{"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":8376000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5546.jpg?v=1767092491"},{"product_id":"tci2510b571112430","title":"TCI B5711 1189560-96-0 Biotin-PEG3-acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBiotin-PEG3-acetic Acid (CAS 1189560-96-0) is a biotin-PEG linker reagent designed for covalent biotinylation of biomolecules such as proteins, peptides, and carbohydrates in laboratory settings. It features a reactive acetic acid moiety that conjugates with primary amine groups on target molecules, enabling highly specific avidin\/streptavidin-based detection and purification workflows. This compound is commonly employed in glycoscience and chemical biology research for glycoconjugate labeling, chemical probe synthesis, and carbohydrate-based biosensor development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085898723546,"sku":"TCI2510B571112430","price":11496000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5711.jpg?v=1767092691"},{"product_id":"tci2510b626513099","title":"TCI B6265 875770-34-6 Biotin-PEG3-Azide (2mg*5)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Biotin-PEG3-Azide (CAS 875770-34-6) is a bifunctional click chemistry reagent combining a biotin affinity tag with an azide reactive group, separated by a PEG3 spacer for enhanced solubility and reduced steric hindrance. This compound enables copper-free or copper-catalyzed conjugation to alkyne-modified biomolecules including proteins, peptides, oligonucleotides, and antibodies. It is widely utilized in chemical biology research for biomolecular labeling, streptavidin-based detection, cell imaging, and proteomics applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48085927067866,"sku":"TCI2510B626513099","price":3598000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6265.jpg?v=1767093384"},{"product_id":"tci2510b626613100","title":"TCI B6266 1309649-57-7 Biotin-PEG4-Azide (2mg*5)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBiotin-PEG4-Azide is a click chemistry conjugation reagent featuring a biotin moiety linked to an azide group via a PEG4 spacer. This compound enables efficient biotin labeling of alkyne-containing molecules through copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. It is widely applied in chemical biology research for biomolecule detection, affinity purification, and the development of bioconjugate probes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48085927133402,"sku":"TCI2510B626613100","price":4863000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6266.jpg?v=1767093388"},{"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":844000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1969000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4975000.0,"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":901000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966258394,"sku":"TCI2510C001613933","price":2306000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966291162,"sku":"TCI2510C001613934","price":6072000.0,"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":564000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085971665114,"sku":"TCI2510C011914065","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085971697882,"sku":"TCI2510C011914066","price":8966000.0,"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":536000.0,"currency_code":"IDR","in_stock":false}],"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":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086004498650,"sku":"TCI2510C049114654","price":1266000.0,"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":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086029369562,"sku":"TCI2510C079515062","price":11018000.0,"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":1378000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086041002202,"sku":"TCI2510C097215328","price":3852000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086041034970,"sku":"TCI2510C097215329","price":11805000.0,"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":704000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086050177242,"sku":"TCI2510C112415549","price":3373000.0,"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":1490000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086068297946,"sku":"TCI2510C140815948","price":4751000.0,"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":3092000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086076915930,"sku":"TCI2510C154516160","price":17173000.0,"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":2025000.0,"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":957000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086090055898,"sku":"TCI2510C180616496","price":4358000.0,"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, particularly in the formation of amide or ester bonds. This compound plays a crucial role in laboratories where functional group manipulation is required, enabling the synthesis of more complex molecules. Its versatility makes it a valuable reagent for chemists working on a variety of synthetic pathways. Due to its reactivity and structural complexity, it is frequently employed in research settings where precise chemical transformations are necessary.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique properties, including its benzyloxycarbonyl (Cbz) group, contribute to its stability under certain conditions while still allowing for controlled reactivity with acids, bases, and metals. This balance of stability and reactivity makes it a preferred choice for synthetic chemists. Its solid form and ease of handling further enhance its appeal in laboratory environments, offering convenience without compromising quality. The compound's ability to undergo reactions such as hydrolysis or reduction expands its utility across multiple synthetic applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-(Benzyloxycarbonylamino)-1-propanol is commonly used in organic chemistry research, particularly in academic and research institutions. Its availability and reliability make it a go-to reagent for synthesizing complex molecules. The compound is especially favored for its role in functional group substitution and its compatibility with various reaction conditions. Its widespread use reflects its importance in advancing chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound due to its ability to form amide and ester bonds, making it ideal for creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eFunctional group manipulation in synthetic pathways is enhanced by its reactivity, allowing for controlled chemical transformations in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry often utilizes this compound for the development of pharmaceutical compounds requiring specific functional groups.\u003c\/li\u003e\n\u003cli\u003eIt is well-suited for hydrolysis and reduction reactions, providing chemists with versatile tools for modifying molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndonesian academic institutions rely on this compound for advanced chemical research, supporting both teaching and experimental work in organic 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: 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 various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and maintain its chemical integrity. When handling, it is important to use appropriate personal protective equipment such as gloves and safety goggles to ensure safety. Due to its reactivity, it should be stored separately from strong acids, bases, and reactive metals. Proper ventilation is also advised when working with this compound to minimize exposure to vapors. Following these guidelines ensures safe and effective use in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086092185818,"sku":"TCI2510C193216551","price":1913000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086092218586,"sku":"TCI2510C193216552","price":4779000.0,"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":536000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086348529882,"sku":"TCI2510D013419468","price":1546000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086348562650,"sku":"TCI2510D013419469","price":3289000.0,"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":536000.0,"currency_code":"IDR","in_stock":true},{"title":"400g","offer_id":48086384443610,"sku":"TCI2510D043619871","price":3598000.0,"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":1687000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086398435546,"sku":"TCI2510D065620210","price":4779000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086398468314,"sku":"TCI2510D065620211","price":12592000.0,"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":732000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086420553946,"sku":"TCI2510D105920767","price":1913000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086420586714,"sku":"TCI2510D105920768","price":5144000.0,"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":901000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086420914394,"sku":"TCI2510D107020778","price":3598000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086420947162,"sku":"TCI2510D107020779","price":18719000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1070.jpg?v=1767102474"},{"product_id":"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":1518000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086449946842,"sku":"TCI2510D160121411","price":4386000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086449979610,"sku":"TCI2510D160121412","price":12592000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086450012378,"sku":"TCI2510D160121413","price":25239000.0,"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":1462000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086651928794,"sku":"TCI2510D402924498","price":4695000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086651961562,"sku":"TCI2510D402924499","price":14025000.0,"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":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086817177818,"sku":"TCI2510E007727743","price":704000.0,"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":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086817308890,"sku":"TCI2510E008127747","price":1490000.0,"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":9135000.0,"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":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48087162519770,"sku":"TCI2510H017232586","price":1378000.0,"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":507000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087168581850,"sku":"TCI2510H020432637","price":816000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0204.jpg?v=1767115883"},{"product_id":"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":1238000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087225008346,"sku":"TCI2510H062333252","price":2419000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087225041114,"sku":"TCI2510H062333253","price":10175000.0,"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":"\u003cp\u003e\u003cstrong\u003eHexyldimethyloctylammonium Bromide\u003c\/strong\u003e (CAS 187731-26-6) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial settings.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C16H36BrN\u003c\/li\u003e\n\u003cli\u003eCAS number: 187731-26-6\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;97.0%(T)\u003c\/li\u003e\n\u003cli\u003eTCI product code: H0989\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087250862298,"sku":"TCI2510H098933767","price":2559000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087250895066,"sku":"TCI2510H098933768","price":7702000.0,"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":"\u003cp\u003e\u003cstrong\u003eHydrazine Acetate\u003c\/strong\u003e (CAS 13255-48-6) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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