{"title":"Chemicals by Class › Compounds by Functional Group › Ethers","description":"\u003cp\u003eEter dari TCI: anisol tersubstitusi, alkil eter alifatik, eter vinil, dan crown ether — pelarut polar aproktik dan building blocks sintesis. Distributor resmi TCI di Indonesia: AMI Scientific.\u003c\/p\u003e","products":[{"product_id":"tci2510b561712305","title":"TCI B5617 117766-40-2 9,9-Bis(4-methoxyphenyl)-9H-fluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5617 9,9-Bis(4-methoxyphenyl)-9H-fluorene (CAS 117766-40-2) is a high-purity small molecule semiconductor building block designed for advanced materials research. This fluorene-based compound serves as a key precursor for synthesizing hole-transporting layers, host materials, and conjugated polymers in organic electronics. It is widely applied in the development of OLEDs, organic photovoltaics, perovskite solar cells, and organic field-effect transistors (OFETs).\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085891317978,"sku":"TCI2510B561712305","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085891350746,"sku":"TCI2510B561712306","price":7471000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5617.jpg?v=1768815838"},{"product_id":"tci2510b564312337","title":"TCI B5643 57234-29-4 1,3-Bis(methoxymethoxy)benzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Bis(methoxymethoxy)benzene (CAS 57234-29-4) is a non-heterocyclic building block from TCI, available in 1g and 5g packaging. This compound features MOM-protected hydroxyl groups at the 1- and 3-positions of the benzene ring, making it a versatile intermediate for selective protection strategies in multi-step organic synthesis. It is widely utilized in pharmaceutical research, functional polymer development, and the synthesis of complex phenolic compounds and bioactive molecules.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085893742810,"sku":"TCI2510B564312337","price":784000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085893775578,"sku":"TCI2510B564312338","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5643.jpg?v=1768815849"},{"product_id":"tci2510b566412364","title":"TCI B5664 26741-53-7 3,9-Bis(2,4-di-tert-butylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,9-Bis(2,4-di-tert-butylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane is an organophosphorus antioxidant and thermal stabilizer widely used in polymer formulation and research. As a phosphite-type stabilizer, it effectively prevents oxidative degradation during polymer processing and extends the service life of finished materials such as polypropylene, polyethylene, and engineering resins. Its spirocyclic structure with sterically hindered 2,4-di-tert-butylphenoxy groups provides excellent thermal stability and resistance to discoloration under high-temperature conditions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085894725850,"sku":"TCI2510B566412364","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085894758618,"sku":"TCI2510B566412365","price":2500000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510b594612721","title":"TCI B5946 101597-25-5 1,1-Bis(4-methoxyphenyl)prop-2-yn-1-ol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,1-Bis(4-methoxyphenyl)prop-2-yn-1-ol is a versatile non-heterocyclic building block featuring both a tertiary propargylic alcohol and two para-methoxyphenyl substituents, making it suitable for carbon-carbon bond-forming reactions in organic synthesis. This compound is frequently employed as a precursor in medicinal chemistry research and the development of functional organic materials. Its dual aromatic methoxy groups and terminal alkyne functionality enable diverse derivatization pathways for constructing complex molecular architectures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085911011546,"sku":"TCI2510B594612721","price":2702000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5946.jpg?v=1768815930"},{"product_id":"tci2510b601212802","title":"TCI B6012 1002355-96-5 tert-Butyl 3-(2-Ethoxy-2-oxoethylidene)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6012 is tert-Butyl 3-(2-Ethoxy-2-oxoethylidene)azetidine-1-carboxylate, an azetidine building block that carries a conjugated α,β-unsaturated ester at the 3-position together with a Boc protecting group on the ring nitrogen. The structure combines two useful elements in a single molecule: a compact four-membered heterocyclic framework and a Michael acceptor group that is ready to react. In organic synthesis laboratories, a material of this kind serves as an efficient bridge for building side-chain substituted azetidine derivatives without having to go through ring-forming steps that normally demand special conditions and give low yields.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound a preferred choice is the directed reactivity of the conjugated double bond attached to the ethyl ester. The carbonyl group withdraws electron density, so the β-carbon becomes strongly electrophilic and is ready to accept nucleophiles in conjugate addition reactions, whether from amines, thiols, malonates, or suitable organometallic reagents. The ethyl ester itself can be hydrolysed to a carboxylic acid, reduced to an alcohol, or converted into an amide, so the range of accessible derivatives is very wide. The Boc group keeps the azetidine nitrogen protected throughout these transformations and can be removed under acidic conditions when the free amine is needed.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, building blocks of this type are used in university research groups, pharmaceutical development units, and contract synthesis facilities that prepare small-molecule libraries. The azetidine motif is valued in medicinal chemistry programmes for the rigidity and reduced conformational freedom it introduces into a candidate structure. Because the material is supplied ready to use, research teams can move directly to the derivatisation step, which shortens experimental timelines and reduces dependence on multi-step in-house ring construction.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugate addition chemistry: the electron-poor β-carbon of the unsaturated ester accepts amine, thiol, malonate, and organometallic nucleophiles cleanly, giving 3-substituted azetidine products in a single controlled step.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry library synthesis: the rigid four-membered azetidine core introduces conformational restriction into candidate molecules, a design element frequently sought when optimising small-molecule leads in drug discovery programmes.\u003c\/li\u003e\n\u003cli\u003eEster functional group interconversion: the ethyl ester can be hydrolysed to the carboxylic acid, reduced to the alcohol, or converted to amides, letting one starting material serve many downstream derivative targets.\u003c\/li\u003e\n\u003cli\u003eProtecting group strategy development: the Boc group on the ring nitrogen survives a wide range of transformations and is cleanly removed under acidic conditions to liberate the free azetidine amine when required.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic scaffold assembly: the compound avoids the demanding ring-closure steps normally needed to build azetidines, letting synthetic chemists access substituted derivatives without low-yielding cyclisation sequences.\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: 1002355-96-5\u003c\/li\u003e\n\u003cli\u003eChemical name: tert-Butyl 3-(2-Ethoxy-2-oxoethylidene)azetidine-1-carboxylate\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale catalogue pack sizes; please confirm the currently listed options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep under 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 container tightly closed in a cool, dry, well-ventilated area away from heat sources, direct sunlight, and incompatible materials, following the storage conditions printed on the manufacturer's label and safety data sheet. Keep the material in its original supplier container or in a clean, chemically compatible amber glass vessel with a secure closure, and label all secondary containers clearly. Handle the compound in a fume hood using safety goggles, nitrile gloves, and a laboratory coat. As an α,β-unsaturated ester, the material is an electrophilic Michael acceptor, so avoid skin and eye contact and avoid inhaling any vapour or dust. Review the manufacturer's safety data sheet before first use, minimise exposure to moisture when transferring, and dispose of residues and contaminated consumables through the laboratory's chemical waste stream.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085914747098,"sku":"TCI2510B601212802","price":784000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085914779866,"sku":"TCI2510B601212803","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6012_734e4b18-5669-44de-92d9-e6fffef3d53a.jpg?v=1767864192"},{"product_id":"tci2510b609812912","title":"TCI B6098 2455-43-8 1,4-Bis(4-phenoxyphenoxy)benzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,4-Bis(4-phenoxyphenoxy)benzene (CAS 2455-43-8) is a non-heterocyclic aromatic building block from TCI, supplied in a 1g package. It is widely used in organic synthesis as a precursor for constructing complex polyaromatic frameworks and polyether-type compounds. Ideal for applications in materials science, polymer chemistry, and supramolecular research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085919858906,"sku":"TCI2510B609812912","price":1566000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6098.jpg?v=1768815975"},{"product_id":"tci2510b610712926","title":"TCI B6107 162558-25-0 (S)-3-(tert-Butoxycarbonylamino)-2-[(9H-fluoren-9-ylmethoxy)carbonylamino]propionic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis compound is a doubly protected amino acid derivative featuring Fmoc and Boc orthogonal protecting groups, widely used as a versatile building block in solid-phase peptide synthesis (SPPS). It enables selective deprotection and stepwise modification of diaminopropionic acid residues in complex peptide chains. Common applications include the development of modified peptides, bioactive peptidomimetics, and molecular probes for biochemical and medicinal chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085920383194,"sku":"TCI2510B610712926","price":2197000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085920415962,"sku":"TCI2510B610712927","price":7572000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6107.jpg?v=1768815983"},{"product_id":"tci2510b615012976","title":"TCI B6150 74774-53-1 1,6-Bis(4-carboxyphenoxy)hexane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,6-Bis(4-carboxyphenoxy)hexane (CAS 74774-53-1) is a non-heterocyclic building block featuring two aromatic carboxylic acid groups bridged by a flexible hexane chain via ether linkages, making it a versatile dicarboxylic monomer. This compound is widely employed in the synthesis of polyesters, polyamides, and other functional polymer materials, as well as in the development of liquid crystals and metal-organic frameworks (MOFs). It is available in 1g and 5g packaging options, suitable for research and development purposes in organic and materials chemistry laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085922283738,"sku":"TCI2510B615012976","price":2500000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085922316506,"sku":"TCI2510B615012977","price":8682000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6150_497df2c8-8e91-4a34-a7b5-75e5bb86b7f1.jpg?v=1767864718"},{"product_id":"tci2510b616913003","title":"TCI B6169 1352745-18-6 [1,3-Bis(ethoxycarbonyl)-2,4,5-trimethylcyclopentadien-1-yl]rhodium(III) Dichloride Dimer","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[1,3-Bis(ethoxycarbonyl)-2,4,5-trimethylcyclopentadien-1-yl]rhodium(III) Dichloride Dimer is a dimeric rhodium(III) catalyst specifically utilized in C–H bond activation reactions, enabling direct functionalization of inert carbon–hydrogen bonds without substrate pre-functionalization. This organometallic complex, featuring a substituted cyclopentadienyl ligand, is widely employed in oxidative annulation and directing-group-assisted cross-coupling methodologies. Its high reactivity and selectivity under mild conditions make it a preferred catalyst for the synthesis of fused heterocycles and the construction of C–C and C–heteroatom bonds in synthetic organic and medicinal chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085923463386,"sku":"TCI2510B616913003","price":10322000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6169.jpg?v=1767093258"},{"product_id":"tci2510b622313051","title":"TCI B6223 182121-12-6 9,9-Bis(methoxymethyl)-9H-fluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9,9-Bis(methoxymethyl)-9H-fluorene (CAS 182121-12-6, TCI B6223) is a non-heterocyclic building block primarily used as a versatile precursor in organic synthesis for constructing substituted fluorene frameworks. It is widely applied in the development of conjugated polymers, electroluminescent materials for OLED devices, and organometallic chemistry. Its dual methoxymethyl groups at the 9-position offer excellent reactivity for further functionalization in advanced material science and sensor research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085925200090,"sku":"TCI2510B622313051","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085925232858,"sku":"TCI2510B622313052","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6223.jpg?v=1768816008"},{"product_id":"tci2510b637613248","title":"TCI B6376 539-30-0 (Ethoxymethyl)benzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6376, (ethoxymethyl)benzene (CAS 539-30-0), also known as benzyl ethyl ether, is a simple aromatic ether that serves as a valuable model substrate in synthetic methodology research. Its benzylic C–H bonds are comparatively weak and readily abstracted, making the compound a common benchmark in C–H functionalisation, selective oxidation, and photoredox catalysis studies. The benzyl–oxygen bond can also be cleaved by hydrogenolysis, so the compound frequently appears in discussions of benzyl protecting-group strategy. AMI Scientific supplies this TCI building block in 1 g and 5 g pack sizes for research and advanced teaching laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085936767194,"sku":"TCI2510B637613248","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085936799962,"sku":"TCI2510B637613249","price":5653000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6376.jpg?v=1768816046"},{"product_id":"tci2510b654813475","title":"TCI B6548 33171-05-0 Bisdemethoxycurcumin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBisdemethoxycurcumin (CAS 33171-05-0) is one of the three principal curcuminoids found in turmeric rhizome, differing from curcumin by the absence of methoxy groups on both aromatic rings. It is commonly used as a reference compound for curcuminoid profiling by HPLC or TLC, and for in vitro bioactivity studies where a single, defined curcuminoid is preferred over a crude extract. Curcuminoids are light sensitive and degrade under alkaline conditions, so the material should be stored cool, dry, and protected from light, with working solutions prepared fresh. AMI Scientific supplies it in a 1 g pack size for research and experimental use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMohammadi et al. (2018). Inhibition of amyloid fibrillation of lysozyme by bisdemethoxycurcumin and diacetylbisdemethoxycurcumin. \u003cem\u003eBiophysical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bpc.2018.02.005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bpc.2018.02.005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLappichetpaiboon (2025). Anticandidal effects of bisdemethoxycurcumin \u0026amp; melatonin with dual light emitting diode in photodynamic therapy. \u003cem\u003ePhotodiagnosis and Photodynamic Therapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.pdpdt.2025.104797\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.pdpdt.2025.104797\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJayaprakasha et al. (2006). Antioxidant activities of curcumin, demethoxycurcumin and bisdemethoxycurcumin. \u003cem\u003eFood Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.foodchem.2005.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.foodchem.2005.06.037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085946630362,"sku":"TCI2510B654813475","price":2953000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6548.jpg?v=1767093878"},{"product_id":"tci2510b656313493","title":"TCI B6563 125401-75-4 2,6-Bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6563 is 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoic acid, the free-acid form of a symmetric pyrimidinyloxy-benzoate structure bearing two methoxylated pyrimidine rings. The free carboxylic acid group gives it distinct acid–base and solubility behaviour compared with its salt form, and provides a ready handle for conversion into esters, amides, or alternative salts. Compounds of this class are studied in agricultural chemistry in connection with acetolactate synthase inhibition in plants. AMI Scientific supplies this TCI product in a 5 g pack; please consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085947384026,"sku":"TCI2510B656313493","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6563.jpg?v=1768816073"},{"product_id":"tci2510b666813627","title":"TCI B6668 1410809-16-3 tert-Butyl 4-[4-(1-Hydroxyethyl)-2-methoxy-5-nitrophenoxy]butanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6668, tert-Butyl 4-[4-(1-Hydroxyethyl)-2-methoxy-5-nitrophenoxy]butanoate (CAS 1410809-16-3), is a functionalized nitrobenzyl-type reagent designed for photolabile protecting group chemistry. Its secondary benzylic alcohol provides an attachment point for caging a target molecule, while the tert-butyl protected butanoate arm acts as a linker toward peptides, surfaces, or carrier molecules. This dual functionality supports caged compound synthesis, light-triggered release studies, and patterned surface fabrication. AMI Scientific supplies this TCI reagent in a 1 g pack size for laboratory-scale synthesis and route optimization.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSmith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-6-heptenoate. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m30\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m30\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSmith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-7-oxo-heptanoate. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m32\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m32\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSmith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-7-hydroxy-heptanoate. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m31\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m31\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085952725210,"sku":"TCI2510B666813627","price":7698000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6668.jpg?v=1767094102"},{"product_id":"tci2510b666913628","title":"TCI B6669 1410809-15-2 tert-Butyl 4-(4-Acetyl-2-methoxy-5-nitrophenoxy)butanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6669, tert-Butyl 4-(4-Acetyl-2-methoxy-5-nitrophenoxy)butanoate (CAS 1410809-15-2), is the ketone counterpart within the same photolabile protecting group series, carrying acetyl, methoxy, and nitro substituents on the aromatic ring. The benzylic acetyl group offers a clear entry point for reduction to the corresponding secondary benzylic alcohol used in caging chemistry. Its tert-butyl protected butanoate arm serves as a linker toward peptides, probes, or functionalized surfaces. AMI Scientific provides this TCI reagent in a 1 g pack size for laboratory-scale synthesis and method development.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSmith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-6-heptenoate. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m30\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m30\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSmith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-7-oxo-heptanoate. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m32\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m32\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSmith (1997). tert-Butyl-3-methoxy-5,5-dimethyl-7-hydroxy-heptanoate. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m31\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m31\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085952954586,"sku":"TCI2510B666913628","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6669.jpg?v=1767094106"},{"product_id":"tci2510b672513651","title":"TCI B6725 7323-63-9 1,4-Di-tert-butyl-2,5-dimethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6725 1,4-Di-tert-butyl-2,5-dimethoxybenzene (CAS 7323-63-9) is a symmetrically substituted aromatic compound bearing two methoxy and two bulky tert-butyl groups. The electron-rich ring together with steric shielding produces oxidised species that are comparatively persistent, which is why the compound features in organic redox flow battery research. It also serves as a useful model substrate for electrochemical studies and as a precursor toward substituted quinone derivatives. AMI Scientific offers 25 g and 100 g pack sizes to cover both exploratory studies and larger electrolyte preparation work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2010). A Comparative Study of 3,5-di-tert-butyl-1,2-dimethoxybezene and 2,5-di-tert-butyl-1,4-dimethoxybenzene for Overcharge Protection of Lithium-Ion Batteries. \u003cem\u003eECS Meeting Abstracts\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1149\/ma2010-02\/5\/330\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1149\/ma2010-02\/5\/330\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKrossing et al. (2008). Dimeric Di(tert-butyl)haloalanes and a Monomeric Di(tert-butyl)phosphino-di(tert-butyl)alane. \u003cem\u003eZeitschrift für Naturforschung B\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1515\/znb-2008-0905\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1515\/znb-2008-0905\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eChen et al. (2007). Degradation pathway of 2,5-di-tert-butyl-1,4-dimethoxybenzene at high potential. \u003cem\u003eElectrochimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.electacta.2007.06.073\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.electacta.2007.06.073\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085953872090,"sku":"TCI2510B672513651","price":2500000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085953904858,"sku":"TCI2510B672513652","price":7445000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6725.jpg?v=1768816095"},{"product_id":"tci2510b679313707","title":"TCI B6793 2373-89-9 4,4'-Dimethoxychalcone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6793 (CAS 2373-89-9) is 4,4'-dimethoxychalcone, a symmetrically methoxy-substituted member of the chalcone family. Its conjugated enone linkage makes it a versatile Michael acceptor and a classic precursor to pyrazolines, isoxazolines, and related heterocycles. The chalcone scaffold is also widely studied in natural product and cell biology research. AMI Scientific supplies this TCI reagent in 5 g and 25 g pack sizes for Indonesian laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAribi et al. (2016). The anodic reactivity of 4,4′-dimethoxychalcone: a synthetic and mechanistic investigation. \u003cem\u003eResearch on Chemical Intermediates\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s11164-016-2607-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s11164-016-2607-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBae et al. (2023). The Effects of 2′-Hydroxy-3,6′-Dimethoxychalcone on Melanogenesis and Inflammation. \u003cem\u003eInternational Journal of Molecular Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/ijms241210393\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/ijms241210393\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSepvianti et al. (2019). Antibacterial Activity of 2 '-hydroxy-4', 6 'dimethoxychalcone. \u003cem\u003eJournal of Health\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.30590\/vol6-no1-p37-39\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.30590\/vol6-no1-p37-39\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":48085956165850,"sku":"TCI2510B679313707","price":2273000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085956198618,"sku":"TCI2510B679313708","price":7926000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6793.jpg?v=1767094233"},{"product_id":"tci2510b691013797","title":"TCI B6910 586400-06-8 Ethyl 4-[[[Benzyl[4-(ethoxycarbonyl)phenyl]amino]methylene]amino]benzoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6910 (CAS 586400-06-8) is a formamidine-type aromatic compound bearing two ethyl benzoate groups, classified by TCI as a polymer additive. Its extended conjugated aromatic system makes it a compound of interest in studies of polymer performance and light-related stability. It is typically incorporated into polymer matrices or coating formulations at the research scale to evaluate compatibility and effect. TCI supplies it in 25 g and 100 g pack sizes; store the material cool, dry and away from direct light, and consult the Safety Data Sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085960163546,"sku":"TCI2510B691013797","price":1844000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085960196314,"sku":"TCI2510B691013798","price":4821000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510c020514197","title":"TCI C0205 2921-14-4 Carboxymethoxylamine Hemihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarboxymethoxylamine Hemihydrochloride (TCI C0205, CAS 2921-14-4), also known as aminooxyacetic acid hemihydrochloride, is a stable salt form of a reactive aminooxy compound. Its aminooxy group readily condenses with aldehydes and ketones, making it useful for carbonyl derivatisation and oxime-based bioconjugation. In biochemistry it is widely applied as an inhibitor of pyridoxal phosphate–dependent enzymes such as transaminases. AMI Scientific supplies this TCI reagent in 25 g and 500 g packs for biochemistry, pharmaceutical, and analytical laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085978448090,"sku":"TCI2510C020514197","price":2576000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085978480858,"sku":"TCI2510C020514198","price":25766000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0205.jpg?v=1767094865"},{"product_id":"tci2510c057814772","title":"TCI C0578 25395-22-6 (2-Carbamoylphenoxy)acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(2-Carbamoylphenoxy)acetic Acid (TCI C0578, CAS 25395-22-6) is an aromatic building block combining a phenoxyacetic acid chain with an ortho-positioned carbamoyl group. The free carboxylic acid is readily activated toward esters, amides, and other acyl derivatives. The close proximity of the amide and oxyacetate groups also makes it a useful precursor for intramolecular cyclisation toward heterocyclic systems. AMI Scientific supplies this TCI product in a 25 g pack for organic synthesis and medicinal chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086011281626,"sku":"TCI2510C057814772","price":1868000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0578.jpg?v=1767095516"},{"product_id":"tci2510c068314917","title":"TCI C0683 22509-74-6 N-Ethoxycarbonylphthalimide [for Peptide Synthesis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0683 N-Ethoxycarbonylphthalimide (CAS 22509-74-6) is a reagent for introducing the phthaloyl protecting group onto primary amines under mild conditions. It is widely used in peptide synthesis and amino acid chemistry, where selective amino protection is essential before coupling steps. Compared with harsher classical methods, it is better suited to substrates bearing sensitive functional groups. This TCI grade is designated for peptide synthesis and is offered in 25 g, 100 g, and 500 g pack sizes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086020391130,"sku":"TCI2510C068314917","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086020423898,"sku":"TCI2510C068314918","price":3207000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086020456666,"sku":"TCI2510C068314919","price":9464000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0683.jpg?v=1767095636"},{"product_id":"tci2510c085815153","title":"TCI C0858 294-93-9 12-Crown 4-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0858 12-Crown 4-Ether (CAS 294-93-9) is the smallest of the commonly used crown ether series, featuring a macrocyclic cavity lined with four oxygen donor atoms. Its cavity dimensions give it a favorable fit for small cations, particularly lithium, which makes it valuable for ion-recognition studies and ion-selective electrode research. As a phase-transfer catalyst, it complexes the cation and leaves the counter-anion more reactive, accelerating substitution and elimination reactions in non-polar media. Supplied in 1mL and 5mL laboratory volumes, it should be stored cool, dry, and tightly sealed, and handled with appropriate personal protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eJunk, (2001). STRUCTURAL ASPECTS OF OXONIUM ION\/CROWN ETHER COMPLEXES. \u003cem\u003eReviews in Inorganic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1515\/revic.2001.21.1-2.93\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1515\/revic.2001.21.1-2.93\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLiu (2007). Ether and crown ether-containing cationic 99mTc complexes useful as radiopharmaceuticals for heart imaging. \u003cem\u003eDalton Transactions\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/b618406e\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/b618406e\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRogers et al. (1992). Crown ether complexes of lead(II) nitrate. Crystal structures of the 12-crown-4, 15-crown-5, benzo-15-crown-5 and 18-crown-6 complexes. \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0020-1693(00)80755-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0020-1693(00)80755-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1mL","offer_id":48086033498330,"sku":"TCI2510C085815153","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5mL","offer_id":48086033531098,"sku":"TCI2510C085815154","price":3711000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0858.jpg?v=1768204568"},{"product_id":"tci2510c085915155","title":"TCI C0859 33100-27-5 15-Crown 5-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0859 15-Crown 5-Ether (CAS 33100-27-5) is a macrocyclic polyether whose five oxygen donor atoms coordinate alkali metal cations, with a cavity size commonly associated with sodium ion binding. It is widely used as a phase-transfer catalyst, solubilizing inorganic salts into organic media and enhancing the reactivity of the accompanying anion. Researchers also employ it as an ionophore in ion-selective membrane formulations and as a host molecule in supramolecular host–guest studies. Offered in 5mL and 25mL packs, the liquid reagent should be kept tightly closed, cool, and dry, and handled with suitable protective equipment in a fume hood.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKijima et al. (2003). Enzymatic Hydrolysis of 4′-(1-Chloro-2-Acetoxyethyl)-Benzo-15-Crown-5-Ether and 4′-Acetoxyethyl-Benzo-15-Crown-5-Ether; a Facile Synthesis of the Optically Active Chlorohydrin Analogue Incorporating Crown Ether. \u003cem\u003eJournal of Chemical Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3184\/030823403103174362\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3184\/030823403103174362\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGROMOV et al. (1996). ChemInform Abstract: Crown Ether Styryl Dyes. Part 14. Synthesis, Luminescence and Complex Formation of trans‐Isomers of Chromogenic 15‐Crown‐5‐ether.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199608202\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199608202\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShubert et al. (2009). Jet-Cooled Electronic and Vibrational Spectroscopy of Crown Ethers: Benzo-15-Crown-5 Ether and 4′-Amino-Benzo-15-Crown-5 Ether. \u003cem\u003eThe Journal of Physical Chemistry A\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jp904231d\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jp904231d\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086033563866,"sku":"TCI2510C085915155","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086033596634,"sku":"TCI2510C085915156","price":4065000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0859.jpg?v=1768204569"},{"product_id":"tci2510c086015157","title":"TCI C0860 17455-13-9 18-Crown 6-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0860 18-Crown 6-Ether (CAS 17455-13-9) is the most widely used member of the crown ether family, with six oxygen donors forming a cavity well matched to the potassium ion. By sequestering K⁺, it liberates the counter-anion and markedly enhances its nucleophilicity and basicity, a principle exploited in phase-transfer catalysis and anion activation. It also serves as a reference ligand in ion-recognition studies, as an ionophore in ion-selective membranes, and as a recognition unit in supramolecular architectures. Supplied in 5g, 25g, and 100g packs, this hygroscopic solid must be stored tightly sealed in a cool, dry place and handled with gloves and eye protection.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMaruyama et al. (2007). Probing cations recognized by a crown ether with the 3D-RISM theory. II. 18-crown-6 ether. \u003cem\u003eCondensed Matter Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5488\/cmp.10.3.315\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5488\/cmp.10.3.315\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWagner et al. (1995). [Cs+(15-Crown-5)(18-Crown-6)e-]6 · (18-Crown-6): Properties of the First Mixed Crown Ether Electride. \u003cem\u003eJournal of Solid State Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/jssc.1995.1278\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/jssc.1995.1278\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBotezatu et al. (2020). Thienyl-phenyl Ethylenes with Crown Ether Fragments and Their Photocyclization Products: UV-Vis, NMR, Redox Response for Complexation. A 18-Crown-6 Ether Restricted with a Tricyclic Aromatic Moiety. \u003cem\u003eMacroheterocycles\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.6060\/mhc200496f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.6060\/mhc200496f\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086033629402,"sku":"TCI2510C086015157","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086033662170,"sku":"TCI2510C086015158","price":1995000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086033694938,"sku":"TCI2510C086015159","price":6008000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0860.jpg?v=1768204570"},{"product_id":"tci2510c088515191","title":"TCI C0885 2182-55-0 Cyclohexyl Vinyl Ether (stabilized with KOH)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0885 Cyclohexyl Vinyl Ether (CAS 2182-55-0), stabilized with KOH, is a vinyl ether monomer used mainly in cationic polymerisation and functional copolymer research. The alkaline stabiliser suppresses acid-initiated premature polymerisation, helping preserve monomer quality during storage. Beyond polymer applications, vinyl ethers also serve as hydroxyl-protecting reagents and as electron-rich components in cycloaddition chemistry. AMI Scientific supplies this TCI product in 25 mL and 500 mL packs; keep it cool, dark, and strictly away from acidic materials.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhou et al. (2004). Synthesis of Poly(cyclohexyl vinyl ether-b-isobutylene-b-cyclohexyl vinyl ether) Triblock Copolymer by Living Cationic Sequential Copolymerization. \u003cem\u003ePolymer Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s00289-004-0306-9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s00289-004-0306-9\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhou et al. (2005). Syntheses and Characterization of Poly(cyclohexyl vinyl ether-stat-vinyl alcohol)-b-polyisobutylene-b-poly(cyclohexyl vinyl ether-stat-vinyl alcohol) Triblock Copolymers and Their Application as Coatings To Deliver Paclitaxel from Coronary Stents. \u003cem\u003eMacromolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ma0508449\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ma0508449\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eCramail et al. (1994). Living cationic polymerization of cyclohexyl vinyl ether. \u003cem\u003eMacromolecular Chemistry and Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/macp.1994.021950120\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/macp.1994.021950120\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086035497178,"sku":"TCI2510C088515191","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086035529946,"sku":"TCI2510C088515192","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0885.jpg?v=1768816360"},{"product_id":"tci2510c102915411","title":"TCI C1029 40912-11-6 Methyl 3-(4-Methoxycarbonylphenyl)propionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1029 Methyl 3-(4-Methoxycarbonylphenyl)propionate (CAS 40912-11-6) is a bifunctional diester building block combining an aromatic ester with a flexible propionate ester chain. The two distinct ester environments allow selective hydrolysis, reduction, or transesterification when designing multi-step routes and molecular linkers. Its para-substituted framework also makes it of interest as a precursor for linear polyester-type materials. AMI Scientific offers this TCI product in 5 g and 25 g research packs; store it dry and tightly closed and consult the official TCI Safety Data Sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086044279002,"sku":"TCI2510C102915411","price":2197000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086044311770,"sku":"TCI2510C102915412","price":7345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1029.jpg?v=1767096212"},{"product_id":"tci2510c116315603","title":"TCI C1163 83482-57-9 4-(4-alpha-Cumylphenoxy)phthalonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(4-α-Cumylphenoxy)phthalonitrile (TCI C1163, CAS 83482-57-9) is a phthalocyanine precursor carrying a bulky cumylphenoxy substituent. Cyclotetramerisation of four such units gives peripherally substituted phthalocyanines whose bulky groups suppress aggregation and improve solubility in organic solvents. Such soluble macrocycles are valuable for near-infrared dyes, photosensitizers, and solution-processed organic semiconductor films. Available in 1 g and 5 g research packs, the solid should be weighed in a ventilated area and stored sealed, cool, dry, and protected from light.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086053650650,"sku":"TCI2510C116315603","price":3005000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086053683418,"sku":"TCI2510C116315604","price":10019000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1163.jpg?v=1768816439"},{"product_id":"tci2510c117615628","title":"TCI C1176 943-03-3 2-Cyano-6-methoxybenzothiazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1176 2-Cyano-6-methoxybenzothiazole (CAS 943-03-3) is a heterocyclic building block that combines a benzothiazole core with a reactive 2-cyano group and a 6-methoxy substituent. It is best known as a key precursor in luciferin chemistry and as a partner for metal-free bioconjugation with 1,2-aminothiol motifs such as N-terminal cysteine. These properties make it valuable for molecular imaging probes, reporter design, and general heterocyclic synthesis. Supplied in a 1 g pack, it should be handled in a fume hood and stored in a cool, dry, light-protected place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086054633690,"sku":"TCI2510C117615628","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1176.jpg?v=1767096476"},{"product_id":"tci2510c117815630","title":"TCI C1178 2032-34-0 3,3-Diethoxypropionitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1178 3,3-Diethoxypropionitrile (CAS 2032-34-0) is a bifunctional liquid building block bearing both a nitrile group and a diethyl acetal, effectively serving as a protected aldehyde equivalent. The acetal remains stable under basic and nucleophilic conditions yet can be hydrolysed under acidic conditions to reveal the free aldehyde. The nitrile can be reduced to an amine, hydrolysed to an acid or amide, or used in heterocycle formation, giving chemists flexible routes for chain elongation. Supplied in a 10 mL pack, it should be dispensed in a fume hood and stored tightly closed away from acids, moisture, and heat.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mL","offer_id":48086054699226,"sku":"TCI2510C117815630","price":2071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1178.jpg?v=1769144505"},{"product_id":"tci2510c171316376","title":"TCI C1713 56683-55-7 4'-Carboxybenzo-15-crown 5-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4'-Carboxybenzo-15-crown 5-Ether is a synthetic reagent widely used in laboratory settings for its ability to form stable complexes with metal ions. This compound belongs to the chelation and complexation compound category, making it essential in organic synthesis and analytical chemistry. Its unique structure allows it to selectively bind to ions such as sodium, potassium, and magnesium, making it a valuable tool in various chemical reactions. The compound is commonly used in research and educational institutions in Indonesia for experiments requiring precise control over metal ion interactions. Its solubility in organic solvents further enhances its versatility in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086085533914,"sku":"TCI2510C171316376","price":8556000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1713.jpg?v=1768197160"},{"product_id":"tci2510c171416377","title":"TCI C1714 60835-75-8 4'-Carboxybenzo-18-crown 6-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4'-Carboxybenzo-18-crown 6-Ether is a synthetic reagent widely used in chemical synthesis and complexation studies. Its unique molecular structure allows it to form stable complexes with metal ions, particularly alkali metals such as sodium and potassium. This compound is commonly utilized in laboratory settings for applications involving metal ion coordination and reaction facilitation. The compound is available in two packaging options: 100mg and 1g, making it suitable for both small-scale experiments and larger research projects. It is a solid powder that dissolves well in organic solvents, ensuring ease of handling and use. Due to its stability and effectiveness, it is a preferred choice in Indonesian laboratories for various chemical research and analytical applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086085566682,"sku":"TCI2510C171416377","price":3484000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086085599450,"sku":"TCI2510C171416378","price":26726000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1714.jpg?v=1768197164"},{"product_id":"tci2510c173616402","title":"TCI C1736 33089-37-1 24-Crown 8-Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e24-Crown 8-Ether is a synthetic reagent widely used in laboratory settings for its ability to form stable complexes with metal ions. This compound, with its unique molecular structure containing eight oxygen atoms, is highly effective in chelation reactions. Its stability and strong binding capacity make it a preferred choice in various chemical applications, including organic synthesis and metal ion analysis. In Indonesian laboratories, this reagent is essential for research and educational purposes, supporting both academic and industrial chemical studies. Its availability in standard packaging ensures ease of use and accessibility for researchers and students.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWilley et al. (2000). Crown ether complexation of p-block metal halides: synthesis and structural characterisation of [InI2(dibenzo-24-crown-8)(H2O)][InI4], [(SnBr4)2(dibenzo-24-crown-8)]·MeCN, [(SbCl3)2(dibenzo-24-crown-8)]·MeCN, [(BiCl3)2(dibenzo-24-crown-8)]·MeCN and [(SbBr3)2(dibenzo-24-crown-8)]. \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0020-1693(00)00029-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0020-1693(00)00029-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eFrańska et al. (2018). Gas-phase relative stabilities of Tl + -crown ether complexes and Rb + -crown ether complexes. \u003cem\u003eEuropean Journal of Mass Spectrometry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1177\/1469066717752794\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1177\/1469066717752794\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTunca (1996). Synthesis of polymers containing crown ether and ferrocene units. \u003cem\u003ePolymer\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0032-3861(96)00628-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0032-3861(96)00628-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086086451418,"sku":"TCI2510C173616402","price":11080000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1736.jpg?v=1768204621"},{"product_id":"tci2510c292517822","title":"TCI C2925 21642-98-8 3-Cyano-4-methoxy-2-pyridone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Cyano-4-methoxy-2-pyridone is a versatile chemical compound widely used in laboratory settings as a building block for the synthesis of heterocyclic compounds. This compound plays a crucial role in organic chemistry by enabling the formation of pyridine-based structures, which are fundamental in many pharmaceutical and industrial applications. Its unique molecular structure allows it to participate in various types of chemical reactions, making it an essential tool for researchers aiming to develop new compounds with specific functional properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and structural complexity make it a preferred choice for a range of synthetic processes. It is particularly useful in substitution reactions, condensation reactions, and cyclic reactions, where its ability to form stable intermediates enhances the efficiency of chemical transformations. Additionally, its stability under certain conditions ensures that it can be easily manipulated and stored, contributing to its popularity among chemists. This stability also supports its use in long-term research projects requiring consistent performance.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Cyano-4-methoxy-2-pyridone is commonly used in chemical, pharmaceutical, and material science research. It is a key component in the development of new compounds with potential applications in medicine and industry. Its availability in the local market facilitates access for researchers, enabling them to conduct experiments and contribute to scientific advancements in various fields.\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 pyridine-based structures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals as a building block for drug molecule design and modification.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the creation of novel polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eChemical reaction studies involving substitution and condensation processes due to its reactivity.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesian universities and research institutions for educational and experimental purposes.\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: 21642-98-8\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 appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a tightly sealed container to avoid exposure to moisture and air, which could affect its reactivity. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn when working with it. Avoid contact with incompatible substances to ensure safe laboratory practices. Proper labeling of containers is essential for safe handling and storage. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086203269338,"sku":"TCI2510C292517822","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086203302106,"sku":"TCI2510C292517823","price":5326000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2925.jpg?v=1769144341"},{"product_id":"tci2510c314718111","title":"TCI C3147 86060-82-4 Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nepsilon-benzyloxycarbonyl-L-lysine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C3147, with the CAS number 86060-82-4, is a specialized chemical compound used in peptide synthesis. This compound, known as Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-Nepsilon-benzyloxycarbonyl-L-lysine, plays a crucial role in the formation of peptide bonds during chemical and biochemical research. It is commonly utilized in laboratories that focus on the development of complex molecular structures, particularly in the field of peptide chemistry. Its unique structure allows for precise and controlled synthesis of peptides, making it an essential tool for researchers working on drug development and molecular biology.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and solubility in organic solvents, which simplifies handling and processing in laboratory settings. Its dual protecting groups—N-alpha and N-epsilon—enable selective peptide bond formation, ensuring accuracy in complex synthetic pathways. These properties make it a preferred choice for scientists aiming to achieve high precision in their synthetic processes. The compound’s ability to withstand various reaction conditions also enhances its versatility in different experimental setups.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in biochemistry, pharmacology, and biotechnology research. It supports the development of new drugs, the analysis of biomolecules, and the study of molecular interactions. Its application is particularly relevant in academic and research institutions that focus on advanced chemical and biological studies. The compound’s reliability and performance make it a key component in the toolkit of Indonesian scientists working on cutting-edge research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing complex peptides due to its dual protecting groups, which allow for controlled and selective bond formation.\u003c\/li\u003e\n\u003cli\u003eDrug Development: Its role in creating peptide-based compounds makes it essential for pharmaceutical research aimed at developing new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: It supports studies involving molecular interactions and structural analysis, contributing to advancements in biotechnology and molecular biology.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: The compound’s stability and solubility make it suitable for use in analytical techniques that require precise chemical handling.\u003c\/li\u003e\n\u003cli\u003eMolecular Modeling: Its well-defined structure aids in the study of molecular behavior, supporting computational and experimental research in chemical biology.\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: 86060-82-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\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 and moisture. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential risks associated with handling. The compound is stable under normal laboratory conditions, making it suitable for long-term storage when properly preserved. Always follow standard laboratory safety protocols when working with this material to ensure a safe and efficient research environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086215983322,"sku":"TCI2510C314718111","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086216016090,"sku":"TCI2510C314718112","price":4695000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3147.jpg?v=1768204735"},{"product_id":"tci2510c315318116","title":"TCI C3153 58743-78-5 4-Cyano-4'-ethoxybiphenyl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Cyano-4'-ethoxybiphenyl is a chemical compound widely used in materials science, particularly in the study and development of liquid crystal (LC) materials. This compound plays a crucial role in laboratories where researchers are working on advanced electronic materials. Its unique molecular structure, consisting of two benzene rings connected by an ethoxy and a cyano group, makes it an essential component in the creation of liquid crystal displays. Due to its specific optical and electronic properties, it is a key material in the production of high-performance electronic devices.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its high polarity and ability to form stable liquid crystal structures. These properties make it ideal for applications requiring precise control over the alignment and behavior of liquid crystal molecules. Its good solubility in organic solvents further enhances its usability in synthesis and processing procedures. The complex molecular structure also contributes to its thermal and chemical stability, ensuring reliable performance in various experimental conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Cyano-4'-ethoxybiphenyl is commonly used in research related to electronic and optical materials. It is a vital component in the development of next-generation display technologies and other advanced applications. Its availability through suppliers like AMI Scientific supports ongoing scientific inquiry and innovation in the field of materials science.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLiquid Crystal Display (LCD) Research: This compound is used to develop and test new liquid crystal materials for use in LCD and OLED technologies, offering precise optical and electrical properties.\u003c\/li\u003e\n\u003cli\u003eElectronic Material Development: It serves as a base material for synthesizing new electronic materials with tailored properties for advanced applications.\u003c\/li\u003e\n\u003cli\u003eOptical Material Testing: Its unique optical characteristics make it suitable for testing and developing materials used in optical devices and sensors.\u003c\/li\u003e\n\u003cli\u003eThermal Stability Studies: The compound's chemical and thermal stability allows it to be used in experiments assessing the performance of materials under varying temperature conditions.\u003c\/li\u003e\n\u003cli\u003eMaterial Characterization: It is frequently used in analytical techniques to study molecular structure, phase behavior, and other material properties in laboratory settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 58743-78-5\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Electronic Materials \u0026gt; Liquid Crystal (LC) Materials\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and maintain its chemical integrity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to avoid skin contact or inhalation. In laboratory settings, it should be kept in a well-ventilated area to minimize exposure. Proper labeling of storage containers is essential for safety and traceability. Regular inspection of storage conditions ensures the material remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086216147162,"sku":"TCI2510C315318116","price":2095000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3153.jpg?v=1769144316"},{"product_id":"tci2510c397819094","title":"TCI C3978 6379-73-3 Carvacrol Methyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCarvacrol Methyl Ether (TCI C3978, CAS 6379-73-3) is a chemical compound widely used in laboratory settings for its role in organic synthesis. It serves as a key building block in the development of complex molecular structures, making it essential for researchers working in chemical and pharmaceutical fields. This compound is particularly valuable for its ability to participate in various chemical reactions without significant degradation, ensuring reliable results in experimental processes. Its versatility allows it to be used in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eCarvacrol Methyl Ether is known for its stable molecular structure and good reactivity, which makes it a preferred choice for synthetic chemists. It is volatile and readily soluble in organic solvents such as ethyl acetate and ethanol, facilitating its use in substitution and oxidation reactions. These properties contribute to its effectiveness in creating bioactive compounds, including antifungal, antiviral, and antiseptic agents. Its chemical stability and reactivity ensure consistent performance in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Carvacrol Methyl Ether is commonly used in research related to bioactive compounds and pharmaceutical development. Its role in synthesizing compounds with biological activity makes it a valuable resource for scientists working on drug discovery and natural product chemistry. The compound's availability and reliability make it an important tool for both academic and industrial research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where Carvacrol Methyl Ether is used to build complex molecular structures due to its reactivity and stability.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of bioactive compounds such as antifungal and antiseptic agents.\u003c\/li\u003e\n\u003cli\u003eFood chemistry applications where its antimicrobial properties are utilized in the formulation of preservatives.\u003c\/li\u003e\n\u003cli\u003eNatural product isolation and modification for the creation of novel compounds with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry for the identification and quantification of Carvacrol Methyl Ether in various sample matrices.\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: 6379-73-3\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 sizes 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 light and heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCarvacrol Methyl Ether should be stored in a cool, dry environment, away from direct light and heat sources to maintain its stability. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent evaporation and contamination. Due to its volatility, it is important to ensure proper ventilation in the laboratory when handling this compound. Avoid exposure to incompatible materials such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is essential to maintain the compound’s integrity and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086310650074,"sku":"TCI2510C397819094","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086310682842,"sku":"TCI2510C397819095","price":5023000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3978.jpg?v=1769144239"},{"product_id":"tci2510d016019497","title":"TCI D0160 622-22-0 Ethylene Glycol Dibenzyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthylene Glycol Dibenzyl Ether (EGDBE) is a chemical compound widely used as a building block in organic synthesis. It plays a crucial role in laboratories by enabling the formation of complex molecular structures through its reactivity and versatility. This compound is particularly valuable in the synthesis of heterocyclic compounds and other complex organic molecules, where controlled reactivity is essential. EGDBE is a key component in the category of non-heterocyclic building blocks, contributing to the development of advanced chemical structures in research and industrial settings.\u003c\/p\u003e\n\u003cp\u003eEGDBE is known for its stable molecular structure, which allows it to remain inert under normal conditions but still participate in chemical reactions when exposed to specific environments, such as moisture or elevated temperatures. Its volatility also makes it an important consideration in thermal processes, requiring precise temperature control during synthesis. These properties make EGDBE a preferred choice for researchers aiming to achieve high-purity results in complex chemical reactions. The compound’s ability to form intricate molecular frameworks further enhances its utility in chemical innovation and product development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, EGDBE is commonly used in organic synthesis and the development of new chemical products. Its availability and effectiveness in creating complex molecular structures make it a favored material for chemical research. It supports innovation in both academic and industrial sectors by enabling the creation of advanced compounds with specific functional properties. Its role in chemical synthesis is vital for advancing scientific knowledge and practical applications in the field of chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application for EGDBE, as it enables the formation of complex molecular structures through its reactivity and stability.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound development benefits from EGDBE’s ability to participate in controlled chemical reactions, making it ideal for creating specialized organic molecules.\u003c\/li\u003e\n\u003cli\u003eChemical research in Indonesian laboratories frequently uses EGDBE to explore new synthetic pathways and develop novel compounds with specific properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development relies on EGDBE for its role in creating advanced materials and products with high functional performance.\u003c\/li\u003e\n\u003cli\u003eMolecular structure optimization is supported by EGDBE’s ability to form intricate frameworks, making it a valuable tool in structural chemistry 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: 622-22-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in 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\u003eEGDBE should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use sealed containers to minimize exposure to moisture and air, which can affect its reactivity. Due to its volatility, proper ventilation is essential when handling EGDBE to ensure safe working conditions. Always wear appropriate personal protective equipment, such as gloves and safety goggles, to avoid direct contact. The compound should be kept away from heat sources and incompatible materials to prevent unwanted reactions. Regular monitoring of storage conditions is advised to maintain the integrity of the material during long-term storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086351053018,"sku":"TCI2510D016019497","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086351085786,"sku":"TCI2510D016019498","price":5150000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0160.jpg?v=1769180480"},{"product_id":"tci2510d045219892","title":"TCI D0452 2050-46-6 1,2-Diethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2-Diethoxybenzene is an organic chemical compound widely used as a building block in the synthesis of complex molecules. It serves as a key intermediate in various chemical reactions where ethoxy groups are required as substituents. In the laboratory, this compound plays a crucial role in the development of aromatic compounds with specific structural features, particularly in the fields of organic synthesis and pharmacology. Its stability and controlled reactivity make it a reliable choice for researchers seeking dependable raw materials.\u003c\/p\u003e\n\u003cp\u003eThe compound's symmetrical molecular structure and low polarity contribute to its favorable solubility in organic solvents such as ethyl acetate and chloroform. These properties make it ideal for reactions that require specific solvent conditions. Additionally, its resistance to degradation under normal conditions ensures a longer shelf life and minimizes the risk of quality loss during storage. This reliability is especially important in laboratory settings where consistency and accuracy are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2-Diethoxybenzene is commonly used in both pure chemical research and industrial applications. It is a fundamental component of the chemical equipment required for the development of new compounds and the advancement of scientific knowledge. Its versatility and reliability make it a valuable resource for chemists and researchers working in various scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 1,2-Diethoxybenzene due to its stable structure and controlled reactivity, enabling the creation of complex aromatic compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for synthesizing drug molecules that require ethoxy substituents for desired biological activity.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories use it as a standard reference material for calibration and quality control in chemical analysis procedures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it as a precursor in the production of specialty chemicals and polymer intermediates.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies may use it as a model compound to study the behavior and degradation of organic pollutants in different environmental matrices.\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: 2050-46-6\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 quantities as per standard laboratory requirements\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\u003e1,2-Diethoxybenzene should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. The compound should be kept in a well-ventilated area to prevent the accumulation of vapors. Avoid contact with strong oxidizing agents or reactive materials to ensure safety. Regular inspection of storage containers is advised to maintain the integrity of the compound. Proper labeling and adherence to standard laboratory safety protocols are essential to ensure safe handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086385197274,"sku":"TCI2510D045219892","price":784000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086385230042,"sku":"TCI2510D045219893","price":2121000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0452.jpg?v=1769144172"},{"product_id":"tci2510d045319894","title":"TCI D0453 2049-73-2 1,3-Diethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Diethoxybenzene is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It plays a crucial role in laboratory settings, particularly in the development of new compounds and the advancement of chemical research. This compound is commonly employed in various chemical reactions, especially in the formation of heterocyclic compounds and more complex aromatic structures. Its versatility makes it an essential tool for chemists working on a wide range of synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 1,3-Diethoxybenzene contribute to its popularity among researchers. It exhibits good stability and moderate reactivity, allowing for efficient chemical reactions under controlled conditions. Additionally, its solubility in organic solvents facilitates easy mixing and separation during experimental processes. These characteristics make it a preferred choice for laboratories aiming to streamline their synthetic procedures and achieve consistent results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,3-Diethoxybenzene is extensively used in chemical research, particularly in academic institutions and research organizations. Its application spans across multiple fields, including pharmaceutical development, material science, and industrial chemistry. Researchers in Indonesia rely on this compound for its reliability and effectiveness in various synthetic applications, making it a fundamental component in modern chemical experimentation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds due to its structural versatility and reactivity in forming complex aromatic rings.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for its role in creating new molecular structures with potential pharmaceutical applications.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments where its chemical stability supports the development of advanced materials.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes that require efficient and reliable building blocks for large-scale production.\u003c\/li\u003e\n\u003cli\u003eAcademic teaching and experimental training to demonstrate key principles of organic synthesis and chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2049-73-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\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 substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1,3-Diethoxybenzene should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in tightly sealed containers to prevent exposure to air and moisture. Suitable storage containers include glass or polyethylene vessels that are resistant to chemical reactions. Laboratory personnel should handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. Avoid contact with incompatible materials like strong oxidizing agents. Regular inspection of storage conditions is essential to maintain the integrity of the compound and ensure safe handling practices are followed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086385262810,"sku":"TCI2510D045319894","price":4240000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0453.jpg?v=1769144170"},{"product_id":"tci2510d045919904","title":"TCI D0459 126-84-1 2,2-Diethoxypropane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2-Diethoxypropane is a chemical compound widely used in various chemical reactions for the synthesis of complex molecules. It serves as a key building block in organic chemistry, commonly found in laboratories as a raw material for the production of organic compounds. In the context of laboratory work, this compound functions as a reagent or solvent, facilitating chemical reactions with efficiency and precision. Its stable chemical properties and controlled reactivity make it a popular choice for a wide range of chemical experiments. The molecular structure of 2,2-Diethoxypropane enables substitution and addition reactions, making it highly suitable for the synthesis of both heterocyclic and non-heterocyclic compounds. Due to its high purity and consistent packaging, it is easily applicable in laboratory settings. Its chemical stability also ensures safety during use under various laboratory conditions. In Indonesia, this compound is extensively used in chemical laboratories, both in universities and research institutions. Its availability and quality make it a preferred choice for synthesis and analytical experiments. Its application supports the development of chemical technologies and research in the field.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 2,2-Diethoxypropane as it enables efficient substitution and addition reactions, supporting the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eIt is commonly used in the preparation of heterocyclic compounds due to its ability to participate in controlled chemical transformations under laboratory conditions.\u003c\/li\u003e\n\u003cli\u003eAs a solvent, it provides a stable environment for various chemical reactions, allowing for better control over reaction pathways and product formation.\u003c\/li\u003e\n\u003cli\u003eIn analytical chemistry, it is employed for its purity and consistency, ensuring accurate and reproducible results in experimental procedures.\u003c\/li\u003e\n\u003cli\u003eIt supports the development of new chemical technologies by serving as a reliable reagent in research and development 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: 126-84-1\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\u003e2,2-Diethoxypropane should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use suitable containers that are resistant to chemical reactions, such as glass or high-density polyethylene. Proper labeling of containers is essential for safe handling. In laboratory settings, it is important to ensure good ventilation to minimize exposure. Avoid contact with incompatible substances such as strong oxidizers. Always follow standard laboratory safety protocols when handling this compound. Regular monitoring of storage conditions ensures the compound remains stable and safe for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mL","offer_id":48086385656026,"sku":"TCI2510D045919904","price":2071000.0,"currency_code":"IDR","in_stock":true},{"title":"250mL","offer_id":48086385688794,"sku":"TCI2510D045919905","price":15522000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0459.jpg?v=1767101325"},{"product_id":"tci2510d049919961","title":"TCI D0499 124-17-4 Diethylene Glycol Monobutyl Ether Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethylene Glycol Monobutyl Ether Acetate (DEGBE Acetate) is a chemical compound widely used in laboratory settings as a versatile solvent. It plays a crucial role in various chemical reactions and synthesis processes due to its ability to dissolve a wide range of organic and inorganic substances. This compound is particularly valued for its stability and low volatility, making it an essential tool in both academic and industrial research environments. Its polar nature allows it to interact effectively with different molecular structures, enhancing its utility in complex chemical systems.\u003c\/p\u003e\n\u003cp\u003eThe properties of DEGBE Acetate that make it a preferred choice include its polarity, solubility in multiple organic solvents, and chemical stability. These characteristics enable it to serve as an effective medium for reactions requiring a stable and non-volatile environment. Additionally, its non-heterocyclic composition ensures that it does not introduce unwanted by-products or contaminants, which is critical in high-purity applications. The compound’s consistent performance across various experimental conditions further solidifies its position as a reliable laboratory reagent.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DEGBE Acetate is commonly used in chemical and pharmaceutical research. It is frequently found in university chemistry labs and research institutions where effective and safe solvents are essential. Its availability in local markets supports its widespread use across different research scales. The compound’s reliability and performance make it a standard choice for many laboratory applications in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in organic synthesis reactions due to its ability to dissolve a wide range of organic compounds and provide a stable reaction environment.\u003c\/li\u003e\n\u003cli\u003eApplied in pharmaceutical research for the preparation of drug compounds and intermediate steps in synthesis processes.\u003c\/li\u003e\n\u003cli\u003eUtilized in analytical chemistry for sample preparation and extraction due to its solubility and polarity.\u003c\/li\u003e\n\u003cli\u003eEmployed in polymer science for the dissolution and processing of various polymer materials.\u003c\/li\u003e\n\u003cli\u003eFound in environmental chemistry studies for the analysis of organic pollutants in water and soil samples.\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: 124-17-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes 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 heat sources\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDEGBE Acetate should be stored in a cool, dry location, away from direct sunlight and heat sources to maintain its chemical stability. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent evaporation and contamination. Due to its polar nature, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound should not be exposed to open flames or ignition sources. Proper ventilation is also essential when working with this solvent to minimize inhalation risks. Regular monitoring of storage conditions helps maintain the integrity and usability of the product in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086387785946,"sku":"TCI2510D049919961","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086387818714,"sku":"TCI2510D049919962","price":581000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0499.jpg?v=1767101398"},{"product_id":"tci2510d050019963","title":"TCI D0500 112-15-2 Diethylene Glycol Monoethyl Ether Acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethylene Glycol Monoethyl Ether Acetate (DEGMEA), with CAS number 112-15-2, is a versatile chemical compound widely used in laboratory settings. This compound is a key component in various chemical processes due to its exceptional solvating properties. It is commonly employed as a solvent in organic synthesis, making it an essential tool for chemists working on complex reactions. Its ability to dissolve a wide range of organic materials makes it a preferred choice for researchers in multiple fields.\u003c\/p\u003e\n\u003cp\u003eDEGMEA is valued for its high solubility in organic compounds and its relatively high boiling point, which contributes to its stability during chemical reactions. Its non-volatile nature ensures that it remains effective even under prolonged heating conditions. Additionally, it is non-corrosive and safe for use in laboratory environments, making it suitable for both small-scale and industrial applications. These properties make it a reliable and efficient solvent for a variety of chemical processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DEGMEA is frequently used in chemical, pharmaceutical, and industrial research settings. It plays a crucial role in the development of new products and the production of chemical compounds that require a stable and effective solvent. Its widespread application in these fields highlights its importance in both academic and industrial research. The compound is an essential part of many laboratory workflows, supporting the synthesis and analysis of various chemical substances.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where a stable and effective solvent is required for complex reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drug compounds and formulations.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production for the creation of solvents and specialty chemicals.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry for dissolving and isolating organic compounds during testing.\u003c\/li\u003e\n\u003cli\u003eCosmetics and food industry applications for the formulation of products requiring organic 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: 112-15-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory requirements\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\u003eDEGMEA 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 such as glass or stainless steel to prevent contamination and evaporation. Since it is a non-corrosive substance, it can be safely stored with other chemical solvents. Proper labeling of containers is essential for safety and identification purposes. In laboratory settings, it is important to ensure that handling is done in well-ventilated areas to minimize exposure. Always follow standard safety protocols when working with chemical solvents to maintain a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086387884250,"sku":"TCI2510D050019963","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086387917018,"sku":"TCI2510D050019964","price":581000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0500.jpg?v=1767101402"},{"product_id":"tci2510d050119965","title":"TCI D0501 112-59-4 Diethylene Glycol Monohexyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethylene Glycol Monohexyl Ether (DEGME), with the CAS number 112-59-4, is a chemical compound widely used as a building block in various chemical reactions. It serves as a versatile reagent in laboratory settings, particularly in the synthesis of organic compounds. Its role is critical in the development of esters and complex molecular structures, making it an essential component for chemists working on diverse synthetic pathways. DEGME is commonly found in research laboratories across Indonesia, supporting both academic and industrial chemical development.\u003c\/p\u003e\n\u003cp\u003eDEGME is valued for its high polarity and excellent solubility in organic solvents such as ethyl acetate and ethanol. These properties make it a preferred choice for applications requiring controlled polarity in chemical reactions. Its stability under normal conditions further enhances its reliability as a reagent. Additionally, its ability to act as both a solvent and a reactant increases its utility in a wide range of chemical processes. The compound’s solubility and reactivity contribute to its effectiveness in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DEGME plays a key role in chemical research and industrial development. It is frequently used in the production of specialty chemicals, including food additives and pharmaceutical intermediates. Its availability through AMI Scientific ensures that researchers and manufacturers have access to this essential compound for their projects. The compound’s relevance in both academic and industrial contexts underscores its importance in the chemical supply chain in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where DEGME is used to facilitate the formation of ester and complex molecular structures due to its polarity and solubility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from DEGME as it supports the development of drug intermediates and active pharmaceutical ingredients through controlled chemical reactions.\u003c\/li\u003e\n\u003cli\u003eCosmetic formulation relies on DEGME for its solubility properties, enabling the creation of stable and effective cosmetic products.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production utilizes DEGME as a solvent and reagent in the manufacture of specialty chemicals and additives.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry employs DEGME as a reference standard or solvent for chromatographic and spectroscopic analyses due to its purity and stability.\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: 112-59-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes 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\u003eDEGME should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the container tightly sealed to prevent evaporation and contamination. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles that are resistant to chemical degradation. Due to its irritant properties, handling should be done with appropriate personal protective equipment, such as gloves and safety goggles. Ensure proper ventilation in the laboratory to minimize exposure. Always follow standard safety protocols when working with chemical substances to maintain a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086387949786,"sku":"TCI2510D050119965","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086387982554,"sku":"TCI2510D050119966","price":1213000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0501.jpg?v=1768817291"},{"product_id":"tci2510d050319967","title":"TCI D0503 89-91-8 Methyl Dimethoxyacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl Dimethoxyacetate (MDMA), with CAS number 89-91-8, is a versatile chemical compound widely used as a building block in organic synthesis. It serves as a foundational material for creating complex organic molecules, playing a crucial role in both academic and industrial research settings. This compound is particularly valued for its ability to participate in various chemical reactions, making it an essential tool for chemists working on the development of new compounds. Its stability and reactivity make it a reliable choice for a wide range of synthetic processes.\u003c\/p\u003e\n\u003cp\u003eMDMA is known for its stable molecular structure and moderate reactivity, which allows it to be used in multiple reaction types such as esterification, reduction, and substitution. Its neutral chemical properties and resistance to spontaneous reactions make it easier to handle in laboratory environments. The compound’s purity and consistency ensure reliable results in experiments, contributing to the accuracy and reproducibility of chemical processes. Its availability in a pure liquid form further enhances its utility in research and development.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, MDMA is commonly used in organic chemistry research and the synthesis of new compounds. It is particularly relevant for academic institutions and research centers focusing on organic chemistry and pharmacology. Its application in both teaching and research settings underscores its importance as a fundamental reagent in the chemical sciences. The compound’s reliability and adaptability make it a preferred choice for both students and experienced researchers.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex compounds due to its reactivity and stability in chemical reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals as a building block for creating new drug molecules.\u003c\/li\u003e\n\u003cli\u003eTeaching and research in academic institutions for demonstrating chemical reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003ePreparation of intermediates for further chemical modifications and compound derivatization.\u003c\/li\u003e\n\u003cli\u003eUse in analytical chemistry for testing and characterizing new chemical 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: 89-91-8\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 standard laboratory supply\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\u003eMDMA should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent contamination and maintain its purity. Due to its chemical stability, it does not require refrigeration but should be protected from moisture and air exposure. In laboratory settings, it is important to handle the compound with appropriate safety measures, such as using gloves and working in a well-ventilated area. Proper labeling of containers is essential to ensure safe handling and prevent accidental use. Always follow standard laboratory safety protocols when working with chemical reagents to maintain a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086388015322,"sku":"TCI2510D050319967","price":2726000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0503.jpg?v=1767101407"},{"product_id":"tci2510d053520016","title":"TCI D0535 122-95-2 1,4-Diethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,4-Diethoxybenzene is an organic chemical compound widely used as a foundational material in various chemical reactions. It belongs to the category of non-heterocyclic building blocks and is commonly utilized in synthetic chemistry for constructing complex molecules. This compound features an aromatic benzene ring with two ethoxy groups attached at positions 1 and 4, making it a versatile intermediate in organic synthesis. Its stability and controlled reactivity make it a reliable choice for researchers aiming to develop new compounds in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eThe properties of 1,4-Diethoxybenzene, such as its non-polar nature and solubility in organic solvents like ethyl acetate and chloroform, enhance its utility in substitution reactions and other chemical processes. Its non-heterocyclic structure ensures chemical stability, making it suitable for applications requiring long-term structural integrity. These characteristics allow it to be easily integrated into a wide range of experimental protocols, contributing to its popularity among chemists working in both research and development environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,4-Diethoxybenzene is frequently employed in organic chemistry research, pharmaceutical compound synthesis, and the development of new chemical materials. Its availability in solid form and ease of handling make it a practical choice for laboratory use. Its role in advancing chemical innovation is significant, particularly in the fields of pharmacology and material science, where it serves as a key component in the creation of novel compounds and functional materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 1,4-Diethoxybenzene due to its aromatic structure and reactivity, enabling the formation of complex molecules with high precision.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for synthesizing bioactive compounds, supporting drug discovery and development efforts.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments leverage its non-polar properties for creating polymers and coatings with specific chemical and physical characteristics.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry uses it as a reference standard for spectroscopic and chromatographic analyses, ensuring accurate and reproducible results.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it for the production of specialty chemicals, enhancing efficiency and product quality in manufacturing.\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: 122-95-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1,4-Diethoxybenzene 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 such as glass or polyethylene to minimize exposure to moisture and air. As a non-polar compound, it does not react readily with most substances, but it is important to keep it away from strong oxidizing agents and incompatible chemicals. In laboratory settings, proper labeling and storage in designated chemical cabinets are essential for safety and organization. Regular inspection of storage conditions ensures that the compound remains in optimal condition for use in experiments and research activities.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086389784794,"sku":"TCI2510D053520016","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086389817562,"sku":"TCI2510D053520017","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0535.jpg?v=1768817299"},{"product_id":"tci2510d057520076","title":"TCI D0575 131-54-4 2,2'-Dihydroxy-4,4'-dimethoxybenzophenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2'-Dihydroxy-4,4'-dimethoxybenzophenone is a chemical compound widely used in laboratory settings as a key reagent in the synthesis of polymers and complex organic compounds. Its unique structure, featuring both hydroxyl and methoxy groups, makes it highly reactive and chemically stable, which is essential for various synthetic processes. This compound plays a crucial role in polymer science, particularly in the development of functional materials and advanced polymers. Its ability to participate in multiple reaction types, such as substitution and condensation, makes it a versatile tool for researchers working on material innovation and organic synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including solubility in organic solvents like ethyl acetate and ethanol, enhance its utility in laboratory applications. These solubility characteristics allow for easier handling and integration into reaction mixtures, improving the efficiency of synthetic procedures. Additionally, its stability under certain conditions ensures that it remains effective throughout the duration of experiments, reducing the risk of degradation and ensuring consistent results. These features make it a preferred choice for scientists engaged in polymer research and organic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,2'-Dihydroxy-4,4'-dimethoxybenzophenone is extensively used in material science and organic chemistry research. It is commonly found in academic institutions and research centers where new materials and polymers are being developed. Its role in quality testing and the study of polymer properties makes it an essential component in the chemical research landscape of Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer synthesis and functional material development due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for creating complex compounds through substitution and condensation reactions.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies to evaluate the properties of synthesized polymers and composites.\u003c\/li\u003e\n\u003cli\u003eQuality control testing of polymer-based products to ensure consistency and performance standards.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical engineering and materials science for educational and experimental purposes.\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: 131-54-4\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Monomers\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of moisture. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and maintain stability. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances, and ensure proper ventilation in the workspace. 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":"25g","offer_id":48086392406234,"sku":"TCI2510D057520076","price":758000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0575.jpg?v=1768817305"},{"product_id":"tci2510d058620090","title":"TCI D0586 131-53-3 2,2'-Dihydroxy-4-methoxybenzophenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2'-Dihydroxy-4-methoxybenzophenone is a chemical compound widely used in scientific and industrial applications, particularly in the fields of materials science and organic chemistry. This compound plays a crucial role in laboratory settings as a monomer for polymer synthesis, where it contributes to the formation of complex molecular structures. Its unique chemical structure, featuring both hydroxyl and methoxy groups, enhances its reactivity and versatility in various chemical reactions. Due to its ability to participate in controlled polymerization processes, it is a valuable tool for researchers working on advanced material development.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and stability under specific conditions make it a preferred choice for chemical synthesis. It exhibits good solubility in organic solvents, which facilitates mixing and reaction processes in the laboratory. Its reactivity can be finely tuned by adjusting reaction conditions, making it suitable for applications requiring precise control over chemical processes. Additionally, its ability to withstand thermal and chemical stress under controlled environments ensures reliable performance in a wide range of experimental setups.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,2'-Dihydroxy-4-methoxybenzophenone is commonly used by researchers and students in material science, organic chemistry, and polymer technology. Its availability and compatibility with various experimental protocols make it a go-to compound for both academic and industrial research. Its role in developing new materials and understanding chemical behavior is essential for advancing scientific knowledge in these fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer synthesis and modification where controlled reactivity and thermal stability are required.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments involving functional group transformations and cross-linking reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of UV-absorbing materials for use in coatings and photostabilizers due to its light-sensitive properties.\u003c\/li\u003e\n\u003cli\u003eResearch in advanced materials science for creating high-performance polymers and composite materials.\u003c\/li\u003e\n\u003cli\u003eAnalytical applications in spectroscopy and chromatography for studying molecular interactions and reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 131-53-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Monomers\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from 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 keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be stored away from strong oxidizing agents and incompatible substances. Proper ventilation is essential when handling this material to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Regular monitoring of storage conditions ensures the material remains stable and safe for use in experimental procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086392930522,"sku":"TCI2510D058620090","price":1010000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0586.jpg?v=1768817305"},{"product_id":"tci2510d062720162","title":"TCI D0627 91-16-7 1,2-Dimethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2-Dimethoxybenzene is an organic chemical compound widely used in laboratory settings for its versatility in chemical reactions. This compound, with its aromatic ring structure and two methoxy groups attached at positions 1 and 2, serves as a fundamental building block in synthetic chemistry. It is commonly employed in the preparation of more complex molecules, including phenolic derivatives and heterocyclic compounds. Its role in laboratory processes is essential for researchers aiming to develop new chemical structures and materials.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its favorable solubility in organic solvents such as ethyl acetate and ethanol, which makes it easy to handle in various synthetic procedures. Its chemical stability under normal conditions also contributes to its reliability in laboratory applications. Additionally, its predictable boiling and melting points aid in purification and separation techniques. These properties make it a preferred choice for chemists working in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2-Dimethoxybenzene is frequently used in organic chemistry research, pharmaceutical synthesis, and industrial chemical development. It is a key reagent in the creation of bioactive compounds and functional materials. Its availability and consistent performance make it a staple in the chemical supply chain for laboratories across Indonesia, supporting a wide range of scientific investigations and innovations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is enhanced by 1,2-Dimethoxybenzene due to its reactivity in electrophilic substitution and condensation reactions, making it ideal for creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its use in the synthesis of bioactive compounds, as it serves as a versatile intermediate in drug development processes.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development relies on this compound for the production of specialty chemicals and functional materials due to its stability and solubility properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications often use it as a reference standard for chromatographic and spectroscopic analyses due to its well-defined physical and chemical properties.\u003c\/li\u003e\n\u003cli\u003eEnvironmental studies may incorporate it in the analysis of organic pollutants, as it is a common component in environmental samples and can be used for comparative 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: 91-16-7\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 practices\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\u003e1,2-Dimethoxybenzene should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container made of glass or high-density polyethylene to prevent evaporation and contamination. Due to its moderate reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure good ventilation when working with this compound to minimize exposure. Avoid contact with incompatible substances such as strong oxidizing agents. Regular monitoring of storage conditions is advised to maintain the integrity and safety of the material in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086395683034,"sku":"TCI2510D062720162","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086395715802,"sku":"TCI2510D062720163","price":683000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086395748570,"sku":"TCI2510D062720164","price":1666000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0627.jpg?v=1768817315"},{"product_id":"tci2510d062820165","title":"TCI D0628 151-10-0 1,3-Dimethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Dimethoxybenzene is a chemical compound widely used as a foundational material in various laboratory reactions. It belongs to the category of non-heterocyclic building blocks and is commonly utilized in organic chemistry for its versatile reactivity. This compound features an aromatic benzene ring with two methoxy groups attached at positions 1 and 3, making it a valuable intermediate in synthetic pathways. Its structural simplicity and predictable behavior make it a go-to reagent for researchers aiming to create more complex molecules.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stability under specific reaction conditions and its ability to participate in multiple types of chemical reactions, including electrophilic substitution, reduction, and coupling reactions. These properties make it a reliable choice for both academic and industrial applications. Its relatively stable boiling and melting points further contribute to its ease of handling and storage, ensuring consistent performance in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,3-Dimethoxybenzene is frequently used in organic chemistry research, particularly in pharmacology and the synthesis of complex compounds. It serves as a key reagent in the development of pharmaceuticals and industrial chemicals. Its role in supporting scientific innovation is vital, especially in research environments where precision and reliability are paramount.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 1,3-Dimethoxybenzene due to its predictable reactivity and structural versatility, enabling the creation of complex molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a building block for drug development, allowing for the modification of molecular structures to enhance therapeutic properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on 1,3-Dimethoxybenzene as a precursor for the synthesis of various chemical intermediates used in manufacturing processes.\u003c\/li\u003e\n\u003cli\u003eFood additive development incorporates this compound in the formulation of flavoring agents and stabilizers, contributing to the quality and safety of food products.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use 1,3-Dimethoxybenzene as a standard reference compound for calibrating instruments and conducting reactivity 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: 151-10-0\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 requirements\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\u003e1,3-Dimethoxybenzene should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent contamination and evaporation. Due to its chemical nature, it should be kept away from strong oxidizing agents and incompatible substances to avoid potential reactions. In laboratory settings, proper ventilation is essential when handling this compound to ensure safe working conditions. Always follow standard safety protocols, including the use of personal protective equipment, to minimize exposure and ensure safe handling practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086396764378,"sku":"TCI2510D062820165","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086396797146,"sku":"TCI2510D062820166","price":1415000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086396829914,"sku":"TCI2510D062820167","price":4544000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0628.jpg?v=1768817314"},{"product_id":"tci2510d062920168","title":"TCI D0629 150-78-7 1,4-Dimethoxybenzene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,4-Dimethoxybenzene is a chemical compound widely used as a foundational material in various chemical reactions, particularly in the synthesis of aromatic and heterocyclic compounds. This compound features an aromatic ring with two methoxy groups positioned at the 1 and 4 positions, which significantly influences its chemical reactivity. Its versatility makes it a key component in organic chemistry, where it serves as a building block for the development of complex molecules. In laboratory settings, it is essential for creating compounds with specific functional groups and structural characteristics.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and ability to participate in substitution and electrophilic reactions make it a preferred choice for synthetic chemists. Its high boiling and melting points facilitate controlled heating and cooling processes during experiments, ensuring precise reaction conditions. These properties contribute to its widespread use in both academic and industrial research environments. Additionally, its chemical inertness under certain conditions allows for predictable outcomes in synthetic pathways, enhancing its reliability in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,4-Dimethoxybenzene is commonly used in organic chemistry research, especially in the study of bioactive compounds and industrial raw materials. Its availability and consistent quality make it a reliable choice for researchers and professionals in educational and industrial institutions. The compound's role in synthesizing pharmaceuticals, dyes, and other chemical products underscores its importance in the chemical industry. Its application is broad, spanning from basic research to advanced industrial processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where 1,4-Dimethoxybenzene serves as a versatile building block for creating complex aromatic and heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its use in the development of bioactive molecules, as it provides a stable platform for functional group modification.\u003c\/li\u003e\n\u003cli\u003eDye and pigment production relies on its aromatic structure, allowing for the synthesis of compounds with specific color properties and chemical stability.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical manufacturing utilizes its reactivity and stability to produce a wide range of chemical intermediates and raw materials.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications include its use as a standard reference material for spectroscopic and chromatographic 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: 150-78-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e1,4-Dimethoxybenzene should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent contamination and evaporation. The compound is generally non-hazardous under normal conditions but should be handled with care to avoid prolonged skin contact. In laboratory settings, it is advisable to work in a well-ventilated area and use appropriate personal protective equipment such as gloves and safety goggles. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Its chemical stability allows for long-term storage when stored correctly, making it a reliable material for research and industrial applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086396862682,"sku":"TCI2510D062920168","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086396895450,"sku":"TCI2510D062920169","price":2045000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0629.jpg?v=1769144156"}],"url":"https:\/\/amiscientific.com\/en\/collections\/chemicals-by-class-compounds-by-functional-group-ethers.oembed?page=43","provider":"AMI Scientific","version":"1.0","type":"link"}