{"title":"Chemicals by Class › Compounds by Functional Group › Carboxylic Acids","description":"\u003cp\u003eAsam karboksilat dari TCI: monoasam dan diasam alifatik, asam aromatik, asam amino, heteroaromatik asam karboksilat untuk sintesis ester, amida, polimer, dan obat. Distributor resmi TCI di Indonesia: AMI Scientific.\u003c\/p\u003e","products":[{"product_id":"tci2510b559512269","title":"TCI B5595 711-02-4 Bicyclo[2.2.2]octane-1,4-dicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5595 Bicyclo[2.2.2]octane-1,4-dicarboxylic Acid (CAS 711-02-4) is a rigid cage-structured dicarboxylic acid used as a non-heterocyclic building block in organic synthesis. This compound serves as a versatile precursor for constructing Metal-Organic Frameworks (MOFs), coordination polymers, and functional porous materials that require high structural rigidity. Its well-defined geometry also makes it suitable for supramolecular chemistry and catalyst design applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085889908954,"sku":"TCI2510B559512269","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5595.jpg?v=1767092548"},{"product_id":"tci2510b579512533","title":"TCI B5795 677010-20-7 [1,1'-Biphenyl]-3,4',5-tricarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[1,1'-Biphenyl]-3,4',5-tricarboxylic Acid is a versatile aromatic polycarboxylic acid building block used for constructing Metal-Organic Frameworks (MOFs) and coordination polymers in materials research. Its three carboxylic acid groups positioned on the biphenyl scaffold provide multiple coordination sites for metal ion binding, making it suitable for gas adsorption, catalysis, and fluorescence-based sensor applications. This compound, supplied by TCI, is ideal for researchers working on advanced porous materials and supramolecular chemistry.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085903671514,"sku":"TCI2510B579512533","price":5982000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5795.jpg?v=1767092758"},{"product_id":"tci2510b608612898","title":"TCI B6086 120728-10-1 N-tert-Butoxycarbonyl-1-aminocyclobutanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6086, N-tert-Butoxycarbonyl-1-aminocyclobutanecarboxylic Acid (CAS 120728-10-1), is a Boc-protected non-proteinogenic amino acid widely employed as a conformationally constrained building block in peptide synthesis. It is commonly utilized in medicinal chemistry research, particularly in the development of modified peptides, peptidomimetics, and cyclic peptide scaffolds for structure-activity relationship studies. This compound supports applications in chemical biology, including enzyme inhibitor design and protein-protein interaction research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085919203546,"sku":"TCI2510B608612898","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085919236314,"sku":"TCI2510B608612899","price":2853000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6086.jpg?v=1768204484"},{"product_id":"tci2510b614412965","title":"TCI B6144 83673-98-7 2-[(tert-Butoxycarbonyl)amino]thiazole-4-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-[(tert-Butoxycarbonyl)amino]thiazole-4-carboxylic Acid is a Boc-protected thiazole amino acid derivative that serves as a versatile heterocyclic building block in organic synthesis. The Boc protecting group safeguards the amine functionality during synthetic transformations and can be readily removed under mild acidic conditions, enabling efficient incorporation of the thiazole scaffold into larger molecular frameworks. This compound is widely utilized in medicinal chemistry research for drug discovery programs, particularly in the development of bioactive thiazole-containing molecules with antimicrobial, anticancer, and anti-inflammatory properties.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085921857754,"sku":"TCI2510B614412965","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085921890522,"sku":"TCI2510B614412966","price":4190000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6144_30b774b8-53f0-43f4-a45f-a11d6bda12b0.jpg?v=1767864684"},{"product_id":"tci2510b617913006","title":"TCI B6179 22803-05-0 [1,1'-Biphenyl]-3,3',4,4'-tetracarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[1,1'-Biphenyl]-3,3',4,4'-tetracarboxylic Acid (CAS 22803-05-0) is a biphenyl-based tetracarboxylic acid building block from TCI, widely employed as a polytopic organic linker for constructing Metal-Organic Frameworks (MOFs) and coordination polymers. Its four carboxylate groups enable strong multi-dentate coordination with metal clusters, making it a versatile precursor in porous crystalline materials research. This compound is commonly applied in studies involving gas adsorption, heterogeneous catalysis, and the synthesis of advanced functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085923594458,"sku":"TCI2510B617913006","price":4266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6179.jpg?v=1767093266"},{"product_id":"tci2510b634313200","title":"TCI B6343 51077-14-6 (S)-1-(tert-Butoxycarbonyl)azetidine-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6343, also known as (S)-1-(tert-butoxycarbonyl)azetidine-2-carboxylic Acid, is a chiral building block essential in asymmetric synthesis. This compound is widely used in laboratories to create complex molecules with specific stereochemistry. Its azetidine ring structure, modified with a tert-butoxycarbonyl group, makes it a versatile tool for chemists aiming to control the spatial arrangement of atoms in organic molecules. This material plays a crucial role in the development of pharmaceuticals and bioactive compounds, where precise stereochemistry is required for biological activity.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its chemical stability under controlled conditions and its solubility in various organic solvents. These properties make it an ideal candidate for use in a wide range of synthetic reactions. Its ability to act as a precursor in asymmetric reactions allows for the selective formation of stereoisomers, which is essential in drug development and fine chemical synthesis. The compound's reliability and reproducibility in laboratory settings make it a preferred choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to pharmacology, organic chemistry, and biochemistry. It is particularly valuable in the development of new drugs and in the study of molecular mechanisms. Many research institutions and universities in Indonesia rely on this material to advance their scientific work and contribute to the field of medicinal chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound enables the selective formation of stereoisomers, crucial for drug development and bioactive compound creation.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its role as a chiral building block, allowing for the synthesis of complex molecules with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drugs, as its stereochemistry can influence biological activity and pharmacological properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies often incorporate this material to investigate molecular interactions and structural requirements for biological function.\u003c\/li\u003e\n\u003cli\u003eIt is also used in the synthesis of fine chemicals, where precise stereochemical control is essential for industrial and research applications.\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: 51077-14-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its organic nature, it is best stored in airtight glass or plastic containers that are resistant to chemical degradation. Proper labeling and storage conditions are essential to ensure the integrity of the material. In laboratory settings, it should be handled with care, using appropriate personal protective equipment. Regular monitoring of storage conditions is advised to maintain the quality and effectiveness of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085931851994,"sku":"TCI2510B634313200","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6343.jpg?v=1767093516"},{"product_id":"tci2510b641513300","title":"TCI B6415 1000931-72-5 4-[(tert-Butoxycarbonyl)amino]-1-cubanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6415 4-[(tert-Butoxycarbonyl)amino]-1-cubanecarboxylic Acid (CAS 1000931-72-5) is a non-heterocyclic building block built on the rigid cubane framework, carrying a free carboxylic acid and a Boc-protected amine on opposite positions. This bifunctional design lets researchers introduce the cubane motif into peptides and small molecules through familiar amide coupling chemistry without an extra protection step. Cubane derivatives are widely studied as benzene bioisosteres, offering a rigid three-dimensional alternative that preserves substituent vectors. AMI Scientific offers this TCI product in a 100 mg pack suited to exploratory synthesis, with full quality details available in the manufacturer's Certificate of Analysis and Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eIHLE et al. (1996). ChemInform Abstract: Preparation of 4‐Alkyl‐2‐(N‐(tert‐butoxycarbonyl)amino)pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2‐(N‐(tert‐ Butoxycarbonyl)amino)‐4‐picoline.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199646162\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199646162\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":"100mg","offer_id":48085938929882,"sku":"TCI2510B641513300","price":7345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6415.jpg?v=1767093637"},{"product_id":"tci2510b643713325","title":"TCI B6437 115951-16-1 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6437 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid (CAS 115951-16-1) is a Boc-protected cyclic amino acid in which the amino and carboxyl groups share a quaternary carbon. Its rigid cyclohexane framework makes it valuable for designing conformationally constrained peptides and peptide analogues. The pre-installed Boc group saves a protection step and can be removed under well-established acidic conditions. Store the solid tightly sealed in a cool, dry place away from strong acids, and refer to the manufacturer's safety data sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBadland et al. (2010). An improved synthesis of (1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetasy.2010.04.049\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetasy.2010.04.049\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\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":48085939912922,"sku":"TCI2510B643713325","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939945690,"sku":"TCI2510B643713326","price":6082000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6437_d1e882c4-5446-4e40-b77f-bf0c8053c12b.jpg?v=1767865775"},{"product_id":"tci2510b652213434","title":"TCI B6522 56842-95-6 Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6522 Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (CAS 56842-95-6) is a rigid, three-dimensional building block widely used in modern medicinal chemistry. The bicyclo[1.1.1]pentane core is frequently explored as a bioisostere for para-substituted benzene rings, offering a fixed linear vector between substituents. Its two bridgehead carboxylic acids can be converted into esters, amides, and rigid linkers for further elaboration. Supplied in a 1 g research pack, it should be weighed in a well-ventilated area and stored cool, dry, and tightly sealed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085944697050,"sku":"TCI2510B652213434","price":4569000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6522.jpg?v=1767093799"},{"product_id":"tci2510b660713563","title":"TCI B6607 1035325-28-0 5-[(tert-Butoxycarbonyl)amino]bicyclo[3.1.1]heptane-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6607 is 5-[(tert-butoxycarbonyl)amino]bicyclo[3.1.1]heptane-1-carboxylic acid, a rigid saturated building block with orthogonal carboxylic acid and Boc-protected amine handles. The bicyclo[3.1.1]heptane core is widely investigated as a three-dimensional bioisostere for meta-substituted benzene rings. Replacing flat aromatic rings with such saturated cages can improve solubility and reduce metabolic liability in lead optimisation programmes. AMI Scientific supplies this TCI building block in a 100 mg pack size for synthetic and medicinal chemistry laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBaenziger et al. (2015). ChemInform Abstract: Development Approaches Towards a 4‐Spiro Cyclopropane Proline Scaffold (S)‐5‐(tert‐Butoxycarbonyl)‐5‐azaspiro[2.4]heptane‐6‐carboxylic Acid. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201536288\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201536288\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMatković (2024). 4-(2-(5-(2-(tert-Butoxycarbonyl)hydrazinecarbonyl)-2-methylthiophen-3-yl)cyclopent-1-enyl)-5-methylthiophene-2-carboxylic Acid. \u003cem\u003eMolbank\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m1760\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m1760\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":"100mg","offer_id":48085950071002,"sku":"TCI2510B660713563","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6607.jpg?v=1767094012"},{"product_id":"tci2510b660913565","title":"TCI B6609 1050886-56-0 4-[(tert-Butoxycarbonyl)amino]bicyclo[2.1.1]hexane-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6609 is 4-[(tert-butoxycarbonyl)amino]bicyclo[2.1.1]hexane-1-carboxylic acid, a compact and rigid saturated building block. It carries orthogonal carboxylic acid and Boc-protected amine handles on opposite bridgehead positions, allowing stepwise elaboration. The bicyclo[2.1.1]hexane core is actively studied as a three-dimensional bioisostere for ortho- and meta-substituted benzene rings in drug discovery. AMI Scientific supplies this TCI building block in a 100 mg pack size for medicinal chemistry and advanced synthesis laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWang et al. (2013). A scalable synthesis of (1R,3S,5R)-2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2013.09.114\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetlet.2013.09.114\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBakonyi et al. (2013). Synthesis of All Four Stereoisomers of 3-(tert-Butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-2-carboxylic Acid. \u003cem\u003eThe Journal of Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jo4013282\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jo4013282\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\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":"100mg","offer_id":48085950136538,"sku":"TCI2510B660913565","price":4771000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6609.jpg?v=1767094020"},{"product_id":"tci2510b661913574","title":"TCI B6619 22287-28-1 Bicyclo[1.1.1]pentane-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6619 is bicyclo[1.1.1]pentane-1-carboxylic acid, a monofunctional derivative of the widely studied BCP cage. The bridgehead-to-bridgehead axis of bicyclo[1.1.1]pentane closely mimics the linear geometry of para-substituted benzene rings, making it a favoured aromatic bioisostere. Replacing arenes with BCP units is frequently associated with improved aqueous solubility, reduced lipophilicity, and enhanced metabolic stability. AMI Scientific supplies this TCI building block in a 100 mg pack size for drug discovery and organic synthesis laboratories.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085950464218,"sku":"TCI2510B661913574","price":8682000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6619.jpg?v=1767094032"},{"product_id":"tci2510b702413876","title":"TCI B7024 612-87-3 [1,1'-Biphenyl]-3,3'-dicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7024 [1,1'-Biphenyl]-3,3'-dicarboxylic acid (CAS 612-87-3) is an aromatic dicarboxylic acid whose meta-substitution pattern gives a distinctive connection geometry. It is commonly used as an organic linker in metal-organic framework and coordination polymer synthesis, where linker geometry governs pore size and network topology. The compound also serves as a monomer for aromatic polyesters and polyamides, and as a precursor to ester and amide derivatives. AMI Scientific supplies it in 1 g and 5 g pack sizes for materials and inorganic chemistry laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhu et al. (2007). Supramolecular assembly of biphenyl dicarboxylic acid on Au(1 1 1). \u003cem\u003eSurface Science\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.susc.2007.02.003\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.susc.2007.02.003\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eImaizumi et al. (2011). Multicolored electrochromism in 4,4′-biphenyl dicarboxylic acid diethyl ester. \u003cem\u003ePhysical Chemistry Chemical Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c1cp20468h\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c1cp20468h\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":48085964095706,"sku":"TCI2510B702413876","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085964128474,"sku":"TCI2510B702413877","price":4140000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7024.jpg?v=1767094487"},{"product_id":"tci2510c038714475","title":"TCI C0387 1759-53-1 Cyclopropanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0387 Cyclopropanecarboxylic Acid, CAS 1759-53-1, is a liquid carboxylic acid building block bearing the increasingly popular cyclopropyl motif. It is readily converted into acid chlorides, esters, amides, and other derivatives, making it a convenient entry point for introducing a conformationally rigid three-membered ring. Common applications include medicinal chemistry research, agrochemical intermediates, and heterocycle synthesis. Supplied by AMI Scientific in 25 mL, 100 mL, and 500 mL sizes, it is corrosive and should be handled in a fume hood with appropriate protective equipment and stored tightly closed in a cool, dry, well-ventilated area.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAkimov et al. (2025). Theoretical conformational analysis of cyclopropanecarboxylic acid fluoride and cyclopropanecarboxylic acid chloride in lowest excited electronic states and investigation of possible torsion–inversion coupling. \u003cem\u003eComputational and Theoretical Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.comptc.2025.115435\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.comptc.2025.115435\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePejlovas et al. (2015). Microwave spectra and structure of the cyclopropanecarboxylic acid-formic acid dimer. \u003cem\u003eThe Journal of Chemical Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1063\/1.4931923\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1063\/1.4931923\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eVereshchagin et al. (2016). ChemInform Abstract: The First Electrocatalytic Stereoselective Multicomponent Synthesis of Cyclopropanecarboxylic Acid Derivatives.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201615072\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201615072\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":48085995421914,"sku":"TCI2510C038714475","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48085995454682,"sku":"TCI2510C038714476","price":3660000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085995487450,"sku":"TCI2510C038714477","price":10019000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0387.jpg?v=1767095155"},{"product_id":"tci2510c045814589","title":"TCI C0458 610-09-3 cis-1,2-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0458 cis-1,2-Cyclohexanedicarboxylic Acid (CAS 610-09-3) is an alicyclic dicarboxylic acid whose two carboxyl groups adopt a cis arrangement on the cyclohexane ring. This defined stereochemistry makes it a useful bridging linker in the assembly of metal organic frameworks and other coordination materials. It also serves as a practical building block for anhydrides, esters, amides, and related synthetic intermediates. Available in 25 g and 500 g packs, it suits both exploratory screening and larger laboratory preparations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086001025242,"sku":"TCI2510C045814589","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086001058010,"sku":"TCI2510C045814590","price":4013000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0458.jpg?v=1768816253"},{"product_id":"tci2510c047014609","title":"TCI C0470 98-89-5 Cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0470 Cyclohexanecarboxylic Acid (CAS 98-89-5) is an alicyclic carboxylic acid that serves as a versatile non-heterocyclic building block. Its carboxyl group readily undergoes esterification, amidation, reduction, and activation to acyl derivatives, while the cyclohexane ring introduces a saturated three-dimensional motif into target molecules. This makes it particularly useful in medicinal chemistry programmes that replace flat aromatic rings with saturated scaffolds. Supplied in 25 g and 500 g packs, it should be stored in a cool, dry place in a tightly closed container, away from strong bases and oxidising agents.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLiu et al. (1994). Pharmacokinetics and Pharmacodynamics of Valproate Analogues in Rats. IV. Anticonvulsant Action and Neurotoxocity of Octanoic Acid, Cyclohexanecarboxylic Acid, and 1‐Methyl‐1 ‐Cyclohexanecarboxylic Acid. \u003cem\u003eEpilepsia\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1111\/j.1528-1157.1994.tb02939.x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1111\/j.1528-1157.1994.tb02939.x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLiu et al. (1992). Pharmacokinetics and pharmacodynamics of valproate analogs in rats. III. Pharmacokinetics of valproic acid, cyclohexanecarboxylic acid, and 1-methyl-1-cyclohexanecarboxylic acid in the bile-exteriorized rat.. \u003cem\u003eDrug Metabolism and Disposition\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0090-9556(25)08799-9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0090-9556(25)08799-9\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLiu et al. (1993). Pharmacokinetics and pharmacodynamics of valproate analogs in rats. II. Pharmacokinetics of octanoic acid, cyclohexanecarboxylic acid, and 1‐methyl‐1‐cyclohexanecarboxylic acid. \u003cem\u003eBiopharmaceutics \u0026amp; Drug Disposition\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/bdd.2510140406\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/bdd.2510140406\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":48086001909978,"sku":"TCI2510C047014609","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086001942746,"sku":"TCI2510C047014610","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0470.jpg?v=1767095302"},{"product_id":"tci2510c047414618","title":"TCI C0474 2305-32-0 trans-1,2-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0474 trans-1,2-Cyclohexanedicarboxylic Acid (CAS 2305-32-0) is an alicyclic dicarboxylic acid whose defined trans geometry makes it a useful organic linker for metal organic framework synthesis. Its two carboxylate groups can bridge metal centres in several coordination modes, offering a flexible alternative to rigid aromatic linkers. The compound also serves as a monomer for polyesters and polyamides and as a precursor to cyclic anhydride derivatives. Supplied in 25 g and 500 g packs, it should be handled with dust precautions and stored in a cool, dry place in a tightly closed container.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086003220698,"sku":"TCI2510C047414618","price":2095000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086003253466,"sku":"TCI2510C047414619","price":20165000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0474.jpg?v=1768816258"},{"product_id":"tci2510c047514620","title":"TCI C0475 619-82-9 trans-1,4-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0475 trans-1,4-Cyclohexanedicarboxylic Acid (CAS 619-82-9) is an alicyclic diacid whose trans-1,4 substitution gives an almost linear arrangement of its two carboxyl groups. This predictable geometry makes it a valuable monomer for polyesters and polyamides, particularly where optical clarity and resistance to UV-induced yellowing are required. It also functions as a rigid symmetrical spacer in organic synthesis and as a linker in coordination polymers. Available in 25 g, 100 g, and 500 g packs, it should be handled with dust precautions and stored cool, dry, and tightly sealed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086003286234,"sku":"TCI2510C047514620","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086003319002,"sku":"TCI2510C047514621","price":5074000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086003351770,"sku":"TCI2510C047514622","price":16631000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0475.jpg?v=1767095310"},{"product_id":"tci2510c047814625","title":"TCI C0478 13149-00-3 cis-1,2-Cyclohexanedicarboxylic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0478 cis-1,2-Cyclohexanedicarboxylic Anhydride (CAS 13149-00-3) is a reactive cyclic anhydride derived from cis-1,2-cyclohexanedicarboxylic acid. Its strained anhydride ring opens readily with alcohols and amines to give mono-esters, mono-amides, and imide precursors bearing a free carboxyl group. The saturated ring also makes it a common choice in epoxy curing chemistry where colour stability and optical clarity matter. Supplied in 25 g, 100 g, and 500 g packs, it is moisture sensitive and should be weighed quickly under dry conditions and stored cool, dry, and tightly sealed.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086003482842,"sku":"TCI2510C047814625","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086003515610,"sku":"TCI2510C047814626","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086003548378,"sku":"TCI2510C047814627","price":2474000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0478.jpg?v=1767095318"},{"product_id":"tci2510c049214655","title":"TCI C0492 2305-26-2 cis-4-Cyclohexene-1,2-dicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0492 cis-4-Cyclohexene-1,2-dicarboxylic Acid (CAS 2305-26-2) is a cyclic dicarboxylic acid that retains an internal double bond. The cis arrangement of its two carboxyl groups favours cyclic anhydride formation and makes the compound a useful acid component for polyesters and polyamides. The remaining alkene provides an additional handle for epoxidation, hydrogenation, or crosslinking, allowing material properties to be tuned. AMI Scientific offers this TCI monomer in small and large packs for formulation trials and laboratory-scale polymer synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086004531418,"sku":"TCI2510C049214655","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086004564186,"sku":"TCI2510C049214656","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0492.jpg?v=1767095367"},{"product_id":"tci2510c049314657","title":"TCI C0493 935-79-5 cis-4-Cyclohexene-1,2-dicarboxylic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0493 cis-4-Cyclohexene-1,2-dicarboxylic Anhydride (CAS 935-79-5) is a cyclic dicarboxylic anhydride widely used as a non-heterocyclic building block in organic synthesis laboratories. Its reactive anhydride group readily undergoes ring opening with amines and alcohols to give imides, amides, and ester derivatives, while the ring double bond allows further functionalization. Researchers commonly apply it in the preparation of specialty monomers, polyester and polyimide precursors, and thermoset resin studies. The material should be kept tightly closed in a cool, dry place away from moisture, and handled with appropriate personal protective equipment in a fume hood.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086004596954,"sku":"TCI2510C049314657","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086004629722,"sku":"TCI2510C049314658","price":934000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0493.jpg?v=1767095370"},{"product_id":"tci2510c051214692","title":"TCI C0512 3400-45-1 Cyclopentanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0512 Cyclopentanecarboxylic Acid (CAS 3400-45-1) is an aliphatic carboxylic acid bearing a carboxyl group directly on a cyclopentane ring. The acid handle is readily converted into esters, amides, acid chlorides, and other acyl derivatives using standard coupling protocols. Its rigid cyclopentyl motif appears frequently in pharmaceutical candidates, making it a practical building block for medicinal chemistry and analog library work. AMI Scientific supplies this TCI grade in 5 g and 25 g packs, and the material should be handled as a corrosive solid-phase reagent with appropriate protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKushev et al. (1999). Synthesis, Cytotoxicity and Antitumor Activity of Platinum(II) Complexes of Cyclopentanecarboxylic Acid Hydrazide. \u003cem\u003eBiological Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1515\/bc.1999.164\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1515\/bc.1999.164\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePark et al. (2024). Exploring helix structures of γ‐peptides based on 2‐(aminomethyl)cyclopentanecarboxylic acid. \u003cem\u003eBiopolymers\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/bip.23575\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/bip.23575\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMahmoudian et al. (1992). Resolution of 4-amino-cyclopentanecarboxylic acid methyl esters using hydrolytic enzymes. \u003cem\u003eEnzyme and Microbial Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0141-0229(92)90055-s\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0141-0229(92)90055-s\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":48086006399194,"sku":"TCI2510C051214692","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086006431962,"sku":"TCI2510C051214693","price":2373000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0512.jpg?v=1767095423"},{"product_id":"tci2510c065214875","title":"TCI C0652 4771-80-6 3-Cyclohexene-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0652 3-Cyclohexene-1-carboxylic Acid is an alicyclic building block that carries both a ring alkene and a carboxylic acid group. The internal double bond can be elaborated through epoxidation, dihydroxylation, hydrogenation, hydroboration, or oxidative cleavage, while the acid group is readily converted into esters, amides, or alcohols. Its structure, classically obtained from a Diels-Alder reaction, provides a stereogenic centre that makes it attractive for chiral resolution studies. AMI Scientific offers this TCI product in 25 g, 100 g, and 500 g packs to suit exploratory work through to larger-scale synthesis.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWang et al. (2014). Dehydro-aromatization of cyclohexene-carboxylic acids by sulfuric acid: critical route for bio-based terephthalic acid synthesis. \u003cem\u003eRSC Advances\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c3ra46670a\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c3ra46670a\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGeiger et al. (1995). (3S,4S,5R)-3,4,5-trihydroxy-1-cyclohexene-carboxylic acid from Sequoiadendron giganteum. \u003cem\u003ePhytochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0031-9422(95)00450-l\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0031-9422(95)00450-l\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eXu et al. (2020). Facile access to chiral β-homoglutamic acid from 3-cyclohexene-carboxylic acid. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397911.2020.1802760\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397911.2020.1802760\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":48086018392282,"sku":"TCI2510C065214875","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086018425050,"sku":"TCI2510C065214876","price":4392000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086018457818,"sku":"TCI2510C065214877","price":12770000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0652.jpg?v=1767095613"},{"product_id":"tci2510c076915019","title":"TCI C0769 5445-51-2 1,1-Cyclobutanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0769 1,1-Cyclobutanedicarboxylic Acid (CAS 5445-51-2) features two carboxyl groups on the same carbon of a strained cyclobutane ring. This gem-dicarboxylate arrangement forms stable bidentate chelates and is well known in platinum coordination chemistry. The compound also serves as a precursor to cyclobutanecarboxylic acid derivatives and to rigid, three-dimensional building blocks. AMI Scientific supplies this TCI product in 5 g and 25 g pack sizes for flexible laboratory use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSANTARSIERO (1990). ChemInform Abstract: The Crystal Structure of 1,1‐Cyclobutanedicarboxylic Acid at 20 K. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199028037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199028037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRao (1993). A Convenient Preparation of 1-Mercapto-3-azidocyclo-butane from 1,1-Cyclobutanedicarboxylic Acid. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919308012613\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919308012613\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRAO (1994). ChemInform Abstract: A Convenient Preparation of 1‐Mercapto‐3‐azidocyclobutane from 1,1‐ Cyclobutanedicarboxylic Acid.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199417106\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199417106\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":48086027174106,"sku":"TCI2510C076915019","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086027206874,"sku":"TCI2510C076915020","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0769.jpg?v=1767095729"},{"product_id":"tci2510c078815048","title":"TCI C0788 1076-97-7 1,4-Cyclohexanedicarboxylic Acid (cis- and trans- mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0788 1,4-Cyclohexanedicarboxylic Acid (CAS 1076-97-7) is supplied as a mixture of cis and trans isomers. As a saturated alicyclic diacid, it serves as a difunctional monomer for polyesters, polyamides, and coating resins where a non-aromatic backbone is desired. Materials researchers also use it as a bridging ligand in coordination polymer studies thanks to its flexible conformation. The 25 g pack size from TCI is well matched to laboratory-scale polymerisation and sample-series preparation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeng et al. (2024). Separation of the cis- and trans-isomers 1,4-cyclohexanedicarboxylic acid by a dynamic MOF. \u003cem\u003eInorganic Chemistry Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.inoche.2024.113302\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.inoche.2024.113302\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBoaz (1999). Enzymatic desymmetrization of cis-1,3-cyclohexanedicarboxylic acid diesters. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0957-4166(99)00060-9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0957-4166(99)00060-9\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBoaz (1999). ChemInform Abstract: Enzymatic Desymmetrization of cis‐1,3‐cyclohexanedicarboxylic Acid Diesters.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199935033\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199935033\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":48276744274138,"sku":"TCI2510C078815048","price":708000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0788.jpg?v=1767095754"},{"product_id":"tci2510c078915050","title":"TCI C0789 619-81-8 cis-1,4-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0789 cis-1,4-Cyclohexanedicarboxylic Acid (CAS 619-81-8) is the pure cis isomer of the alicyclic diacid, offered as a raw material for Metal Organic Frameworks. Its cis geometry places both carboxyl groups on the same face of the ring, giving coordination motifs distinct from those of the trans isomer. As a flexible aliphatic linker, it is studied in the assembly of porous frameworks for gas adsorption, separation, and heterogeneous catalysis. TCI offers 25 g and 100 g packs, covering both condition screening and larger repeat syntheses.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086028517594,"sku":"TCI2510C078915050","price":5527000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086028550362,"sku":"TCI2510C078915051","price":14385000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0789.jpg?v=1768816337"},{"product_id":"tci2510c085615149","title":"TCI C0856 3724-52-5 1,2,3,4-Cyclopentanetetracarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0856 1,2,3,4-Cyclopentanetetracarboxylic Acid (CAS 3724-52-5) is an alicyclic tetracarboxylic acid with four carboxyl groups arranged around a compact, rigid cyclopentane ring. It is widely studied as a precursor to alicyclic dianhydrides used in the synthesis of optically transparent polyimide films for optoelectronic and coating applications. Its multidentate carboxylate functionality also makes it a valuable linker in metal-organic frameworks and coordination polymers. AMI Scientific supplies this TCI building block in a 5 g pack; store it cool, dry, and tightly closed, and follow the official TCI Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAgrawal (2026). Complexation Behavior of all-cis-1,2,3,4-Cyclopentanetetracarboxylic Acid and Hippuric Acid toward Transition Metal Ions: A Potentiometric Study. \u003cem\u003eInternational Journal of Scientific Research in Science and Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.32628\/ijsrst2613437\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.32628\/ijsrst2613437\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHuang et al. (2022). Three coordination polymers of manganese(II), cadmium(II) with a flexible ligand of cis, cis, cis-1,2,3,4-cyclopentanetetracarboxylic acid: crystal structures, thermal decomposition mechanisms and magnetic properties. \u003cem\u003eResearch on Chemical Intermediates\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s11164-022-04784-9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s11164-022-04784-9\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eCui et al. (2013). Four 3D “brick-wall”-like metal–organic frameworks with a flexible ligand of (S,S,R,R)-1,2,3,4-cyclopentanetetracarboxylic acid: crystal structures, luminescent and magnetic properties. \u003cem\u003eDalton Trans.\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c2dt32022c\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c2dt32022c\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":48276743028954,"sku":"TCI2510C085615149","price":1112000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0856.jpg?v=1767095892"},{"product_id":"tci2510c088815198","title":"TCI C0888 3721-95-7 Cyclobutanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0888 Cyclobutanecarboxylic Acid (CAS 3721-95-7) is a strained four-membered cyclic carboxylic acid widely used as a non-heterocyclic building block in organic synthesis. Its carboxyl group is readily converted into amides, esters, and other acyl derivatives, making it a practical entry point for multi-step synthetic routes. The cyclobutyl motif is frequently explored in medicinal chemistry to introduce conformational rigidity and modulate the three-dimensional profile of target molecules. Available through AMI Scientific in 10 g and 25 g packs, it should be stored in a tightly closed container in a cool, dry, well-ventilated area in line with the official TCI documentation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDEHMLOW et al. (1990). ChemInform Abstract: Synthesis of Stereoisomeric 3‐Substituted Cyclobutanecarboxylic Acid Derivatives.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199036116\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199036116\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGrigor’ev et al. (2018). Complexes of An(VI) with Cyclobutanecarboxylic Acid Anions and Outer-Sphere Alkali Metal Cations. \u003cem\u003eRadiochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1134\/s1066362218050065\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1134\/s1066362218050065\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKabalka et al. (2005). Synthesis of a boronated amino acid as a potential neutron therapy agent: 1-amino-3-[(dihydroxyboryl)ethyl]cyclobutanecarboxylic acid. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2005.04.130\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetlet.2005.04.130\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":"10g","offer_id":48086035792090,"sku":"TCI2510C088815198","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086035824858,"sku":"TCI2510C088815199","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0888.jpg?v=1767095945"},{"product_id":"tci2510c094515284","title":"TCI C0945 5660-81-1 Cyclopentylmalonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0945 Cyclopentylmalonic Acid (CAS 5660-81-1) is a substituted malonic acid derivative bearing a cyclopentyl group at the alpha position. Its dicarboxylic framework and acidic alpha proton make it a versatile non-heterocyclic building block for alkylation, condensation, esterification, and controlled decarboxylation chemistry. The compound is widely used in multi-step organic synthesis and medicinal chemistry research where a compact cyclic aliphatic scaffold is required. Available in 5 g and 25 g packs, it should be kept tightly closed in a cool, dry place, with the manufacturer's Safety Data Sheet consulted before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086039298266,"sku":"TCI2510C094515284","price":3055000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086039331034,"sku":"TCI2510C094515285","price":10651000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0945.jpg?v=1767096051"},{"product_id":"tci2510c129615788","title":"TCI C1296 636-82-8 1-Cyclohexene-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1296 1-Cyclohexene-1-carboxylic Acid is an α,β-unsaturated cyclic carboxylic acid offering two complementary reactive sites. The carboxyl group supports amide, ester, and acid chloride formation, while the conjugated alkene enables epoxidation, dihydroxylation, and catalytic hydrogenation. It is frequently chosen as a model substrate when evaluating chiral catalysts in asymmetric hydrogenation studies. AMI Scientific offers this TCI building block in 1 g and 5 g pack sizes for small to medium scale research.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWang et al. (2014). Dehydro-aromatization of cyclohexene-carboxylic acids by sulfuric acid: critical route for bio-based terephthalic acid synthesis. \u003cem\u003eRSC Advances\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c3ra46670a\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c3ra46670a\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGeiger et al. (1995). (3S,4S,5R)-3,4,5-trihydroxy-1-cyclohexene-carboxylic acid from Sequoiadendron giganteum. \u003cem\u003ePhytochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0031-9422(95)00450-l\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0031-9422(95)00450-l\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eXu et al. (2020). Facile access to chiral β-homoglutamic acid from 3-cyclohexene-carboxylic acid. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397911.2020.1802760\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397911.2020.1802760\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":48086061711578,"sku":"TCI2510C129615788","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086061744346,"sku":"TCI2510C129615789","price":4292000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1296.jpg?v=1767096691"},{"product_id":"tci2510c130915802","title":"TCI C1309 598-10-7 1,1-Cyclopropanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1309 1,1-Cyclopropanedicarboxylic Acid carries two carboxyl groups on a single carbon of a strained three-membered ring. This gem-disubstituted arrangement makes it a valuable building block for introducing rigid cyclopropane motifs into target molecules. Both acid groups can be converted into esters or amides, or used as handles for ring construction and decarboxylation studies. AMI Scientific offers this TCI product in 1 g and 5 g packs for laboratory research and medicinal chemistry work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHELL et al. (1996). ChemInform Abstract: Efficient Method for Removal of a Carboxylic Acid Moiety from Sterically Crowded Cyclopropanedicarboxylic Acid Derivatives.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199636063\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199636063\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHell et al. (1996). Efficient Method for Removal of a Carboxylic Acid Moiety from Sterically Crowded Cyclopropanedicarboxylic Acid Derivatives. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919608003571\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919608003571\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKvaratskhelia et al. (2011). The Regularities of Electrolytic Dissociation of 1,2-Cyclopropanedicarboxylic Acids. \u003cem\u003eECS Transactions\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1149\/1.3646092\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1149\/1.3646092\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":48086062366938,"sku":"TCI2510C130915802","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086062399706,"sku":"TCI2510C130915803","price":2474000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1309.jpg?v=1767096715"},{"product_id":"tci2510c141815959","title":"TCI C1418 31982-85-1 (-)-trans-1,2-Cyclohexanedicarboxylic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1418 (-)-trans-1,2-Cyclohexanedicarboxylic anhydride (CAS 31982-85-1) is a chiral cyclic anhydride built on a rigid cyclohexane framework. Nucleophilic ring opening with alcohols or amines yields chiral monoesters and monoamides that retain a free carboxylic acid handle. These intermediates are valuable for asymmetric synthesis, chiral ligand preparation, and catalyst desymmetrisation studies. The material is moisture sensitive and is supplied by AMI Scientific in convenient 100 mg and 1 g research quantities.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086068723930,"sku":"TCI2510C141815959","price":431000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086068756698,"sku":"TCI2510C141815960","price":2045000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1418.jpg?v=1767096907"},{"product_id":"tci2510c142715971","title":"TCI C1427 2216-84-4 1,2,3,4,5,6-Cyclohexanehexacarboxylic Acid Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1427 1,2,3,4,5,6-Cyclohexanehexacarboxylic Acid Monohydrate (CAS 2216-84-4) is a highly functionalized polycarboxylic acid bearing six carboxyl groups on a single cyclohexane ring. Its exceptional density of coordinating groups makes it a powerful linker for metal-organic frameworks and coordination polymers with high connectivity. It is also employed as a chelating agent and as a crystallization modifier in materials research. AMI Scientific supplies this TCI reagent in 5 g and 25 g research packages.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eThuéry (2010). A Lanthanide Ion-Decorated Uranyl−Organic Two-Dimensional Assembly with all-cis 1,2,3,4,5,6-Cyclohexanehexacarboxylic Acid. \u003cem\u003eCrystal Growth \u0026amp; Design\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/cg1003534\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/cg1003534\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eThuéry et al. (2010). Two- and Three-Dimensional Europium−Organic Assemblies with the all-cis and all-trans Isomers of 1,2,3,4,5,6-Cyclohexanehexacarboxylic Acid. \u003cem\u003eCrystal Growth \u0026amp; Design\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/cg100500p\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/cg100500p\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":48086069149914,"sku":"TCI2510C142715971","price":2373000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086069182682,"sku":"TCI2510C142715972","price":6058000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1427.jpg?v=1767096919"},{"product_id":"tci2510c165716316","title":"TCI C1657 14166-21-3 (+\/-)-trans-1,2-Cyclohexanedicarboxylic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-trans-1,2-Cyclohexanedicarboxylic Anhydride is a chemical compound widely used in organic synthesis as a building block. It is a stable and reactive compound with an anhydride structure, making it suitable for esterification and amide formation reactions. This compound is commonly utilized in laboratory settings for the synthesis of complex organic molecules, pharmaceutical development, and research on chemical reactivity. Its availability in various packaging options facilitates its use in both small-scale and large-scale experiments. The compound is ideal for applications requiring precise chemical reactions and is a valuable resource in Indonesian laboratories for advancing research in organic chemistry and related fields.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086083240154,"sku":"TCI2510C165716316","price":2802000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086083272922,"sku":"TCI2510C165716317","price":8506000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1657.jpg?v=1767097289"},{"product_id":"tci2510c170116361","title":"TCI C1701 2426-02-0 1-Cyclohexene-1,2-dicarboxylic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Cyclohexene-1,2-dicarboxylic Anhydride is a chemical compound widely used as a building block in organic synthesis. It is a versatile reagent that participates in various chemical reactions, particularly in esterification and anhydride formation. Its unique molecular structure makes it suitable for the synthesis of complex organic compounds. This compound is commonly used in laboratory settings for research and development in the field of chemistry. Its reactivity and stability under controlled conditions make it a preferred choice for both academic and industrial applications. The compound is essential for producing intermediates in pharmaceutical and polymer industries. Its application in Indonesia is significant, especially in academic and research institutions where precision and quality are paramount.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086084976858,"sku":"TCI2510C170116361","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086085009626,"sku":"TCI2510C170116362","price":4266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1701.jpg?v=1767097342"},{"product_id":"tci2510c170216363","title":"TCI C1702 1560-11-8 1-Cyclopentenecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Cyclopentenecarboxylic Acid is a chemical compound widely used in organic synthesis and laboratory research. With a unique molecular structure featuring a cyclopentene ring and a carboxylic acid group, this compound is highly reactive and suitable for various chemical reactions. It is commonly utilized in the development of pharmaceuticals and industrial chemicals due to its reactivity and structural versatility. The compound is available in two packaging options, making it accessible for both small-scale and moderate laboratory use. Its stability under controlled conditions and ease of handling make it a reliable choice for researchers in Indonesia. This product is ideal for applications requiring precise chemical synthesis and is an essential tool in organic chemistry laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBespalova et al. (1994). New synthesis of 3-cyclopentenecarboxylic acid esters by olefin metathesis. \u003cem\u003eRussian Chemical Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/bf00703712\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/bf00703712\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":48086085042394,"sku":"TCI2510C170216363","price":2071000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086085075162,"sku":"TCI2510C170216364","price":6385000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1702.jpg?v=1767097346"},{"product_id":"tci2510c191416545","title":"TCI C1914 7686-77-3 3-Cyclopentene-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Cyclopentene-1-carboxylic Acid is a chemical compound widely used as a foundational building block in organic synthesis. Its unique molecular structure, featuring a cyclopentene ring connected to a carboxylic acid group, makes it a versatile reagent in laboratory settings. This compound is essential for the development of complex organic molecules, particularly in reactions involving substitution or addition mechanisms. Its role in creating heterocyclic compounds, esters, and other functional derivatives is critical in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for synthetic chemists. It exhibits stability under controlled conditions but is sensitive to oxidation and moisture, requiring careful handling. Its simple yet adaptable structure allows for a wide range of chemical modifications, making it suitable for high reactivity applications. The flexibility of its molecular framework enables it to participate in various reaction pathways, enhancing its utility in organic synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Cyclopentene-1-carboxylic Acid is commonly used by researchers, students, and pharmaceutical industries. It plays a vital role in the synthesis of bioactive compounds, drug development, and industrial chemical production. Its availability in the local market ensures accessibility for those requiring high-quality raw materials for their experiments and projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its cyclopentene ring structure and carboxylic acid functionality.\u003c\/li\u003e\n\u003cli\u003ePreparation of ester derivatives through esterification reactions with alcohols and acid catalysts.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive compounds in pharmaceutical research for drug discovery and formulation.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where functional group modification is required for polymer synthesis.\u003c\/li\u003e\n\u003cli\u003eResearch in chemical modification of organic molecules requiring high reactivity and structural versatility.\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: 7686-77-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and oxidizing agents\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 prevent degradation due to moisture and oxidation. It is recommended to use airtight containers made of glass or polyethylene to minimize exposure to air and humidity. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with strong oxidizing agents to prevent unwanted reactions. Ensure proper ventilation in the workspace to reduce the risk of inhalation of any vapors. Regular monitoring of storage conditions is advised to maintain the compound's integrity and effectiveness for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086091956442,"sku":"TCI2510C191416545","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086091989210,"sku":"TCI2510C191416546","price":2650000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1914.jpg?v=1767097536"},{"product_id":"tci2510c195316564","title":"TCI C1953 46022-05-3 (1R,2R)-1,2-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1,2)-Cyclohexanedicarboxylic Acid is a chiral building block widely used in asymmetric synthesis to construct molecules with optical activity. This compound plays a crucial role in chemical research by enabling precise control over molecular configuration, which is essential in pharmaceutical and biochemical applications. Its unique structure allows it to participate in a variety of chemical reactions, making it a versatile tool for synthetic chemists. As a key component in the development of bioactive compounds, it supports the creation of complex molecules with specific stereochemical properties.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and reactivity make it a preferred choice for researchers working in asymmetric synthesis. Its cyclohexane ring provides a rigid framework, which is beneficial for maintaining stereochemical integrity during chemical transformations. Additionally, its ability to undergo substitution and reduction reactions allows for the synthesis of a wide range of derivatives. These properties make it an ideal candidate for applications requiring high precision and specificity in molecular design.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (1,2)-Cyclohexanedicarboxylic Acid is commonly used in research focused on asymmetric synthesis and the development of bioactive compounds. It is a valuable resource for academic institutions and research centers aiming to advance knowledge in organic chemistry and pharmacology. Its use is particularly prevalent in studies involving chiral molecule synthesis and drug development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is essential for creating chiral molecules with specific stereochemistry, which is critical in pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: Its role in constructing complex structures makes it ideal for synthesizing compounds with biological activity.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: It supports the study of molecular reactivity and structural modifications in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Compound Synthesis: Its stability and reactivity enable the production of drug candidates with precise stereochemical configurations.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is widely used in educational and research settings to explore advanced synthetic methodologies and molecular design.\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: 46022-05-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: 1R,2R\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\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 sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible substances to ensure safety. Proper labeling of containers is essential for safe handling and storage in a laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086092644570,"sku":"TCI2510C195316564","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086092677338,"sku":"TCI2510C195316565","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1953.jpg?v=1769180370"},{"product_id":"tci2510c195416566","title":"TCI C1954 21963-41-7 (1S,2S)-1,2-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1S,2S)-1,2-Cyclohexanedicarboxylic Acid is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in organic chemistry laboratories, where it is employed to create molecules with specific stereochemistry. Its importance lies in its ability to influence the stereochemical outcome of reactions, making it a valuable tool in the development of pharmaceuticals and other chiral compounds. As a key component in asymmetric synthesis, it enables chemists to achieve precise control over the spatial arrangement of atoms in target molecules.\u003c\/p\u003e\n\u003cp\u003eThe compound's stable cyclic structure and two carboxylic acid groups make it highly reactive and versatile in various chemical reactions. These functional groups allow for a wide range of chemical transformations, including substitution, esterification, and asymmetric reactions. Its chemical stability under controlled conditions ensures consistent performance in laboratory settings, making it a preferred choice for researchers. The compound's ability to participate in multiple reaction pathways enhances its utility in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the development of bioactive compounds. It is a fundamental reagent in experiments requiring precise molecular control, and its availability in pure form supports high-quality research. Many research institutions and universities rely on it as a key reagent in their synthetic processes, contributing to the advancement of chemical sciences in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules with specific stereochemistry, essential in pharmaceutical development.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its stable structure and reactivity make it a key reagent in complex molecule synthesis and structural analysis.\u003c\/li\u003e\n\u003cli\u003eBioactive Compound Development: Used in the synthesis of compounds with biological activity, supporting drug discovery efforts.\u003c\/li\u003e\n\u003cli\u003eStructural Elucidation Studies: Its well-defined stereochemistry aids in determining molecular structures through spectroscopic analysis.\u003c\/li\u003e\n\u003cli\u003eTeaching and Training: Frequently used in academic settings to demonstrate asymmetric synthesis principles and molecular construction techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 21963-41-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct 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 to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent moisture absorption, which could affect its reactivity. Due to its carboxylic acid groups, it may require storage in a non-corrosive container to avoid degradation. Laboratory personnel should handle it with care, using appropriate personal protective equipment when necessary. It is important to ensure that the storage area is well-ventilated to minimize exposure to vapors. Proper labeling of containers is essential to ensure safe handling and prevent accidental misuse.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086092710106,"sku":"TCI2510C195416566","price":1718000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086092742874,"sku":"TCI2510C195416567","price":5781000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1954.jpg?v=1769144430"},{"product_id":"tci2510c202916656","title":"TCI C2029 25357-95-3 1,3,5-Cyclohexanetricarboxylic Acid (cis- and trans- mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3,5-Cyclohexanetricarboxylic Acid (cis- and trans- mixture) is a versatile organic compound widely used in chemical and materials science research. This compound is a key component in the synthesis of complex molecules, particularly in the development of organic-inorganic hybrid materials. Its cyclic structure with three carboxylic acid groups positioned at specific sites makes it a valuable reagent for creating stable and functional chemical structures. In laboratory settings, it serves as a foundational material for various experimental processes, including the formation of metal-organic frameworks (MOFs) and other advanced materials.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and controlled reactivity make it a preferred choice for researchers aiming to achieve precise chemical reactions or crystalline structures. Its non-toxic nature and availability in the chemical market further enhance its appeal for routine laboratory use. Additionally, its non-volatile properties and good solubility in both organic solvents and water allow it to be used in a wide range of experimental conditions. These characteristics ensure that it remains a reliable and efficient material for diverse applications in modern research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,3,5-Cyclohexanetricarboxylic Acid is commonly used in the study and development of hybrid materials, especially in the synthesis of Metal Organic Frameworks (MOFs). Its role in creating stable and functional materials has made it an essential reagent in both academic and industrial research settings. The compound's reliability and adaptability make it a go-to choice for researchers working on advanced material science projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMetal Organic Frameworks (MOFs) synthesis benefits from its cyclic structure and carboxylic acid groups, enabling coordination with metal ions to form stable porous materials.\u003c\/li\u003e\n\u003cli\u003eOrganic-inorganic hybrid material development utilizes its chemical stability and reactivity to create functional composite structures with unique properties.\u003c\/li\u003e\n\u003cli\u003eChemical reaction intermediates in synthesis processes rely on its controlled reactivity and solubility, making it suitable for a variety of reaction conditions.\u003c\/li\u003e\n\u003cli\u003eCrystal growth experiments take advantage of its non-volatile nature and solubility, allowing for the formation of well-defined crystalline structures.\u003c\/li\u003e\n\u003cli\u003eMaterial characterization studies use its consistent properties to ensure reproducibility and accuracy in analytical techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 25357-95-3\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 various quantities as per standard chemical supply specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline powder\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain its chemical integrity. As a non-volatile and non-toxic material, it does not require special handling beyond standard laboratory safety protocols. When working with this compound, it is advisable to use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Its good solubility in both organic and aqueous solvents means it can be safely used in a wide range of experimental setups without significant risk. Proper storage and handling ensure its effectiveness and safety in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086097035482,"sku":"TCI2510C202916656","price":4165000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086097068250,"sku":"TCI2510C202916657","price":11104000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2029.jpg?v=1768816743"},{"product_id":"tci2510c203616669","title":"TCI C2036 34771-04-5 trans-4-(Carbobenzoxyamino)cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTrans-4-(Carbobenzoxyamino)cyclohexanecarboxylic Acid is a chemical compound widely used in synthetic chemistry applications. It serves as a key building block in the synthesis of complex organic molecules, particularly those with cyclic structures and amino substitutions. This compound is commonly found in chemical laboratories as a raw material for the development of various functional compounds. Its versatility makes it an essential component in the creation of bioactive substances, including pharmaceuticals and pharmacological agents.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure features both carboxylate and amino functional groups, which contribute to its high reactivity. These functional groups enable it to participate in a variety of chemical reactions, such as substitution, coupling, and structural modification. Its reactivity and functional versatility make it a preferred choice for organic chemists and researchers. The compound's ability to interact with a wide range of reagents enhances its applicability in diverse synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in both fundamental and applied chemical research. It plays a crucial role in the development of chemical materials for the pharmaceutical, cosmetic, and industrial sectors. Researchers in educational institutions and research organizations frequently utilize this compound for experimental purposes, contributing to advancements in chemical sciences and drug development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This compound is ideal for synthesizing complex organic molecules due to its reactive functional groups and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It is used in the creation of bioactive compounds, supporting the development of new drugs and pharmacological agents.\u003c\/li\u003e\n\u003cli\u003eCosmetic Formulation: Its chemical properties make it suitable for use in the formulation of cosmetic products, contributing to the development of new ingredients.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemistry: It is applied in the production of various chemical materials, supporting industrial applications in different sectors.\u003c\/li\u003e\n\u003cli\u003eResearch and Education: It is widely used in academic and research settings for experimental studies and teaching purposes in chemical sciences.\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: 34771-04-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in 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 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 light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Protective gloves and safety goggles should be worn when handling to ensure personal safety. Avoid contact with incompatible substances to prevent unwanted chemical reactions. Proper labeling and storage conditions are essential to ensure the compound remains effective for research and application purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086097756378,"sku":"TCI2510C203616669","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086097789146,"sku":"TCI2510C203616670","price":4266000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086097821914,"sku":"TCI2510C203616671","price":13880000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2036.jpg?v=1767097690"},{"product_id":"tci2510c206216709","title":"TCI C2062 76784-95-7 (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2062 is (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid, an alicyclic tricarboxylic acid carrying three carboxyl groups on a cyclohexane framework at positions 1, 2, and 4, with a uniform spatial orientation on one face of the ring. In organic synthesis and materials science laboratories, this compound serves as a non-heterocyclic building block — a small starting material that carries several reactive points at once, allowing it to be developed into far larger molecules. Its three acid groups are readily converted into esters, amides, acid chlorides, or metal salts, making it an efficient point of departure for researchers constructing branched structures and cross-linked networks alike.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this material a preferred choice are the combination of a saturated cyclohexane framework and a defined stereochemical arrangement. Unlike its aromatic analogues, the saturated aliphatic ring does not absorb ultraviolet light strongly and is more resistant to yellowing, so polymers or resins derived from it tend to retain optical clarity for longer. The (1alpha,2alpha,4alpha) stereochemical designation ensures that all three carboxyl groups point to the same face of the ring, giving a predictable and reproducible spatial geometry that is valuable whenever the shape of the resulting molecule governs its performance. Sourcing the material from TCI gives laboratories a consistent, well-characterised grade suitable for reproducible synthetic work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic synthesis, polymer chemistry, and coordination chemistry, as well as in industrial R\u0026amp;D units developing coatings, resins, and specialty materials. It is generally handled at bench scale for method development and small-batch preparation, where a defined multi-functional starting material shortens synthetic routes and where consistent supply of a catalogued reference compound supports work that must be repeated and reported.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolyester and polyamide synthesis — its three carboxyl groups act as multiple condensation points, allowing researchers to introduce branching or cross-linking into a polymer backbone from a single well-defined monomer.\u003c\/li\u003e\n\u003cli\u003eCoordination polymer and metal–organic framework studies — the carboxyl groups convert readily into metal salts and coordinate to metal centres, while the fixed stereochemistry gives predictable connectivity between nodes.\u003c\/li\u003e\n\u003cli\u003eOptically clear coating and resin development — the saturated aliphatic ring resists ultraviolet absorption and yellowing, helping formulators produce cured films that keep their clarity over extended service periods.\u003c\/li\u003e\n\u003cli\u003eMulti-step organic synthesis as a scaffold — chemists selectively derivatise the acid groups into esters, amides, or acid chlorides to build larger, structurally elaborate target molecules from a compact core.\u003c\/li\u003e\n\u003cli\u003eStructure–property investigations in materials science — the defined (1alpha,2alpha,4alpha) geometry lets researchers correlate spatial arrangement of functional groups with the mechanical and optical behaviour of the resulting material.\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: 76784-95-7\u003c\/li\u003e\n\u003cli\u003eProduct Code: C2062\u003c\/li\u003e\n\u003cli\u003eChemical Name: (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in standard TCI research-scale packaging; please confirm the size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: Keep the container tightly closed in a cool, dry, well-ventilated place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong bases and strong oxidising agents. Glass or chemically resistant containers with secure closures are suitable, and the container should be reclosed promptly after each use to limit moisture uptake. Handle the solid in a fume hood or a well-ventilated area, and weigh it carefully to avoid generating airborne dust. Laboratory personnel should wear safety goggles, chemical-resistant gloves, and a laboratory coat, and should avoid contact with skin and eyes as well as inhalation of dust. Wash hands thoroughly after handling. Always consult the manufacturer's Safety Data Sheet before use, and dispose of residues and contaminated materials in accordance with applicable institutional and local chemical waste regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48276098318554,"sku":"TCI2510C206216709","price":2147000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2062.jpg?v=1767097739"},{"product_id":"tci2510c206316711","title":"TCI C2063 16526-68-4 (1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetricarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2063 is (1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetricarboxylic Acid, an alicyclic tricarboxylic acid bearing three carboxyl groups arranged alternately at positions 1, 3, and 5 of the cyclohexane ring, all oriented toward the same face of the ring. This arrangement produces a molecule with highly distinctive three-fold symmetry, which has made the compound one of the most widely used building blocks in supramolecular chemistry and crystal engineering. In the laboratory it serves as a three-directional connector that links metal centres or other organic units into two-dimensional and three-dimensional networks.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material such a frequent choice is its cis,cis-1,3,5 geometry, which forces all three carboxyl groups to occupy equatorial positions in the chair conformation, so that the directions of bonding become ordered and predictable. It is this regularity that makes the compound the aliphatic analogue of trimesic acid, but built on a flexible, saturated framework rather than a rigid aromatic plane. That flexibility allows network topologies and pore shapes to form that cannot be reached with flat ligands. The three acid groups are also readily deprotonated in a stepwise manner, giving further control over how the linker binds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically encountered in university research groups and institutional materials-chemistry facilities working on coordination polymers, framework materials, and supramolecular assemblies. It is normally handled at the bench scale during ligand preparation and solvothermal synthesis, weighed out as a solid starting material and combined with metal salts or organic partners. Research and teaching laboratories also use it in synthetic organic chemistry work where a symmetric, multi-functional carboxylic acid scaffold is required.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCoordination polymer and framework synthesis: the three-fold symmetric carboxyl arrangement acts as a tritopic linker that ties metal centres into extended two- and three-dimensional networks with predictable connectivity.\u003c\/li\u003e\n\u003cli\u003eCrystal engineering studies: the fixed cis,cis-1,3,5 geometry gives ordered, predictable bonding directions, allowing researchers to design and rationalise packing arrangements and hydrogen-bonded assemblies with confidence.\u003c\/li\u003e\n\u003cli\u003eSupramolecular chemistry research: as one of the most popular building blocks in this field, it assembles metal centres and organic units into higher-order structures through its three convergent acid groups.\u003c\/li\u003e\n\u003cli\u003ePorous material design: its flexible saturated framework, unlike rigid aromatic ligands, allows access to network topologies and pore shapes that planar linkers such as trimesic acid cannot achieve.\u003c\/li\u003e\n\u003cli\u003eStepwise coordination chemistry experiments: the three acid groups deprotonate progressively, letting researchers tune charge and binding mode of the ligand across different reaction conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 16526-68-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical name: (1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetricarboxylic Acid\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes offered for this catalogue item; please refer to the current listing\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this material in its original tightly closed container in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as strong bases and strong oxidising agents. Use clean, dry glass or chemically compatible plastic containers when transferring or subdividing the solid, and reseal promptly to limit moisture uptake. Handle in a fume hood or well-ventilated workspace, and wear standard laboratory personal protective equipment including safety glasses, gloves, and a laboratory coat. Avoid raising dust during weighing, and clean spills promptly using dry collection methods. Always consult the manufacturer's safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086100672730,"sku":"TCI2510C206316711","price":2778000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086100705498,"sku":"TCI2510C206316712","price":8959000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2063.jpg?v=1767097743"},{"product_id":"tci2510c218616856","title":"TCI C2186 3971-31-1 1,3-Cyclohexanedicarboxylic Acid (cis- and trans- mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2186 1,3-Cyclohexanedicarboxylic Acid is supplied as a mixture of cis and trans isomers. It is an alicyclic dicarboxylic acid in which two carboxyl groups are attached at the 1 and 3 positions of a cyclohexane ring. The material is categorised as a raw material for Metal Organic Frameworks within the organic-inorganic hybrid materials group. Its role in the laboratory is to act as an organic linker — the bridging unit that connects metal nodes to build three-dimensional porous frameworks. Beyond framework construction, the compound is also used as a monomer and as an intermediate in polymer research and in general organic synthesis that calls for a cycloaliphatic backbone.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound attractive is its saturated and flexible cyclohexane backbone, which differs from rigid aromatic linkers such as terephthalic acid. Conformational flexibility of the ring allows a variety of framework topologies to form, including structures that can respond to changes in their environment. The mixture of cis and trans isomers presents two different bond-angle geometries, and researchers frequently exploit this to explore structural diversity during exploratory work. The absence of an aromatic ring also means the resulting framework carries a distinctly different electronic and steric character from aromatic-linker systems.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically used in university and institutional research settings where porous materials, coordination polymers, and polymer chemistry are studied. It suits exploratory synthesis programmes in which several linker geometries are screened before a target framework is selected. Working groups in materials science and organic synthesis draw on it when a saturated cycloaliphatic diacid is required, and it is normally handled in ordinary bench-scale glassware alongside other MOF raw materials held in the laboratory chemical inventory.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMetal organic framework synthesis — serves as the organic linker bridging metal nodes into three-dimensional porous frameworks, with ring flexibility permitting topologies unavailable to rigid aromatic linkers.\u003c\/li\u003e\n\u003cli\u003eCoordination polymer research — the two carboxyl groups at the 1 and 3 ring positions provide reliable coordination sites for building extended metal-carboxylate networks under exploratory conditions.\u003c\/li\u003e\n\u003cli\u003eFramework topology screening — the cis and trans isomer mixture supplies two distinct bond-angle geometries in a single material, letting researchers survey structural diversity efficiently at the exploratory stage.\u003c\/li\u003e\n\u003cli\u003ePolymer research as a monomer — the dicarboxylic acid functionality supports polycondensation chemistry where a saturated cycloaliphatic unit is wanted instead of an aromatic one.\u003c\/li\u003e\n\u003cli\u003eGeneral organic synthesis intermediate — used wherever a synthetic route requires a cycloaliphatic diacid backbone, contributing a non-aromatic scaffold with different steric and electronic character.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: C2186\u003c\/li\u003e\n\u003cli\u003eCAS number: 3971-31-1\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\u003eComposition: mixture of cis and trans isomers\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in a tightly closed container, following the supplier'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, and well-ventilated area, away from direct sunlight, moisture, and incompatible materials. The original supplier container is preferred; if transfer is necessary, use clean, chemically compatible, and clearly labelled containers, and reseal promptly after each use to limit moisture uptake. Handle the material in a fume hood or a well-ventilated workspace, and wear standard laboratory personal protective equipment including a lab coat, safety glasses, and suitable chemical-resistant gloves. Avoid the generation and inhalation of dust, and avoid contact with skin and eyes. Use dedicated clean spatulas when weighing to prevent cross-contamination of the stock. Always consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable laboratory waste regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086109126874,"sku":"TCI2510C218616856","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086109159642,"sku":"TCI2510C218616857","price":6184000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2186.jpg?v=1767097878"},{"product_id":"tci2510c219716873","title":"TCI C2197 2305-31-9 cis-1,3-Cyclohexanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003ecis-1,3-Cyclohexanedicarboxylic Acid (CAS 2305-31-9) is an organic compound belonging to the class of cyclic aliphatic dicarboxylic acids and serves as an important building block in chemical synthesis. The molecule features a cyclohexane ring carrying two carboxyl groups (–COOH) attached at positions 1 and 3 in the cis configuration. In the laboratory, this material acts as a versatile precursor for assembling more complex molecules through esterification, amidation, or coordination with metal ions. The presence of two reactive acid groups makes it an ideal starting point for designing ligands, polymer monomers, and pharmaceutical or agrochemical intermediates, allowing synthetic chemists to build target structures step by step with predictable reactivity.\u003c\/p\u003e\n\u003cp\u003eThe main advantage of this compound lies in the cis geometry of its two carboxyl groups, which produces a characteristic bond angle and functional-group density that offer stereochemical flexibility not available in the trans isomer. This arrangement positions the two acid groups on the same face of the ring, enabling selective and well-defined interactions in both solution-phase and coordination chemistry. The compound is a stable dicarboxylic acid that is straightforward to weigh, dissolve, and handle under routine laboratory conditions, and its well-characterized reactivity supports reproducible results across repeated syntheses. For researchers seeking a dependable aliphatic diacid scaffold, this TCI-grade reagent offers consistent quality that simplifies method development and scale-up work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly applied in organic chemistry, inorganic chemistry, and materials science research groups, where it is used to construct new molecular architectures in a systematic and controlled manner. Academic and industrial researchers employ it in esterification and amidation studies to generate monomers, crosslinkers, and coordination complexes, while polymer chemists use it as a rigid aliphatic dicarboxylic acid component in polyamide and polyester formulations. As a stocked item supplied by AMI Scientific, it supports both teaching laboratories and active research projects, ensuring that chemists across Indonesia can obtain a consistent, traceable building block for exploratory synthesis and method development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLigand Design – The two cis-oriented carboxyl groups provide two well-defined metal-binding sites, making this compound a practical scaffold for constructing chelating ligands and coordination complexes in inorganic synthesis.\u003c\/li\u003e\n\u003cli\u003ePolymer Monomer Synthesis – As a rigid aliphatic dicarboxylic acid, it can be incorporated into polyester and polyamide backbones through esterification or amidation, giving polymer chemists a useful building block for chain extension and crosslinking studies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical and Agrochemical Intermediates – Its reactive carboxyl groups allow straightforward derivatization into esters, amides, and other functional handles, enabling stepwise assembly of bioactive molecules in medicinal chemistry programs.\u003c\/li\u003e\n\u003cli\u003eMaterials Science Research – The defined cis geometry and predictable reactivity make it a useful component for constructing coordination polymers, metal–organic frameworks, and functional organic materials with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003eTeaching and Method Development – As a well-characterized dicarboxylic acid with a defined CAS registry number, it serves as a dependable substrate for teaching esterification reactions and for validating analytical methods such as titration and chromatography.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C2197)\u003c\/li\u003e\n\u003cli\u003eChemical name: cis-1,3-Cyclohexanedicarboxylic Acid\u003c\/li\u003e\n\u003cli\u003eCAS number: 2305-31-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI container sizes; confirm the current pack options with AMI Scientific at the time of ordering.\u003c\/li\u003e\n\u003cli\u003eStorage note: keep the container tightly closed in a cool, dry area, protected from moisture and direct sunlight.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and incompatible materials such as strong bases or oxidizing agents. Keep it in its original, tightly sealed container, preferably the TCI-supplied bottle, and reseal immediately after each use to prevent moisture uptake and contamination. Wear appropriate personal protective equipment, including laboratory gloves and safety glasses, when handling the material, and avoid inhaling any dust by working in a fume hood when transferring larger quantities. Keep the product labeled with its CAS number and batch information, and follow standard laboratory waste-disposal procedures applicable to organic acids.\u003c\/p\u003e\n\u003cp\u003e*Note: Assumptions made where the Indonesian reference was silent — pack sizes, physical form, and purity are not specified and are therefore left to confirmation at the time of ordering.*\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086110666970,"sku":"TCI2510C219716873","price":4039000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086110699738,"sku":"TCI2510C219716874","price":13603000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2197.jpg?v=1767097890"},{"product_id":"tci2510c219816875","title":"TCI C2198 15383-49-0 1,2,4,5-Cyclohexanetetracarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2,4,5-Cyclohexanetetracarboxylic acid is an organic compound built around a cyclohexane ring that carries four carboxylic acid groups at the 1,2,4,5 positions. In the laboratory, it serves as a versatile building block for the synthesis of a wide range of derivative compounds, including esters, imides, coordination ligands, and functional polymer monomers. The presence of four reactive carboxyl groups makes it an ideal starting material for condensation reactions and structural modification, and it is widely used in organic chemistry research, polymer chemistry, materials chemistry, and the development of intermediates for both industrial and academic applications. This product is supplied by TCI under catalog number C2198 and CAS number 15383-49-0, and is available in 5 g and 25 g pack sizes tailored to laboratory working scales.\u003c\/p\u003e\n\u003cp\u003eResearchers select this compound primarily because of its relatively rigid and symmetric cyclohexane framework, which provides a stable molecular scaffold and facilitates control over the geometry of the final synthetic products. The four carboxylic acid groups distributed around the ring allow the molecule to act as a multi-functional linker or ligand, offering multiple points of attachment in coordination chemistry and enabling stepwise derivatization in organic synthesis. Its symmetry reduces the number of possible isomers and side reactions, giving cleaner reaction profiles and more predictable outcomes. These characteristics make it a dependable and preferred choice when constructing complex molecular architectures, cross-linked networks, or well-defined coordination compounds in advanced research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically employed in academic and industrial research programs focused on organic synthesis, polymer development, and materials science. It is commonly used in the preparation of polyimide precursors, coordination ligands, and functional monomers for specialty polymers, particularly in university chemistry departments and research institutes. The availability of 5 g and 25 g packaging allows researchers to match the quantity to the scale of their work, whether for small exploratory reactions or longer synthetic campaigns. Its stable, symmetric structure is especially valued when reproducible results and consistent product quality are required in ongoing research projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEster synthesis: The four carboxylic acid groups can be converted into ester derivatives in a stepwise manner, making this compound a practical scaffold for building functional esters used in fine chemical and materials research.\u003c\/li\u003e\n\u003cli\u003eImide and polyimide precursors: Its symmetric tetra-acid structure reacts readily with amines to form imide linkages, supporting the preparation of thermally stable polymer intermediates in polymer chemistry laboratories.\u003c\/li\u003e\n\u003cli\u003eCoordination chemistry ligands: The multiple carboxylate binding sites allow the molecule to coordinate metal ions in well-defined geometries, making it a suitable ligand for designing coordination complexes and framework materials.\u003c\/li\u003e\n\u003cli\u003eFunctional polymer monomers: The rigid cyclohexane core can be incorporated into polymer backbones as a cross-linking or branching unit, enabling controlled network architectures in functional polymer synthesis.\u003c\/li\u003e\n\u003cli\u003eIntermediate development: Organic and medicinal chemistry teams use this compound as a versatile intermediate for condensation and ring-modification steps, enabling access to more complex non-heterocyclic target molecules.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 15383-49-0\u003c\/li\u003e\n\u003cli\u003eCatalog number: C2198\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eAvailable pack sizes: 5 g and 25 g\u003c\/li\u003e\n\u003cli\u003ePhysical form: not specified in the available product data\u003c\/li\u003e\n\u003cli\u003eStorage note: keep the container tightly closed and store in a cool, dry place protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the product in a cool, dry place, protected from moisture and direct sunlight, inside a tightly sealed original container. Use containers made of glass or compatible laboratory plastics that resist acidic compounds, and avoid metal containers that may react with carboxylic acids. Keep the container closed when not in use and reseal it promptly after each weighing to minimize exposure to humid air. Wear appropriate personal protective equipment, such as laboratory gloves, safety goggles, and a laboratory coat, when handling the material. Work in a well-ventilated area or fume hood to avoid inhaling any dust from the powder. Keep the material away from strong bases, oxidizing agents, and open flames, and follow standard laboratory waste-disposal procedures when discarding unused material.\u003c\/p\u003e\n\u003cp\u003e*Note: This description is based solely on the facts provided in the Indonesian reference; no additional technical data was added.*\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086110732506,"sku":"TCI2510C219816875","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086110765274,"sku":"TCI2510C219816876","price":3560000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2198.jpg?v=1767097894"},{"product_id":"tci2510c236717119","title":"TCI C2367 39079-62-4 Chromone-3-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChromone-3-carboxylic Acid (TCI C2367), with CAS number 39079-62-4, is a chemical compound widely used in laboratory settings as a building block for the synthesis of heterocyclic compounds. This compound serves as a fundamental component in the development of complex organic structures, particularly in the field of medicinal chemistry. Its role is essential in the creation of biologically active molecules, such as flavonoids and other natural products. Due to its structural versatility, it is a key reagent in various synthetic pathways, enabling the formation of diverse chemical entities with potential pharmaceutical applications.\u003c\/p\u003e\n\u003cp\u003eThe stability and controlled reactivity of Chromone-3-carboxylic Acid make it a preferred choice for organic chemists. Its ability to participate in multiple reaction types, including Diels-Alder, substitution, and condensation reactions, enhances its utility in synthetic chemistry. The compound’s chemical properties allow for predictable and reproducible outcomes in laboratory experiments, making it a reliable material for both research and development purposes. Its molecular structure also provides opportunities for functional group modifications, expanding its applicability in drug discovery and biochemical studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chromone-3-carboxylic Acid is a vital component for organic chemistry research, especially in pharmaceutical and biotechnology sectors. Its availability in solid form and ease of handling make it practical for a wide range of experimental applications. Researchers in Indonesia frequently use this compound to explore new synthetic routes and develop novel compounds with potential therapeutic benefits. Its role in advancing chemical research is significant, supporting both academic and industrial innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its versatile molecular structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules such as flavonoids and natural products for pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eFacilitation of Diels-Alder reactions for the construction of complex ring systems in medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eUse in substitution and condensation reactions to modify functional groups for drug design applications.\u003c\/li\u003e\n\u003cli\u003eSupport in biochemical studies for the investigation of compound interactions with biological targets.\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: 39079-62-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eChromone-3-carboxylic Acid should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its solid form, it is suitable for storage in glass or plastic containers that are resistant to chemical degradation. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental contamination. Regular inspection of storage conditions is advised to maintain optimal chemical stability and safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086122528986,"sku":"TCI2510C236717119","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086122561754,"sku":"TCI2510C236717120","price":3434000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2367.jpg?v=1767098207"},{"product_id":"tci2510c239717162","title":"TCI C2397 952616-39-6 (+\/-)-cis-3-(Carbobenzoxyamino)cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-cis-3-(Carbobenzoxyamino)cyclohexanecarboxylic Acid is a chemical compound widely used in organic synthesis reactions within laboratory settings. This compound plays a crucial role in the development of complex molecules, particularly in the synthesis of bioactive compounds such as pharmaceuticals and pharmacological agents. Its unique structural features make it an essential building block for researchers aiming to create new chemical entities with specific biological activities. Due to its versatility, it is frequently utilized in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and reactivity under controlled conditions make it a preferred choice for synthetic chemists. Its ability to interact with various functional groups allows for the creation of diverse molecular structures, enhancing its applicability in advanced chemical synthesis. The presence of a cyclohexane ring and the carboxylic acid functionality provide multiple points of reactivity, making it suitable for a wide range of chemical transformations. These properties contribute to its popularity among researchers working in organic chemistry and medicinal chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in scientific research and pharmaceutical product development. Researchers rely on its complex structure and high reactivity to conduct experiments that require precise molecular modifications. Its limited availability further underscores its value in advanced research, making it a sought-after material for those engaged in drug discovery and chemical innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a primary application where this compound serves as a key building block for creating complex molecules with biological activity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its ability to participate in various chemical reactions, enabling the synthesis of active pharmaceutical ingredients.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry studies often use this compound to develop new drugs, leveraging its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003eMolecular modification processes rely on its stable chemical properties and reactivity to create novel compounds with desired functionalities.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects utilize this compound to explore new chemical pathways and optimize the properties of potential therapeutic agents.\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: 952616-39-6\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 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 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, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances, and ensure proper ventilation in the workspace. Regular inspection of storage conditions is advised to maintain the integrity of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086124658906,"sku":"TCI2510C239717162","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2397.jpg?v=1767098282"},{"product_id":"tci2510c240017167","title":"TCI C2400 1259278-10-8 (1R,3S)-3-(Carbobenzoxyamino)cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1R,3S)-3-(Carbobenzoxyamino)cyclohexanecarboxylic Acid is a specialized organic compound used as a building block in chemical synthesis. This compound plays a crucial role in laboratories where complex molecular structures are being developed. Its unique chemical structure, featuring a cyclohexane ring modified with an amino and a carboxylic acid group, makes it a versatile tool for synthetic chemists. Due to its reactivity and compatibility with various reagents, it is widely used in research settings to create new compounds with specific functional groups.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and predictable chemical behavior make it a preferred choice for synthetic chemists. Its ability to undergo substitution, coupling, and modification reactions allows it to be integrated into a wide range of synthetic pathways. The presence of the carbobenzoxy (Cbz) group adds an additional layer of functionality, enabling controlled deprotection in later stages of synthesis. These properties make it a reliable and efficient reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in the synthesis of bioactive compounds. It is a key component in the development of pharmaceuticals and advanced materials. Researchers in universities and research institutions rely on its chemical versatility to create compounds with specific biological activities. Its application in drug discovery and material science underscores its importance in modern chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBioactive Compound Synthesis: This compound is ideal for creating bioactive molecules due to its reactivity and structural versatility, enabling the synthesis of pharmaceuticals and functional materials.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its use in organic synthesis allows for the development of complex molecules, making it a valuable tool for academic and industrial research.\u003c\/li\u003e\n\u003cli\u003eDrug Development: The compound's ability to undergo various chemical transformations makes it suitable for the synthesis of drug candidates with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Applications: Its structural characteristics make it useful in the development of advanced materials with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eSynthetic Pathway Optimization: The compound's predictable behavior and compatibility with reagents make it a preferred choice for optimizing synthetic routes 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: 1259278-10-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: 10 g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store at room temperature in a dry, cool 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 dry, cool environment away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound. Avoid contact with incompatible substances to prevent unwanted chemical reactions. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086124855514,"sku":"TCI2510C240017167","price":2273000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2400.jpg?v=1767098286"},{"product_id":"tci2510c250217277","title":"TCI C2502 53159-92-5 1,2,3,4-Cyclobutanetetracarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2,3,4-Cyclobutanetetracarboxylic Acid is a chemical compound widely used as a fundamental building block in the synthesis of complex molecules. Its unique cyclic structure with four carboxylate groups makes it highly versatile in organic chemistry applications. In the laboratory, this compound plays a critical role in the development of new compounds, including pharmaceuticals, industrial chemicals, and organic materials. Its ability to participate in various chemical reactions and form stable intermediates makes it an essential tool for researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high reactivity and compatibility with a wide range of functional groups, which allows for the creation of diverse molecular structures. Its stability under controlled conditions further enhances its utility in precise chemical synthesis. These properties make it a preferred choice for chemists aiming to modify complex molecular frameworks. The compound’s predictable behavior and consistent performance contribute to its reliability in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2,3,4-Cyclobutanetetracarboxylic Acid is commonly used in organic chemistry, pharmaceutical research, and material science. It is a key component in experiments involving the synthesis of new compounds and the development of advanced chemical techniques. Its availability and reliability make it a staple in research institutions and universities across Indonesia, supporting a wide range of scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its cyclic structure and multiple carboxylate groups, enabling the creation of complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drug molecules through structural modifications and functional group manipulations.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments rely on its reactivity and stability to create advanced polymers and chemical intermediates.\u003c\/li\u003e\n\u003cli\u003eAcademic research institutions use it as a standard building block for teaching and experimental purposes in organic chemistry courses.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production incorporates it to synthesize specialty chemicals and functional materials with specific properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 53159-92-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity. Since it is a solid powder, it should be kept in a sealed container to avoid exposure to air and contaminants. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to ensure safety. Regular monitoring of storage conditions is advised to maintain the compound’s integrity and usability in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086129344730,"sku":"TCI2510C250217277","price":2071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2502.jpg?v=1767098414"}],"url":"https:\/\/amiscientific.com\/en\/collections\/chemicals-by-class-compounds-by-functional-group-carboxylic-acids.oembed?page=25","provider":"AMI Scientific","version":"1.0","type":"link"}