 1309649-57-7 Biotin-PEG4-Azide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c001613932\"\u003eTCI C0016 5872-08-2 (+\/-)-10-Camphorsulfonic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b571112430\"\u003eTCI B5711 1189560-96-0 Biotin-PEG3-acetic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0262372\"\u003eTCI A0262 88-68-6 2-Aminobenzamide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b626513099\"\u003eTCI B6265 875770-34-6 Biotin-PEG3-Azide (2mg*5)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0411594\"\u003eTCI A0411 504-29-0 2-Aminopyridine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b626613100\"\u003eTCI B6266 1309649-57-7 Biotin-PEG4-Azide (2mg*5)\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan panjang rantai PEG, gugus fungsi reaktif (azida, asam karboksilat, ester aktif) yang sesuai dengan strategi konjugasi, serta kemurnian reagen pelabelan untuk hasil analisis glikan yang konsisten. 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 Glycoscience, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-monosaccharides-glycoscience\"\u003eMonosaccharides [Glycoscience]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-monosaccharides-glycoscience\"\u003eMonosaccharides [Glycoscience]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-functional-oligosaccharides\"\u003eFunctional Oligosaccharides\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-functional-oligosaccharides\"\u003eFunctional Oligosaccharides\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-applications-using-glyco-materials\"\u003eApplications Using Glyco-materials\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-glyco-building-blocks\"\u003eGlyco Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l2-glycoscience\"\u003eGlycoscience\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":"tci2510b554612203","title":"TCI B5546 1309649-57-7 Biotin-PEG4-Azide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Biotin-PEG4-Azide (B5546, CAS 1309649-57-7) is a click chemistry reagent featuring a biotin affinity tag linked via a PEG4 spacer to an azide reactive group. It is primarily used for biotinylation of alkyne-modified biomolecules through copper-catalyzed or strain-promoted azide-alkyne cycloaddition reactions. This reagent is ideal for applications in protein labeling, affinity purification, pull-down assays, and various streptavidin-based detection systems.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085886304474,"sku":"TCI2510B554612203","price":7521000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5546.jpg?v=1767092491"},{"product_id":"tci2510c001513929","title":"TCI C0015 3144-16-9 (+)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0015 (+)-10-Camphorsulfonic Acid, CAS 3144-16-9, is a strong, optically active sulfonic acid built on the camphor framework. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallisation. The compound also serves as a convenient solid Brønsted acid catalyst for protection and deprotection steps, and as an ion-pairing additive in chromatography. AMI Scientific offers this TCI product in 25 g, 100 g, and 500 g pack sizes; because it is hygroscopic, keep the container tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYan et al. (1999). Thermoelectric Properties of Alternatively Layered Films of Polyaniline and (±)-10-Camphorsulfonic Acid-Doped Polyaniline. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1999.1217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1999.1217\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\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":48085966127322,"sku":"TCI2510C001513929","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4468000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0015.jpg?v=1767094558"},{"product_id":"tci2510c001613932","title":"TCI C0016 5872-08-2 (+\/-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0016 (+\/-)-10-Camphorsulfonic Acid, CAS 5872-08-2, is the racemic form of this strong, solid organic sulfonic acid. It is valued as an easily weighed Brønsted acid catalyst for acetal and ketal formation and cleavage, including protecting-group work on carbohydrate substrates. The compound is also used to form crystalline amine salts and as an ion-pairing additive in chromatographic analysis. AMI Scientific supplies this TCI product in 25 g, 100 g, and 500 g pack sizes; store it tightly closed and protected from moisture.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYan et al. (1999). Thermoelectric Properties of Alternatively Layered Films of Polyaniline and (±)-10-Camphorsulfonic Acid-Doped Polyaniline. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1999.1217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1999.1217\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\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":48085966225626,"sku":"TCI2510C001613932","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966258394,"sku":"TCI2510C001613933","price":2071000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966291162,"sku":"TCI2510C001613934","price":5452000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0016.jpg?v=1767094562"},{"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":505000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085971665114,"sku":"TCI2510C011914065","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085971697882,"sku":"TCI2510C011914066","price":8051000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0119.jpg?v=1767094704"},{"product_id":"tci2510c017614149","title":"TCI C0176 501-53-1 Benzyl Chloroformate (30-35% in Toluene)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0176 Benzyl Chloroformate (30–35% in Toluene), CAS 501-53-1, is a widely used acylating reagent for introducing the Cbz (benzyloxycarbonyl) protecting group onto amines. Supplied as a toluene solution in a 25 mL pack, it is convenient to measure and dispense for research-scale organic and peptide synthesis. The resulting carbamates are stable under many reaction conditions yet can be removed by hydrogenolysis, supporting orthogonal protection strategies. Handle it in a fume hood with appropriate protective equipment, keep the container tightly closed, and store it in a cool, dry, well-ventilated area away from ignition sources.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLezama et al. (2014). Kinetics of the Gas-Phase Elimination Reaction of Benzyl Chloroformate and Neopentyl Chloroformate. \u003cem\u003eInternational Journal of Chemical Kinetics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/kin.20896\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/kin.20896\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePati et al. (2004). Synthesis of N‐Benzylated Anilines from the Reaction of Anilines and Benzyl Chloroformate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200431064\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200431064\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMizuno et al. (2003). Non‐phosgene Synthesis of Benzyl Chloroformate (CbzCl).. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200301081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200301081\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48276754235610,"sku":"TCI2510C017614149","price":481000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0176.jpg?v=1767094820"},{"product_id":"tci2510c049114653","title":"TCI C0491 110-83-8 Cyclohexene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0491 Cyclohexene (CAS 110-83-8) is a simple cyclic alkene and one of the most widely used model substrates for double-bond chemistry. It supports bromination, hydration, epoxidation, hydroboration, and oxidative cleavage, with results that are easy to observe in a teaching laboratory. Researchers also use it as a benchmark olefin when evaluating new catalysts. AMI Scientific supplies this TCI reagent in small and large liquid packs; it is highly flammable and can form peroxides on prolonged exposure to air and light, so careful storage is essential.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZELLNER et al. (2005). Supporting monolayer Pt on W(110) and C\/W(110): Modification effects on the reaction pathways of cyclohexene. \u003cem\u003eJournal of Catalysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jcat.2005.09.007\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jcat.2005.09.007\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eChen et al. (1996). Similarities in the decomposition and dehydrogenation of cyclohexene on (4 × 4)-CMo(110) and Pt(111). \u003cem\u003eSurface Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0039-6028(96)00993-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0039-6028(96)00993-4\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShah et al. (1993). Hydrogenation of cyclohexene using polymer-supported ruthenium (III) complexes as catalysts. \u003cem\u003eJournal of Molecular Catalysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0304-5102(93)87007-u\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0304-5102(93)87007-u\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086004465882,"sku":"TCI2510C049114653","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086004498650,"sku":"TCI2510C049114654","price":1137000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0491.jpg?v=1767095362"},{"product_id":"tci2510c079515061","title":"TCI C0795 17341-93-4 2,2,2-Trichloroethyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0795 2,2,2-Trichloroethyl Chloroformate (CAS 17341-93-4) is the standard reagent for introducing the Troc protecting group onto amines and alcohols. Troc protection is valued for its orthogonality, since it can be removed reductively — typically with zinc — without disturbing acid- or base-labile protecting groups. The reagent is also used to prepare carbamates and carbonates in carbohydrate, peptide, and natural product synthesis. Supplied by TCI in 25 g and 250 g packs, it is moisture-sensitive and corrosive, and must be handled dry in a fume hood.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHE et al. (1991). ChemInform Abstract: Di‐(2,2,2‐Trichloroethyl) Carbonate: By‐Product in Reactions with 2,2, 2‐Trichloroethyl Chloroformate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199110106\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199110106\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHe et al. (1990). DI-(2,2,2-Trichloroethyl)-Carbonate: Byproduct in Reactions with 2,2,2-Trichloroethyl Chloroformate. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919008053155\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919008053155\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eOliveira dos Reis (2007). 2,2,2-Trichloroethyl Chloroformate (TrocCl). \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2007-980374\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2007-980374\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086029336794,"sku":"TCI2510C079515061","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086029369562,"sku":"TCI2510C079515062","price":9893000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0795.jpg?v=1767095774"},{"product_id":"tci2510c097215327","title":"TCI C0972 35963-20-3 (-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0972 (-)-10-Camphorsulfonic Acid (CAS 35963-20-3) is a crystalline chiral sulfonic acid available in 25 g, 100 g, and 500 g pack sizes. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallization. The compound also serves as a strong Brønsted acid catalyst for acetal formation, deprotection, and related transformations. Store it tightly sealed in a cool, dry place and wear gloves and eye protection when weighing, as the solid is corrosive.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSong et al. (2013). Improved thermoelectric performance of PEDOT:PSS film treated with camphorsulfonic acid. \u003cem\u003eJournal of Polymer Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10965-013-0316-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10965-013-0316-0\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":48086040969434,"sku":"TCI2510C097215327","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086041002202,"sku":"TCI2510C097215328","price":3458000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086041034970,"sku":"TCI2510C097215329","price":10600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0972.jpg?v=1767096117"},{"product_id":"tci2510c112415548","title":"TCI C1124 13139-17-8 N-Carbobenzoxyoxysuccinimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1124 N-Carbobenzoxyoxysuccinimide (Z-OSu, CAS 13139-17-8) is an activated succinimidyl ester used to install the carbobenzyloxy (Cbz) protecting group on amines. As a solid reagent it offers easier weighing and cleaner reaction profiles than benzyl chloroformate, with N-hydroxysuccinimide as the readily removed by-product. It is widely applied in peptide synthesis, medicinal chemistry, and chemical biology where selective N-terminal protection and orthogonal deprotection by hydrogenolysis are required. AMI Scientific supplies this TCI product in 25 g and 250 g pack sizes for Indonesian research laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086050144474,"sku":"TCI2510C112415548","price":633000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086050177242,"sku":"TCI2510C112415549","price":3029000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1124.jpg?v=1767096390"},{"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":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086068297946,"sku":"TCI2510C140815948","price":4266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1408.jpg?v=1767096891"},{"product_id":"tci2510c154516159","title":"TCI C1545 3724-43-4 (Chloromethylene)dimethyliminium Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1545, (Chloromethylene)dimethyliminium Chloride (CAS 3724-43-4), is the isolated form of the Vilsmeier reagent, supplied as a ready-to-use solid rather than generated in situ. It acts as a powerful electrophilic and dehydrating agent, enabling Vilsmeier–Haack formylation of electron-rich aromatics, activation of carboxylic acids, dehydration of amides to nitriles, and conversion of alcohols to chlorides. Within glycoscience, its dehydrative activation chemistry is applied to carbohydrate donors and related transformations. Offered by AMI Scientific in 25 g and 250 g packs, this highly moisture-sensitive solid must be weighed under dry inert conditions and stored tightly closed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086076883162,"sku":"TCI2510C154516159","price":2778000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086076915930,"sku":"TCI2510C154516160","price":15420000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1545.jpg?v=1767097106"},{"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":1818000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1639.jpg?v=1767097255"},{"product_id":"tci2510c180616495","title":"TCI C1806 16774-21-3 Ammonium Cerium(IV) Nitrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eAmmonium Cerium(IV) Nitrate (TCI C1806) is a chemical compound widely used in laboratory settings for its strong oxidizing properties and stability. This compound, with the CAS number 16774-21-3, is commonly applied in catalytic reactions, quantitative analysis, and organic synthesis. It serves as a reliable source of cerium(IV) ions, which are essential in various oxidation processes. Its solubility in polar solvents like water and ethanol makes it convenient for use in different experimental conditions. In Indonesian laboratories, this compound is an essential tool for researchers in chemistry, particularly in catalysis and analytical chemistry. Its versatility and effectiveness make it a preferred choice for both academic and industrial applications.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHORIUCHI et al. (1997). ChemInform Abstract: A New α‐Iodination of Ketones Using Iodine‐Ammonium Cerium(IV) Nitrate in Alcohol or Acetic Acid.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199721065\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199721065\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTAKESHITA et al. (1992). ChemInform Abstract: Treatment of Dimethoxyparacyclophanes with Ammonium Cerium(IV) Nitrate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199248102\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199248102\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":"50g","offer_id":48086090023130,"sku":"TCI2510C180616495","price":860000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086090055898,"sku":"TCI2510C180616496","price":3913000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1806.jpg?v=1767097475"},{"product_id":"tci2510c193216551","title":"TCI C1932 34637-22-4 3-(Benzyloxycarbonylamino)-1-propanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(Benzyloxycarbonylamino)-1-propanol is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block in the development of complex molecules, including peptides, pharmaceuticals, and industrial chemicals. Its role as a substrate or reagent in deprotection or molecular coupling reactions makes it essential for synthetic chemists. This compound is particularly valuable due to its controlled reactivity and stability, allowing for precise manipulation in various chemical processes.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure, featuring an alcohol chain and a benzyloxycarbonyl group, enables it to participate in specific chemical reactions such as hydrolysis, reduction, and substitution. These properties make it a reliable choice for researchers requiring consistent and predictable chemical behavior. Its high purity and consistent packaging ensure that it meets the rigorous demands of scientific research, especially in applications where accuracy and reproducibility are critical.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-(Benzyloxycarbonylamino)-1-propanol is commonly used in chemical research, particularly in organic synthesis and the development of new chemical materials. It is a preferred reagent in academic and industrial settings due to its versatility and reliability. Many research institutions and universities in Indonesia rely on this compound for experiments that require high-quality starting materials. Its application is widespread in both basic and applied research projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where this compound serves as a building block for creating complex molecules, including pharmaceuticals and peptides.\u003c\/li\u003e\n\u003cli\u003ePeptide synthesis benefits from its reactivity, allowing for the controlled coupling of amino acid residues in the formation of peptides.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development utilizes this compound in the synthesis of various chemical intermediates and specialty compounds.\u003c\/li\u003e\n\u003cli\u003eMolecular coupling reactions rely on its stability and controlled reactivity to facilitate the formation of new molecular structures.\u003c\/li\u003e\n\u003cli\u003eDe protection processes use this compound to selectively remove protective groups from molecules during synthetic sequences.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 34637-22-4\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 as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Proper labeling of storage containers is essential for safe handling and identification. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid exposure to heat or direct sunlight to ensure long-term stability. Regular inspection of storage conditions is advised to maintain optimal laboratory safety and product quality.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086092185818,"sku":"TCI2510C193216551","price":1718000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086092218586,"sku":"TCI2510C193216552","price":4292000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1932.jpg?v=1767097544"},{"product_id":"tci2510d013419467","title":"TCI D0134 280-57-9 1,4-Diazabicyclo[2.2.2]octane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,4-Diazabicyclo[2.2.2]octane (DABCO) is a nitrogen-donor ligand widely used in chemical reactions, particularly in catalysis. This compound plays a crucial role in laboratory settings by facilitating the formation of metal complexes through its ability to coordinate with transition metals. Its cyclic structure provides stability and enhances its reactivity in various synthetic processes. DABCO is a versatile reagent that supports the development of new materials and compounds in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eDABCO is valued for its chemical stability, non-toxicity, and lack of odor, making it a safe and reliable choice for laboratory use. It exhibits excellent resistance to degradation under a wide range of reaction conditions, allowing for repeated use without significant loss of activity. These properties contribute to its popularity among chemists who require consistent performance and minimal safety concerns. Additionally, its inert nature ensures that it does not interfere with the intended chemical reactions, maintaining the integrity of experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DABCO is commonly used in chemical research, especially in catalytic processes and organic synthesis. Its availability through suppliers like AMI Scientific ensures that researchers have access to high-quality materials necessary for advanced scientific investigations. The compound's reliability and safety profile make it an essential component in both educational institutions and research facilities across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCatalytic reactions benefit from DABCO's ability to coordinate with transition metals, enhancing reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis relies on DABCO as a ligand to facilitate complex bond formations and improve reaction yields.\u003c\/li\u003e\n\u003cli\u003ePolymerization processes utilize DABCO to stabilize metal catalysts, ensuring controlled and consistent polymer chain growth.\u003c\/li\u003e\n\u003cli\u003eHydrolysis reactions use DABCO to modulate the activity of metal-based catalysts, improving reaction rates and product purity.\u003c\/li\u003e\n\u003cli\u003eSubstitution reactions benefit from DABCO's stability and inertness, allowing precise control over reaction pathways and side products.\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: 280-57-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Nitrogen-Donor Ligands [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\u003eDABCO should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air, which may affect its performance. Due to its non-toxic and odorless nature, DABCO is generally safe to handle, but standard laboratory precautions should still be followed, such as wearing appropriate personal protective equipment. It is advisable to store DABCO in a well-ventilated area to ensure safe handling and long-term preservation. Proper storage conditions help maintain the compound's effectiveness and ensure its suitability for repeated use in various chemical applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086348497114,"sku":"TCI2510D013419467","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086348529882,"sku":"TCI2510D013419468","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086348562650,"sku":"TCI2510D013419469","price":2953000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0134.jpg?v=1767100911"},{"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":481000.0,"currency_code":"IDR","in_stock":true},{"title":"400g","offer_id":48086384443610,"sku":"TCI2510D043619871","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0436.jpg?v=1767101296"},{"product_id":"tci2510d065620209","title":"TCI D0656 605-65-2 Dansyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDansyl Chloride (D0656), with CAS number 605-65-2, is a chemical compound widely used in laboratory settings, particularly in the fields of chemical biology and glycoscience. It serves as a versatile reagent for labeling and detecting specific molecules such as proteins, peptides, and carbohydrates. Its ability to form stable covalent bonds makes it an essential tool for structural analysis and compound identification. This compound is commonly employed in analytical techniques like spectroscopy and chromatography, where its fluorescent properties aid in the visualization and quantification of target molecules.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make Dansyl Chloride a preferred choice is its high reactivity and the capacity to bind to amino or hydroxyl groups on target molecules. This characteristic allows for precise and reliable labeling, which is crucial in molecular studies and diagnostic applications. Additionally, its chemical structure ensures compatibility with a wide range of experimental conditions, making it adaptable to various research needs. The compound’s stability and consistent performance contribute to its reliability in both academic and industrial laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dansyl Chloride is extensively used in biomedical, pharmaceutical, and analytical chemistry research. It plays a significant role in the study of metabolic diseases, drug development, and the analysis of biological components. Its availability in different packaging formats supports its use across various research scales, from basic scientific investigations to more complex analytical projects. This compound remains a valuable resource for researchers seeking accurate and efficient molecular labeling solutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolecular labeling in protein and peptide analysis due to its ability to form stable covalent bonds with amino groups.\u003c\/li\u003e\n\u003cli\u003eFluorescent detection in chromatographic and spectroscopic techniques for enhanced visualization of target molecules.\u003c\/li\u003e\n\u003cli\u003eGlycoscience research for studying carbohydrate-protein interactions and structural analysis of glycoproteins.\u003c\/li\u003e\n\u003cli\u003eMetabolic disease research for tracking and identifying biomarkers in biological samples.\u003c\/li\u003e\n\u003cli\u003eDrug development applications for labeling and characterization of therapeutic compounds during preclinical studies.\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: 605-65-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes to suit different experimental needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\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\u003eDansyl Chloride 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 humidity and air, which can affect its reactivity. Since it is a reactive chemical, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is essential when working with this compound to minimize inhalation risks. It is important to keep it away from incompatible substances to prevent any unwanted chemical reactions. Following these storage and handling guidelines ensures the compound remains effective and safe for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086398402778,"sku":"TCI2510D065620209","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086398435546,"sku":"TCI2510D065620210","price":4292000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086398468314,"sku":"TCI2510D065620211","price":11306000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0656.jpg?v=1767101712"},{"product_id":"tci2510d105920766","title":"TCI D1059 2524-64-3 Diphenyl Chlorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiphenyl Chlorophosphate is a chemical compound widely used as a building block in organic synthesis. It serves as a versatile reagent that enables substitution reactions and other chemical transformations under various laboratory conditions. This compound is particularly valuable for its ability to participate in the formation of ester and phosphate bonds, making it essential in the development of complex molecular structures. Its role in organic chemistry is critical, especially in research settings where precise control over chemical reactions is required.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Diphenyl Chlorophosphate make it a preferred choice for laboratory applications. It exhibits stability under certain conditions but is highly reactive towards water and other polar substances. This reactivity necessitates careful handling and storage to maintain its integrity. Its ability to engage in multiple types of chemical reactions also makes it a valuable tool for chemists seeking to explore diverse synthetic pathways. The compound’s reactivity and versatility contribute to its widespread use in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diphenyl Chlorophosphate is commonly used in organic chemistry research, particularly in universities and research institutions focused on the synthesis of new compounds. Its application is prevalent in projects involving esterification, phosphate ester formation, and other synthetic processes. The compound’s utility in creating complex molecules has made it an essential component of many chemical research programs in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: Diphenyl Chlorophosphate is widely used in the synthesis of esters and phosphate esters due to its reactivity and versatility in forming complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is a key reagent in the development of new pharmaceutical compounds, particularly in the formation of phosphate ester linkages.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: Universities and research institutions use it extensively in teaching and research to demonstrate chemical reactivity and synthetic techniques.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry: It is employed in industrial settings for the production of various chemical intermediates and specialty compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It serves as a standard reagent for testing and characterizing other chemical compounds in analytical laboratories.\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: 2524-64-3\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 or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a cool, dry place away from moisture and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiphenyl Chlorophosphate should be stored in a cool, dry environment to prevent degradation. It is essential to keep the compound away from moisture and polar solvents to maintain its chemical integrity. Suitable containers should be sealed and made of materials that do not react with the compound, such as glass or inert polymer. Due to its reactivity, it is recommended to handle the material with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation should be maintained in the laboratory to minimize exposure. Regular monitoring of storage conditions is necessary to ensure the compound remains stable and safe for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086420521178,"sku":"TCI2510D105920766","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086420553946,"sku":"TCI2510D105920767","price":1718000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086420586714,"sku":"TCI2510D105920768","price":4619000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1059.jpg?v=1767102466"},{"product_id":"tci2510d107020777","title":"TCI D1070 84-58-2 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DCDCQ) is a chemical compound widely used in laboratory settings for its catalytic and photocatalytic properties. As a key reagent in chemical reactions, DCDCQ plays a vital role in accelerating and controlling oxidation and reduction processes. Its unique molecular structure, featuring two chlorine atoms and two cyanide groups attached to a benzoquinone ring, makes it highly reactive and versatile. This compound is particularly valuable in research involving light-sensitive reactions, where it can act as a photosensitizer to initiate chemical transformations under UV exposure.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of DCDCQ, including its ability to interact with various substrates and generate free radicals, make it a preferred choice for advanced chemical applications. Its molecular structure contains multiple electron-active groups, enabling it to participate in a wide range of chemical interactions. Additionally, DCDCQ exhibits stability under controlled conditions, which allows for consistent performance in laboratory experiments. These characteristics make it an essential tool for researchers working in catalysis and photoreactive systems.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DCDCQ is commonly used in academic and industrial research settings. It supports studies in photocatalytic processes, environmental remediation, and organic synthesis. Due to its reactivity and sensitivity to light and moisture, it is often employed in controlled environments where precise chemical reactions are required. Its role in advancing chemical research in Indonesia underscores its importance as a reliable and effective reagent.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePhotocatalytic degradation of pollutants in environmental chemistry research due to its ability to absorb light and generate reactive species.\u003c\/li\u003e\n\u003cli\u003eOxidation reactions in organic synthesis where DCDCQ acts as a catalyst to facilitate electron transfer processes.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new materials in inorganic chemistry by leveraging its structural properties for functional group modification.\u003c\/li\u003e\n\u003cli\u003eControlled chemical reactions in analytical chemistry for the synthesis of complex compounds under specific conditions.\u003c\/li\u003e\n\u003cli\u003ePhotoredox catalysis in green chemistry applications to reduce energy consumption and improve reaction efficiency.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 84-58-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Photocatalysts [Catalysis]\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 powder\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\u003eDCDCQ should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers made of materials that do not react with the compound, such as glass or high-density polyethylene. Due to its sensitivity to UV light, it is advisable to keep the material in a dark, sealed container when not in use. Laboratory personnel should handle DCDCQ with care, using appropriate personal protective equipment to avoid exposure. Proper ventilation is essential during handling to minimize inhalation risks. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086420881626,"sku":"TCI2510D107020777","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086420914394,"sku":"TCI2510D107020778","price":3231000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086420947162,"sku":"TCI2510D107020779","price":16809000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1070.jpg?v=1767102474"},{"product_id":"tci2510d127020984","title":"TCI D1270 6674-22-2 1,8-Diazabicyclo[5.4.0]-7-undecene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,8-Diazabicyclo[5.4.0]-7-undecene is a chemical compound classified under heterocyclic compounds, widely utilized in chemical biology research. This compound plays a crucial role in laboratories where complex molecular structures and biological interactions are studied. It is particularly valuable in glycoscience, where it aids in the investigation of glycosylation processes and carbohydrate-based reactions. Its unique molecular architecture allows for precise interactions with biological molecules such as proteins and enzymes, making it an essential tool for advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability under controlled conditions and high reactivity in substitution and conjugation reactions, make it a preferred choice for researchers. Its ability to participate in specific chemical transformations enhances its utility in synthetic chemistry and molecular modification studies. The compound's sensitivity to moisture and air necessitates careful handling, but its reactivity and specificity make it a powerful reagent in specialized laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,8-Diazabicyclo[5.4.0]-7-undecene is commonly used in research focused on molecular biology and chemical synthesis. Its role in glycoscience and biochemical studies makes it an important material for scientists working on complex molecular structures and functional group modifications. The compound's unique properties support a wide range of experimental approaches, contributing to advancements in chemical and biological research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGlycoscience Research: This compound is ideal for studying carbohydrate-based reactions and glycosylation processes due to its ability to interact with biological molecules.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: Its reactivity and specificity make it suitable for modifying complex biological molecules and synthetic compounds.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry Applications: The compound is used in the synthesis of complex organic structures, particularly in substitution and conjugation reactions.\u003c\/li\u003e\n\u003cli\u003eEnzymatic Reaction Studies: Its interaction with enzymes and proteins makes it valuable for investigating biochemical pathways and catalytic mechanisms.\u003c\/li\u003e\n\u003cli\u003eStructural Analysis in Biochemistry: The compound's unique molecular structure supports research into molecular recognition and interaction dynamics.\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: 6674-22-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\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 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\u003eThis compound should be stored in a dry, cool environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its reactivity and purity. Due to its sensitivity, it should be handled in a controlled laboratory setting with proper ventilation. Always use appropriate personal protective equipment when working with this compound. Avoid direct contact with skin and eyes, and ensure that the workspace is free from potential contaminants. Regular monitoring of storage conditions is essential to ensure the compound remains suitable for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086432186586,"sku":"TCI2510D127020984","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086432219354,"sku":"TCI2510D127020985","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086432252122,"sku":"TCI2510D127020986","price":3787000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1270.jpg?v=1767102806"},{"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":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086449946842,"sku":"TCI2510D160121411","price":3937000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086449979610,"sku":"TCI2510D160121412","price":11306000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086450012378,"sku":"TCI2510D160121413","price":22663000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1601.jpg?v=1767103323"},{"product_id":"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":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086651928794,"sku":"TCI2510D402924498","price":4216000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086651961562,"sku":"TCI2510D402924499","price":12593000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4029.jpg?v=1767106964"},{"product_id":"tci2510e007727742","title":"TCI E0077 107-15-3 Ethylenediamine Anhydrous","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthylenediamine Anhydrous (EDA) is a chemical compound widely used in laboratory settings for its versatility and reactivity. As a building block in chemical synthesis, EDA plays a crucial role in the development of complex molecules, including heterocyclic compounds and polymers. Its simple molecular structure allows it to participate in various reactions such as condensation, substitution, and the formation of covalent bonds. This makes it an essential reagent for chemists working on diverse synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of EDA make it a preferred choice in controlled laboratory environments. It is chemically stable under specific conditions but highly sensitive to moisture and oxidation. Being anhydrous, it avoids the complications associated with water content, ensuring consistent results in reactions that require dry conditions. This characteristic is particularly valuable in high-precision synthesis processes where purity and stability are critical.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethylenediamine Anhydrous is commonly used in chemical research, pharmaceutical development, and industrial chemical production. It is frequently found in university laboratories, research institutions, and manufacturing companies that produce chemical products. Its broad applications make it a fundamental component of chemical supplies in these settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChemical synthesis is a primary application where EDA is used to build complex molecules through various reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from EDA's role in the synthesis of drug compounds and intermediates.\u003c\/li\u003e\n\u003cli\u003ePolymer development relies on EDA as a key component in creating cross-linked structures and functional materials.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry uses EDA in the preparation of reagents and standards for precise measurements.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production incorporates EDA in the manufacturing of specialty chemicals and additives.\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: 107-15-3\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: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and oxidizing agents\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthylenediamine Anhydrous should be stored in a cool, dry environment to prevent moisture absorption and oxidation. It is recommended to use airtight containers made of materials such as glass or polyethylene to ensure long-term stability. Due to its sensitivity, it should be kept away from sources of heat and direct sunlight. In laboratory settings, proper ventilation is essential to minimize exposure. Always handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safe usage and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086817145050,"sku":"TCI2510E007727742","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086817177818,"sku":"TCI2510E007727743","price":633000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0077.jpg?v=1767110603"},{"product_id":"tci2510e008127746","title":"TCI E0081 6780-13-8 Ethylenediamine Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E0081 Ethylenediamine Monohydrate is the hydrated form of ethylenediamine, a simple aliphatic diamine paired with one molecule of water in its structure. This monohydrate form is supplied as a liquid and offers a practical middle ground in the laboratory: the chemical character of the diamine is fully preserved, while handling is noticeably easier than that of the strongly hygroscopic anhydrous form. Its two primary amine groups make the compound a useful starting material for building ligands, forming metal complexes, and preparing nitrogen-bearing intermediates across a wide range of synthetic research programmes.\u003c\/p\u003e\n\u003cp\u003eThe property that most often drives its selection is the ability to clamp onto metal ions through both nitrogen atoms, producing robust chelate complexes that hold together under working conditions. This is accompanied by strongly basic behaviour, which is valuable in reactions that require an alkaline environment to proceed. The accompanying water content, far from being a drawback, is an advantage in reactions run in aqueous media: the material is already fully dissolved and requires no additional adjustment before use. The monohydrate form also tends to be easier to pour and measure accurately at the ambient temperatures of a tropical laboratory.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories the reagent fits naturally into coordination chemistry, synthesis, and chemical biology work, where it is placed under the Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience category. The two available pack sizes give a genuine choice between occasional use for orientation trials and more sustained consumption in routine method work, so laboratories can match their purchase to how frequently the reagent actually turns over on the bench.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMetal complex preparation — the two primary amine groups bind a single metal centre simultaneously, giving sturdy chelate complexes suitable for coordination chemistry studies and structural characterisation work.\u003c\/li\u003e\n\u003cli\u003eLigand construction — the diamine backbone serves as a reliable framework onto which larger multidentate ligands are assembled for research into metal binding and complex design.\u003c\/li\u003e\n\u003cli\u003eSynthesis of nitrogen-bearing intermediates — both amine functions provide reactive handles for building intermediates that carry nitrogen into subsequent steps of a synthetic route.\u003c\/li\u003e\n\u003cli\u003eReactions requiring alkaline conditions — the strongly basic nature of the diamine establishes and maintains the alkaline environment that certain transformations demand without additional base.\u003c\/li\u003e\n\u003cli\u003eAqueous-phase reaction work — because the monohydrate arrives already fully dissolved in its water of hydration, it enters water-based reaction systems without further adjustment or dissolution steps.\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: 6780-13-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: 25 mL and 500 mL\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid (monohydrate form)\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in its original container, following the storage guidance on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, kept upright in a well-ventilated area away from heat and incompatible substances. Because the compound is strongly basic, work with it in a fume hood and wear gloves, safety glasses, and a laboratory coat to avoid contact with skin and eyes. Dispense using clean, dry glassware and reseal the container promptly after each withdrawal to limit exposure to air and moisture from the surrounding laboratory atmosphere. Always consult the manufacturer's safety data sheet before first use and follow the institutional waste-handling procedures in place at your facility.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086817276122,"sku":"TCI2510E008127746","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086817308890,"sku":"TCI2510E008127747","price":1339000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0081.jpg?v=1767110611"},{"product_id":"tci2510f078330747","title":"TCI F0783 18861-78-4 Fluorescein 6-Isothiocyanate (isomer II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI F0783 Fluorescein 6-Isothiocyanate (isomer II) is a fluorescent labelling reagent widely known in molecular biology and biochemistry laboratories, commonly referred to as FITC. The compound consists of a fluorescein core that emits bright green fluorescence when excited by blue light, combined with an isothiocyanate group that acts as a reactive anchor toward amine functionalities. Its role in the laboratory is to link an easily detected optical signal to biological molecules such as proteins, antibodies, peptides, or oligosaccharides, so that the presence and distribution of those molecules can be observed directly.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this reagent a preferred choice are the combination of strong fluorescence output and selective labelling reactivity. The isothiocyanate group reacts with primary amines, particularly free amino groups at chain termini as well as on lysine side chains, forming a thiourea linkage that is covalently stable and not readily lost during washing steps. Offering this product as a single isomer, namely isomer II, is an important advantage, because labelling with an isomer mixture can produce heterogeneous conjugates and complicate reproducibility between batches. A single isomer supports more consistent conjugation chemistry and more comparable results from one preparation to the next.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university research groups, biochemistry and molecular biology teaching laboratories, and analytical service units that prepare their own fluorescent conjugates rather than purchasing ready-made labelled reagents. It is drawn on where fluorescence microscopy, flow cytometry, or fluorescence-based detection is part of the routine workflow, and where glycoscience and chemical biology studies require biological molecules to be tagged with a visible optical reporter before observation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProtein and antibody labelling, because the isothiocyanate group couples covalently to primary amines on lysine residues and chain termini, producing stable fluorescent conjugates that survive repeated washing.\u003c\/li\u003e\n\u003cli\u003eFluorescence microscopy of cells and tissues, since the fluorescein core emits bright green fluorescence under blue-light excitation and is readily visualised with standard filter configurations used for FITC.\u003c\/li\u003e\n\u003cli\u003eFlow cytometry sample preparation, where labelled antibodies and binding proteins give a strong optical signal that allows individual cells to be distinguished and counted reliably.\u003c\/li\u003e\n\u003cli\u003eGlycoscience research on oligosaccharides and glycoconjugates, in which amine-bearing sugar derivatives are tagged so that their presence and distribution can be tracked during separation and detection.\u003c\/li\u003e\n\u003cli\u003ePeptide labelling for binding and localisation studies, because the single-isomer format gives more homogeneous conjugates and improves reproducibility between preparations compared with isomer mixtures.\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: 18861-78-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003eProduct code: F0783\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed on this product page\u003c\/li\u003e\n\u003cli\u003eStorage note: store under the conditions stated on the manufacturer's label, protected from light\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, protected from light, since fluorescein derivatives are light sensitive and the isothiocyanate group is reactive toward moisture and amines. Amber glass vials or containers wrapped in foil are suitable, and the container should be allowed to reach room temperature before opening to limit condensation. Handle the solid in a well-ventilated area or fume hood while wearing gloves, safety glasses, and a laboratory coat, and avoid contact with skin, eyes, and inhalation of dust. Prepare working solutions fresh where possible, keep them shielded from light during use, and consult the manufacturer's safety data sheet before handling and for waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48087031578842,"sku":"TCI2510F078330747","price":8203000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0783.jpg?v=1767113860"},{"product_id":"tci2510h017232585","title":"TCI H0172 7803-57-8 Hydrazine Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydrazine Monohydrate from TCI is a hydrazine hydrate supplied as a colourless liquid, and it ranks among the most versatile reagents available in a chemistry laboratory. Within the field of glycoscience, it serves as the reagent for hydrazinolysis, the process that releases glycan chains from glycoproteins so that the sugar structures can be analysed separately from their protein component. Beyond that specific role, hydrazine hydrate is widely used as a reducing agent, as a source of the N–N unit in heterocyclic synthesis, and as a deprotection reagent for phthalimide groups. Because it is supplied in liquid form, the material is easy to measure by pipette for reactions at any scale.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this reagent a preferred choice begin with its strong nucleophilic reactivity toward carbonyl and imide groups, which drives the condensation and deprotection chemistry it is chosen for. It also reduces without leaving any metal residue behind, since its by-products are simply nitrogen and water — a considerable advantage when the reaction product must stay free of metallic contamination. Its solubility in water and in alcohols is excellent, and the liquid form allows rapid, homogeneous mixing so that reactions can proceed at relatively low temperatures rather than requiring forcing conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this reagent is typically found in glycoscience and synthetic organic chemistry work, where the same properties that make it useful also define how it must be handled. Hydrazine hydrate evaporates readily and is highly reactive toward oxidising materials, so its use always demands that work be carried out inside a fume hood. Analysts measuring it by pipette for glycan release or heterocyclic synthesis should plan every transfer with that requirement in mind.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHydrazinolysis of glycoproteins — the reagent releases intact glycan chains from the protein backbone so that sugar structures can be analysed independently of the protein portion.\u003c\/li\u003e\n\u003cli\u003eReduction reactions — hydrazine hydrate reduces without leaving metal residues behind, because its by-products are only nitrogen and water, keeping the product free of metallic contamination.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic synthesis — it supplies the N–N unit required to build nitrogen-containing ring systems, making it a standard building block in synthetic organic chemistry programmes.\u003c\/li\u003e\n\u003cli\u003ePhthalimide deprotection — its strong nucleophilic reactivity toward imide groups cleaves phthalimide protecting groups efficiently, liberating the free amine for the next synthetic step.\u003c\/li\u003e\n\u003cli\u003eSmall- and large-scale reaction work — the liquid form is easily measured by pipette and mixes rapidly and homogeneously, allowing reactions to run at relatively low temperatures.\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: 7803-57-8\u003c\/li\u003e\n\u003cli\u003eCatalogue number: H0172\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePhysical form: colourless liquid (hydrazine hydrate)\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly closed and away from oxidising materials; handle in a fume hood\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Hydrazine Monohydrate in a tightly closed container, kept well away from oxidising materials, as the reagent is highly reactive toward them. Because the liquid evaporates readily, containers should be resealed immediately after each transfer and kept in a well-ventilated storage area reserved for reactive chemicals. All dispensing, pipetting, and reaction set-up should be performed inside a fume hood without exception. Analysts should wear appropriate laboratory gloves, eye protection, and a lab coat, and should avoid any contact between the reagent and oxidising agents anywhere in the work area.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087162487002,"sku":"TCI2510H017232585","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48087162519770,"sku":"TCI2510H017232586","price":1237000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0172.jpg?v=1767115807"},{"product_id":"tci2510h020432636","title":"TCI H0204 7803-57-8 Hydrazine Monohydrate (79%)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0204 Hydrazine Monohydrate (79%) is a solution of hydrazine in its monohydrate form, supplied as a liquid with exceptionally strong reducing power and high nucleophilic character. In the laboratory it is recognised as one of the most versatile reagents available, and at the same time one of the most demanding in terms of careful handling. Within glycoscience, hydrazine monohydrate plays a central role in hydrazinolysis, the release of glycan chains from glycoproteins so that the carbohydrate structures can be analysed separately from the protein backbone. This role makes it a key material in glycomics research and in glycoprotein characterisation work that depends on recovering intact glycans.\u003c\/p\u003e\n\u003cp\u003eThe property that leads researchers to select this reagent is the combination of reducing strength with the ability to cleave amide bonds selectively under controlled conditions. As a nucleophile carrying two adjacent nitrogen atoms, hydrazine reacts rapidly with aldehydes and ketones to form hydrazones, and it is used widely in Wolff-Kishner reduction chemistry and in the construction of heterocyclic ring systems. In the liquid monohydrate form the compound is easier to pour and to measure accurately than the anhydrous material, although it must still be treated at every stage as a hazardous substance. Hydrazine is highly toxic, corrosive, and readily absorbed, so the practical convenience of the liquid form never removes the need for strict control.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this reagent is generally found in university research groups, glycobiology and biochemistry units, and analytical laboratories that carry out structural work on carbohydrates and glycoproteins. It is normally handled in a fume hood by trained personnel, dispensed in small working volumes rather than bulk transfers, and reserved for procedures where its reducing power or selective amide cleavage is genuinely required. Institutions that stock it typically pair it with defined handling procedures and restricted access to the storage area.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHydrazinolysis of glycoproteins — releases glycan chains from the protein backbone so the intact carbohydrate structures can be recovered and analysed independently for glycomics work.\u003c\/li\u003e\n\u003cli\u003eGlycoprotein characterisation and glycomics profiling — provides the cleavage chemistry needed to obtain whole glycans for downstream structural study rather than fragmented carbohydrate pieces.\u003c\/li\u003e\n\u003cli\u003eHydrazone formation from aldehydes and ketones — the doubly nitrogenated nucleophile reacts rapidly with carbonyl groups, making it a dependable reagent for derivatisation and condensation chemistry.\u003c\/li\u003e\n\u003cli\u003eWolff-Kishner reduction procedures — the strong reducing character of hydrazine drives the conversion of carbonyl compounds in this classical synthetic transformation under laboratory conditions.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic ring construction in synthetic chemistry — the two adjacent nitrogen atoms serve as a building block for forming nitrogen-containing ring systems in preparative organic synthesis.\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: 7803-57-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, hydrazine monohydrate solution (79%)\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard laboratory pack sizes offered by TCI for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in the original container, in a cool, well-ventilated place away from incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydrazine monohydrate is highly toxic, corrosive, and readily absorbed, and must be treated as a hazardous material throughout handling and storage. Store the container tightly closed in a cool, well-ventilated area, away from oxidising agents, acids, heat sources, and ignition sources, and keep it in the original supplier container or another compatible chemically resistant vessel. All dispensing should be carried out inside a functioning fume hood by trained personnel wearing chemical-resistant gloves, safety goggles, and a laboratory coat. Although the liquid monohydrate is easier to pour and measure than the anhydrous form, that convenience does not reduce the need for strict control. Avoid skin contact and inhalation of vapour, transfer only the volume required for the procedure, and keep spill control materials and eyewash facilities accessible.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087168549082,"sku":"TCI2510H020432636","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087168581850,"sku":"TCI2510H020432637","price":733000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0204.jpg?v=1767115883"},{"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":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"200g","offer_id":48087212327130,"sku":"TCI2510H046833023","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0468.jpg?v=1767116459"},{"product_id":"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":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087225008346,"sku":"TCI2510H062333252","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087225041114,"sku":"TCI2510H062333253","price":9137000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0623.jpg?v=1767116767"},{"product_id":"tci2510h098933767","title":"TCI H0989 187731-26-6 Hexyldimethyloctylammonium Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHexyldimethyloctylammonium Bromide is a chemical compound widely used in research applications within the fields of chemistry and biochemistry. As a quaternary ammonium salt, it plays a crucial role in various laboratory processes, particularly in the synthesis of complex molecules. Its unique molecular structure, consisting of long hydrocarbon chains and ionic groups, makes it a versatile reagent for both polar and non-polar interactions. This compound is essential in experiments that require stable and reactive ionic components, contributing to the advancement of scientific research in multiple disciplines.\u003c\/p\u003e\n\u003cp\u003eThe compound's properties, including its non-volatile nature and chemical stability, make it a preferred choice for laboratory use. It dissolves easily in organic solvents, which enhances its utility in a wide range of chemical reactions. Its ability to maintain structural integrity under various experimental conditions ensures reliable results in research settings. Additionally, its ionic characteristics allow it to interact effectively with other molecules, making it an important tool in biochemical studies. These features collectively position it as a valuable reagent for scientific investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hexyldimethyloctylammonium Bromide is commonly used in biochemistry, pharmacology, and materials science research. Its availability in the local market ensures that researchers have access to this compound for their experiments. Institutions and universities rely on it for experiments requiring stable and reactive ionic compounds, supporting ongoing scientific inquiry and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical research utilizes this compound for its ability to interact with polar and non-polar molecules, aiding in the study of molecular interactions and complex compound synthesis.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development benefits from its role in the synthesis of bioactive compounds, supporting the creation of new drug candidates with desired chemical properties.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments leverage its stability and solubility to develop new materials with specific functional properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications take advantage of its ionic nature for use in chromatographic and spectroscopic techniques to analyze complex mixtures.\u003c\/li\u003e\n\u003cli\u003eMolecular biology studies incorporate it in the preparation of reagents for DNA and RNA manipulation, facilitating precise biochemical 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: 187731-26-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\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 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\u003eHexyldimethyloctylammonium Bromide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air, which could affect its integrity. Due to its ionic nature, it is important to handle it with care to avoid contamination. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. It should be stored away from incompatible substances to ensure safety. Regular inspection of storage conditions is advised to ensure optimal preservation of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087250862298,"sku":"TCI2510H098933767","price":2297000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087250895066,"sku":"TCI2510H098933768","price":6916000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0989.jpg?v=1767117359"},{"product_id":"tci2510h111233890","title":"TCI H1112 13255-48-6 Hydrazine Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHydrazine Acetate (TCI H1112, CAS 13255-48-6) is a chemical compound widely utilized in laboratory settings, particularly in organic chemistry and biochemical research. It serves as a key reagent in various chemical reactions, facilitating the synthesis of complex organic molecules. Its versatility makes it an essential component in the development of bioactive compounds, including pharmaceuticals and diagnostic agents. This compound plays a crucial role in enabling researchers to manipulate molecular structures through bond formation and substitution reactions.\u003c\/p\u003e\n\u003cp\u003eThe unique chemical properties of Hydrazine Acetate make it a preferred choice for laboratory applications. It has the ability to react with a variety of functional groups, such as carbonyl and carboxyl groups, which enhances its utility in synthetic pathways. Its stability under controlled conditions ensures reliable performance during experiments. These characteristics allow it to be used in a wide range of chemical processes, contributing to the efficiency and accuracy of laboratory work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hydrazine Acetate is commonly used by researchers in pharmaceutical, biochemical, and organic chemistry fields. It supports the development of new compounds and has applications in health and environmental research. Its availability and effectiveness make it a valuable tool for scientific investigation and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where hydrazine acetate facilitates bond formation and molecular modification due to its reactivity with functional groups.\u003c\/li\u003e\n\u003cli\u003eBiochemical research involving the creation of bioactive compounds, as it enables the synthesis of molecules with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eDiagnostic agent development, where it contributes to the production of compounds used in medical testing and analysis.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research, as it supports the synthesis of drug molecules through substitution and coupling reactions.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies, where it is used in the analysis and modification of organic pollutants in chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 13255-48-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHydrazine Acetate 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 can affect its reactivity. Due to its potential hazards, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and goggles, should be worn. Avoid contact with skin and eyes, and ensure proper disposal according to local regulations. Regular monitoring of storage conditions is advised to ensure the compound remains safe and effective for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087256760538,"sku":"TCI2510H111233890","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087256793306,"sku":"TCI2510H111233891","price":6639000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1112.jpg?v=1767117514"},{"product_id":"tci2510i000134904","title":"TCI I0001 288-32-4 Imidazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eImidazole is a chemical compound with a heterocyclic structure containing two nitrogen atoms in an aromatic ring. It serves as a fundamental building block in various chemical reactions, often acting as a starting material or intermediate in the synthesis of complex compounds. In the laboratory, Imidazole plays a crucial role in the development of pharmaceuticals, industrial chemicals, and organic compounds. Its stability and reactivity make it a preferred choice for researchers and scientists.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make Imidazole a preferred choice is its ability to form bonds with a wide range of functional groups, including carboxylic acids, amines, and sulfonates. This versatility allows it to participate in diverse chemical reactions, enhancing its utility in synthetic chemistry. Additionally, Imidazole exhibits relatively high melting and boiling points, which facilitates heating and cooling processes in laboratory settings. These characteristics contribute to its widespread use in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Imidazole is widely utilized in chemical, pharmaceutical, and industrial research. It is commonly found in research institutions and universities, where it supports the development of new products, the refinement of synthesis methods, and the improvement of production efficiency. Its availability in various packaging options ensures that it meets the needs of different laboratory applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical synthesis where Imidazole serves as a key intermediate in the creation of complex drug molecules due to its ability to form stable bonds with functional groups.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research where it is used to create a variety of heterocyclic compounds, contributing to the development of new chemical structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where its reactivity and stability make it suitable for the synthesis of specialty chemicals and polymers.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications where it is used as a reagent in various qualitative and quantitative tests due to its predictable chemical behavior.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies where it is employed in the modification of biomolecules, aiding in the development of new therapeutic agents and diagnostic tools.\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: 288-32-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes to meet different laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline form\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\u003eImidazole should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be stored separately from strong acids and bases to avoid potential chemical interactions. Proper labeling of containers is essential for safe handling and to ensure that all laboratory personnel are aware of its properties and precautions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087344808154,"sku":"TCI2510I000134904","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087344840922,"sku":"TCI2510I000134905","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087344873690,"sku":"TCI2510I000134906","price":3079000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0001.jpg?v=1767118780"},{"product_id":"tci2510l004236916","title":"TCI L0042 123-76-2 Levulinic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI L0042 Levulinic Acid is a short-chain keto acid that carries two functional groups at once — a ketone group and a carboxylic acid group — within a single, relatively simple molecule. It is widely recognised as one of the principal platform chemicals obtainable from cellulose-based biomass, which gives it an important position in renewable chemistry research. In the laboratory, levulinic acid serves as a versatile building block for constructing more complex molecules, as well as a reference material in studies of biomass conversion.\u003c\/p\u003e\n\u003cp\u003eThe main advantage of levulinic acid lies in its bifunctional structure. The carboxyl group allows the formation of esters, amides, and salts, while the ketone group opens pathways for nucleophilic addition, condensation, reduction, and the construction of heterocyclic rings. The close proximity of these two groups promotes intramolecular cyclisation reactions that yield lactone and pyrrolidinone derivatives efficiently. Its good solubility in both water and a range of polar organic solvents gives researchers considerable freedom in choosing a reaction system. In addition, its origin in renewable biomass sources makes it a highly relevant material for sustainable chemistry programmes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in university research groups, government research institutes, and industrial R\u0026amp;D units working on renewable chemistry and organic synthesis. It is typically handled at bench scale for exploratory synthesis, method development, and student research projects, where a well-characterised bifunctional building block from an established supplier such as TCI supports reproducible results across repeated experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis building block — the combination of ketone and carboxylic acid functionality within one small molecule allows chemists to construct more complex target structures through selective transformation at either site.\u003c\/li\u003e\n\u003cli\u003eBiomass conversion research — as a recognised platform chemical derived from cellulose-based biomass, it serves as a reference substance for studies tracking the conversion of renewable feedstocks into useful chemicals.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound preparation — the ketone group supports ring-forming chemistry, and the proximity of the two functional groups promotes efficient intramolecular cyclisation toward lactone and pyrrolidinone derivatives.\u003c\/li\u003e\n\u003cli\u003eEsterification and amidation studies — the carboxyl group readily forms esters, amides, and salts, making the material a convenient substrate for teaching and investigating classical carboxylic acid derivatisation reactions.\u003c\/li\u003e\n\u003cli\u003eRenewable and sustainable chemistry programmes — its origin in renewable biomass makes it a suitable model compound for research groups developing greener synthetic routes and evaluating bio-based starting materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCatalogue number: L0042\u003c\/li\u003e\n\u003cli\u003eCAS Number: 123-76-2\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 TCI research packaging; please confirm the pack size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the product label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials, following the conditions stated on the product label and Safety Data Sheet. Keep the material in its original supplier container or in a chemically compatible, clearly labelled vessel, and reseal it promptly after each use to limit moisture uptake. As with any carboxylic acid, handle it in a fume hood while wearing safety glasses, chemical-resistant gloves, and a laboratory coat. Avoid contact with skin and eyes, and consult the Safety Data Sheet before use, handling, and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":50506735288538,"sku":"TCI2510L004236916","price":455000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510L0042.jpg?v=1767121297"},{"product_id":"tci2510m012337678","title":"TCI M0123 150-76-5 4-Methoxyphenol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Methoxyphenol is an organic chemical compound widely used in various chemical reactions and the synthesis of complex molecules. It is a phenolic compound with a methoxy group substituted at the para position, which contributes to its high reactivity. In the laboratory, it serves as a fundamental building block for the development of aromatic compounds, pharmaceuticals, and industrial chemicals. Due to its chemical versatility, it is frequently employed in substitution and oxidation reactions, making it a key reagent in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits polar characteristics and is soluble in organic solvents such as ethyl acetate and acetone, which facilitates its use in a wide range of chemical processes. Its solubility and reactivity make it a preferred choice for researchers and scientists. Additionally, 4-Methoxyphenol demonstrates reasonable stability under normal conditions, simplifying its storage and handling in laboratory settings. These properties ensure its reliability and consistency in chemical applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Methoxyphenol is utilized in diverse chemical research activities, including the synthesis of new compounds, qualitative analysis, and the development of chemical materials for industrial applications. Its reliability and versatility make it a highly sought-after reagent among researchers. Its role in supporting scientific innovation and industrial development is well recognized in the local scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of aromatic compounds due to its phenolic structure and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drug molecules and derivatives.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production as a key intermediate in the creation of various chemical products.\u003c\/li\u003e\n\u003cli\u003eQualitative analysis in chemical testing for the identification of functional groups.\u003c\/li\u003e\n\u003cli\u003eOrganic reaction studies for substitution and oxidation processes in synthetic chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 150-76-5\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\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Methoxyphenol should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be stored away from strong oxidizing agents and incompatible substances. Proper labeling of storage containers is essential to ensure safe handling. In laboratory settings, personal protective equipment such as gloves and goggles should be worn when handling this compound. Regular inspection of storage conditions is advised to ensure compliance with safety standards and to maintain the integrity of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087514218714,"sku":"TCI2510M012337678","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087514251482,"sku":"TCI2510M012337679","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087514284250,"sku":"TCI2510M012337680","price":1491000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0123.jpg?v=1767122277"},{"product_id":"tci2510m013737699","title":"TCI M0137 74-89-5 Methylamine (ca 40% in Water, ca 12mol\/L)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethylamine (ca 40% in Water, ca 12mol\/L) is a versatile chemical compound widely used in laboratory settings for its reactivity and utility in various chemical and biochemical experiments. As a primary amine, it plays a crucial role in the synthesis of organic compounds, particularly in glycoscience and chemical biology. Its ability to participate in multiple reaction mechanisms makes it an essential reagent for researchers working on complex molecular structures. This solution is commonly found in laboratories where the development of new pharmaceuticals, biotechnology applications, and analytical chemistry procedures are conducted.\u003c\/p\u003e\n\u003cp\u003eThe high concentration of methylamine in aqueous solution (12mol\/L) enhances its effectiveness in chemical reactions, allowing for efficient and controlled synthesis processes. Its reactivity with functional groups in other compounds makes it a preferred choice for those seeking to modify molecular structures or create new compounds. The solubility in water further simplifies its handling and integration into experimental protocols. These properties make methylamine a reliable and powerful tool in the hands of skilled researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, methylamine is frequently used in biochemical and organic chemistry research. It supports studies in pharmacology, biotechnology, and chemical synthesis, enabling scientists to explore new compounds and understand molecular interactions. Its availability in the local market ensures that researchers have access to this essential reagent for their experimental needs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGlycoscience research benefits from methylamine’s ability to modify carbohydrate structures, aiding in the study of glycoproteins and glycolipids.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis relies on methylamine as a key reagent for forming amine bonds, facilitating the creation of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments use methylamine to investigate enzyme activity and protein interactions, supporting molecular biology studies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development incorporates methylamine in the synthesis of drug compounds, enhancing the efficiency of compound creation.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications utilize methylamine for sample preparation and reaction control in various testing procedures.\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: 74-89-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Aqueous solution\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eMethylamine should be stored in a cool, dark location, away from heat and direct sunlight to maintain its stability. It is recommended to use sealed, corrosion-resistant containers to prevent evaporation and contamination. Due to its high reactivity, it should be kept away from strong oxidizers and acids to avoid hazardous reactions. Laboratory personnel should wear appropriate personal protective equipment, including gloves and goggles, when handling this material. Proper ventilation is essential to minimize exposure to vapors. Always ensure that the storage area is well-ventilated and accessible only to authorized personnel to prevent accidental contact or misuse.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087515529434,"sku":"TCI2510M013737699","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48087515562202,"sku":"TCI2510M013737700","price":531000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0137.jpg?v=1767122317"},{"product_id":"tci2510m157339625","title":"TCI M1573 51010-74-3 Morpholinosulfur Trifluoride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMorpholinosulfur Trifluoride (MSTF), also known as TCI M1573 with CAS number 51010-74-3, is a chemical compound widely used in laboratory research, particularly in the fields of chemical biology and glycoscience. This compound plays a crucial role in the synthesis of bioactive molecules, including pharmaceuticals and enzyme inhibitors. Its unique structure, combining morpholino and sulfon trifluoride groups, enables specific interactions with biological molecules such as proteins and nucleic acids. MSTF is a versatile reagent that supports the development of new compounds with therapeutic potential.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of MSTF make it a preferred choice for researchers. It exhibits stability under various conditions, ensuring consistent performance in experiments. MSTF is soluble in organic solvents, which facilitates its use in a wide range of chemical reactions. Its ability to interact with diverse biological substrates makes it an essential tool in molecular modification and functional group manipulation. These characteristics contribute to its reliability and effectiveness in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, MSTF is commonly used in applied research, such as the synthesis of pharmacological compounds and drug development. Its role in creating bioactive molecules aligns with the goals of both academic and industrial research institutions. Researchers rely on MSTF for its chemical versatility and stability, making it a valuable component in the development of new therapeutic agents and biochemical applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBioactive Compound Synthesis: MSTF is used to create molecules with therapeutic potential, supporting drug development and pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eEnzyme Inhibitor Development: Its ability to interact with biological substrates makes it ideal for designing compounds that inhibit specific enzymes.\u003c\/li\u003e\n\u003cli\u003eGlycoscience Research: MSTF is utilized in studies involving carbohydrate-based molecules, aiding in the understanding of glycosylation processes.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: Its chemical flexibility allows for the synthesis of modified compounds used in functional group analysis and structural studies.\u003c\/li\u003e\n\u003cli\u003ePharmacological Compound Design: MSTF supports the creation of new drug candidates by enabling the synthesis of complex molecular structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 51010-74-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\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\u003eMorpholinosulfur Trifluoride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical nature, it is important to handle MSTF with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid contact with incompatible materials, and ensure proper ventilation when working with this compound. MSTF should be stored away from heat sources and flammable materials to minimize potential hazards. Regular inspection of storage conditions is advised to maintain the integrity of the compound over time.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087614619866,"sku":"TCI2510M157339625","price":1718000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087614652634,"sku":"TCI2510M157339626","price":5452000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1573.jpg?v=1767125133"},{"product_id":"tci2510n015542804","title":"TCI N0155 552-16-9 2-Nitrobenzoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Nitrobenzoic Acid is a chemical compound widely used in laboratory settings as a fundamental building block for various chemical reactions, particularly in the synthesis of complex organic compounds. It plays a crucial role in organic chemistry by serving as a versatile reagent that can participate in multiple reaction types due to its functional groups. This compound is commonly utilized in research and development processes across multiple scientific fields, including pharmaceuticals and industrial chemistry. Its chemical structure allows for easy modification through various chemical transformations, making it a valuable tool in the hands of chemists and researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique properties, such as the presence of both nitro and carboxyl groups, contribute to its high reactivity and polarity. These characteristics make it suitable for a wide range of chemical reactions, including substitution, esterification, and redox processes. The stability of 2-Nitrobenzoic Acid under normal conditions ensures that it remains effective for extended periods, which is essential for consistent results in laboratory experiments. Its reactivity and stability make it a preferred choice for many synthetic pathways in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Nitrobenzoic Acid is frequently used in academic and industrial research settings. It is a key component in the development of new chemical compounds and is often employed in the synthesis of heterocyclic compounds, esters, and other derivatives. Its availability and reliability make it a popular choice among researchers working on pharmaceutical and organic chemistry projects in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in the synthesis of heterocyclic compounds due to its reactive nitro and carboxyl groups, enabling the formation of complex organic structures.\u003c\/li\u003e\n\u003cli\u003eApplied in esterification reactions because of its carboxylic acid functionality, allowing for the creation of ester derivatives in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eUtilized in redox reactions due to the presence of the nitro group, which can be reduced to various nitrogen-containing compounds.\u003c\/li\u003e\n\u003cli\u003eEmployed in pharmaceutical research for the development of new drug molecules, as it can serve as a precursor in the synthesis of bioactive compounds.\u003c\/li\u003e\n\u003cli\u003eIncorporated in industrial chemical processes for the production of specialty chemicals, where its reactivity and stability are advantageous.\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: 552-16-9\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 direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Nitrobenzoic Acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air, which can affect its reactivity. Suitable storage containers include glass or polyethylene vessels that are resistant to chemical corrosion. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is generally stable under normal conditions, it should be kept away from strong oxidizing agents to prevent unwanted reactions. Proper storage and handling ensure the compound remains effective and safe for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087793402074,"sku":"TCI2510N015542804","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087793434842,"sku":"TCI2510N015542805","price":7572000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0155.jpg?v=1767129363"},{"product_id":"tci2510n022042881","title":"TCI N0220 100-02-7 4-Nitrophenol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Nitrophenol is a versatile chemical compound widely used in various chemical reactions and the synthesis of complex molecules. As a fundamental building block in chemistry, it plays a crucial role in the development of aromatic and heterocyclic compounds. This compound is commonly found in chemical laboratories, particularly in research involving substitution reactions, structural coupling, and organic compound modification. Its reactivity makes it an essential reagent for the production of more complex chemical products, including pharmaceuticals, industrial chemicals, and synthetic precursors.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 4-Nitrophenol make it a preferred choice for laboratory applications. It exhibits a stable molecular structure and is highly reactive under various chemical conditions. It is soluble in organic solvents such as ethyl acetate and ethanol, but it is not soluble in water. This solubility profile allows it to be easily used in reactions requiring non-aqueous solvents. Additionally, its well-defined melting and boiling points facilitate precise heating and cooling processes in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Nitrophenol is frequently used in chemical research and educational settings. It is a common reagent in academic and industrial research institutions, supporting both teaching and experimental work. Its availability and chemical properties make it an essential component in the chemical supply chain within the country, contributing to the advancement of scientific studies and technological development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in organic synthesis for the preparation of substituted aromatic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eApplied in pharmaceutical research for the development of drug molecules requiring nitro group functionality.\u003c\/li\u003e\n\u003cli\u003eUtilized in analytical chemistry for the detection and quantification of aromatic compounds through spectroscopic methods.\u003c\/li\u003e\n\u003cli\u003eEmployed in environmental studies to analyze the presence of nitrophenolic compounds in water and soil samples.\u003c\/li\u003e\n\u003cli\u003eIncorporated in teaching laboratories for demonstrating substitution reactions and functional group transformations.\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: 100-02-7\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 supply options\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\u003e4-Nitrophenol should be stored in a cool, dry place away from direct sunlight and incompatible materials. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and maintain chemical integrity. Due to its reactivity, it should be kept away from strong oxidizing agents and strong acids. Proper labeling and safe handling procedures are essential to ensure laboratory safety. Always use appropriate personal protective equipment when handling this compound to minimize exposure risks. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087798022362,"sku":"TCI2510N022042881","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087798055130,"sku":"TCI2510N022042882","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087798087898,"sku":"TCI2510N022042883","price":3913000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0220.jpg?v=1767129439"},{"product_id":"tci2510o008244383","title":"TCI O0082 79-37-8 Oxalyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eOxalyl Chloride from TCI is the diacyl chloride of oxalic acid. It is a highly reactive liquid reagent and one of the core tools of the synthetic chemist. In the laboratory it has two main roles. First, it activates dimethyl sulfoxide in the Swern oxidation, which converts primary and secondary alcohols into aldehydes and ketones. Second, it converts carboxylic acids into acyl chlorides. In glycoscience, the reagent is important for the selective oxidation and modification of hydroxyl groups on carbohydrates.\u003c\/p\u003e\n\u003cp\u003eChemists choose oxalyl chloride because its reactions run under relatively mild conditions and its by-products are all gases: carbon monoxide, carbon dioxide and hydrogen chloride. These gases leave the reaction mixture easily, which makes the workup simpler. With a small amount of DMF as catalyst, acyl chloride formation can proceed at room temperature or below, so the method suits sensitive substrates. In the Swern oxidation, the reagent lets chemists oxidize alcohols without heavy metals and without over-oxidation to carboxylic acids. This gives cleaner product profiles for delicate carbohydrate and natural product intermediates.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, oxalyl chloride is widely needed by synthetic organic chemistry laboratories at universities, research institutes and pharmaceutical development facilities. Research groups working on carbohydrate chemistry, glycoconjugate synthesis and medicinal chemistry use it routinely to prepare aldehyde intermediates and activated acid derivatives. As a TCI product supplied through AMI Scientific, it gives Indonesian researchers access to a trusted reagent brand for multistep synthesis, method development and teaching laboratories that demonstrate classical oxidation and acylation chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSwern oxidation: oxalyl chloride activates dimethyl sulfoxide, so primary and secondary alcohols can be oxidized to aldehydes and ketones under mild conditions without heavy metal oxidants.\u003c\/li\u003e\n\u003cli\u003eAcyl chloride preparation: with catalytic DMF it converts carboxylic acids into acyl chlorides at room temperature or below, and its gaseous by-products make workup and isolation simple.\u003c\/li\u003e\n\u003cli\u003eCarbohydrate modification in glycoscience: it enables selective oxidation and functionalization of sugar hydroxyl groups, which supports the synthesis of modified monosaccharides, oligosaccharide building blocks and glycoconjugates.\u003c\/li\u003e\n\u003cli\u003eSynthesis of sensitive intermediates: because the reactions run under mild conditions and do not over-oxidize to carboxylic acids, it suits delicate substrates in natural product and medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eAmide and ester formation workflows: the acyl chlorides it generates react readily with amines and alcohols, making it a practical first step for building amide and ester linkages.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code O0082)\u003c\/li\u003e\n\u003cli\u003eCAS number: 79-37-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003ePack sizes: Several pack sizes are available; please confirm current options with AMI Scientific\u003c\/li\u003e\n\u003cli\u003eStorage note: Moisture-sensitive; keep tightly sealed in a cool, dry, well-ventilated place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eOxalyl chloride reacts vigorously with water and moisture, releasing hydrogen chloride and other toxic gases. Keep it in its original tightly closed container, ideally under an inert atmosphere such as nitrogen or argon, in a cool, dry, well-ventilated area away from water, alcohols, bases and oxidizers. Handle it only inside a properly working fume hood and wear chemical-resistant gloves, safety goggles or a face shield, and a lab coat. Transfer it with dry syringes or cannulas and add it slowly, because reactions give off gas. Always consult the supplier's Safety Data Sheet before use and dispose of waste according to local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48275527499994,"sku":"TCI2510O008244383","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48275527532762,"sku":"TCI2510O008244384","price":2197000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0082.jpg?v=1767131330"},{"product_id":"tci2510o057745003","title":"TCI O0577 16940-66-2 Sodium Borohydride (Granulated)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eSodium Borohydride (Granulated), with the CAS number 16940-66-2, is a chemical compound widely used in laboratory settings for its strong reducing properties. It plays a crucial role in various chemical reactions, particularly in reduction processes, where it acts as a powerful hydride source. This granulated form is especially useful in chemical synthesis, offering controlled reactivity and ease of handling. Its versatility makes it an essential reagent in both inorganic and organic chemistry applications, supporting a wide range of experimental needs in research and education.\u003c\/p\u003e\n\u003cp\u003eThe granulated form of sodium borohydride is preferred due to its stability in controlled environments and its ability to be safely handled in laboratory conditions. It is a white powder that reacts vigorously with water and air, necessitating careful storage and use. Its reactivity with oxygen and moisture means it must be stored in a dry, sealed container to prevent decomposition. Despite its reactivity, its granulated form allows for precise dosing and controlled reactions, making it a reliable choice for many chemical processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, sodium borohydride is commonly used in chemical synthesis, analytical chemistry, and catalytic testing. It is an integral part of both academic and industrial research, supporting the development of new compounds and materials. Its role in educational curricula and research projects highlights its importance in advancing chemical knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where sodium borohydride is used to reduce carbonyl compounds to alcohols, offering a reliable and efficient method for producing complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eInorganic chemistry experiments that require a strong reducing agent for the synthesis of various metal compounds and hydrides.\u003c\/li\u003e\n\u003cli\u003eCatalytic testing in which sodium borohydride serves as a hydride source, enabling the evaluation of catalyst efficiency in reduction reactions.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications where it is used for the reduction of metal ions, aiding in the detection and quantification of specific elements.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories where it is employed to demonstrate redox reactions and the properties of strong reducing agents in a controlled setting.\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: 16940-66-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Main-group Elements\u003c\/li\u003e\n\u003cli\u003ePack sizes: Granulated form available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: White granules\u003c\/li\u003e\n\u003cli\u003eStorage note: Must be stored in a dry, sealed container away from moisture and air\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eSodium borohydride should be stored in a cool, dry place, away from moisture and sources of heat. It is essential to use airtight containers to prevent exposure to air and humidity, which can lead to decomposition. Due to its reactivity with water and oxygen, it should never be handled near open flames or in environments with high humidity. When working with this compound, it is recommended to use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Proper ventilation is also necessary to minimize the risk of inhalation of any vapors that may be released during handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087919395034,"sku":"TCI2510O057745003","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087919427802,"sku":"TCI2510O057745004","price":1995000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0577.jpg?v=1767132072"},{"product_id":"tci2510p080146243","title":"TCI P0801 838-85-7 Diphenyl Phosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiphenyl phosphate is a chemical compound widely used in laboratory settings as a foundational reagent for various organic reactions. It serves as a key building block in the synthesis of complex organic molecules, particularly in reactions involving substitution, esterification, and phosphorus bond formation. Due to its structural composition of two phenyl groups attached to a phosphate group, it exhibits high reactivity and versatility in chemical transformations. This compound is essential for researchers aiming to develop new synthetic pathways and functional materials.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Diphenyl phosphate make it a preferred choice in laboratory applications. It is chemically stable under specific conditions, yet retains high reactivity towards various substrates. Its purity and consistent chemical behavior ensure reliable results in experimental processes. The compound’s ability to participate in multiple reaction types, combined with its stability, makes it a valuable asset in both academic and industrial research environments. Its non-colored nature and solid or liquid form, depending on storage conditions, further enhance its usability in diverse laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diphenyl phosphate is extensively used in organic chemistry research and pharmaceutical development. It plays a crucial role in the synthesis of pharmaceutical compounds and other complex molecules. Its availability and performance make it a preferred material for laboratories seeking precision and quality in their chemical experiments. The compound’s reliability and effectiveness contribute to its widespread use in both academic and industrial sectors across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from Diphenyl phosphate due to its reactivity and role in phosphorus bond formation.\u003c\/li\u003e\n\u003cli\u003eEsterification processes utilize this compound for its ability to form ester linkages efficiently in controlled environments.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in chemical reactions rely on Diphenyl phosphate for its stability and participation in multiple reaction pathways.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical compound development uses Diphenyl phosphate as a building block for synthesizing complex drug molecules.\u003c\/li\u003e\n\u003cli\u003eResearch in phosphorus chemistry leverages this compound for its structural versatility and reactivity in various synthetic strategies.\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: 838-85-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on storage conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiphenyl phosphate should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid exposure to incompatible materials such as strong acids or bases. The compound should be stored in airtight containers made of materials resistant to chemical degradation, such as glass or high-density polyethylene. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087993843930,"sku":"TCI2510P080146243","price":884000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087993876698,"sku":"TCI2510P080146244","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P0801.jpg?v=1767133751"},{"product_id":"tci2510p112046714","title":"TCI P1120 1623-08-1 Dibenzyl Phosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzyl phosphate is a chemical compound widely used in laboratory settings as a building block for various organic synthesis reactions. It serves as a versatile reagent in chemical processes, particularly in the creation of complex organic molecules. Its unique structure, consisting of two benzyl groups attached to a phosphorus atom, provides it with high reactivity and functional versatility. This makes it an essential material for chemists working on synthetic pathways that require precise control over reaction conditions. Its ability to participate in multiple types of chemical transformations enhances its value in both research and industrial applications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability under normal conditions, combined with its reactivity toward specific reagents and functional groups, makes it a preferred choice for many laboratory applications. Its ability to form phosphodiester bonds and its compatibility with a wide range of functional groups, such as hydroxyl, amine, and carbonyl groups, further contribute to its popularity. These properties allow it to be used in a variety of synthetic strategies, making it a valuable tool for chemists aiming to develop new compounds or optimize existing synthesis routes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzyl phosphate is commonly used in both academic and applied research settings. It plays a key role in the development of new chemical materials, pharmaceutical compounds, and analytical methods. Its relevance in the chemical industry and research institutions in Indonesia underscores its importance as a fundamental reagent in modern chemical experimentation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where Dibenzyl phosphate is used to create complex molecules by participating in substitution and esterification reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its ability to form phosphodiester bonds, which are crucial in the development of new drug compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry utilizes its reactivity to detect and quantify specific functional groups in various samples.\u003c\/li\u003e\n\u003cli\u003ePolymer science applies it as a building block in the synthesis of phosphorus-containing polymers with unique properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies use it to modify biomolecules, enabling the study of enzyme mechanisms 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: 1623-08-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: 100g, 500g, 1kg\u003c\/li\u003e\n\u003cli\u003ePhysical form: White crystalline 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\u003eDibenzyl phosphate 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, which can affect its reactivity. Due to its high reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential fumes. Avoid contact with incompatible substances, and ensure that it is kept away from heat sources. Proper labeling and storage conditions are essential to ensure safety and maintain the integrity of the compound in a laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088028610778,"sku":"TCI2510P112046714","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088028643546,"sku":"TCI2510P112046715","price":6487000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1120.jpg?v=1767134302"},{"product_id":"tci2510p122346863","title":"TCI P1223 990-91-0 Tetrabenzyl Pyrophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTetrabenzyl Pyrophosphate is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It serves as a key reagent in various chemical reactions where phosphorus-containing functionalities are required. Its unique molecular structure, consisting of two benzyl groups attached to a phosphorus core, makes it highly versatile in organic chemistry applications. This compound is particularly valuable for its ability to act as a phosphorus donor, enabling the formation of phosphorus-based intermediates in synthetic pathways. Due to its stability and controlled reactivity, it is a reliable choice for researchers working in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eTetrabenzyl Pyrophosphate is preferred for its chemical stability and controlled reactivity, which allow for predictable outcomes in chemical reactions. It exhibits good solubility in organic solvents such as ethyl acetate and dimethyl sulfoxide, facilitating ease of handling and incorporation into reaction mixtures. Its resistance to degradation under normal conditions ensures long-term storage and consistent performance in laboratory experiments. These properties make it a reliable and efficient reagent for a wide range of chemical processes, especially in the synthesis of phosphorus-containing compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Tetrabenzyl Pyrophosphate is commonly used in organic chemistry research, particularly in academic institutions and research centers. It plays a vital role in the development of new chemical compounds and the study of reaction mechanisms. Its availability and reliability make it a standard component in many laboratory workflows, supporting both teaching and research activities in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of phosphorus-containing compounds due to its role as a phosphorus donor in chemical reactions.\u003c\/li\u003e\n\u003cli\u003ePreparation of phosphorus-based intermediates in complex molecule construction for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003cli\u003eResearch in catalytic processes where phosphorus functionality is essential for reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical methodologies in academic and industrial research settings requiring stable phosphorus reagents.\u003c\/li\u003e\n\u003cli\u003eUse in analytical chemistry for the study of phosphorus-containing compounds and their reactivity in different environments.\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: 990-91-0\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 options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTetrabenzyl Pyrophosphate 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 may affect its reactivity. The compound is generally stable under normal storage conditions but should be handled with care to avoid contamination. In laboratory settings, it is important to follow standard safety protocols, including the use of appropriate personal protective equipment. Proper labeling and storage away from incompatible materials ensure safe handling and long-term usability of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088037097690,"sku":"TCI2510P122346863","price":1920000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1223.jpg?v=1767134508"},{"product_id":"tci2510p148947218","title":"TCI P1489 7647-10-1 Palladium(II) Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePalladium(II) Chloride (TCI P1489), with CAS number 7647-10-1, is a key chemical compound used in catalytic reactions and C-H activation processes. It plays a crucial role in organic synthesis by facilitating reactions that require the activation of carbon-hydrogen bonds. This compound is widely utilized in laboratory settings for its ability to accelerate chemical reactions without altering the structure of the main molecular components. Its versatility makes it an essential reagent for researchers working in catalysis and inorganic chemistry.\u003c\/p\u003e\n\u003cp\u003ePalladium(II) Chloride is known for its high density and solubility in organic solvents such as ethyl acetate and acetone. These properties make it ideal for applications requiring high reactivity and concentration. Additionally, it has the ability to form complexes with various ligands, which expands its utility in chemical synthesis. The compound is chemically stable under certain conditions but is highly reactive towards water and organic compounds. This reactivity necessitates careful handling and storage to maintain its effectiveness.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Palladium(II) Chloride is extensively used in organic chemistry and catalysis research. Its application is particularly relevant for institutions and researchers focused on developing new synthetic methods and catalytic processes. The compound's performance in controlled environments supports advanced research and innovation in chemical sciences, making it a valuable resource for academic and industrial laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from Palladium(II) Chloride's ability to activate carbon-hydrogen bonds, enabling complex molecule formation through efficient catalytic mechanisms.\u003c\/li\u003e\n\u003cli\u003eC-H activation processes rely on this compound's reactivity to facilitate selective bond-breaking, which is critical in creating novel chemical structures with high precision.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions are enhanced by the compound's capacity to act as a catalyst, promoting the formation of carbon-carbon bonds under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eIsomerization processes utilize Palladium(II) Chloride to rearrange molecular structures efficiently, offering a reliable method for structural transformation.\u003c\/li\u003e\n\u003cli\u003eSubstitution reactions benefit from its high reactivity, allowing for the replacement of functional groups in organic compounds with minimal byproduct formation.\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: 7647-10-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [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 dry, cool, and well-ventilated area away from moisture and organic solvents\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003ePalladium(II) Chloride should be stored in a dry, cool, and well-ventilated area to prevent moisture exposure, which can lead to degradation. It is recommended to use airtight containers made of glass or polyethylene to ensure chemical stability. Due to its reactivity with water and organic compounds, it should be kept away from these substances during storage. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper ventilation is essential to minimize inhalation risks. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48088058691802,"sku":"TCI2510P148947218","price":2929000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48088058724570,"sku":"TCI2510P148947219","price":11912000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1489.jpg?v=1767134951"},{"product_id":"tci2510p149047220","title":"TCI P1490 7440-05-3 Palladium 5% on Carbon (wetted with ca 55% Water)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePalladium 5% on Carbon (wetted with ca 55% Water) from TCI is a heterogeneous catalyst made of palladium metal dispersed on an activated carbon support, with a palladium loading of 5%. The product is deliberately wetted with approximately 55% water to make it safer to handle. Pd\/C is one of the most widely used catalysts in organic synthesis laboratories. It is used mainly to hydrogenate multiple bonds, reduce nitro groups, and remove benzyl and Cbz protecting groups with hydrogen gas or a hydrogen donor.\u003c\/p\u003e\n\u003cp\u003eChemists choose this catalyst because it is active, selective in many reductive transformations, and easy to separate from the reaction mixture by simple filtration. Activated carbon has a very large surface area, so the palladium is spread evenly and many active sites are available. The 5% loading is active enough for many routine reactions and uses less precious metal than higher loadings. The water-wetted form, at about 55% water, greatly lowers the pyrophoric risk, which is the tendency of dry catalyst to ignite when it meets air and organic solvent vapours.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5% Pd\/C is widely used in university research on drug synthesis, natural products, and organic chemistry. Researchers rely on it when they prepare intermediates, modify natural product scaffolds, or remove protecting groups in multistep syntheses. Because it is a reliable and well-documented catalyst, it is also a practical choice for teaching laboratories and for groups developing reduction methods. In all of these settings, the wetted form makes everyday weighing, transfer, and filtration safer.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHydrogenation of carbon–carbon double and triple bonds: the evenly dispersed palladium on activated carbon gives many active sites, so unsaturated compounds can be saturated efficiently with hydrogen gas or a suitable hydrogen donor.\u003c\/li\u003e\n\u003cli\u003eReduction of nitro groups to amines: Pd\/C is a standard catalyst for this transformation, and chemists can recover it from the reaction mixture by filtration once the reduction is complete.\u003c\/li\u003e\n\u003cli\u003eRemoval of benzyl protecting groups: the catalyst cleaves benzyl ethers and related groups by hydrogenolysis, which makes it a key tool in multistep synthesis of drugs and natural products.\u003c\/li\u003e\n\u003cli\u003eCleavage of Cbz (benzyloxycarbonyl) protecting groups: Pd\/C removes Cbz groups from amines under reductive conditions, which supports work in peptide chemistry and the preparation of amine intermediates.\u003c\/li\u003e\n\u003cli\u003eTransfer hydrogenation with hydrogen donors: when handling hydrogen gas is impractical, this catalyst can work with a hydrogen donor, so reductive transformations stay accessible in laboratories with limited hydrogenation equipment.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code P1490)\u003c\/li\u003e\n\u003cli\u003eCAS number: 7440-05-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Hydrogenation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eComposition: 5% palladium on an activated carbon support, wetted with approximately 55% water\u003c\/li\u003e\n\u003cli\u003ePack sizes: as listed in the TCI catalogue for product P1490\u003c\/li\u003e\n\u003cli\u003eStorage note: keep in its wetted state in a tightly closed container, away from ignition sources\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the catalyst in its original, tightly closed container in a cool, well-ventilated area away from heat, open flames, and other ignition sources. Do not let the material dry out, because dry Pd\/C can ignite when it meets air and organic solvent vapours. Store it away from oxidizing agents and flammable solvents. When charging a reaction, add the catalyst under an inert atmosphere where possible, before adding the organic solvent. Never let used catalyst dry on filter paper. Keep filter cakes wet and dispose of them according to local regulations for precious metal waste. Wear safety glasses, gloves, and a lab coat, and work in a fume hood. Always consult the TCI Safety Data Sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088058822874,"sku":"TCI2510P149047220","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088058855642,"sku":"TCI2510P149047221","price":3711000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1490.jpg?v=1767134955"},{"product_id":"tci2510p149147222","title":"TCI P1491 7440-05-3 Palladium 10% on Carbon (wetted with ca 55% Water)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePalladium 10% on Carbon (wetted with ca 55% Water) from TCI is a heterogeneous hydrogenation catalyst with 10% palladium on an activated carbon support. Like the 5% grade, it is wetted with about 55% water so it is safer to handle. The higher metal loading makes it the grade of choice for chemists who need stronger catalytic activity. Typical cases are substrates that are hard to reduce, slow hydrogenolysis of protecting groups, and reactions that need to finish faster with less solid catalyst in the flask.\u003c\/p\u003e\n\u003cp\u003eThe main advantage of the 10% loading is that each gram of catalyst carries more palladium sites. Researchers can therefore use a smaller mass of catalyst to deliver the same amount of metal. Less solid makes filtration easier and reduces the amount of product lost by adsorption onto the carbon. The activated carbon support keeps the palladium well dispersed, which helps it stay active. The water content of about 55% greatly lowers the risk of the catalyst igniting on contact with air or organic solvent vapours. Dry Pd\/C is well known for this hazard.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, 10% Pd\/C is a routine purchase for organic synthesis laboratories at universities, research institutions and industrial R\u0026amp;D groups. Postgraduate researchers and synthetic chemists use it to reduce multiple bonds, remove benzyl-type protecting groups and convert nitro groups into amines while building target molecules. Its water-wetted form also suits teaching and research laboratories that want a more forgiving catalyst for everyday hydrogenation work. This is especially useful where staff and students vary in experience with pyrophoric materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCatalytic hydrogenation of alkenes and alkynes: the high palladium loading gives strong activity, so carbon–carbon multiple bonds can be saturated efficiently under a hydrogen atmosphere.\u003c\/li\u003e\n\u003cli\u003eHydrogenolysis of benzyl and Cbz protecting groups: the stronger activity of the 10% grade helps with deprotections that run slowly over lower-loading catalysts and shortens overall reaction times.\u003c\/li\u003e\n\u003cli\u003eReduction of nitro compounds to amines: the catalyst is widely used to make aromatic amines as intermediates in pharmaceutical, dye and fine chemical synthesis research.\u003c\/li\u003e\n\u003cli\u003eTransfer hydrogenation with hydrogen donors: the supported palladium also works with donor reagents, so laboratories can run reductions without handling hydrogen gas cylinders directly.\u003c\/li\u003e\n\u003cli\u003eDifficult or sterically hindered substrate reductions: more palladium per gram gives the activity needed for substrates that respond poorly to 5% Pd\/C, while keeping the catalyst mass manageable for filtration.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code P1491)\u003c\/li\u003e\n\u003cli\u003eCAS number: 7440-05-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Hydrogenation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eComposition: palladium 10% on activated carbon support\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid catalyst wetted with ca 55% water\u003c\/li\u003e\n\u003cli\u003ePack sizes: as listed on the product page; storage: keep tightly closed and away from ignition sources\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the catalyst in its original, tightly closed container in a cool, well-ventilated place, away from heat, sparks, open flames and oxidising agents. Do not let the material dry out, because the water content is what lowers its ignition risk. Weigh and transfer it carefully, preferably under an inert gas such as nitrogen when adding it to flammable solvents. Never add it to a flask that already contains hydrogen. After filtration, keep used catalyst wet with water and do not let the filter cake dry in air, because spent Pd\/C can ignite. Wear safety glasses, gloves and a lab coat, work in a fume hood, and follow the supplier's safety data sheet and your institution's rules for disposing of precious-metal waste.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088058921178,"sku":"TCI2510P149147222","price":1944000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088058953946,"sku":"TCI2510P149147223","price":6134000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1491.jpg?v=1767134958"},{"product_id":"tci2510p152847242","title":"TCI P1528 12135-22-7 Palladium Hydroxide (contains Pd, PdO) on Carbon (wetted with ca 50% Water)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePalladium Hydroxide (contains Pd, PdO) on Carbon, with approximately 50% water content, is a chemical compound widely used in catalytic reactions, particularly in hydrogenation processes. This material serves as a versatile catalyst in laboratory settings, offering high reactivity and efficiency in various chemical transformations. It is a metal-based catalyst supported on carbon, which enhances its surface area and adsorption capacity, making it suitable for a wide range of applications. Its ability to facilitate hydrogenation reactions makes it an essential tool for researchers working in organic and inorganic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe unique properties of Palladium Hydroxide make it a preferred choice for catalytic applications. Its high surface area and strong adsorption capacity allow it to interact effectively with reactants, promoting efficient reaction pathways. The presence of water in its structure further aids in the activation process, improving its performance in reactive environments. Additionally, the carbon support provides mechanical stability, ensuring the catalyst remains active and uniform during reactions. These characteristics make it ideal for use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Palladium Hydroxide is commonly used in chemical research, particularly in the fields of catalysis and hydrogenation. It is a key component in experiments involving the hydrogenation of alkenes and aromatic compounds. Its availability and effectiveness make it a popular choice among researchers and institutions in Indonesia. The material is also used in the development of new chemical processes and the optimization of existing ones, contributing to scientific advancements in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHydrogenation Reactions: Palladium Hydroxide is ideal for hydrogenation due to its high catalytic activity and ability to facilitate the reduction of unsaturated compounds.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It supports the synthesis of complex organic molecules by promoting efficient and selective hydrogenation processes.\u003c\/li\u003e\n\u003cli\u003eCatalytic Testing: Its stability and reactivity make it suitable for testing new catalytic systems and reaction conditions in research settings.\u003c\/li\u003e\n\u003cli\u003eIndustrial Process Development: The material is used in developing and optimizing chemical processes that require efficient hydrogenation catalysts.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is employed in analytical procedures where precise control of hydrogenation reactions is necessary for accurate results.\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: 12135-22-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Hydrogenation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Wetted with approximately 50% water, supported on carbon\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\u003ePalladium Hydroxide should be stored in a cool, dry environment to maintain its stability and catalytic activity. It is recommended to use airtight containers to prevent moisture absorption, which can affect its performance. Due to its wetted nature, it should be kept away from strong oxidizing agents to avoid unwanted reactions. Proper labeling of storage containers is essential for safe handling. In laboratory settings, it is important to wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this material. Regular inspection of storage conditions ensures the material remains in optimal condition for use in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10g","offer_id":48088060199130,"sku":"TCI2510P152847242","price":8329000.0,"currency_code":"IDR","in_stock":true},{"title":"50g","offer_id":48088060231898,"sku":"TCI2510P152847243","price":27760000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1528.jpg?v=1767134974"},{"product_id":"tci2510p174347419","title":"TCI P1743 7789-60-8 Phosphorus Tribromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePhosphorus Tribromide (PBr₃), with the CAS number 7789-60-8, is a highly reactive chemical compound widely used in laboratory settings for its versatility in chemical reactions. As a key reagent in organic and inorganic chemistry, it plays a crucial role in the synthesis of brominated compounds and the modification of organic molecules. Its ability to act as both a reagent and a catalyst makes it indispensable in various synthetic pathways. Due to its reactivity, PBr₃ is often employed in substitution reactions and bond-forming processes, where it facilitates the introduction of bromine atoms into organic structures.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of PBr₃, including its high reactivity, corrosiveness, and tendency to vaporize, make it a preferred choice for specific applications. Its high density and volatility require careful handling, but these characteristics also make it effective in reactions that demand extreme conditions. The compound's ability to react with alcohols, ethers, and other organic compounds under controlled conditions ensures its utility in both academic and industrial research. Its reactivity and effectiveness in promoting chemical transformations justify its use in specialized laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, PBr₃ is commonly used in research and development projects involving the synthesis of brominated compounds. It is a reliable choice for chemists working in educational institutions and research organizations due to its availability and effectiveness. However, its hazardous nature necessitates strict safety protocols to ensure safe handling and use in laboratory settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of brominated compounds due to its ability to introduce bromine atoms into organic molecules.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions in substitution processes where bromine is needed for structural modification.\u003c\/li\u003e\n\u003cli\u003ePreparation of bromides from alcohols and ethers through nucleophilic substitution mechanisms.\u003c\/li\u003e\n\u003cli\u003eResearch in inorganic chemistry for the formation of phosphorus-based compounds under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical materials requiring reactive brominating agents for functional group introduction.\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: 7789-60-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Phosphorous Compounds\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a cool, dry, and well-ventilated area away from moisture and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003ePhosphorus Tribromide should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible materials. It is recommended to use sealed containers made of inert materials such as glass or stainless steel to prevent chemical reactions. Due to its corrosive and toxic nature, proper personal protective equipment, including gloves, goggles, and a fume hood, must be used during handling. The compound should never be stored near flammable materials or in areas with high humidity. Regular monitoring of storage conditions is essential to ensure safety and maintain the integrity of the chemical.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"300g","offer_id":48088070062298,"sku":"TCI2510P174347419","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48088070095066,"sku":"TCI2604P1743335","price":581000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1743.jpg?v=1767135151"},{"product_id":"tci2510p174847423","title":"TCI P1748 584-08-7 Potassium Carbonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePotassium carbonate (K2CO3), with CAS number 584-08-7, is an inorganic salt supplied as a white powder that is very commonly used in chemistry laboratories as a mild to moderately strong inorganic base. In organic synthesis, this compound plays an important role as a proton acceptor (base) that helps activate substrates, for example in the deprotonation of acidic groups or phenols, and it facilitates nucleophilic substitution reactions as well as cross-coupling reactions involving transition metal catalysts. As a base, it supports a broad range of routine laboratory procedures by providing controlled basicity that drives reactions toward the desired products while minimizing unwanted side reactions.\u003c\/p\u003e\n\u003cp\u003eIn cross-coupling reactions such as the Suzuki–Miyaura and Sonogashira reactions, potassium carbonate is frequently selected as the base to accelerate the transmetalation step and keep the catalytic cycle running smoothly. The TCI P1748 product is packaged in a 300 gram bottle, making it practical for laboratory-scale preparative work, whether for academic research or industrial development in Indonesia. With consistent purity and stable availability, TCI potassium carbonate is one of the essential reagents that supports the success of a wide variety of organic chemistry experiments. Its main advantage over other inorganic bases, such as sodium carbonate or potassium hydroxide, lies in its convenient balance of basicity, solubility, and ease of handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI P1748 potassium carbonate is commonly used in organic synthesis courses, academic research projects, and industrial process development where a dependable base is required. It is especially valued in pharmaceutical and fine-chemical research settings that routinely perform palladium-catalyzed coupling reactions, where consistent base quality directly affects reproducibility. Because the product is supplied in a convenient 300 gram pack, laboratories can maintain a steady working stock for routine experiments, ensuring that researchers in Indonesia can rely on the same dependable reagent performance from one batch to another.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: Potassium carbonate acts as the base that drives the transmetalation step, helping transfer the organic group from the boronic acid to the palladium catalyst efficiently and keeping the catalytic cycle productive.\u003c\/li\u003e\n\u003cli\u003eSonogashira coupling: As a mild inorganic base, it neutralizes the acidic proton of terminal alkynes and supports the copper–palladium catalytic cycle under relatively mild conditions, making it a practical choice for this reaction.\u003c\/li\u003e\n\u003cli\u003eDeprotonation of phenols and acidic groups: Its moderate basicity activates acidic substrates such as phenols or carboxylic acids, enabling subsequent nucleophilic substitution or alkylation steps to proceed under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions: Potassium carbonate facilitates SN2-type transformations in polar solvents by generating the required nucleophilic species from less reactive starting materials, which makes it a versatile base for routine synthesis.\u003c\/li\u003e\n\u003cli\u003eGeneral base for organic synthesis: Its white powder form dissolves readily in aqueous or mixed solvent systems, making it a convenient and reliable base for a wide range of laboratory-scale reactions and preparative procedures.\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\u003eProduct code: P1748\u003c\/li\u003e\n\u003cli\u003eCAS number: 584-08-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]\u003c\/li\u003e\n\u003cli\u003ePack size: 300 gram bottle\u003c\/li\u003e\n\u003cli\u003ePhysical form: white powder\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003ePotassium carbonate should be stored in its original, tightly closed container in a cool, dry, and well-ventilated area, protected from moisture and humidity because the salt is hygroscopic and may absorb water from the surrounding air. A desiccator or a sealed bottle with a tight-fitting lid is suitable for long-term storage. When handling the powder, wear appropriate personal protective equipment such as laboratory gloves and safety goggles to avoid contact with skin and eyes. Avoid generating dust, and work in a fume hood if large amounts are handled. Keep the container away from acids and strong oxidizing agents, and always recap the bottle immediately after use to preserve product quality and ensure reliable results in subsequent experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"300g","offer_id":48088070586586,"sku":"TCI2510P174847423","price":481000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1748.jpg?v=1767135163"},{"product_id":"tci2510p178547466","title":"TCI P1785 7440-05-3 Palladium 10% on Carbon (wetted with ca 55% Water) [Useful catalyst for coupling reaction, etc]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ePalladium 10% on Carbon (wetted with ca 55% Water) is a widely used catalyst in chemical reactions, particularly in coupling reactions. This material is a composite of palladium metal evenly distributed on the surface of activated carbon, with approximately 55% water content. It serves as an essential tool in laboratories for accelerating chemical reactions without being consumed in the process. Its versatility makes it a valuable asset in various synthetic processes, enabling efficient and controlled chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe unique properties of Palladium 10% on Carbon make it a preferred choice for many chemical applications. The combination of palladium and activated carbon provides a large surface area for adsorption, enhancing reactivity. The presence of water helps maintain the stability of the catalyst and prevents precipitation. Additionally, its high reactivity and selectivity allow it to function effectively in a variety of reaction conditions. These characteristics ensure consistent performance and reliability in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Palladium 10% on Carbon is commonly used in both academic and industrial research. It is frequently employed in hydrogenation processes and coupling reactions, such as the Suzuki and Heck reactions. Its stability and efficiency make it a go-to material for chemists working on complex synthetic pathways. The material is also favored for its safety profile compared to pure metal catalysts, making it a reliable choice for routine laboratory operations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHydrogenation reactions benefit from this catalyst due to its high surface area and reactivity, enabling efficient hydrogen transfer in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions, such as the Suzuki and Heck reactions, rely on this material for its stability and ability to activate substrates under mild conditions.\u003c\/li\u003e\n\u003cli\u003eCatalytic reduction processes utilize this catalyst to facilitate the conversion of functional groups in a controlled and selective manner.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis workflows often incorporate this material to enhance reaction rates and improve product yields in complex transformations.\u003c\/li\u003e\n\u003cli\u003eEnvironmental remediation applications may use this catalyst to break down pollutants in aqueous solutions through catalytic degradation.\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: 7440-05-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Hydrogenation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Powder or slurry, depending on the specific 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 material should be stored in a cool, dry environment to maintain its catalytic activity and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its performance. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with strong oxidizing agents or acids to prevent unwanted side reactions. In laboratory settings, it is important to ensure proper ventilation when working with this material to maintain a safe and controlled environment. Always follow standard safety protocols to ensure safe handling and storage practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088073404634,"sku":"TCI2510P178547466","price":1944000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088073437402,"sku":"TCI2510P178547467","price":6134000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P1785.jpg?v=1767135226"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-reagents-for-oligosaccharide-synthesis-glycoscience.oembed?page=6","provider":"AMI Scientific","version":"1.0","type":"link"}