{"title":"C-X(Non-Halogen) Bond Formation [Synthetic Reagents]","description":"\u003cp\u003e\u003cstrong\u003eC-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/strong\u003e — compiles synthetic reagents for forming non-halogen carbon-heteroatom bonds such as C-N, C-S, C-B, C-P, and C-C through amination, boration, cyanation, formylation, phosphorylation, and C-H activation. This group also includes reagents for azidation, guanidinylation, nitration, ethynylation, vinylation, and Mitsunobu reactions that expand functional groups on molecular frameworks.\u003c\/p\u003e\u003cp\u003eC-X(Non-Halogen) Bond Formation reagents are widely used by synthetic organic chemistry and medicinal chemistry researchers to introduce amine, cyano, phosphonate, or vinyl groups into aromatic and aliphatic frameworks during compound library build-up. Reagents such as iodonium salts and phosphorodiamidites are often used in Mitsunobu, boration, or electrophilic functionalization reactions to assemble complex intermediates efficiently. This group also supports building block synthesis for functional materials and catalysis research.\u003c\/p\u003e\u003cp\u003eExample products in this collection: \u003ca href=\"\/en\/products\/tci2510a0419611\"\u003eTCI A0419 578-66-5 8-Aminoquinoline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b557312236\"\u003eTCI B5573 1868173-47-0 4-Biphenylyl(2,4,6-trimethoxyphenyl)iodonium Trifluoromethanesulfonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x004156728\"\u003eTCI X0041 7647-01-0 Hydrogen Chloride - Methanol Reagent (5-10%) [for Esterification]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b568712395\"\u003eTCI B5687 68014-21-1 tert-Butyl (Triphenylphosphoranylidene)carbamate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x003956727\"\u003eTCI X0039 7647-01-0 Hydrogen Chloride - Butanol Reagent (5-10%) [for Esterification] (1mL*10)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b595712735\"\u003eTCI B5957 325773-62-4 2,2'-Bis[bis(3,5-dimethylphenyl)phosphino]-1,1'-biphenyl\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x003656726\"\u003eTCI X0036 373-57-9 Boron Trifluoride - Methanol Reagent (10-20%) [for Esterification] (1mL*10)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b599712781\"\u003eTCI B5997 108549-21-9 Benzyl N,N,N',N'-Tetraisopropylphosphorodiamidite\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003eReagent selection in this category should consider purity, stability against moisture, and physical form such as ready-to-use solutions, crystalline powder, or single-use ampoule packaging according to reaction scale. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on each item's page.\u003c\/p\u003e\u003cp\u003eOther parallel categories under Synthetic Organic Reagents, often used together in one laboratory workflow:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-c-c-bond-formation-synthetic-reagents\"\u003eC-C Bond Formation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-protection-deprotection-derivatization\"\u003eProtection, Deprotection, Derivatization\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-acids-bases-synthetic-reagents\"\u003eAcids, Bases [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chelation-complexation-compounds\"\u003eChelation\/Complexation Compounds\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-phase-transfer-catalysts\"\u003ePhase Transfer Catalysts\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-coupling-synthetic-reagents\"\u003eCoupling [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eThis collection is further divided into 12 more specific groups:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-c-h-bond-activation-reaction-synthetic-reagents\"\u003eC-H Bond Activation Reaction [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-formylation-synthetic-reagents\"\u003eFormylation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phosphorylation-synthetic-reagents\"\u003ePhosphorylation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-mitsunobu-reaction-synthetic-reagents\"\u003eMitsunobu Reaction [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-vinylation-synthetic-reagents\"\u003eVinylation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-amination-synthetic-reagents\"\u003eAmination [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-c-s-bond-formation-synthetic-reagents\"\u003eC-S Bond Formation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-ethynylation-synthetic-reagents\"\u003eEthynylation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-guanidinylation-synthetic-reagents\"\u003eGuanidinylation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-cyanation-synthetic-reagents\"\u003eCyanation [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-boration-synthetic-reagents\"\u003eBoration [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-c-x-non-halogen-bond-formation-other-synthetic-reagents\"\u003eC-X(Non-Halogen) Bond Formation (Other) [Synthetic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eBack to \u003ca href=\"\/en\/collections\/reagen-sintesis-organik\"\u003eSynthetic Organic Reagents\u003c\/a\u003e. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — authorized TCI Japan distributor in Indonesia — to check availability and lead time directly from Japan.\u003c\/p\u003e","products":[{"product_id":"tci2510b643513320","title":"TCI B6435 2488525-05-7 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6435 [[[1,1'-Biphenyl]-4-yloxy]imino]-lambda4-sulfanone (CAS 2488525-05-7) is a specialty synthetic reagent classified for non-halogen C–X bond formation. Reagents of this N-sulfinylamine type are used to introduce sulfur- and nitrogen-containing fragments into organic frameworks, typically through reactions with nucleophiles or organometallic partners. It is aimed at researchers exploring modern synthetic methodology and medicinal chemistry applications. Handle the reagent in a fume hood, protect it from moisture, and consult the manufacturer's technical documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939749082,"sku":"TCI2510B643513320","price":3913000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939781850,"sku":"TCI2510B643513321","price":17893000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6435_e9fb4a3b-01c3-4d53-8ed4-d4eec33ad2f2.jpg?v=1792631536"},{"product_id":"tci2510b655213480","title":"TCI B6552 2763205-15-6 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 is a spiro-linked building block bearing two pinacol boronate groups at the 2' and 7' positions of a spiro[cyclopenta-dipyridine-fluorene] framework. Its difunctional boronate handles make it a convenient monomer for palladium-catalysed Suzuki–Miyaura cross-coupling and for the assembly of conjugated oligomers and polymers. The rigid, orthogonal spiro geometry combined with electron-poor pyridine nitrogens is of particular interest in organic optoelectronic material research and in nitrogen-donor ligand design. AMI Scientific supplies this TCI product in 100 mg and 500 mg pack sizes; always consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085946859738,"sku":"TCI2510B655213480","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":6890000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552_2f2f4c5c-80a2-4de2-8583-9ea22d2ceb26.jpg?v=1792631678"},{"product_id":"tci2510b708213900","title":"TCI B7082 3075704-21-8 [1,2-Bis(ethoxycarbonyl)hydrazineyl]triphenylphosphonium Trifluoromethanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7082 is a preformed phosphonium salt derived from triphenylphosphine and a dialkyl azodicarboxylate, stabilized as its trifluoromethanesulfonate. It streamlines Mitsunobu-type dehydrative couplings by combining both reagent components in a single, easily weighed solid. This avoids handling heat- and shock-sensitive liquid azodicarboxylates while fixing the reagent stoichiometry. Offered in 1 g, 5 g, and 25 g sizes, it should be kept dry, cool, and away from heat sources and strong reducing agents.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085964980442,"sku":"TCI2510B708213900","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085965013210,"sku":"TCI2510B708213901","price":1894000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085965045978,"sku":"TCI2510B708213902","price":5805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7082_d1432c49-a384-4e26-9073-814d32f0614a.jpg?v=1792631961"},{"product_id":"tci2510c038414469","title":"TCI C0384 13395-16-9 Bis(2,4-pentanedionato)copper(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0384 Bis(2,4-pentanedionato)copper(II), CAS 13395-16-9, is the well-known copper(II) acetylacetonate chelate used as a versatile copper source in synthesis and materials science. Its stable β-diketonate framework makes the complex convenient to weigh and dissolve, while the ligands are readily displaced once the active catalytic species forms. It is commonly applied as a catalyst precursor in copper-mediated coupling and C–H functionalisation studies, and as a precursor for copper-based thin films and nanoparticles. AMI Scientific supplies it in 25 g and 250 g packs; store in a tightly closed container in a cool, dry place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085995159770,"sku":"TCI2510C038414469","price":607000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085995192538,"sku":"TCI2510C038414470","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0384_41752859-403b-4ada-a50a-a897263ae333.jpg?v=1792632473"},{"product_id":"tci2510c044114561","title":"TCI C0441 105-56-6 Ethyl Cyanoacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyanoacetate from TCI is an ester that contains an active methylene group. In this compound, the CH2 group sits between two electron-withdrawing groups: a nitrile and an ethyl ester. Because of this structure, the methylene protons are fairly acidic and readily form a stabilized carbanion. This makes Ethyl Cyanoacetate one of the oldest and most widely used building blocks in organic synthesis laboratories. Chemists use it to form carbon-carbon bonds and to build many kinds of heterocyclic rings, from small exploratory reactions to multi-step synthetic routes.\u003c\/p\u003e\n\u003cp\u003eResearchers choose Ethyl Cyanoacetate because one small molecule offers three reactive sites: the active methylene carbon, the nitrile group and the ester group. The active carbon takes part in Knoevenagel condensations, alkylations and Michael additions. The nitrile and ester groups can join cyclization reactions that form pyrimidines, pyridones, thiophenes (through the Gewald reaction) and other heterocyclic frameworks that matter in medicinal chemistry. These reactions usually need only simple, easy-to-obtain base catalysts, so the reagent is practical for both research and teaching.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, Ethyl Cyanoacetate is in steady demand at organic chemistry and pharmacy laboratories in universities. There it supports undergraduate practical courses, final-year projects and graduate research on synthetic methods and heterocyclic compounds. Research groups working on bioactive molecules use it as a dependable starting material for building compound libraries. Its well-documented reactivity also makes it a good choice for showing students the basic ideas of carbanion chemistry. AMI Scientific supplies this TCI reagent to help these laboratories run their synthesis work smoothly.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKnoevenagel condensation: the acidic active methylene group condenses easily with aldehydes and ketones under mild base catalysis, giving dependable access to substituted alkenes for further synthesis.\u003c\/li\u003e\n\u003cli\u003eAlkylation reactions: the stabilized carbanion formed at the methylene carbon reacts with suitable electrophiles, so chemists can add new carbon substituents in a controlled way.\u003c\/li\u003e\n\u003cli\u003eMichael addition: as a soft, stabilized nucleophile, the carbanion adds to activated alkenes and builds new carbon-carbon bonds that are useful in longer synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eHeterocycle synthesis: the nitrile and ester groups take part in cyclization reactions that form pyrimidines, pyridones and related frameworks that are important in medicinal chemistry research.\u003c\/li\u003e\n\u003cli\u003eGewald reaction and teaching laboratories: it is a classic component for making thiophenes, and its simple base-catalyzed chemistry makes it a strong choice for showing students how carbanion reactions work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0441)\u003c\/li\u003e\n\u003cli\u003eCAS number: 105-56-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: please confirm the available pack sizes with AMI Scientific when you order\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: keep the container tightly closed in a cool, dry, well-ventilated area and follow the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore Ethyl Cyanoacetate in its original tightly closed container, such as the supplier's glass bottle, in a cool, dry and well-ventilated place. Keep it away from heat, ignition sources, direct sunlight, and strong acids, bases and oxidizing agents. Handle it in a fume hood and wear suitable personal protective equipment, including chemical-resistant gloves, safety glasses and a laboratory coat. Do not inhale vapors and avoid contact with skin and eyes. Before use, read the Safety Data Sheet supplied with the product for hazard details, first-aid measures and disposal guidance, and dispose of waste according to your institution's rules and local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085998829786,"sku":"TCI2510C044114561","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085998862554,"sku":"TCI2510C044114562","price":1036000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0441_38a0d21b-b644-4bce-93cb-ef314b97135b.jpg?v=1792632547"},{"product_id":"tci2510c097615333","title":"TCI C0976 15074-54-1 2-Chlorophenyl Phosphorodichloridate [Phosphorylating Agent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chlorophenyl Phosphorodichloridate is a phosphorylating agent supplied by TCI. Chemists use it to introduce a phosphate group into organic molecules. Its structure has a phosphorus atom bonded to a 2-chlorophenoxy group and two reactive chlorine atoms. The reagent is widely known in synthetic chemistry laboratories for preparing phosphate esters. It is also used in the phosphotriester method, where it forms internucleotide linkages during oligonucleotide synthesis. This makes it an important tool for researchers in bioorganic chemistry and nucleic acid chemistry who need a reliable way to build phosphorus-containing structures.\u003c\/p\u003e\n\u003cp\u003eThe reagent's main advantage is the two chlorine atoms on phosphorus. They can react one at a time with two different nucleophiles, such as two separate hydroxyl groups. This allows phosphate diester linkages to be formed in a controlled order rather than all at once. The 2-chlorophenyl group protects the phosphorus atom while the synthesis proceeds and can be removed later under suitable conditions. High reactivity combined with a removable protecting group is why chemists choose this reagent to assemble phosphate-bearing molecules systematically. Because it is highly sensitive to moisture, it needs careful handling to keep that reactivity.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, phosphorylating reagents like this one are relevant to synthetic organic chemistry laboratories at universities, research institutes, and industrial research and development groups. Researchers working on phosphate esters, nucleotide chemistry, or oligonucleotide assembly can use it in multistep synthesis programs. It also suits teaching and research groups that study phosphorus chemistry and protecting-group strategies. AMI Scientific supplies this TCI reagent to laboratories that need a well-characterised building block for phosphorylation work as part of their routine or exploratory synthesis.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePhosphate ester synthesis: the reactive phosphorus–chlorine bonds let chemists attach a phosphate group to organic alcohols, which makes this reagent a direct route to phosphate esters.\u003c\/li\u003e\n\u003cli\u003eOligonucleotide synthesis by the phosphotriester method: the reagent is well known for forming internucleotide bonds, which supports the stepwise assembly of nucleotide chains in nucleic acid research.\u003c\/li\u003e\n\u003cli\u003eStepwise coupling of two different nucleophiles: the two chlorine atoms react one after the other, so two distinct hydroxyl-bearing molecules can be joined through a controlled phosphate diester linkage.\u003c\/li\u003e\n\u003cli\u003eProtecting-group strategies in phosphorus chemistry: the 2-chlorophenyl group protects the phosphorus atom during synthesis and can be removed later, which suits multistep routes that need temporary protection.\u003c\/li\u003e\n\u003cli\u003eBioorganic chemistry research: groups studying phosphorylated biomolecules can use this reagent to build phosphate-containing structures systematically, combining high reactivity with a protecting group that can be removed later.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0976)\u003c\/li\u003e\n\u003cli\u003eCAS number: 15074-54-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eReagent type: Phosphorylating agent\u003c\/li\u003e\n\u003cli\u003ePack sizes: See the available options on the product listing\u003c\/li\u003e\n\u003cli\u003eStorage note: Highly sensitive to moisture; keep tightly sealed under dry conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Chlorophenyl Phosphorodichloridate is highly sensitive to moisture, so keep it away from humidity and water at all times. Store it in its original, tightly closed container in a cool, dry, well-ventilated area, preferably under a dry inert atmosphere once opened. Reseal the container promptly after each use to limit exposure to air. Handle the reagent in a fume hood and use dry glassware and equipment. Wear suitable personal protective equipment, including chemical-resistant gloves, safety goggles, and a laboratory coat. Keep it apart from incompatible materials, and always read the supplier's Safety Data Sheet before use for full hazard, handling, and disposal information.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086041231578,"sku":"TCI2510C097615333","price":683000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0976_28de8976-bcdf-4cf7-8a30-eb1a8b02898a.jpg?v=1792633317"},{"product_id":"tci2510c097815336","title":"TCI C0978 207121-42-4 Barium 2-Cyanoethylphosphate Hydrate [Phosphorylating Agent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0978 Barium 2-Cyanoethylphosphate Hydrate (CAS 207121-42-4) is a solid phosphorylating reagent available in 5 g and 25 g packs. It delivers a phosphate unit already carrying a 2-cyanoethyl protecting group, which can later be removed under mild basic conditions. The reagent is commonly applied to nucleosides, sugars, and simple alcohols, typically with a coupling activator, and the barium counterion is exchanged or precipitated as required. Because barium salts are toxic, weigh the material with gloves and dust protection, keep it dry and tightly closed, and dispose of residues through heavy-metal waste channels.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086041362650,"sku":"TCI2510C097815336","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086041395418,"sku":"TCI2510C097815337","price":5326000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0978_d9ca5751-9caf-4a24-898c-942b570da452.jpg?v=1792633320"},{"product_id":"tci2510c121015673","title":"TCI C1210 5381-99-7 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1210 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one, CAS 5381-99-7, is a cyclic phosphorus(III) chloride reagent widely used for phosphitylation of free hydroxyl groups. It reacts readily with nucleosides, sugars, and other alcohols to give phosphorus(III) intermediates that can subsequently be oxidised, sulfurised, or cyclised. Because of this, it is a standard tool in nucleotide chemistry, cyclic phosphate synthesis, and phosphorus-containing prodrug research. AMI Scientific supplies 5 g and 25 g packs; the reagent is highly moisture sensitive and must be handled under dry, inert conditions in line with the manufacturer's Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086056534234,"sku":"TCI2510C121015673","price":1716000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086056567002,"sku":"TCI2510C121015674","price":5048000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1210_f3642225-4ad8-4eb0-af74-b633b59ebfb1.jpg?v=1792633533"},{"product_id":"tci2510c124215716","title":"TCI C1242 2942-58-7 Diethyl Cyanophosphonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1242 Diethyl Cyanophosphonate (DEPC) is a well-established coupling reagent for activating carboxylic acids toward amide and ester bond formation. It is frequently applied in peptide synthesis, where it offers effective coupling under comparatively mild conditions. The reagent is highly toxic and moisture-sensitive, and hydrolysis can release extremely hazardous gas, so it must be handled only by trained personnel in a fume hood. Available in 5 g and 25 g packs, it must be stored, used, and disposed of strictly in accordance with the official TCI safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGUZMAN et al. (1997). ChemInform Abstract: A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199747196\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199747196\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGuzmán et al. (1997). A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919708005008\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919708005008\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDemir et al. (2009). Cyanide Ion Promoted Addition of Acylphosphonates to Diethyl Cyanophosphonate: Synthesis of Phosphonocyanohydrin O-Phosphates. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1216634\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1216634\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086058598618,"sku":"TCI2510C124215716","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086058631386,"sku":"TCI2510C124215717","price":5350000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1242_4cf408c6-d600-4c54-ba66-a7a22565c7bf.jpg?v=1792633561"},{"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":2828000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086076915930,"sku":"TCI2510C154516160","price":15470000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1545_cbaa1698-59e4-429e-9bbb-23a71f52375c.jpg?v=1792633826"},{"product_id":"tci2510c175716420","title":"TCI C1757 245365-64-4 N-Benzyloxycarbonyl-2-nitrobenzenesulfonamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Benzyloxycarbonyl-2-nitrobenzenesulfonamide is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound is known for its ability to participate in substitution reactions and molecular coupling processes, making it essential in the synthesis of complex organic compounds. Its stable structure allows it to react selectively with various reagents such as amines, acids, and bases. In laboratory applications, it is commonly used in research related to the development of bioactive compounds and pharmaceuticals. Due to its reactivity and specificity, this compound is a preferred choice for experiments requiring precision and controlled chemical reactions. Its versatility makes it a valuable tool for both academic and industrial research in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086087106778,"sku":"TCI2510C175716420","price":2600000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086087139546,"sku":"TCI2510C175716421","price":7976000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1757_078584fb-51bf-4982-9a61-51eedb13bb87.jpg?v=1792634031"},{"product_id":"tci2510c216016823","title":"TCI C2160 534-17-8 Cesium Carbonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Cesium Carbonate, catalog code C2160, is an inorganic salt of the alkali metal cesium that has become one of the most popular bases in modern organic synthesis. In the laboratory this compound is used primarily as a proton-scavenging base in alkylation reactions, transition-metal-catalyzed cross-coupling reactions, and nucleophilic aromatic substitution reactions. Its presence on the reagent shelf of a synthesis laboratory means that many transformations that previously proceeded only with difficulty under conventional bases can now be carried out under considerably milder conditions.\u003c\/p\u003e\n\u003cp\u003eThe property that most often leads chemists to select cesium carbonate is its relatively good solubility in polar aprotic organic solvents such as DMF, DMSO, and acetonitrile, far exceeding that of the corresponding potassium or sodium carbonate salts. The cesium cation is large and has low polarizing power, so its ion pairing is loose; this leaves the accompanying nucleophilic anion more reactive, an effect widely known as the cesium effect. Its basicity is moderate, strong enough to deprotonate phenols, thiols, amides, or dicarbonyl compounds, yet mild enough to leave sensitive functional groups intact. The compound is also hygroscopic, which must be taken into account during handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically found in university organic synthesis and medicinal chemistry groups, in research institute laboratories, and in pharmaceutical and fine chemical development units where coupling and alkylation reactions are run routinely. Because the local climate is humid throughout the year, laboratories here pay particular attention to keeping the container tightly closed and limiting exposure to open air, so that the reagent retains its performance from one experiment to the next.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAlkylation of phenols and thiols — the moderate basicity deprotonates these substrates cleanly while the loose cesium ion pair keeps the resulting anion highly nucleophilic toward the alkylating agent.\u003c\/li\u003e\n\u003cli\u003eTransition-metal-catalyzed cross-coupling reactions — serves as the proton-scavenging base that keeps the catalytic cycle turning over without attacking sensitive functional groups elsewhere in the substrate.\u003c\/li\u003e\n\u003cli\u003eNucleophilic aromatic substitution — good solubility in DMF, DMSO, and acetonitrile allows the base to work in the homogeneous polar aprotic media these substitutions normally require.\u003c\/li\u003e\n\u003cli\u003eN-alkylation of amides and related nitrogen nucleophiles — basicity sufficient to deprotonate the amide nitrogen while remaining mild enough to preserve other functionality in the molecule.\u003c\/li\u003e\n\u003cli\u003eDeprotonation and functionalization of dicarbonyl compounds — generates the stabilized enolate under milder conditions than conventional carbonate bases permit, which is useful for multi-step synthetic sequences.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 534-17-8\u003c\/li\u003e\n\u003cli\u003eCatalog code: C2160\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Main-group Elements [Catalysis and Inorganic Chemistry]\u003c\/li\u003e\n\u003cli\u003eChemical class: inorganic alkali metal salt (cesium carbonate)\u003c\/li\u003e\n\u003cli\u003eStorage note: hygroscopic material; keep the container tightly closed and protected from moisture. Pack sizes available on request.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore cesium carbonate in its original tightly closed container, in a dry place away from direct exposure to humid air, since the material is hygroscopic and readily takes up atmospheric moisture. Chemically resistant containers with well-sealed caps are appropriate, and transferring the reagent inside a glove box or under a dry inert atmosphere is advisable when reaction results are sensitive to water content. Weigh out only the quantity needed and close the container immediately afterwards. Handle the material in a fume hood using safety glasses, gloves, and a laboratory coat, avoid contact with skin and eyes and inhalation of the dust, and consult the manufacturer's safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086107914458,"sku":"TCI2510C216016823","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086107947226,"sku":"TCI2510C216016824","price":3357000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2160_f52e716d-0e0e-4dc7-b156-683ac334bbcd.jpg?v=1792634282"},{"product_id":"tci2510c223116927","title":"TCI C2231 3570-58-9 2-Chloroethyl Methanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2231 2-Chloroethyl Methanesulfonate is a non-heterocyclic building block belonging to the mesylate ester family, widely applied as a two-ended alkylating reagent in organic synthesis. Its molecular structure carries a mesylate group serving as an excellent leaving group at one end and a chlorine atom at the other, giving researchers two reactive sites with clearly differentiated levels of reactivity. This configuration is particularly useful for introducing a two-carbon bridge into a target molecule in stepwise fashion, then closing it through a cyclization reaction. The compact size of the molecule makes it an economical choice from an atom-economy standpoint in synthetic design.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of a mesylate over aromatic sulfonates lies in its lower molecular weight, so the mass of reagent required per mole is smaller and the methanesulfonate by-product is more easily separated during the purification stage. The mesylate group is also far more readily displaced than chloride or bromide, which means nucleophilic substitution can proceed at low temperature with a weak base, making it suitable for substrates that are sensitive to harsh conditions. The reactivity difference between the mesylate end and the chloride end allows reactions to be directed selectively to one site before the second site is engaged.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically found in university organic chemistry research groups, pharmaceutical and medicinal chemistry programmes, and industrial R\u0026amp;D units engaged in intermediate preparation. It is handled in fume hoods on a research and pilot scale, where the ability to run substitution steps under mild conditions is valued in facilities that do not always have access to specialised low-temperature or inert-atmosphere equipment. Its role as a compact bifunctional linker makes it a practical stock item for multi-step synthesis work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eStepwise alkylation of nucleophiles, where the highly labile mesylate end reacts first under mild conditions while the chloride end remains available for a later, separate transformation.\u003c\/li\u003e\n\u003cli\u003eIntroduction of two-carbon bridges into target molecules, allowing researchers to extend a scaffold by a short ethylene linker before closing the structure through a subsequent cyclization step.\u003c\/li\u003e\n\u003cli\u003eRing-closing and cyclization chemistry, in which the two differentiated reactive ends are engaged in sequence so that intramolecular bond formation completes the desired ring system.\u003c\/li\u003e\n\u003cli\u003ePreparation of synthetic intermediates in medicinal and pharmaceutical chemistry research, where mild substitution conditions protect sensitive functional groups elsewhere in the substrate molecule.\u003c\/li\u003e\n\u003cli\u003eBifunctional linker chemistry for joining two distinct nucleophilic partners, exploiting the clear reactivity gap between the mesylate and chloride termini to control the order of coupling.\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: 3570-58-9\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-Chloroethyl Methanesulfonate\u003c\/li\u003e\n\u003cli\u003eCatalogue code: C2231\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original tightly closed container under 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 the container tightly closed in a cool, dry, well-ventilated area away from heat, ignition sources, moisture, and incompatible materials such as strong bases and strong oxidising agents, following the conditions specified on the manufacturer's label and safety data sheet. Keep the material in its original supplier container, or in a chemically compatible, clearly labelled vessel if transfer is necessary. Handle only inside a functioning fume hood, wearing safety glasses, chemical-resistant gloves, and a laboratory coat. As an alkylating agent, this compound should be treated with particular care: avoid skin contact, eye contact, and inhalation of vapours, minimise the quantity handled on the open bench, and consult the safety data sheet before use, spill clean-up, or waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086113190106,"sku":"TCI2510C223116927","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2231_c90a815e-de18-4181-82d0-93188a221fb0.jpg?v=1792634348"},{"product_id":"tci2510c230417037","title":"TCI C2304 578743-87-0 Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I) is a copper-based chemical compound widely used in catalytic reactions, particularly in carbon-hydrogen (C-H) activation processes. This compound plays a crucial role in modern laboratory settings by enabling the efficient transformation of complex organic molecules. Its unique structure, containing a copper(I) ion and an imidazol-2-ylidene ligand, allows it to act as a highly effective catalyst in various synthetic pathways. Due to its stability and reactivity, it is an essential tool for researchers working in catalysis and inorganic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its exceptional catalytic activity and chemical stability. It maintains its structural integrity under a range of reaction conditions, making it suitable for both academic and industrial applications. Its ability to selectively activate C-H bonds makes it particularly valuable in the development of new synthetic methods. Additionally, its compatibility with a wide range of organic substrates enhances its versatility in laboratory settings. These properties make it a preferred choice for chemists seeking reliable and efficient catalytic solutions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in research focused on organic chemistry, catalysis, and inorganic chemistry. It supports the development of new chemical processes and the synthesis of complex molecules. Its application is especially relevant in academic and research institutions where advanced catalytic techniques are required. The compound’s reliability and performance make it a key component in the chemical research toolkit of Indonesian scientists.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Reactions: This compound is ideal for C-H activation due to its ability to selectively activate carbon-hydrogen bonds, enabling the synthesis of complex organic molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in organic synthesis to facilitate various reactions such as substitution and oxidation, providing a stable and reactive catalytic environment.\u003c\/li\u003e\n\u003cli\u003eCatalytic Oxidation Processes: The compound's unique structure allows it to act as a catalyst in oxidation reactions, enhancing reaction rates and selectivity in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eInorganic Chemistry Research: Its role in inorganic chemistry is significant, particularly in the study of metal-ligand interactions and catalytic mechanisms.\u003c\/li\u003e\n\u003cli\u003eAdvanced Catalytic Studies: Researchers use it to explore new catalytic pathways and improve existing synthetic methods, contributing to the advancement of chemical 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: 578743-87-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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 moisture and direct sunlight to maintain its stability and effectiveness. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation to minimize exposure to any potential vapors. Always follow standard safety protocols when working with catalytic materials to ensure a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086118629594,"sku":"TCI2510C230417037","price":1212000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086118662362,"sku":"TCI2510C230417038","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2304_74545967-ff2d-4b02-959f-322019d956f3.jpg?v=1792634426"},{"product_id":"tci2510c240517170","title":"TCI C2405 852445-83-1 Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]gold(I)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]gold(I) is a chemical compound used in catalytic reactions, particularly in C-H activation processes. This compound is a metal complex with a unique structure and highly effective catalytic properties. In the laboratory, it plays a crucial role in accelerating chemical reactions that require C-H bond activation, such as the synthesis of complex organic compounds. Its stability and reactivity make it a valuable tool for researchers working in catalysis and organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high catalytic efficiency and stability under specific conditions make it a preferred choice for various scientific applications. Its structure, featuring a gold(I) ion bonded to an imidazole ligand, allows it to interact effectively with relevant substrates. This unique molecular configuration enhances its ability to facilitate complex chemical transformations. The compound’s reactivity and stability ensure consistent performance in laboratory settings, making it a reliable option for advanced research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to organic chemistry, catalysis, and the synthesis of complex compounds. It supports studies that require precise and efficient C-H activation, contributing to advancements in chemical research. Its versatility and effectiveness make it a key component in various scientific investigations conducted in Indonesian academic and research institutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Reactions: This compound is ideal for activating carbon-hydrogen bonds, enabling the synthesis of complex organic molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the development of new organic compounds, particularly in reactions requiring selective and efficient catalytic activity.\u003c\/li\u003e\n\u003cli\u003eCatalytic Research: Its unique structure and catalytic properties make it a valuable tool for studying catalytic mechanisms and improving reaction conditions.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry Applications: It supports the development of new chemical processes in industrial settings, particularly those involving complex catalytic systems.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is frequently used in academic laboratories for teaching and research purposes, helping students and researchers explore advanced catalytic techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 852445-83-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid direct contact with skin and inhalation of vapors. Ensure proper ventilation in the laboratory when working with this material. Regular inspection of storage conditions is advised to ensure long-term integrity and safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086124953818,"sku":"TCI2510C240517170","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2405_318a3182-8ee3-4d28-a30e-1f77b388849d.jpg?v=1792634542"},{"product_id":"tci2510c270917560","title":"TCI C2709 152120-62-2 N-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine is a chemical compound widely used in organic synthesis reactions, particularly in the formation of heterocyclic compounds. This material plays a crucial role in laboratory settings where researchers aim to develop complex molecular structures. Its unique chemical structure enables it to participate in various substitution and reaction mechanisms under controlled conditions. As a versatile building block, it supports the creation of compounds with potential applications in pharmaceutical and medicinal chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability under specific conditions, combined with its reactivity towards acids, bases, and organic solvents, makes it a preferred choice for synthetic chemists. Its ability to undergo substitution reactions and its compatibility with a range of reagents contribute to its utility in advanced synthetic pathways. The structural complexity of N-(Carbobenzoxy)-1H-pyrazole-1-carboxamidine also allows for the design of molecules with tailored biological activities, making it a key component in drug discovery and development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used by chemists and pharmacologists to synthesize new compounds with potential medical or industrial applications. Its availability in solid form and its reactivity in substitution reactions make it a valuable resource for researchers working on complex molecular synthesis projects. The compound is essential for advancing chemical research and innovation in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for creating heterocyclic compounds due to its reactive functional groups and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for developing compounds with biological activity, as it can be modified to target specific molecular interactions.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry applications where the compound serves as a building block for drug molecule design and optimization.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry departments focusing on synthetic methodologies and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development for producing specialized compounds used in various sectors such as agriculture and materials science.\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: 152120-62-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and contaminants. Due to its reactivity with acids and bases, it should be handled with appropriate personal protective equipment. Storage conditions should avoid direct sunlight and high humidity to prevent degradation. Laboratory personnel should ensure proper ventilation when working with this compound to minimize any potential hazards. Regular monitoring of storage conditions is advised to maintain the integrity of the material during long-term use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086192783578,"sku":"TCI2510C270917560","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086192816346,"sku":"TCI2510C270917561","price":2347000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2709_52ab1bfb-6e0e-483a-9d8c-10656bc0cb88.jpg?v=1792634786"},{"product_id":"tci2510c332618356","title":"TCI C3326 1620086-77-2 5-Chlorosaligenyl-N,N-diisopropylphosphoramidite","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Chlorosaligenyl-N,N-diisopropylphosphoramidite is a chemical compound widely used in chemical biology, particularly in nucleic acid chemistry. It serves as a key precursor in the synthesis of phosphoramidite nucleotides, which are essential components in the production of oligonucleotides. This compound plays a crucial role in molecular biology laboratories where the construction of DNA or RNA strands is required for various experimental applications. Its chemical structure enables specific reactions under controlled conditions, making it a versatile tool in modern biochemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its reactivity and stability under specific conditions. Its ability to selectively bind to nucleotide bases ensures accuracy and precision in nucleic acid synthesis. This makes it particularly suitable for applications requiring high fidelity, such as DNA sequencing or probe design. The compound’s stability also allows for reliable performance in laboratory settings, contributing to the reproducibility of experimental results. These properties make it a preferred choice for researchers working in nucleic acid chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Chlorosaligenyl-N,N-diisopropylphosphoramidite is commonly used by researchers in universities, research centers, and biotechnology labs. It supports studies in genetics, biomedicine, and chemical biology, which are rapidly growing fields in Indonesia. Its application is essential for advancing research in molecular biology and related disciplines, providing a foundation for innovative scientific discoveries.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA sequencing relies on this compound to synthesize oligonucleotide probes with high specificity and accuracy.\u003c\/li\u003e\n\u003cli\u003eOligonucleotide synthesis benefits from its reactivity, enabling the precise construction of DNA and RNA strands.\u003c\/li\u003e\n\u003cli\u003ePCR experiments use this compound to create primers that ensure accurate amplification of target DNA sequences.\u003c\/li\u003e\n\u003cli\u003eProbe design in molecular biology requires its selective binding properties to generate reliable hybridization results.\u003c\/li\u003e\n\u003cli\u003eGenetic research utilizes this compound to develop custom nucleic acid sequences for functional and structural 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: 1620086-77-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Nucleic Acid Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its chemical integrity. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid contact with skin and eyes, and ensure that spill containment measures are in place. Proper disposal should follow local regulations to ensure safety and environmental compliance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086233317594,"sku":"TCI2510C332618356","price":2323000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086233350362,"sku":"TCI2510C332618357","price":8051000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3326_8f2441f9-114b-407a-b1df-0c535009101e.jpg?v=1792635221"},{"product_id":"tci2510c402619136","title":"TCI C4026 2413767-30-1 tert-Butyl [(3-Chloro-5,6-dicyanopyrazin-2-yl)oxy]carbamate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C4026 2413767-30-1 tert-Butyl [(3-Chloro-5,6-dicyanopyrazin-2-yl)oxy]carbamate is a synthetic chemical compound widely used in laboratory settings for the formation of C-X (non-halogen) bonds during complex molecule synthesis. This reagent plays a crucial role in organic chemistry by enabling the creation of specific molecular structures through substitution and coupling reactions. Its unique chemical structure allows it to participate in a variety of synthetic pathways, making it a versatile tool for researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and reactivity under controlled conditions. It exhibits high reactivity towards various substrates, which makes it ideal for applications requiring precise chemical transformations. Its molecular design supports efficient participation in organic reactions, allowing for the synthesis of a wide range of compounds. These properties make it a preferred choice for laboratories aiming to achieve high-quality results in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in both academic and applied research. It is a key component in the development of new chemical compounds and is utilized in various research projects. Its reliability and effectiveness in synthetic reactions have made it a standard material in chemical laboratories across Indonesia, supporting both fundamental and applied scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where precise bond formation is required due to its reactivity and structural specificity.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the development of new pharmaceutical compounds through targeted molecular modifications.\u003c\/li\u003e\n\u003cli\u003eChemical analysis and testing in academic institutions to support teaching and experimental research activities.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production processes that require high-purity reagents for consistent results.\u003c\/li\u003e\n\u003cli\u003eAdvanced synthetic pathways in research laboratories focusing on complex molecule creation and modification.\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: 2413767-30-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation and packaging\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, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical properties to prevent contamination and degradation. Proper labeling of containers is essential for safety and traceability. In laboratory settings, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to minimize exposure. Regular monitoring of storage conditions ensures the compound remains stable and effective for use in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48086315106522,"sku":"TCI2510C402619136","price":4871000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/tci2510c402619136-struktur-1000.png?v=1792635703"},{"product_id":"tci2510d068620257","title":"TCI D0686 137-18-8 p-Xyloquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ep-Xyloquinone is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a building block in organic chemistry, it plays a crucial role in the development of heterocyclic compounds and other specialized chemical structures. Its unique reactivity and stability make it a valuable tool for chemists working on a variety of synthetic pathways. This compound is commonly found in pharmaceutical and chemical industries, where it serves as a key intermediate in the production of drugs and industrial chemicals.\u003c\/p\u003e\n\u003cp\u003eThe chemical and physical properties of p-Xyloquinone contribute to its popularity among researchers. It possesses a stable aromatic structure and exhibits high reactivity, making it suitable for substitution and oxidation reactions. These characteristics allow it to be used in a wide range of experimental applications, from basic research to advanced chemical synthesis. Its consistent performance and high purity ensure reliable results in laboratory experiments, making it a preferred choice for scientists seeking precision and reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, p-Xyloquinone is frequently used in organic chemistry research, particularly in academic institutions and research organizations. It is an essential component in the synthesis of various compounds with specific structural requirements. Due to its availability and reliability, it is commonly selected for experiments that require high accuracy and consistency. Its role in chemical synthesis supports the development of new compounds with potential applications in medicine and industry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from p-Xyloquinone due to its reactivity and ability to form complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for the synthesis of drug molecules and active pharmaceutical ingredients.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on p-Xyloquinone for the creation of specialized compounds used in various commercial applications.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry uses p-Xyloquinone to explore new synthetic pathways and molecular structures.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry experiments incorporate p-Xyloquinone to test reaction mechanisms and chemical behavior under different conditions.\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: 137-18-8\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 sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003ep-Xyloquinone should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. Due to its reactivity, it is important to handle p-Xyloquinone with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the laboratory when working with this compound. Regular monitoring of storage conditions will help ensure the compound remains in optimal condition for use in experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086400172250,"sku":"TCI2510D068620257","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086400205018,"sku":"TCI2510D068620258","price":2297000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086400237786,"sku":"TCI2510D068620259","price":8580000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0686_f9bdbdde-ac47-4be5-8494-db4e9614a39d.jpg?v=1792636328"},{"product_id":"tci2510d072020315","title":"TCI D0720 110-70-3 N,N'-Dimethylethylenediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N’-Dimethylethylenediamine (DMEDA), with the CAS number 110-70-3, is a versatile chemical compound widely used in laboratory settings for its reactivity and functional properties. As a building block in organic synthesis, DMEDA plays a crucial role in the development of complex molecules, including pharmaceuticals, industrial chemicals, and food additives. Its unique structure, featuring two amine groups connected by an ethylene chain, allows it to participate in various chemical reactions, making it a valuable tool for chemists. Due to its ability to act as a strong base and electron donor, DMEDA is frequently employed in reactions requiring pH control or bond cleavage.\u003c\/p\u003e\n\u003cp\u003eDMEDA is particularly favored for its strong basicity and reactivity towards electrophilic and reactive species. These characteristics make it an ideal choice for applications such as condensation, reduction, and the formation of new chemical bonds. Its high boiling point also allows for its use in reactions that require elevated temperatures without significant evaporation. The compound’s stability and reactivity ensure that it remains a preferred reagent in many synthetic pathways, especially in the production of pharmaceutical intermediates and specialty chemicals.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMEDA is commonly used in the synthesis of organic compounds, particularly in the pharmaceutical and chemical industries. It is a key component in the development of new drugs and industrial materials. Its availability through suppliers like AMI Scientific ensures that researchers have access to this essential building block for their experiments and production processes. The compound’s reliability and effectiveness make it a staple in both academic and industrial research settings in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where DMEDA is used to build complex molecules due to its reactivity and ability to act as a nucleophile.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from DMEDA’s role in the synthesis of drug intermediates, where its basicity and reactivity aid in forming key molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on DMEDA for the creation of specialty chemicals, as its stability and reactivity support efficient synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eFood additive development uses DMEDA in the formulation of flavor compounds and preservatives, leveraging its chemical versatility and safety profile.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications benefit from DMEDA’s use in pH control and as a reagent in various spectroscopic and chromatographic techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 110-70-3\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 direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMEDA should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its strong basicity and reactivity, it should be kept separate from acids, oxidizing agents, and other reactive substances. Proper ventilation is essential during handling to minimize exposure to vapors. Always wear appropriate personal protective equipment, including gloves, goggles, and a lab coat, when working with DMEDA to ensure safety in the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086402334938,"sku":"TCI2510D072020315","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086402367706,"sku":"TCI2510D072020316","price":3584000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0720_4cb46a26-4da1-49d3-bae9-35a411d5e567.jpg?v=1792636377"},{"product_id":"tci2510d090520562","title":"TCI D0905 1662-01-7 Bathophenanthroline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBathophenanthroline is a chemical compound widely used in laboratory settings, particularly in catalysis and inorganic chemistry. As a nitrogen-donor ligand, it plays a crucial role in forming stable metal complexes, which are essential in various catalytic reactions. Its ability to coordinate with transition metals makes it an important tool for researchers aiming to enhance reaction efficiency without undergoing chemical change itself. This compound is commonly found in chemical research, where it supports the development of new synthetic methods and analytical techniques.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure features multiple nitrogen atoms, enabling strong and selective binding with metal ions. This structural characteristic contributes to its high stability and reactivity, making it a preferred choice for both synthetic and analytical applications. Its solubility in organic solvents such as ethylamine and dimethylformamide further enhances its versatility in laboratory experiments. These properties ensure that Bathophenanthroline remains a reliable and effective reagent in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Bathophenanthroline is extensively used in scientific research across various institutions, including universities and research centers. It supports both catalytic and analytical studies, contributing to advancements in chemical sciences. Its role in quantitative analysis, particularly in detecting and measuring metal concentrations in solution, makes it an essential component in many experimental protocols.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCatalytic Reaction Development: Bathophenanthroline is used to form stable metal complexes, enhancing reaction efficiency in catalytic processes.\u003c\/li\u003e\n\u003cli\u003eMetal Ion Detection and Quantification: Its strong binding affinity with metal ions allows for accurate detection and measurement in analytical chemistry.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry Research: The compound supports the creation of new chemical structures by facilitating metal coordination in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Analysis: It is employed in the analysis of trace metal contaminants in environmental samples due to its high selectivity and sensitivity.\u003c\/li\u003e\n\u003cli\u003eBioinorganic Chemistry Studies: Bathophenanthroline aids in studying metal-ligand interactions in biological systems, contributing to understanding metal-based biochemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1662-01-7\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 standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the specific product variant\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\u003eBathophenanthroline should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. As a nitrogen-donor ligand, it is generally non-toxic but should be handled with care, following standard laboratory safety protocols. Proper labeling and storage conditions ensure the compound remains effective for its intended applications. Laboratory personnel should wear appropriate personal protective equipment when handling this material to ensure safe and efficient use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086412656858,"sku":"TCI2510D090520562","price":3055000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086412689626,"sku":"TCI2510D090520563","price":11887000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0905_62007bd3-b760-4e9c-91ad-dcbe56a75e1a.jpg?v=1792636550"},{"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":707000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086420553946,"sku":"TCI2510D105920767","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086420586714,"sku":"TCI2510D105920768","price":4669000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1059_fba3eaef-b98b-4ce3-96f9-e2e739ac411f.jpg?v=1792636670"},{"product_id":"tci2510d129421008","title":"TCI D1294 1188-33-6 N,N-Dimethylformamide Diethyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1294 N,N-Dimethylformamide Diethyl Acetal [for Esterification] is an organic synthesis reagent from the formamide acetal family, formulated specifically for esterification work. The reagent supplies an ethyl group, allowing carboxylic acids to be converted into their corresponding ethyl esters without a strong acid catalyst and without prolonged reflux in an excess of alcohol. As a non-heterocyclic building block, it holds an important position in both synthesis and analytical laboratories, because it shortens the working sequence and reduces the risk of damaging other sensitive functional groups present on the target molecule.\u003c\/p\u003e\n\u003cp\u003eThe principal advantage of this reagent lies in its mild, essentially neutral reaction conditions. Substrates carrying acid-labile groups, additional ester linkages, or stereogenic centres can therefore be processed with a lower risk of racemisation and decomposition than would be expected under classical acid-catalysed esterification. Beyond esterification, the formamide acetal framework is also able to react with active methylene compounds to form enaminone derivatives, although the product's primary intended use is genuinely directed towards esterification reactions. It is supplied as a moisture-sensitive liquid, so the best results are obtained only when the reagent is handled and stored correctly.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on organic synthesis, in medicinal and natural-product chemistry projects where sensitive intermediates must be esterified, and in analytical laboratories that prepare ester derivatives prior to instrumental measurement. Because it removes the need for strongly acidic conditions and extended reflux, it fits well into routine bench workflows where sample quantities are limited and functional-group integrity has to be preserved.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEthyl ester preparation from carboxylic acids: supplies the ethyl group directly, so conversion proceeds without a strong acid catalyst or a large excess of ethanol under prolonged reflux.\u003c\/li\u003e\n\u003cli\u003eEsterification of acid-sensitive substrates: the mild, nearly neutral conditions allow molecules bearing acid-labile protecting groups or additional ester linkages to be converted with reduced decomposition.\u003c\/li\u003e\n\u003cli\u003eDerivatisation of stereogenic compounds: because harsh acidic media are avoided, substrates containing stereogenic centres can be esterified with a lower risk of racemisation during the reaction.\u003c\/li\u003e\n\u003cli\u003eEnaminone synthesis from active methylene compounds: the formamide acetal framework reacts with active methylene substrates to build enaminone derivatives useful as intermediates in further synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eSample derivatisation in analytical laboratories: forming ester derivatives shortens the preparation sequence and helps preserve other sensitive functional groups on the analyte before instrumental analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1188-33-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct designation: D1294, N,N-Dimethylformamide Diethyl Acetal [for Esterification]\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, moisture sensitive\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed and protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBecause this reagent is a moisture-sensitive liquid, it should be stored in a tightly closed original container and protected from atmospheric humidity; best results are obtained only when the reagent is kept dry. Store in a cool, well-ventilated area away from heat, ignition sources, and incompatible materials, and keep the container closed when not in use. Dispense in a fume hood using dry glassware and dry syringes or cannulas, and minimise the time the container remains open. Wear safety glasses, chemical-resistant gloves, and a laboratory coat while handling. Return the container to storage promptly after use and follow the manufacturer's safety data sheet together with local laboratory waste-disposal procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433038554,"sku":"TCI2510D129421008","price":1060000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433071322,"sku":"TCI2510D129421009","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1294_a12d25e5-66ea-4634-a39f-d45a9caa8396.jpg?v=1792636887"},{"product_id":"tci2510d130121014","title":"TCI D1301 6006-65-1 N,N-Dimethylformamide Dipropyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1301 N,N-Dimethylformamide Dipropyl Acetal [for Esterification] is a member of the formamide acetal family carrying two propoxy groups, prepared specifically for esterification reactions in both synthesis and analytical laboratories. The reagent allows carboxylic acids to be converted directly into their propyl esters without a strong acid catalyst and without the need to add excess alcohol under prolonged reflux conditions. As a non-heterocyclic building block, it complements the dimethyl and diethyl variants within the same family of reagents, giving researchers a choice of ester alkyl group according to the demands of a particular analysis or synthetic target.\u003c\/p\u003e\n\u003cp\u003eThe distinguishing feature of this reagent lies in its propyl chain, which is longer than either the methyl or ethyl equivalent, producing ester derivatives with different polarity and different retention behaviour in chromatographic analysis. This difference is especially valuable when the peak of a methyl or ethyl derivative overlaps with components of the sample matrix, since the analyst can select propyl derivatisation instead to obtain better separation. The reaction conditions are mild and close to neutral, which preserves the integrity of other functional groups present in the molecule and reduces the risk of unwanted side reactions during derivatisation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, reagents of this type are used in university synthesis groups, government research institutes, and analytical service laboratories that prepare samples for chromatographic determination. Because it works under gentle, near-neutral conditions and avoids the handling of strong acid catalysts, it fits well into routine sample-preparation workflows where a straightforward and reproducible derivatisation step is required before instrumental measurement, and where the choice of alkyl group must be adapted to the sample matrix at hand.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDirect esterification of carboxylic acids: converts the acid group into the corresponding propyl ester in a single step, without a strong acid catalyst or a large excess of alcohol under long reflux.\u003c\/li\u003e\n\u003cli\u003eDerivatisation for chromatographic analysis: forms propyl ester derivatives with polarity and retention characteristics that differ from methyl and ethyl analogues, giving analysts an alternative when peaks overlap.\u003c\/li\u003e\n\u003cli\u003eResolution of matrix interference problems: when methyl or ethyl derivative peaks coincide with sample matrix components, switching to propyl derivatisation shifts retention and delivers better chromatographic separation.\u003c\/li\u003e\n\u003cli\u003eSynthesis of propyl esters on substrates with sensitive functionality: the mild, near-neutral reaction conditions preserve other functional groups on the molecule that acidic esterification methods could damage.\u003c\/li\u003e\n\u003cli\u003eBuilding block work in non-heterocyclic organic synthesis: serves alongside the dimethyl and diethyl acetal variants so researchers can select the ester alkyl group that matches their synthetic target.\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: 6006-65-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D1301\u003c\/li\u003e\n\u003cli\u003eApplication grade: supplied as a reagent designated for esterification\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the packaging options offered by the manufacturer for this catalogue item\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 moisture, in a cool and well-ventilated area away from direct sunlight and sources of ignition. Acetal reagents of this type are moisture-sensitive, so containers should be resealed promptly after use and, where practical, handled under a dry inert atmosphere. Dispense and transfer the material inside a fume hood using clean, dry glassware and dry syringes or cannulas. Laboratory personnel should wear safety goggles, chemical-resistant gloves, and a laboratory coat, and should avoid inhaling vapours or allowing contact with skin and eyes. Keep the reagent separate from strong acids and strong oxidising agents, and consult the manufacturer's safety data sheet before use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433267930,"sku":"TCI2510D130121014","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433300698,"sku":"TCI2510D130121015","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1301_a0a374c8-7b56-49d2-b647-fc0dde725e8f.jpg?v=1792636893"},{"product_id":"tci2510d130221016","title":"TCI D1302 18503-90-7 N,N-Dimethylformamide Dibutyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Dibutyl Acetal (DMFDBA), with CAS number 18503-90-7, is a chemical compound widely utilized in laboratory settings for esterification reactions. As a key building block in organic synthesis, it plays a vital role in the formation of esters from carboxylic acids. Its stability and reactivity make it a versatile reagent for creating complex molecular structures. This compound is particularly favored for its ability to participate in both esterification and other organic transformations, making it an essential component in synthetic chemistry workflows.\u003c\/p\u003e\n\u003cp\u003eDMFDBA is known for its excellent solubility in organic solvents, which facilitates mixing and reaction processes in laboratory experiments. Its chemical properties allow it to react efficiently with a variety of acids and alcohols, enhancing its utility in esterification reactions. The compound’s stability under various reaction conditions ensures consistent results, making it a reliable choice for researchers. Additionally, its dual role as both a reagent and a solvent increases its flexibility in different experimental setups, contributing to its widespread use in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMFDBA is commonly used in organic chemistry research, compound development, and industrial chemical production. It supports academic institutions and research centers in advancing chemical knowledge and innovation. Its availability and effectiveness make it a standard material in both educational and industrial chemical applications within the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for esterification reactions due to its reactivity with carboxylic acids and alcohols.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical compounds in research laboratories requiring reliable reagents for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where DMFDBA is used as a building block for ester formation processes.\u003c\/li\u003e\n\u003cli\u003eEducational institutions for teaching and conducting experiments in organic chemistry courses.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the synthesis of ester-based compounds used in drug development.\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: 18503-90-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMFDBA should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent evaporation and contamination. Due to its chemical nature, it should be stored separately from strong oxidizing agents and acids to avoid potential reactions. Proper ventilation is essential when handling this compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with DMFDBA to ensure safe handling and reduce exposure risks. Regular monitoring of storage conditions is advised to maintain the compound's integrity and ensure compliance with safety standards.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433333466,"sku":"TCI2510D130221016","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433366234,"sku":"TCI2510D130221017","price":4165000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1302_8027a39b-178f-415e-834a-be26e223d3d4.jpg?v=1792636896"},{"product_id":"tci2510d130321018","title":"TCI D1303 36805-97-7 N,N-Dimethylformamide Di-tert-butyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Di-tert-butyl Acetal is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key building block in organic synthesis, it enables the formation of esters through efficient and controlled chemical processes. This compound is particularly valued for its ability to react with various carboxylic acids, making it a versatile reagent in synthetic chemistry. Its stability and reactivity make it a reliable choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability and reactivity, make it a preferred choice for laboratory applications. It is known for its ability to undergo esterification efficiently, which is crucial in the synthesis of ester compounds with diverse industrial and pharmaceutical applications. Its non-heterocyclic nature allows it to be used in a wide range of chemical reactions without interfering with other functional groups. This makes it a go-to material for chemists seeking reliable and consistent results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N,N-Dimethylformamide Di-tert-butyl Acetal is commonly used in organic chemistry research. It is a staple in both academic and industrial settings, where its reliability and efficiency are highly appreciated. Its availability in liquid form and ease of use further contribute to its popularity among researchers. Its non-volatile nature also ensures safety during handling and storage, making it a trusted reagent in controlled laboratory environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for esterification reactions due to its efficient and stable chemical properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of ester-based compounds with therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemistry applications where ester compounds are required for product formulation.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical laboratories for teaching and experimental purposes.\u003c\/li\u003e\n\u003cli\u003ePolymer science for the synthesis of ester-functionalized polymers with specific properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 36805-97-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. While it is relatively stable under normal storage conditions, it should not be exposed to extreme temperatures or incompatible substances. Proper labeling and safe storage practices are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086433431770,"sku":"TCI2510D130321018","price":3710000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086433464538,"sku":"TCI2510D130321019","price":12795000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1303_78b6d684-4f4a-40d5-9223-24dce614594d.jpg?v=1792636898"},{"product_id":"tci2510d133221062","title":"TCI D1332 4637-24-5 N,N-Dimethylformamide Dimethyl Acetal [for Esterification] (0.5mL*10)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D1332 N,N-Dimethylformamide Dimethyl Acetal [for Esterification] is a methylating reagent supplied in a specially prepared format of ten glass ampoules, each containing 0.5 mL. Widely known by the abbreviation DMF-DMA, this reagent converts carboxylic acids into their corresponding methyl esters quickly and cleanly, without requiring a strong acid catalyst or an excess of solvent. In the laboratory it plays an essential role during sample preparation prior to gas chromatographic analysis, because free carboxylic acids tend to produce broadened, asymmetric peaks on the column.\u003c\/p\u003e\n\u003cp\u003eThe qualities that make analysts choose this reagent lie in its single-dose ampoule packaging and the purity maintained specifically for esterification work. Each ampoule holds a pre-measured quantity, so the analyst does not need to open a large bulk container repeatedly, and the risk of quality deterioration through contact with atmospheric moisture is kept to a minimum. The methylation reaction proceeds at moderate temperature within a short time and generates volatile by-products, which therefore do not interfere with chromatographic injection.\u003c\/p\u003e\n\u003cp\u003eBeyond esterification, DMF-DMA is also widely used as an enaminone-forming reagent and as a one-carbon unit source in synthetic chemistry. In Indonesian laboratories this combination of roles suits analytical services, university research groups, and quality control units that prepare acidic samples for gas chromatography while also running small-scale building block synthesis. The ten-ampoule set allows a single delivery to cover several separate work sessions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMethyl ester preparation from carboxylic acids: the reagent performs the conversion rapidly and cleanly without a strong acid catalyst or excess solvent, simplifying the workflow.\u003c\/li\u003e\n\u003cli\u003eSample derivatisation before gas chromatography: free carboxylic acids give broad, asymmetric peaks, so converting them to methyl esters improves peak shape on the column.\u003c\/li\u003e\n\u003cli\u003eRoutine analytical sample preparation: each pre-measured ampoule removes the need to repeatedly open a bulk container, which keeps handling consistent between analytical batches.\u003c\/li\u003e\n\u003cli\u003eEnaminone formation in synthetic chemistry: DMF-DMA is widely employed as an enaminone-forming reagent, making this pack useful for building block work beyond esterification.\u003c\/li\u003e\n\u003cli\u003eOne-carbon unit introduction: the reagent serves as a source of a single carbon unit, supporting synthetic routes that require this fragment in non-heterocyclic building block 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: 4637-24-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack size: 0.5 mL × 10 ampoules per set\u003c\/li\u003e\n\u003cli\u003eGrade note: supplied as a reagent for esterification\u003c\/li\u003e\n\u003cli\u003eStorage: keep ampoules sealed and protected from moisture until use\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the ampoules in their original packaging in a cool, dry place away from direct sunlight and sources of heat, keeping each unit sealed until the moment of use so that contact with atmospheric moisture is avoided. Because the material is sensitive to water vapour, the single-dose ampoule format should be used as intended: open one ampoule per working session rather than transferring the contents into a larger shared container. Handle the reagent in a fume hood with appropriate gloves, safety glasses, and a laboratory coat, and open glass ampoules carefully to avoid cuts. Prepare and transfer the reagent using clean, dry glassware, and dispose of residues and empty ampoules through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1set","offer_id":48086435168474,"sku":"TCI2510D133221062","price":2020000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1332_19e382b6-f647-40b0-8dd1-654e74ca543e.jpg?v=1792636937"},{"product_id":"tci2510d159521401","title":"TCI D1595 4909-78-8 N,N-Dimethylformamide Dineopentyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N-Dimethylformamide Dineopentyl Acetal (DMF-DIPA) is a chemical compound widely used in laboratory settings for its role in esterification reactions. As a key reagent, it serves as a versatile source of ester groups that can react with various substrates to form new organic compounds. This compound is particularly valuable in synthetic chemistry due to its ability to act both as a solvent and a reactive component, streamlining the synthesis process without the need for additional reagents. Its application spans multiple areas of organic chemistry, making it an essential material for researchers and chemists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eDMF-DIPA is preferred for its chemical stability under controlled conditions and its reactivity in a wide range of chemical environments. It possesses a high boiling point, which allows it to be used in reactions requiring elevated temperatures. Its ability to participate in esterification reactions makes it a reliable choice for producing ester derivatives. Additionally, its dual functionality as a solvent and reagent enhances its utility in complex synthesis pathways. These properties make DMF-DIPA a go-to compound in Indonesian laboratories where efficiency and reliability are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMF-DIPA is commonly used in organic chemistry research, especially in the pharmaceutical and chemical industries. It plays a crucial role in the synthesis of complex organic molecules, contributing to the development of new drugs and materials. Its availability and effectiveness make it a staple in many research facilities across Indonesia, supporting both academic and industrial chemical innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEsterification Reactions: DMF-DIPA is ideal for esterification due to its ability to provide ester groups, facilitating the formation of ester derivatives in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the synthesis of complex organic compounds, acting as both a solvent and reactive component to enhance reaction efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its role in producing ester derivatives makes it valuable in drug development and compound modification processes.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry: DMF-DIPA supports the production of various chemical products by enabling efficient and reliable esterification pathways.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a solvent in analytical procedures to dissolve and process organic compounds for further analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4909-78-8\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: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from heat and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMF-DIPA should be stored in a cool, dry environment, away from heat and direct sunlight to maintain its chemical stability. It is recommended to use sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to oxygen and heat to prevent degradation. Proper storage ensures the compound remains effective for its intended applications in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086449520858,"sku":"TCI2510D159521401","price":1136000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086449553626,"sku":"TCI2510D159521402","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1595_b443f15f-5f3e-4d32-9ce1-e0824bc0b1da.jpg?v=1792637138"},{"product_id":"tci2510d207122115","title":"TCI D2071 4637-24-5 N,N-Dimethylformamide Dimethyl Acetal [for Esterification]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2071 N,N-Dimethylformamide Dimethyl Acetal, commonly abbreviated as DMF-DMA, is a versatile liquid reagent prepared specifically for esterification work. In the laboratory it acts as a mild methylating agent that rapidly converts carboxylic acids into their methyl esters without requiring strong mineral acids or hazardous diazomethane. This role is particularly important during sample preparation prior to gas chromatographic analysis, because many organic acids are insufficiently volatile and are difficult to separate cleanly until they have been converted into their more readily analysed ester derivatives.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this reagent a preferred choice are its selective reactivity and its comparatively gentle reaction conditions. The aminal acetal group in its structure readily releases methanol and forms a reactive intermediate species, so esterification can proceed under moderate heating with by-products that are easily evaporated away. DMF-DMA is also well known as an enaminone-forming reagent and as a one-carbon source for heterocyclic synthesis, including pyrazoles, pyrimidines, and isoxazoles, so a single bottle can support several different kinds of work at once.\u003c\/p\u003e\n\u003cp\u003eBecause it is supplied in liquid form, the reagent is straightforward to measure and to add directly to a reaction mixture or to a derivatisation vial. In Indonesian laboratories this suits routine analytical service work, teaching and research laboratories in organic synthesis, and quality control settings where organic acid content is determined by gas chromatography. Its dual usefulness in both derivatisation and synthetic chemistry makes it a practical item to keep on hand where a single reagent inventory has to serve mixed workloads.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMethyl ester derivatisation for gas chromatography — converts poorly volatile organic acids into methyl esters that elute and separate far more cleanly, improving peak shape and quantitation in routine GC analysis.\u003c\/li\u003e\n\u003cli\u003eMild esterification of carboxylic acids — provides a route to methyl esters without strong mineral acid catalysts or hazardous diazomethane, which simplifies both the procedure and the safety controls required.\u003c\/li\u003e\n\u003cli\u003eEnaminone formation in organic synthesis — reacts with activated methyl and methylene compounds to give enaminone intermediates that serve as flexible platforms for further ring-forming chemistry.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic building block chemistry — acts as a one-carbon source in the construction of pyrazoles, pyrimidines, and isoxazoles, supporting medicinal and materials-oriented synthetic programmes.\u003c\/li\u003e\n\u003cli\u003eTeaching and research laboratory synthesis exercises — its moderate reaction conditions and easily evaporated by-products make reaction workup and product isolation more manageable for students and researchers alike.\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: 4637-24-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D2071\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid reagent, specified for esterification use\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry, well-ventilated area away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, and well-ventilated chemical store, away from heat sources, ignition sources, and direct sunlight. Because the acetal group releases methanol on reaction, keep the container sealed against atmospheric moisture and reclose it promptly after each withdrawal; amber glass or the supplier's original glass packaging is appropriate. Handle and dispense in a fume hood, wearing safety glasses, chemically resistant gloves, and a laboratory coat. Use clean, dry glassware and dry syringes or pipettes when transferring, avoid contact with strong acids and oxidising agents, and consult the manufacturer's safety data sheet before first use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086491660506,"sku":"TCI2510D207122115","price":1818000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2071_4dbe9011-4484-4d53-8742-8c4f373e1807.jpg?v=1792637573"},{"product_id":"tci2510d223422345","title":"TCI D2234 527-61-7 2,6-Dimethyl-1,4-benzoquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Dimethyl-1,4-benzoquinone is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. As a building block in chemical reactions, it plays a crucial role in the development of complex organic molecules. Its aromatic structure, featuring two methyl groups at positions 2 and 6, along with two keto groups at positions 1 and 4, makes it a valuable intermediate in various synthetic pathways. This compound is particularly useful in oxidation and reduction reactions due to its stable yet reactive nature. It is commonly found in both academic and industrial research environments, where its chemical properties support a wide range of experimental applications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice for laboratory use. It is non-colored, solid in form, and soluble in organic solvents, which simplifies its handling and integration into chemical processes. Its relatively high melting and boiling points allow for efficient thermal processing in laboratory settings. These physical characteristics contribute to its reliability in synthetic procedures, enabling consistent results. The compound’s stability under controlled conditions ensures that it remains effective for multiple applications without degrading prematurely.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Dimethyl-1,4-benzoquinone is frequently used in organic chemistry research and pharmaceutical development. Its role in synthesizing compounds with pharmaceutical and industrial applications makes it an essential material for researchers. Many institutions and laboratories in Indonesia rely on this compound for its predictable performance and compatibility with various chemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 2,6-Dimethyl-1,4-benzoquinone is used for its ability to participate in oxidation and reduction reactions, making it ideal for creating complex organic molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from this compound due to its role in the synthesis of various drug compounds, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes often incorporate this material because of its stability and reactivity, allowing it to be used in the production of specialty chemicals and intermediates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories use it as a reference standard for identifying and quantifying compounds in various samples through spectroscopic and chromatographic methods.\u003c\/li\u003e\n\u003cli\u003ePolymer science research employs this compound in the development of new materials, leveraging its chemical structure to create polymers with specific functional properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 527-61-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its stability. Due to its chemical nature, it should be kept away from strong oxidizing or reducing agents to avoid unwanted reactions. Proper labeling of storage containers is essential for safety and identification. In laboratory settings, personal protective equipment such as gloves and goggles should be worn when handling this material to ensure safe usage. Regular inspection of storage conditions is advised to ensure optimal preservation of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086505881818,"sku":"TCI2510D223422345","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086505914586,"sku":"TCI2510D223422346","price":3686000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086505947354,"sku":"TCI2510D223422347","price":12820000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2234_5884d687-9973-433a-a1b3-8f5565e9c85a.jpg?v=1792637748"},{"product_id":"tci2510d258022850","title":"TCI D2580 79791-38-1 Dodecylbenzenesulfonyl Azide (soft type) (mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2580 Dodecylbenzenesulfonyl Azide (soft type) (mixture) is a synthetic reagent belonging to the group of reagents used for carbon–heteroatom (non-halogen) bond formation. Its primary laboratory function is as a diazo transfer reagent, meaning it delivers a diazo group to compounds bearing an active hydrogen — such as 1,3-dicarbonyl compounds, beta-ketoesters, and malonates — to form alpha-diazocarbonyl compounds. The diazo compounds produced in this reaction are highly useful intermediates, because they can be decomposed into carbenes or metal carbenoids for cyclopropanation, C–H insertion, and rearrangement reactions.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this reagent a preferred choice is its handling profile. Short-chain aryl sulfonyl azides such as tosyl azide are known to be sensitive to impact and heat, whereas this \"soft type\" product is supplied as a mixture formulation with a long dodecyl chain that appreciably reduces that sensitivity and makes the reagent far more convenient to use in a research laboratory setting. The long alkyl chain on the benzene ring also improves solubility in non-polar organic solvents and simplifies separation of the sulfonamide by-product during work-up, which together support smoother, more reproducible synthetic procedures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in organic synthesis and methodology research groups at universities, research institutes, and industrial R\u0026amp;D units that prepare alpha-diazocarbonyl intermediates in-house. It suits work programmes in which diazo transfer is performed on a bench scale for further carbene-based transformations, and where a less impact- and heat-sensitive alternative to short-chain sulfonyl azides is preferred so that routine synthetic work can proceed with more comfortable handling requirements.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDiazo transfer to 1,3-dicarbonyl compounds — the reagent delivers the diazo group to active-hydrogen substrates directly, giving access to alpha-diazocarbonyl products without resorting to more impact-sensitive short-chain sulfonyl azides.\u003c\/li\u003e\n\u003cli\u003ePreparation of alpha-diazo beta-ketoesters — beta-ketoesters are classic active-methylene substrates for this reagent, and the resulting diazo esters serve as stable-handling intermediates for downstream carbene chemistry.\u003c\/li\u003e\n\u003cli\u003eDiazo functionalisation of malonate derivatives — malonates possess the activated hydrogens required for diazo transfer, and the reagent's good solubility in non-polar solvents helps keep such reaction mixtures homogeneous.\u003c\/li\u003e\n\u003cli\u003ePrecursor synthesis for cyclopropanation studies — diazocarbonyl compounds made with this reagent decompose to carbenes or metal carbenoids, which are the working species used to build cyclopropane rings.\u003c\/li\u003e\n\u003cli\u003eSubstrate preparation for C–H insertion and rearrangement work — the same metal carbenoid intermediates generated from these diazo compounds are used in C–H insertion and rearrangement reactions in methodology research.\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: 79791-38-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eProduct code: D2580\u003c\/li\u003e\n\u003cli\u003ePhysical form: supplied as a \"soft type\" mixture formulation containing the long-chain dodecylbenzenesulfonyl azide\u003c\/li\u003e\n\u003cli\u003eStorage note: store according to the manufacturer's stated conditions on the product label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container, kept in a cool, dry, well-ventilated area away from heat sources, direct sunlight, ignition sources, and incompatible materials, and follow the storage conditions stated by the manufacturer on the label and Safety Data Sheet. Although the soft type mixture formulation is markedly less sensitive to impact and heat than short-chain aryl sulfonyl azides, sulfonyl azides as a class still warrant careful handling: avoid friction, shock, and unnecessary heating or concentration to dryness. Handle in a fume hood using appropriate gloves, safety glasses, and a laboratory coat, keep containers closed when not in use, and review the Safety Data Sheet before work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086566469850,"sku":"TCI2510D258022850","price":1263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/tci2510d258022850-struktur-1000.png?v=1792638123"},{"product_id":"tci2510d260422885","title":"TCI D2604 12107-56-1 Dichloro(1,5-cyclooctadiene)palladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2604 Dichloro(1,5-cyclooctadiene)palladium(II) is an organopalladium complex in which a 1,5-cyclooctadiene diene ligand is bound to palladium together with two chloride ligands. In catalysis laboratories, this compound serves as a highly practical palladium catalyst precursor: the cyclooctadiene ligand binds firmly enough to keep the complex stable during storage, yet remains labile enough to be displaced by other ligands such as phosphines, N-heterocyclic carbenes, bipyridine, or other nitrogen donor ligands when an active catalyst needs to be formed in situ. For that reason, this reagent has become a flexible starting point for many palladium-based catalytic systems.\u003c\/p\u003e\n\u003cp\u003eThe properties that make it a widely chosen reagent are the ease of ligand exchange and the clearly defined palladium content in the +2 oxidation state. Researchers can design catalysts with ligands of their own choosing without having to prepare palladium complexes from raw metal, so stoichiometry is better controlled and reaction outcomes are more reproducible. Because the complex is supplied as a solid, it is also easier to weigh and measure out than a precursor solution, while remaining straightforward to store under ordinary laboratory conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on catalysis and synthetic organic chemistry, particularly in studies of C–H bond activation and related transformations. Its solid form suits laboratories that prepare catalyst systems batch by batch on a small scale, where accurate weighing and predictable ligand substitution behaviour matter more than bulk handling. It fits naturally into method development work in which several ligand sets are screened against the same palladium source.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC–H bond activation studies: the complex delivers a well-defined palladium(II) source whose labile diene ligand can be exchanged for the directing ligand required by the activation system under investigation.\u003c\/li\u003e\n\u003cli\u003eIn situ catalyst generation: researchers combine the precursor with phosphines or N-heterocyclic carbenes directly in the reaction vessel, forming the active palladium species without isolating an intermediate complex.\u003c\/li\u003e\n\u003cli\u003eLigand screening in method development: a single palladium source can be paired with many different donor ligands, allowing systematic comparison of catalytic performance while keeping the metal input constant.\u003c\/li\u003e\n\u003cli\u003eCoordination chemistry teaching and research: the straightforward substitution of 1,5-cyclooctadiene by nitrogen donor ligands such as bipyridine illustrates ligand exchange behaviour clearly for synthesis and characterisation exercises.\u003c\/li\u003e\n\u003cli\u003eReproducible small-scale synthetic work: because the palladium oxidation state is clearly defined, stoichiometry can be calculated precisely, which supports repeatable results across successive experimental runs.\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: 12107-56-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C–H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eChemical name: Dichloro(1,5-cyclooctadiene)palladium(II)\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the available TCI catalogue packaging options for this product code\u003c\/li\u003e\n\u003cli\u003eStorage: store under ordinary laboratory storage conditions in a closed container\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 dry and protected from moisture, in a cool and well-ventilated chemical storage area away from incompatible reagents. Glass or the manufacturer's supplied container is suitable; reseal promptly after each use to limit exposure to air and humidity. Handle the solid in a fume hood using gloves, safety glasses, and a laboratory coat, and avoid generating dust when weighing. Transfer with clean, dry spatulas to prevent contamination that could affect catalytic performance. Collect residues and spent catalyst as heavy-metal chemical waste according to institutional disposal procedures, and consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086567715034,"sku":"TCI2510D260422885","price":4039000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086567747802,"sku":"TCI2510D260422886","price":15520000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2604_cd36f0e0-1fa7-4747-90dc-0061b3add86d.jpg?v=1792638132"},{"product_id":"tci2510d354423843","title":"TCI D3544 870-50-8 Di-tert-butyl Azodicarboxylate (20% in Toluene)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDi-tert-butyl Azodicarboxylate (DTBAC), with the CAS number 870-50-8, is a synthetic reagent widely used in chemical laboratories for forming C-X bonds, particularly in organic synthesis. It is a versatile compound that plays a crucial role in reactions involving carbon-carbon or carbon-halogen bond formation. Its utility extends across various research fields, including pharmaceutical and organic chemistry, where it is employed to create complex molecular structures. DTBAC is known for its reactivity and stability, making it an essential component in many synthetic processes.\u003c\/p\u003e\n\u003cp\u003eDTBAC is favored for its high reactivity and controlled stability, which allow it to participate in a wide range of chemical reactions under specific conditions. Its ability to form stable intermediates and its compatibility with various substrates make it a preferred choice for chemists. The compound remains stable under certain conditions, ensuring consistent performance in laboratory settings. Its non-degradative nature also ensures reliability in long-term storage and use, contributing to its widespread adoption in chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DTBAC is commonly used in organic chemistry research and the synthesis of complex compounds. It is a key reagent in the development of new pharmaceuticals and specialty chemicals. Its application is particularly prevalent in academic and industrial research settings where precision and reliability are essential. The compound's versatility and effectiveness make it a staple in many laboratory workflows across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where C-X bond formation is required due to its ability to facilitate carbon-carbon and carbon-halogen bond formation.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research applications for the development of complex molecular structures due to its reactivity and stability.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis processes that require controlled reactivity and high efficiency in bond formation.\u003c\/li\u003e\n\u003cli\u003eAcademic research in organic chemistry where precise and reliable reagents are essential for experimental success.\u003c\/li\u003e\n\u003cli\u003eCustom compound synthesis projects that demand a versatile and stable reagent for multiple reaction conditions.\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: 870-50-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 20% in Toluene\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from heat and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDTBAC should be stored in a cool, dark place, away from heat and direct light to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid exposure to moisture and incompatible substances to ensure safety and effectiveness. Regular monitoring of storage conditions is advised to maintain the integrity of the reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086622961882,"sku":"TCI2510D354423843","price":2449000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3544_a6f77762-0f64-457c-8bfc-178565d10054.jpg?v=1792638664"},{"product_id":"tci2510d389124310","title":"TCI D3891 14783-09-6 Dichloro(1,10-phenanthroline)copper(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDichloro(1,10-phenanthroline)copper(II) is a chemical compound widely used in catalytic reactions and C-H activation processes within laboratory settings. As a copper-based inorganic catalyst, it plays a crucial role in accelerating chemical reactions without being consumed in the process. This compound is particularly valuable in organic and inorganic chemistry research, where it contributes to the efficiency and selectivity of various reaction pathways. Its ability to form stable complexes with ligands like 1,10-phenanthroline makes it a versatile tool for synthetic chemists.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and stability under diverse reaction conditions make it a preferred choice for laboratory applications. Its capacity to act as a catalyst in substitution and oxidation reactions is enhanced by its coordination properties. The presence of the 1,10-phenanthroline ligand contributes to the formation of a highly active and stable complex, which is essential for maintaining catalytic efficiency. These characteristics ensure that the compound remains effective across a range of experimental setups, from solution-based to vacuum conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to C-H activation, organic synthesis, and metal-based catalysis. Its reliability and performance in various chemical processes make it a staple in both academic and industrial research environments. Scientists and researchers rely on its consistent behavior to achieve reproducible results in complex chemical transformations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Research - This compound is ideal for C-H activation studies due to its ability to facilitate selective bond-breaking in hydrocarbon molecules.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis - It serves as a key catalyst in the synthesis of complex organic compounds, enhancing reaction efficiency and yield.\u003c\/li\u003e\n\u003cli\u003eMetal-Based Catalysis - Its copper content makes it suitable for catalytic reactions involving metal coordination and complex formation.\u003c\/li\u003e\n\u003cli\u003eOxidation Reactions - The compound is effective in promoting oxidation processes, particularly in the presence of appropriate ligands.\u003c\/li\u003e\n\u003cli\u003eSubstitution Reactions - It is widely used in substitution reactions where it facilitates the replacement of functional groups with high selectivity.\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: 14783-09-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and catalytic activity. It is recommended to use airtight containers to prevent exposure to moisture and air, which can degrade its effectiveness. 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 keep it away from incompatible substances to avoid any potential chemical reactions. In laboratory settings, it should be stored in a designated chemical storage area that is well-ventilated and accessible only to authorized personnel. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086643769562,"sku":"TCI2510D389124310","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086643802330,"sku":"TCI2510D389124311","price":2953000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3891_c6605bc5-e22c-41ff-9f04-40be4bed55c9.jpg?v=1792638936"},{"product_id":"tci2510d422424759","title":"TCI D4224 16466-61-8 Di-tert-butyl Hydrazodicarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4224 Di-tert-butyl Hydrazodicarboxylate (CAS 16466-61-8) is a hydrazine derivative in which both nitrogen atoms are protected by tert-butoxycarbonyl groups, which is why it is commonly referred to as a doubly Boc-protected hydrazide. The reagent plays an important role in organic synthesis as a protected nitrogen source for carbon–heteroatom bond formation, particularly in electrophilic amination reactions and in the preparation of hydrazine-based compounds. Its protected form allows researchers to introduce an N–N unit into a molecular framework safely and in a controlled manner, then remove the protecting groups in a final step under acidic conditions that are already very well established.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this reagent so widely used is its stability as a solid that is easy to weigh out, compared with free hydrazine, which is far more reactive and carries greater risk. The two Boc groups lower the nucleophilicity of the nitrogen atoms, so reactions become more selective, while at the same time providing a clean deprotection pathway using acids such as TFA or HCl without the need for specialised reagents. The compound is also known as the redox partner of di-tert-butyl azodicarboxylate: this reduced form is both the by-product of, and the precursor to, that azodicarboxylate.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research settings and in industrial R\u0026amp;D groups working on organic synthesis and medicinal chemistry. Because it belongs to the C-X (Non-Halogen) Bond Formation class of synthetic reagents, it is generally ordered together with other building blocks for multi-step synthesis programmes, where a protected nitrogen source that can be handled as a stable solid on the open bench is preferred over free hydrazine.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eElectrophilic amination reactions, where the doubly Boc-protected nitrogen serves as a controlled, attenuated nitrogen source rather than a highly reactive free hydrazine.\u003c\/li\u003e\n\u003cli\u003eCarbon–heteroatom bond formation, providing a defined C–N bond-forming partner within the C-X (Non-Halogen) Bond Formation class of synthetic reagents for multi-step routes.\u003c\/li\u003e\n\u003cli\u003eSynthesis of hydrazine-based compounds, letting researchers install an intact N–N unit into a molecular framework and unmask it later under standard acidic conditions.\u003c\/li\u003e\n\u003cli\u003ePreparation and regeneration of di-tert-butyl azodicarboxylate, since this reduced compound is both the by-product of and the precursor to that azodicarboxylate reagent.\u003c\/li\u003e\n\u003cli\u003eProtecting-group strategies in medicinal and organic chemistry research, where clean Boc removal with TFA or HCl avoids the need for specialised or exotic deprotection reagents.\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: 16466-61-8\u003c\/li\u003e\n\u003cli\u003eChemical name: Di-tert-butyl Hydrazodicarboxylate\u003c\/li\u003e\n\u003cli\u003eProduct code: D4224\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X (Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, stable and easy to weigh; store in a closed container away from moisture and acidic vapours\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, moisture and acids, since acidic conditions are what remove the Boc protecting groups. Keep the material in its original supplier container or in a clean, chemically compatible, well-sealed glass or plastic vessel with a clear label. Because the compound is supplied as a stable solid, it can be weighed on the bench, but handling should still take place in a fume hood where practical, using safety glasses, gloves and a laboratory coat. Avoid dust formation, close the container immediately after use, and follow institutional chemical waste procedures for residues and contaminated materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086679879898,"sku":"TCI2510D422424759","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086679912666,"sku":"TCI2510D422424760","price":4316000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4224_e43a6485-7ded-42df-bdd7-c1466efeeb48.jpg?v=1792639212"},{"product_id":"tci2510d435724932","title":"TCI D4357 185990-03-8 2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound plays a crucial role in laboratory settings where complex molecular structures need to be synthesized with high precision. Its unique chemical structure enables it to participate in various reaction mechanisms, making it an essential tool for chemists working on advanced synthetic pathways. It is particularly valuable in applications that require controlled reactivity and compatibility with a wide range of substrates.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability under specific conditions, combined with its reactivity in targeted chemical environments, makes it a preferred choice in modern synthetic chemistry. Its molecular framework, containing both boron and silicon atoms, provides versatility in reaction types such as coupling and substitution. These properties allow it to be used in a variety of synthetic strategies, including those involving boron-based reagents. Its ability to maintain structural integrity during synthesis processes ensures consistent results, which is vital for research and development in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in academic and research institutions. It supports the development of new synthetic techniques and contributes to the advancement of chemical knowledge. Its application in molecular modification and complex compound synthesis makes it a key component in the toolkit of chemists working on innovative projects. The compound's relevance in both educational and industrial research contexts underscores its importance in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this reagent's ability to form stable C-X bonds, enabling the creation of complex molecular structures with high efficiency.\u003c\/li\u003e\n\u003cli\u003eBoron-based reaction systems often require reagents with specific reactivity profiles, and this compound provides the necessary chemical versatility for such processes.\u003c\/li\u003e\n\u003cli\u003eMolecular modification projects rely on its capacity to undergo substitution and coupling reactions, making it ideal for functional group transformations.\u003c\/li\u003e\n\u003cli\u003eResearch in synthetic chemistry frequently involves the use of non-halogen bond-forming agents, and this compound is a reliable choice for such investigations.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis in Indonesian laboratories utilizes this reagent to develop new methodologies and improve existing synthetic routes.\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: 185990-03-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure, which can affect its reactivity. In laboratory settings, it should be handled with appropriate personal protective equipment to ensure safety. Due to its chemical nature, it should be stored separately from incompatible substances to avoid potential reactions. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in laboratory applications. Proper labeling and storage practices are essential to maintain the integrity of the compound and ensure safe handling in research environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086688465114,"sku":"TCI2510D435724932","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086688497882,"sku":"TCI2510D435724933","price":5906000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4357_e2db3010-d154-4890-a7b3-83c78fb57404.jpg?v=1792639312"},{"product_id":"tci2510d458725220","title":"TCI D4587 54648-79-2 N,N'-Diisopropyl-O-methylisourea","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N'-Diisopropyl-O-methylisourea (DMIM), also known as TCI D4587 with CAS number 54648-79-2, is a synthetic reagent widely used in organic chemistry laboratories. This compound plays a crucial role in the formation of C-X bonds, particularly in carbon-carbon bond formation reactions. Its versatility makes it a valuable tool for chemists engaged in synthetic reactions, enabling the synthesis of complex organic molecules. DMIM is commonly used in substitution and replacement reactions, depending on the reaction conditions applied. Its presence in laboratory settings supports the development of new compounds and the modification of molecular structures.\u003c\/p\u003e\n\u003cp\u003eDMIM is valued for its chemical stability under specific conditions, although it is highly sensitive to moisture and air exposure. This sensitivity necessitates careful handling and storage to maintain its reactivity. The presence of the isourea group in its molecular structure contributes to its reactivity, making it suitable for various synthetic applications. Its chemical properties allow it to participate in a wide range of reactions, making it a preferred choice for researchers in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMIM is extensively used in organic chemistry research by universities and research institutions. It is particularly relevant in the development of synthetic compounds, including pharmaceutical applications. Its role in facilitating chemical reactions makes it an essential component in the synthesis of new materials and drug compounds. The compound's utility in laboratory settings underscores 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 applications benefit from DMIM's ability to facilitate C-X bond formation, supporting the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for substitution reactions where the isourea group enhances reactivity and selectivity under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eDMIM is commonly used in the development of pharmaceutical compounds, aiding in the synthesis of drug molecules through targeted chemical modifications.\u003c\/li\u003e\n\u003cli\u003eResearch institutions rely on DMIM for molecular structure modification, enabling the design of new compounds with desired properties.\u003c\/li\u003e\n\u003cli\u003eIts role in carbon-carbon bond formation makes it a key reagent in the synthesis of polymers and specialty chemicals.\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: 54648-79-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Should be stored in a sealed container, away from heat and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMIM should be stored in a sealed container to prevent exposure to moisture and air, which can degrade its chemical properties. It is recommended to keep the material in a cool, dry place away from direct heat sources to maintain its stability. Laboratory personnel should handle DMIM with care, using appropriate personal protective equipment such as gloves and safety goggles to avoid skin contact or inhalation. Due to its sensitivity, it is essential to ensure that the storage area is well-ventilated and free from potential contaminants. Proper labeling and secure storage are necessary to prevent accidental exposure and ensure safe handling in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086698492122,"sku":"TCI2510D458725220","price":3686000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4587.jpg?v=1768818147"},{"product_id":"tci2510d536526253","title":"TCI D5365 19740-72-8 Diisopropyl Hydrazine-1,2-dicarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiisopropyl Hydrazine-1,2-dicarboxylate is a chemical compound widely used in synthetic laboratory applications. It serves as a key reagent in the formation of C-X (non-halogen) bonds, which are essential in organic synthesis. This compound is particularly valuable for its ability to participate in complex chemical reactions, making it a versatile tool for researchers. Its role in hydrazinization and substitution reactions further enhances its utility in the laboratory. Due to its reactivity, it is often employed in the development of new compounds with specific functional groups.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical structure and reactivity make it a preferred choice for synthetic chemists. It exhibits stability under certain conditions, allowing for controlled reaction environments. Its ability to form new bonds and its participation in multiple reaction mechanisms make it suitable for a wide range of chemical transformations. The compound’s reactivity also enables it to be used in advanced synthetic strategies, contributing to the development of pharmaceutical and organic compounds. These properties ensure its reliability in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diisopropyl Hydrazine-1,2-dicarboxylate is commonly used in scientific research and chemical product development. It is particularly favored for its role in organic synthesis and pharmaceutical applications. Researchers in Indonesia rely on this compound for its consistent performance in complex reactions. However, due to its reactivity, careful handling is required to ensure safety and effectiveness in experimental processes. Its use is integral to advancing chemical research and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where C-X bond formation is required, due to its ability to participate in hydrazinization and substitution reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new compounds with specific functional groups, as it enables the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications for the synthesis of advanced polymers and functional materials, owing to its reactivity in forming new chemical bonds.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical laboratories for teaching and experimental purposes, due to its versatility in various synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development for the production of specialty chemicals, as it supports the creation of compounds with tailored properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 19740-72-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory reagent packaging\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid (may vary depending on supplier and formulation)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment like gloves and safety goggles. Avoid contact with incompatible substances such as strong oxidizers or acids. Ensure proper ventilation in the laboratory to minimize exposure risks. Regular monitoring of storage conditions is essential to maintain its stability and effectiveness for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086756360410,"sku":"TCI2510D536526253","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086756393178,"sku":"TCI2510D536526254","price":3181000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5365_b0c25104-0dd5-4cd5-bc51-d4b55ec68743.jpg?v=1792639900"},{"product_id":"tci2510d551426430","title":"TCI D5514 7321-55-3 Dimethylmalononitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDimethylmalononitrile (DMN), with the CAS number 7321-55-3, is a synthetic reagent widely used in organic chemistry for the formation of carbon-carbon bonds. This compound features a central carbon atom bonded to two nitrile groups, enabling it to participate in a variety of chemical reactions. Its unique structure makes it a valuable tool in the synthesis of complex organic molecules. In laboratory settings, DMN plays a crucial role in advancing research in both academic and industrial environments. Its versatility and reactivity make it an essential component in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eDMN is known for its stability under controlled conditions, yet it exhibits high reactivity when exposed to elevated temperatures or humidity. This reactivity is advantageous in reactions requiring high selectivity and efficiency, such as Michael additions and alkylation processes. Its ability to undergo various chemical transformations makes it a preferred choice for chemists seeking reliable and effective reagents. The solid form of DMN also simplifies handling and processing, making it ideal for use in laboratory environments that require precision and consistency.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMN is commonly used in organic chemistry research, particularly in pharmaceutical and material science applications. Its role in synthesizing heterocyclic compounds and other complex structures has made it an essential reagent for researchers. The demand for high-quality synthetic reagents has further solidified DMN’s position as a key component in ongoing scientific investigations. Its availability and performance make it a reliable choice for laboratories focused on innovation and discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where DMN is used to form carbon-carbon bonds through reactions like Michael additions and alkylation.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from DMN’s ability to participate in the synthesis of complex heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications rely on DMN for creating functional organic materials with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry uses DMN as a reagent in the preparation of standard solutions for qualitative and quantitative analysis.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate DMN to produce intermediates for a wide range of chemical 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: 7321-55-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDMN should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or polyethylene, to minimize exposure to moisture and air. Due to its reactivity, it is important to handle DMN with care, using appropriate personal protective equipment like gloves and safety goggles. Avoid exposure to high temperatures and direct sunlight to ensure safe storage. In laboratory settings, proper ventilation and adherence to standard safety protocols are essential to prevent any potential hazards. Always ensure that DMN is kept away from incompatible substances to maintain a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086763143386,"sku":"TCI2510D551426430","price":3029000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086763176154,"sku":"TCI2510D551426431","price":10498000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5514_3bd705ed-5f5b-4ab7-98fa-994fdf7cb9a4.jpg?v=1792639985"},{"product_id":"tci2510d588626877","title":"TCI D5886 2247605-87-2 Dichloro[8-(diisopropylphosphino)-5-fluoro-2-(2-pyridinyl)quinoline]iron(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5886 Dichloro[8-(diisopropylphosphino)-5-fluoro-2-(2-pyridinyl)quinoline]iron(II), CAS 2247605-87-2, is a divalent iron complex bound by a multidentate ligand built on a functionalised quinoline framework. The ligand brings three coordinating elements together within a single scaffold: an electron-rich diisopropylphosphine group, a quinoline nitrogen, and a pyridine nitrogen, together with a fluorine substituent on the aromatic backbone. The complex is classified under catalysis for C–H bond activation, a field that attracts considerable attention in modern synthetic chemistry because it allows new bonds to be formed directly from carbon–hydrogen bonds that are normally inert.\u003c\/p\u003e\n\u003cp\u003eThe added value of this catalyst lies in its use of iron as the metal centre. Iron is an abundant and relatively inexpensive metal with a milder toxicity profile than noble metals such as palladium, rhodium, or iridium, which makes it an attractive direction for more sustainable catalysis development. The rigid ligand framework, with its combined phosphorus and nitrogen donor arrangement, helps to control the geometry around the metal centre and to stabilise the active species throughout the catalytic cycle. The isopropyl substituents on phosphorus contribute to the steric environment surrounding the metal, while the fluorine substituent modulates the electronic character of the aromatic system.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a well-defined complex of this type is typically used in university and institutional research settings where synthetic methodology and catalysis are studied. It suits work in organic synthesis groups, chemistry departments, and research institutes exploring earth-abundant metal catalysis as an alternative to precious metal systems. Because it arrives as a discrete, pre-formed complex, it removes the need for in-house ligand–metal assembly and gives researchers a reproducible starting point for comparative studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC–H bond activation studies — the complex is supplied specifically for this catalysis category, giving researchers a defined iron-based system for converting normally inert carbon–hydrogen bonds into new functional groups.\u003c\/li\u003e\n\u003cli\u003eEarth-abundant metal catalysis research — iron's abundance, lower cost, and milder toxicity profile make this complex a direct comparison point against palladium, rhodium, or iridium catalyst systems in methodology work.\u003c\/li\u003e\n\u003cli\u003eSynthetic methodology development — the pre-formed, well-defined structure allows chemists to test and refine reaction conditions without first preparing and characterising the ligand–metal combination themselves.\u003c\/li\u003e\n\u003cli\u003eLigand design and coordination chemistry investigations — the tridentate phosphine–quinoline–pyridine donor set offers a concrete example for studying how mixed P,N,N donors control geometry around a divalent iron centre.\u003c\/li\u003e\n\u003cli\u003eStructure–activity relationship experiments — the fluorine substituent on the aromatic backbone and the isopropyl groups on phosphorus provide defined electronic and steric handles for correlating ligand features with catalytic behaviour.\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: 2247605-87-2\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D5886\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the research-scale pack sizes listed by the manufacturer for this catalogue number\u003c\/li\u003e\n\u003cli\u003eStorage: follow the storage 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 the material in its original tightly closed container in a cool, dry, and well-ventilated place, away from heat sources, direct sunlight, and incompatible chemicals, and follow the specific storage conditions printed on the manufacturer's label and safety data sheet. Phosphine-containing metal complexes are generally handled under an inert atmosphere and protected from moisture and air where the manufacturer indicates this is required. Handle in a fume hood using appropriate personal protective equipment, including safety glasses, gloves, and a laboratory coat. Keep containers clearly labelled, avoid generating dust, and dispose of residues in accordance with applicable laboratory waste regulations. Consult the safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086782378202,"sku":"TCI2510D588626877","price":6864000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5886_65180c70-767e-4e81-bc01-b3314b0695e5.jpg?v=1792640211"},{"product_id":"tci2510e049528283","title":"TCI E0495 6780-49-0 Ethyl N-Phenylformimidate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl N-Phenylformimidate is a chemical compound widely used as a building block in organic synthesis, particularly in the development of heterocyclic compounds and complex organic molecules. This versatile reagent plays a crucial role in laboratory settings where researchers aim to create compounds with specific structural and functional properties. Its ability to participate in various chemical reactions makes it an essential tool for chemists working on synthetic pathways. The compound is commonly employed in the formation of amide bonds and cyclic nitrogen structures, which are fundamental in the synthesis of pharmaceuticals and industrial chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and reactivity under controlled conditions make it a preferred choice for synthetic chemists. Its molecular structure allows for substitution and addition reactions, offering flexibility in the design of new compounds. This reactivity, combined with its chemical stability, ensures that it remains a reliable material for use in both academic and industrial research. Its predictable behavior in different reaction environments enhances its utility in laboratory workflows, making it a go-to reagent for those seeking to optimize synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl N-Phenylformimidate is extensively used in organic chemistry research, especially in the development of pharmacological compounds and industrial chemicals. It is also a valuable tool in educational settings, where it is used to teach synthesis techniques and the application of chemical reagents. Its availability in the local market ensures that researchers and educators have consistent access to this essential compound for their work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its ability to form stable amide bonds and cyclic nitrogen structures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and industrial chemicals through its participation in substitution and addition reactions.\u003c\/li\u003e\n\u003cli\u003eEducational use in teaching synthesis techniques and the application of chemical reagents in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the creation of bioactive molecules with specific structural requirements.\u003c\/li\u003e\n\u003cli\u003eSupport for industrial chemical production where controlled reactivity and stability are essential for process optimization.\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: 6780-49-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl N-Phenylformimidate should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be stored separately from incompatible substances to avoid any potential chemical interactions. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. Regular inspection of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086867476698,"sku":"TCI2510E049528283","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086867509466,"sku":"TCI2510E049528284","price":2271000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0495_fcb6a311-5619-40eb-b8d5-af06ed539dc7.jpg?v=1792641055"},{"product_id":"tci2510e099828855","title":"TCI E0998 13124-15-7 Ethyl 3-(3,4-Dichlorophenyl)carbazate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 3-(3,4-Dichlorophenyl)carbazate is a synthetic reagent widely used in laboratory settings for its role in chemical synthesis. This compound is part of the broader category of synthetic reagents designed for C-X bond formation, particularly in substitution reactions involving halogen atoms. Its molecular structure includes a carbonyl group attached to a carbazole ring, making it a versatile intermediate in the synthesis of complex organic molecules. Due to its chemical stability and reactivity, it is a valuable tool for researchers working on organic chemistry and pharmaceutical development.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and reactivity make it a preferred choice for synthetic chemists. Its non-volatile nature simplifies handling and processing in laboratory environments, reducing the risk of evaporation or loss during reactions. Additionally, its ability to participate in substitution reactions involving carbon-halogen bonds allows for precise control over reaction pathways. These properties make it suitable for applications requiring high specificity and controlled reaction conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 3-(3,4-Dichlorophenyl)carbazate is commonly used in organic chemistry research, especially in the synthesis of complex organic compounds and drug development. Its role in creating ester and carboxylic acid derivatives makes it a key reagent in the production of pharmaceutical intermediates and specialty chemicals.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules where ester functionality is required for structural modification.\u003c\/li\u003e\n\u003cli\u003ePreparation of pharmaceutical intermediates involving halogenated aromatic rings for drug development.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions requiring stable reagents with controlled reactivity in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the development of new therapeutic agents with specific molecular structures.\u003c\/li\u003e\n\u003cli\u003eAnalytical applications where precise chemical reactivity and stability are essential for accurate results.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 13124-15-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl 3-(3,4-Dichlorophenyl)carbazate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which may affect its stability. Due to its non-volatile nature, it is less prone to evaporation but should still be handled with care to avoid contamination. Laboratory personnel should ensure proper ventilation when working with this compound and use appropriate personal protective equipment. Storage should be away from incompatible materials to ensure safety and maintain the compound's effectiveness in synthetic applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086916038874,"sku":"TCI2510E099828855","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086916071642,"sku":"TCI2510E099828856","price":6006000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0998_edf39107-cb29-4549-a205-e6293d31070c.jpg?v=1792641439"},{"product_id":"tci2510e105828941","title":"TCI E1058 60683-30-9 O-Ethyl-N,N'-diisopropylisourea","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI E1058 60683-30-9 O-Ethyl-N,N'-diisopropylisourea is a synthetic reagent widely used in laboratory settings for its role in organic synthesis. This compound is specifically designed for reactions involving the formation of C-X bonds, where X is not a halogen. Its chemical structure includes an isourea group and an ethyl group, making it a versatile reagent in the creation of complex organic molecules. It is commonly employed in substitution reactions and bond-forming processes, contributing to the development of new chemical compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's preference in laboratory applications stems from its stability under controlled conditions and its ability to act as an electron donor in specific chemical reactions. This property enhances reaction rates and improves the efficiency of synthetic processes. Its sensitivity to moisture and high temperatures necessitates careful handling, but its reactivity and effectiveness make it a valuable tool in organic chemistry. The compound's role in accelerating reactions and improving yields makes it a preferred choice for researchers working on complex synthesis projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, O-Ethyl-N,N'-diisopropylisourea is frequently used in chemical research, especially in the synthesis of organic compounds. Its application spans various experimental setups, including those requiring high reactivity and precise chemical transformations. Researchers rely on this reagent for its consistent performance and reliability in synthetic processes, making it an essential component in many laboratory workflows.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This reagent is ideal for organic synthesis due to its ability to participate in bond-forming reactions and facilitate the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eSubstitution Reactions: Its role in substitution reactions makes it suitable for modifying existing molecules by replacing functional groups with desired substituents.\u003c\/li\u003e\n\u003cli\u003eC-X Bond Formation: It is specifically used in reactions that involve the formation of C-X bonds without halogen atoms, aligning with its classification in synthetic reagents.\u003c\/li\u003e\n\u003cli\u003eResearch and Development: Its reactivity and effectiveness make it a preferred choice for R\u0026amp;D in chemical laboratories aiming to develop new compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used in analytical procedures where precise chemical transformations are required for the identification and characterization of compounds.\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: 60683-30-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and high temperatures\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity, which can affect its chemical integrity. Due to its sensitivity to high temperatures, it should be kept away from heat sources and direct sunlight. Laboratory personnel should handle the compound with appropriate personal protective equipment to ensure safety during use and storage. Proper labeling of storage containers is essential to prevent accidental exposure and ensure safe handling in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086920724698,"sku":"TCI2510E105828941","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1058-struktur.jpg?v=1791525030"},{"product_id":"tci2510e129929263","title":"TCI E1299 700371-70-6 Ethyl 2-(4-Cyanophenyl)hydrazinecarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-(4-Cyanophenyl)hydrazinecarboxylate is a synthetic reagent widely used in laboratory settings for its role in organic chemistry reactions. This compound is essential for the formation of C-X bonds, particularly in reactions involving hydrazine derivatives. Its molecular structure enables it to participate in various synthetic pathways, making it a versatile tool for chemists. It is commonly employed in the synthesis of heterocyclic compounds and complex organic molecules, contributing to the development of new chemical entities.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice in controlled laboratory environments. It exhibits stability under specific conditions, which ensures reliable performance in synthetic processes. However, it is highly sensitive to moisture and air exposure, necessitating careful handling and storage. This sensitivity, combined with its high reactivity, allows it to be an effective reagent in reactions requiring precision and speed. Its ability to participate in multiple reaction mechanisms enhances its utility across different synthetic applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 2-(4-Cyanophenyl)hydrazinecarboxylate is frequently used in organic chemistry research. It plays a crucial role in the synthesis of complex compounds and drug development. Research institutions and universities in Indonesia rely on this reagent for experimental work, particularly in the field of heterocyclic chemistry. Its availability and effectiveness make it a valuable component in academic and industrial chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its ability to form C-X bonds in controlled environments.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds as it facilitates the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry where precise reactivity and stability are required for synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eAcademic teaching and experimentation in chemistry laboratories focusing on synthetic reagent applications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production processes that require high reactivity and controlled reaction conditions.\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: 700371-70-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on the specific formulation and supplier packaging\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-(4-Cyanophenyl)hydrazinecarboxylate should be stored in a cool, dry place away from moisture and air exposure. It is recommended to use airtight containers to prevent degradation. The compound is sensitive to humidity, so maintaining a controlled environment is essential. It should be kept in a well-ventilated area to minimize exposure to airborne contaminants. Proper labeling and storage conditions ensure the reagent remains effective for its intended use. Laboratory personnel should always wear appropriate personal protective equipment when handling this compound to ensure safety and compliance with standard operating procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086946185434,"sku":"TCI2510E129929263","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086946218202,"sku":"TCI2510E129929264","price":4063000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1299_f06e5506-53e5-4c47-b008-98c5451abf20.jpg?v=1792641726"},{"product_id":"tci2510f005329740","title":"TCI F0053 109-94-4 Ethyl Formate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Formate is a chemical compound widely used in various synthetic reactions within laboratory settings. As an ester derived from formic acid and ethanol, it plays a crucial role in organic chemistry by participating in esterification and hydrolysis reactions. Its chemical stability and reactivity under specific conditions make it a versatile reagent for chemists. Ethyl Formate is commonly utilized as a building block for the synthesis of other organic compounds, contributing to the development of new materials and pharmaceuticals.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes that make Ethyl Formate a preferred choice is its distinct aroma and clear liquid form, which facilitate easy identification and handling in the lab. Its relatively low boiling point allows for efficient evaporation or distillation processes, making it ideal for applications requiring controlled temperature and pressure conditions. Additionally, its chemical properties enable it to be used in a variety of experimental setups, enhancing its utility in both research and educational environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl Formate is extensively used across multiple disciplines, including organic chemistry, pharmaceutical research, and analytical chemistry. It is a fundamental component in the teaching and research activities of educational institutions and research centers. Its reliability and consistent performance have made it a trusted reagent in both academic and industrial laboratory settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from Ethyl Formate due to its ability to participate in esterification and hydrolysis reactions, making it ideal for creating complex organic molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes Ethyl Formate as a reagent in the development of new drugs, where precise chemical reactions are essential for synthesizing active pharmaceutical ingredients.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories use Ethyl Formate for sample preparation and as a standard in chromatographic analysis due to its stable chemical properties and distinct aroma.\u003c\/li\u003e\n\u003cli\u003eEducational institutions incorporate Ethyl Formate into their curriculum to teach fundamental chemical reactions and synthesis techniques to students.\u003c\/li\u003e\n\u003cli\u003eIndustrial laboratories rely on Ethyl Formate for the production of specialty chemicals, where controlled chemical processes are necessary for quality and consistency.\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: 109-94-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities to suit different laboratory needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Clear liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl Formate should be stored in a cool, dry place away from direct sunlight and sources of heat to maintain its chemical stability. It is recommended to use sealed, airtight containers made of glass or high-density polyethylene to prevent evaporation and contamination. Due to its flammable nature, it should be kept away from open flames and potential ignition sources. In laboratory settings, proper ventilation is essential to avoid inhalation of vapors. Regular monitoring of storage conditions ensures the compound remains safe and effective for use. Always follow standard safety protocols when handling this reagent to minimize risks associated with its chemical properties.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086976397530,"sku":"TCI2510F005329740","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086976430298,"sku":"TCI2510F005329741","price":1289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0053_326abc9a-8cca-4858-ab33-00236da0ea11.jpg?v=1792642046"},{"product_id":"tci2510f015729870","title":"TCI F0157 4394-85-8 4-Formylmorpholine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Formylmorpholine is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds and their derivatives. As a building block in organic chemistry, it plays a crucial role in the development of complex molecular structures. Its unique molecular structure, featuring a morpholine ring with an aldehyde group at the fourth position, makes it highly versatile for various chemical reactions. This compound is particularly valuable in the creation of bioactive molecules, industrial chemicals, and materials science applications due to its reactivity and functional group versatility.\u003c\/p\u003e\n\u003cp\u003eThe reactivity of 4-Formylmorpholine is a key factor in its popularity among chemists. The aldehyde group enables participation in substitution, redox, and cross-linking reactions, while the morpholine ring provides structural stability. These properties allow it to be used in the synthesis of a wide range of compounds, including pharmaceuticals and functional materials. Its ability to undergo further modifications through reduction, oxidation, or bond formation makes it an essential tool in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Formylmorpholine is commonly used in organic chemistry research, especially in the development of bioactive compounds and functional materials. Its availability and chemical properties make it a preferred choice for researchers working on drug discovery, polymer synthesis, and advanced material development. The compound’s role in creating complex structures with high reactivity and stability is vital in both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactive aldehyde group and stable morpholine ring.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules for pharmaceutical research and drug discovery applications.\u003c\/li\u003e\n\u003cli\u003eSynthesis of functional materials used in polymer science and advanced material research.\u003c\/li\u003e\n\u003cli\u003ePreparation of intermediates for industrial chemical production requiring structural complexity.\u003c\/li\u003e\n\u003cli\u003eUse in redox and substitution reactions to create diverse chemical derivatives and molecular structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4394-85-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline or powder, depending on production\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\u003e4-Formylmorpholine should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can affect its reactivity. Due to its reactive nature, it should be handled in a well-ventilated laboratory setting, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong oxidizing agents. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in chemical synthesis. Proper labeling and safe storage practices are essential to prevent accidental exposure and ensure laboratory safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086982754522,"sku":"TCI2510F015729870","price":607000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086982787290,"sku":"TCI2510F015729871","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0157_5aedc1eb-9ee6-427c-99fd-93f75ea8615a.jpg?v=1792642109"},{"product_id":"tci2510f035630146","title":"TCI F0356 150760-95-5 Cyanomethyl Formate [Formylating Reagent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyanomethyl Formate (TCI F0356), with CAS number 150760-95-5, is a formylating reagent widely utilized in organic chemistry laboratories. It plays a critical role in the synthesis of complex compounds by introducing formyl groups into organic molecules. This reagent is particularly valuable in reactions that require precise functional group modifications. Its versatility makes it an essential tool for chemists working on a variety of synthetic pathways. In research settings, it supports the development of new compounds, including pharmaceuticals and industrial chemicals, by enabling controlled and efficient chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Cyanomethyl Formate make it a preferred choice for specialized reactions. It exhibits stability under certain conditions but is highly reactive toward water and heat. This reactivity is advantageous in organic synthesis, allowing for the formation of complex structures that are difficult to achieve through alternative methods. Its ability to function effectively in organic solvents and under vacuum conditions further enhances its utility. These characteristics ensure that it remains a reliable and efficient reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyanomethyl Formate is commonly used in organic chemistry research, especially in higher education institutions and research organizations. Its ability to produce compounds with high accuracy and reliability makes it a favored choice among researchers. The reagent's consistent performance across various experimental conditions supports its widespread application in both teaching and research settings. Its role in advancing chemical synthesis is well recognized in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where formyl groups are needed for functional group modification.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds requiring precise chemical transformations.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis processes involving complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the creation of bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications requiring controlled reagent behavior in specific solvents.\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: 150760-95-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per 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 heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyanomethyl Formate should be stored in a cool, dry location, away from moisture and heat to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and moisture, which can affect its reactivity. Due to its sensitivity to water, it should be kept in a controlled environment to avoid unintended chemical reactions. Proper labeling of containers is essential for safety and identification. Laboratory personnel should handle the reagent with care, using appropriate personal protective equipment to ensure safe handling. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086997074138,"sku":"TCI2510F035630146","price":2928000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086997106906,"sku":"TCI2510F035630147","price":9767000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0356_438a3312-9ef1-425e-9cae-1de87d85ca1f.jpg?v=1792642203"},{"product_id":"tci2510f051330377","title":"TCI F0513 64-18-6 Formic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eFormic acid (TCI F0513, CAS 64-18-6) is a fundamental chemical compound widely used in laboratory settings. As a key building block in organic chemistry, it plays a critical role in various synthetic processes. Its strong acidic properties make it an essential reagent for reactions requiring acidic conditions, such as esterification and hydrolysis. In the laboratory, formic acid is valued for its versatility and effectiveness in a wide range of chemical applications. It is commonly used in both qualitative and quantitative analyses, supporting research in diverse scientific fields.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of formic acid, including its volatility and reactivity, make it a preferred choice for many laboratory procedures. Its ability to dissolve in water and its low molecular weight allow for rapid reaction kinetics, enhancing the efficiency of chemical processes. Additionally, its availability in pure liquid form ensures consistent performance in experiments. These characteristics make it a reliable and essential component in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, formic acid is frequently used in research and development activities. It is a common reagent in chemical synthesis, analytical chemistry, and organic reactions. Its presence in various scientific institutions supports the advancement of chemical studies and innovation. Due to its widespread use and effectiveness, formic acid remains a staple in the laboratory supply chain across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEsterification reactions benefit from formic acid's acidic properties, enabling efficient ester formation in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eAromatic compound synthesis often utilizes formic acid as a catalyst or reagent due to its reactivity and solubility.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications rely on formic acid for pH adjustment and as a solvent in chromatographic techniques.\u003c\/li\u003e\n\u003cli\u003eHydrolysis reactions are commonly performed using formic acid to break down complex molecules under acidic conditions.\u003c\/li\u003e\n\u003cli\u003eComplex compound synthesis requires formic acid to facilitate protonation and reaction pathways in multi-step processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 64-18-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes, including liquid form\u003c\/li\u003e\n\u003cli\u003ePhysical form: Pure liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eFormic acid should be stored in a cool, dry location, away from direct sunlight and incompatible materials. It is recommended to use sealed containers made of materials resistant to corrosion, such as glass or high-density polyethylene. Due to its volatility and reactivity, proper ventilation is essential when handling the substance. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to prevent skin and eye contact. Storage areas should be clearly labeled and kept secure to prevent accidental exposure. Regular monitoring of storage conditions ensures the stability and safety of the chemical.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"300mL","offer_id":48087010148570,"sku":"TCI2510F051330377","price":505000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0513_6e8f87da-504b-4543-bb8e-c26a48919bbe.jpg?v=1792642250"},{"product_id":"tci2510f085430846","title":"TCI F0854 50978-45-5 N-Formylsaccharin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Formylsaccharin (TCI F0854, CAS 50978-45-5) is a chemical compound widely used in synthetic laboratory applications. It serves as a reagent in various chemical reactions, particularly those involving the formation of carbon-carbon bonds. This compound is essential for researchers conducting organic synthesis, as it facilitates reactions such as substitution and condensation. Its utility makes it a valuable tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eN-Formylsaccharin is known for its chemical stability under controlled conditions, yet it exhibits high reactivity when exposed to specific chemical environments. This reactivity makes it ideal for reactions requiring precision and efficiency. Its ability to participate actively in chemical processes ensures reliable results in laboratory experiments. Additionally, its availability in multiple packaging formats allows for flexibility in experimental scale, from small-scale research to larger production processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N-Formylsaccharin is commonly used in organic chemistry research, particularly in higher education institutions and research organizations. Its availability, reliability, and compatibility with various synthetic methods make it a preferred choice for chemists. Researchers rely on its consistent performance to achieve accurate and reproducible outcomes in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from N-Formylsaccharin due to its role in promoting carbon-carbon bond formation and facilitating substitution reactions.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for condensation reactions where functional groups such as amines or hydroxyls are involved, enhancing reaction efficiency and product yield.\u003c\/li\u003e\n\u003cli\u003eIn academic research settings, it supports the development of complex organic molecules, providing a reliable reagent for students and researchers.\u003c\/li\u003e\n\u003cli\u003eIts use in industrial applications allows for the production of specialized compounds used in pharmaceuticals and chemical manufacturing.\u003c\/li\u003e\n\u003cli\u003eN-Formylsaccharin is well-suited for laboratory-scale experiments, offering flexibility in both small and large-scale chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 50978-45-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-C Bond Formation\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various packaging formats for different experimental needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN-Formylsaccharin should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent moisture exposure, which could affect its reactivity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the compound is stored away from incompatible substances to avoid any potential chemical interactions. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in experiments. Proper handling and storage practices help maintain the integrity and effectiveness of N-Formylsaccharin in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087040065754,"sku":"TCI2510F085430846","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087040098522,"sku":"TCI2510F085430847","price":5124000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0854_45098023-5d1b-4202-a388-f00d511702cc.jpg?v=1792642428"},{"product_id":"tci2510g016431769","title":"TCI G0164 506-93-4 Guanidine Nitrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGuanidine Nitrate is the nitrate salt of guanidine, a high-nitrogen compound known in the laboratory both as a source of the guanidine group and as a material carrying the nitrate anion as an oxidising component. Its ionic structure combines the nitrogen-rich guanidinium cation with the nitrate anion, which is why this compound is widely studied in energetic materials research, gas generant chemistry, and heterocyclic synthesis. The material also serves as a starting substance in the preparation of guanidine derivatives and other nitrogen compounds at laboratory scale.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound attractive is its very high nitrogen content together with a distinctive oxygen balance, so that its decomposition produces a large volume of gas with minimal solid residue. This property is the basis for its study as a gas generant material in materials research. From a synthetic point of view, the nitrate salt of guanidine is a solid form that is stable at room temperature, easy to weigh out, and soluble in water as well as in certain polar solvents, making it practical for supplying the guanidine group used to build pyrimidine rings, triazines, and aminopyrimidine derivatives.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, this material is used by laboratories working on synthetic reagent chemistry and nitrogen-compound research, where a stable, easily weighed solid source of the guanidine group is preferred over handling less convenient forms. It suits academic research groups, materials laboratories, and organic synthesis units that prepare heterocyclic scaffolds and guanidine derivatives on a routine bench scale, and that require a consistent reagent grade from an established supplier.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic synthesis: supplies the guanidine group for constructing pyrimidine rings, triazines, and aminopyrimidine derivatives, with the solid salt form making stoichiometric weighing straightforward at the bench.\u003c\/li\u003e\n\u003cli\u003eEnergetic materials research: studied for its very high nitrogen content and distinctive oxygen balance, properties that are central to characterising decomposition behaviour in this field of investigation.\u003c\/li\u003e\n\u003cli\u003eGas generant chemistry: investigated because decomposition yields a large volume of gas with minimal solid residue, which is exactly the behaviour gas generant formulation studies are designed to evaluate.\u003c\/li\u003e\n\u003cli\u003ePreparation of guanidine derivatives: serves as a laboratory-scale starting material where a stable, room-temperature solid provides the guanidinium cation for onward functionalisation and derivative work.\u003c\/li\u003e\n\u003cli\u003eNitrogen compound synthesis: acts as a starting substance for other nitrogen-containing compounds, with good solubility in water and certain polar solvents simplifying solution preparation and reaction setup.\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: 506-93-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Oxidation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eProduct Code: G0164\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid at room temperature; soluble in water and certain polar solvents\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI laboratory pack sizes; please confirm the size required when ordering\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from heat sources, direct sunlight, and any incompatible materials, particularly reducing agents and combustible substances, given that the nitrate anion acts as an oxidising component. Keep the material in its original tightly sealed container or an equivalent chemically resistant vessel, clearly labelled and kept off the floor. Handle in a fume hood using standard laboratory personal protective equipment, including safety goggles, gloves, and a laboratory coat. Avoid generating dust during weighing and transfer, keep the container closed when not in use, and consult the manufacturer's safety data sheet before first use and before disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087094984922,"sku":"TCI2510G016431769","price":884000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0164_b5da2d87-b49f-4468-ad39-64f58cf45190.jpg?v=1792643007"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-c-x-non-halogen-bond-formation-synthetic-reagents.oembed?page=13","provider":"AMI Scientific","version":"1.0","type":"link"}