{"title":"Dicarbonyl Chlorides and Dicarboxylic Acids [Polybenzoxazole Raw Materials]","description":"\u003cp\u003e\u003cstrong\u003eDicarbonyl Chlorides and Dicarboxylic Acids [Polybenzoxazole Raw Materials]\u003c\/strong\u003e — mencakup asam dikarboksilat dan turunan diklorida asamnya, seperti adipic acid, sebacoyl chloride, hingga senyawa aromatik terfluorinasi, yang menjadi bahan baku monomer untuk sintesis polibenzoksazol dan poliamida berkinerja tinggi. Gugus karbonil ganda pada strukturnya memungkinkan reaksi polikondensasi membentuk rantai polimer.\u003c\/p\u003e\u003cp\u003eDicarbonyl Chlorides and Dicarboxylic Acids dipakai peneliti kimia polimer dan material untuk sintesis polibenzoksazol, poliimida, serta poliester melalui reaksi polikondensasi dengan diamina atau diol, menghasilkan bahan dengan ketahanan panas dan sifat mekanik yang diinginkan. Turunan diklorida seperti sebacoyl chloride umumnya lebih reaktif sehingga cocok untuk polimerisasi antarmuka pada suhu rendah.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0161245\"\u003eTCI A0161 124-04-9 Adipic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b687313775\"\u003eTCI B6873 1102-92-7 4,4'-(Perfluoropropane-2,2-diyl)dibenzoyl Chloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b14016663\"\u003eTCI B1401 1171-47-7 2,2-Bis(4-carboxyphenyl)hexafluoropropane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d054520029\"\u003eTCI D0545 110-99-6 Diglycolic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510s003049887\"\u003eTCI S0030 111-19-3 Sebacoyl Chloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d211522171\"\u003eTCI D2115 2215-89-6 4,4'-Dicarboxydiphenyl Ether\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510s002249874\"\u003eTCI S0022 111-20-6 Sebacic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d236722552\"\u003eTCI D2367 2449-35-6 4,4'-Dicarboxydiphenyl Sulfone\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan reaktivitas gugus diklorida asam yang sensitif terhadap kelembapan sehingga membutuhkan penanganan dan kemasan kedap air, serta kemurnian asam dikarboksilat yang memengaruhi bobot molekul polimer hasil polikondensasi. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Polybenzoxazole Raw Materials, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-bis-2-aminophenol-s-polybenzoxazole-raw-materials\"\u003eBis(2-aminophenol)s [Polybenzoxazole Raw Materials]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-monomers\"\u003eMonomers\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-polymer-additives\"\u003ePolymer Additives\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-polymerization-reagents\"\u003ePolymerization Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-polyimide-raw-materials\"\u003ePolyimide Raw Materials\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-polymers\"\u003ePolymers\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-polybenzoxazole-raw-materials\"\u003ePolybenzoxazole Raw Materials\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b687313775","title":"TCI B6873 1102-92-7 4,4'-(Perfluoropropane-2,2-diyl)dibenzoyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6873 (CAS 1102-92-7) is 4,4'-(perfluoropropane-2,2-diyl)dibenzoyl chloride, a difunctional acid chloride monomer containing the hexafluoroisopropylidene (\"6F\") linkage. Polycondensation with diamines or bisphenols gives fluorinated aromatic polyamides and polyesters that are widely studied for their solubility and membrane behaviour. Because acid chlorides react readily with moisture and liberate hydrogen chloride, dry glassware and an inert atmosphere are strongly recommended. TCI supplies this monomer in 5 g and 25 g pack sizes; always review the Safety Data Sheet before handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085959344346,"sku":"TCI2510B687313775","price":3429000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085959377114,"sku":"TCI2510B687313776","price":11974000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6873.jpg?v=1768816110"},{"product_id":"tci2510d054520029","title":"TCI D0545 110-99-6 Diglycolic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiglycolic Acid (DGA), with CAS number 110-99-6, is a chemical compound widely used in various laboratory reactions. It is a carboxylic acid featuring two hydroxyl groups attached to a central carbon atom. In the laboratory, DGA serves as a building block for the synthesis of complex organic compounds, including esters, amides, and heterocyclic compounds. Its versatility makes it an essential reagent in chemical synthesis and functional group transformations.\u003c\/p\u003e\n\u003cp\u003eThe reactivity of Diglycolic Acid is a key factor in its popularity among chemists. It readily reacts with bases and electrophilic compounds, making it ideal for substitution and esterification reactions. The presence of two hydroxyl groups allows it to participate in a wide range of chemical reactions, such as those involving carbodiimides or nitrogen-containing compounds. These properties make DGA a preferred choice for the synthesis of complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diglycolic Acid is commonly used in organic chemistry research and industrial applications. Its solubility in organic solvents like ethyl acetate and acetone facilitates its use in various synthetic processes. The compound is also used in the development of pharmaceuticals and specialty chemicals, contributing to the advancement of scientific research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of esters and amides due to its reactivity and functional group versatility.\u003c\/li\u003e\n\u003cli\u003ePreparation of heterocyclic compounds through its ability to form stable intermediates.\u003c\/li\u003e\n\u003cli\u003eEsterification reactions with carboxylic acids and alcohols in the presence of catalysts.\u003c\/li\u003e\n\u003cli\u003eFunctional group transformations in the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eUse in pharmaceutical research for the development of drug molecules and intermediates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 110-99-6\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: Solid, crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiglycolic Acid should be stored in a cool, dry place, away from moisture and direct sunlight. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with strong bases and electrophilic reagents to prevent unwanted reactions. Proper ventilation is essential when working with this compound to ensure safe laboratory practices. Always follow standard chemical safety protocols to minimize risks during handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086390243546,"sku":"TCI2510D054520029","price":1153000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086390276314,"sku":"TCI2510D054520030","price":10681000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0545.jpg?v=1767101483"},{"product_id":"tci2510d211522171","title":"TCI D2115 2215-89-6 4,4'-Dicarboxydiphenyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2115 4,4'-Dicarboxydiphenyl Ether is an aromatic dicarboxylic acid built from two benzene rings joined by an ether bridge, with a carboxyl group at the para position of each ring. The compound is classified as a raw material for Metal Organic Frameworks (MOFs), a family of porous materials formed by connecting metal ions with organic linkers. In laboratory work, this compound serves as the linker or bridging ligand that determines the geometry, pore size, and framework stability of the porous material a researcher intends to synthesise.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it a frequent choice lies in its two widely separated, opposed carboxyl groups, combined with an ether bridge that introduces a small degree of angular flexibility between the two aromatic rings. Carboxyl groups are strong coordination sites toward a wide range of metal ions, so the resulting framework tends to be robust, while the not-quite-linear angle of the ether bridge opens the possibility of framework topologies different from those obtained with fully rigid aromatic linkers. This combination of coordination strength and limited flexibility is what makes diphenyl ether type linkers attractive to researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, materials of this kind are typically used in university and institutional research groups working on porous materials, where the linker is combined with a metal salt under solvothermal conditions and the resulting framework is then characterised. Because the compound functions as a structural building block rather than a routine reagent, it is generally purchased in research-scale quantities and handled as part of a defined synthesis plan rather than as a general-purpose stock chemical.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMetal Organic Framework synthesis — the two para-oriented carboxyl groups coordinate strongly to metal ions, allowing the linker to define pore dimensions and framework connectivity during assembly.\u003c\/li\u003e\n\u003cli\u003eFramework topology studies — the ether bridge gives an angular, partially flexible geometry that lets researchers access network topologies unavailable to fully rigid aromatic dicarboxylic linkers.\u003c\/li\u003e\n\u003cli\u003eCoordination polymer preparation — as a ditopic bridging ligand, it links metal centres into extended one, two, or three dimensional coordination networks for structural investigation.\u003c\/li\u003e\n\u003cli\u003ePorous materials research — because the linker length and geometry govern pore size, it is used when a specific pore environment is targeted for adsorption or separation studies.\u003c\/li\u003e\n\u003cli\u003eOrganic-inorganic hybrid materials development — it provides the organic component that bonds to inorganic metal nodes, forming hybrid materials whose properties depend on the linker chosen.\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: 2215-89-6\u003c\/li\u003e\n\u003cli\u003eChemical name: 4,4'-Dicarboxydiphenyl Ether\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D2115\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Organic-Inorganic Hybrid Materials \u0026gt; Metal Organic Frameworks (MOF) and Their Raw Materials\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale pack sizes according to the TCI catalogue; storage in a cool, dry place as indicated on the product label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from moisture, direct sunlight, and incompatible materials, and keep it in the original manufacturer packaging or an equivalent chemically resistant, clearly labelled container. Because the material is a fine organic solid, weigh and transfer it in a fume hood or well-ventilated workspace to limit dust generation, and use a spatula rather than pouring where possible. Wear a laboratory coat, safety glasses, and suitable gloves during handling, avoid contact with skin and eyes, and wash hands after use. Follow the manufacturer safety data sheet for detailed guidance, and dispose of residues and contaminated materials through the laboratory chemical waste stream.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48275718308058,"sku":"TCI2510D211522171","price":1069000.0,"currency_code":"IDR","in_stock":false}]},{"product_id":"tci2510d272323046","title":"TCI D2723 5659-93-8 Dimethylmalonyl Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDimethylmalonyl Dichloride (DMMD), with the CAS number 5659-93-8, is a versatile chemical compound widely used in organic synthesis as a building block. It serves as a fundamental reagent in laboratories where the creation of complex organic molecules is required. Its unique structure allows for various chemical reactions, including substitution and nucleophilic or electrophilic reactions, making it a key component in the development of new compounds. This compound is particularly valued for its reactivity and ability to undergo functional group modifications, which opens up a wide range of synthetic possibilities in both academic and industrial settings.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of DMMD, such as its two chlorine atoms on the central carbon, contribute to its reactivity and utility in synthetic chemistry. These chlorine atoms make it an excellent candidate for substitution reactions, enabling the introduction of various functional groups. This flexibility allows chemists to tailor the final product to meet specific applications in pharmaceuticals, materials science, and chemical industries. The compound's stability under controlled conditions further enhances its appeal for use in laboratory environments where precision and reproducibility are essential.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DMMD is commonly used by researchers and chemical industries to develop new products such as pharmaceuticals, polymers, and industrial chemicals. Its role in organic modification and the synthesis of new compounds makes it an essential tool for innovation in chemical research. The compound's availability and reliability have made it a preferred choice for both academic and industrial applications in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where DMMD is used to build complex molecules through substitution and functional group modifications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from DMMD as it enables the creation of new drug compounds with specific biological activities.\u003c\/li\u003e\n\u003cli\u003ePolymer development utilizes DMMD to introduce functional groups into polymer chains, enhancing material properties.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications leverage DMMD's reactivity to synthesize advanced materials with tailored characteristics.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on DMMD for the synthesis of various chemical intermediates used in manufacturing 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: 5659-93-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or crystalline, depending on the supplier\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDimethylmalonyl Dichloride should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Protective gloves and goggles should be worn when handling the compound to ensure safety. Avoid contact with incompatible materials such as strong bases or reducing agents. Regular monitoring of storage conditions is essential to ensure the compound remains stable and suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086574203098,"sku":"TCI2510D272323046","price":3852000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086574235866,"sku":"TCI2510D272323047","price":12255000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2723.jpg?v=1767105232"},{"product_id":"tci2510g020231815","title":"TCI G0202 2873-74-7 Glutaryl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGlutaryl Chloride is the acid dichloride of glutaric acid — a five-carbon chain compound bearing highly reactive acid chloride groups at both ends. Its role in the laboratory is that of a bifunctional acylating reagent, capable of joining two nucleophiles at once or building polymer chains through polycondensation reactions. Because acid chlorides are far more reactive than free carboxylic acids, reactions proceed rapidly at low temperature, which makes this reagent well suited to substrates that cannot tolerate prolonged heating or harsh acid-catalyst conditions.\u003c\/p\u003e\n\u003cp\u003eIts principal characteristics are a liquid form at room temperature, which makes volumetric measurement straightforward, together with high reactivity toward amines, alcohols, and water. The two acyl chloride groups are separated by three methylene units, giving exactly the chain spacing and flexibility needed to form amides, esters, and cyclic imides. This property is what makes the compound a mainstay in the synthesis of polyamides and polyesters via interfacial polycondensation — a classic experiment that is also frequently demonstrated in polymer chemistry teaching laboratories.\u003c\/p\u003e\n\u003cp\u003eAs a consequence of that reactivity, the compound is highly sensitive to moisture and must be handled with appropriate care in Indonesian laboratories, where ambient humidity is consistently high throughout the year. Academic research groups, polymer chemistry teaching laboratories, and synthetic organic laboratories preparing amide and ester derivatives are the typical users. Work is generally carried out under dry conditions, with the container kept closed between transfers so that reagent quality is preserved across repeated use.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eInterfacial polycondensation for polyamide synthesis, where the two terminal acid chloride groups react rapidly with a diamine at the boundary between two immiscible phases without heating.\u003c\/li\u003e\n\u003cli\u003ePolyester preparation through polycondensation with diols, taking advantage of acid chloride reactivity that far exceeds that of the corresponding free carboxylic acid under mild conditions.\u003c\/li\u003e\n\u003cli\u003eBifunctional acylation of amines to form diamides, where a single reagent links two nucleophile molecules through a flexible three-methylene spacer between the carbonyl centres.\u003c\/li\u003e\n\u003cli\u003eCyclic imide construction, in which the chain length and flexibility of the glutaryl backbone allow ring closure onto a single nitrogen nucleophile under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eTeaching demonstrations in polymer chemistry practicals, where the classic interfacial polycondensation experiment illustrates step-growth polymerisation visibly and rapidly at room temperature.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2873-74-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed on this product page\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid at room temperature\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed under dry conditions, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a dry, well-ventilated area, away from moisture and from incompatible materials such as water, alcohols, and amines. Glass containers with a secure, chemically resistant closure are appropriate; keep the original packaging sealed between uses. Handle in a fume hood, using gloves, safety goggles, and a laboratory coat, since acid chlorides react vigorously with water and release corrosive by-products. Transfer under dry conditions and minimise the time the container remains open, particularly in humid environments. 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