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4-Aminocyclohexanecarboxylic Acid

    • Product Name 4-Aminocyclohexanecarboxylic Acid
    • Alias AmCHA
    • Einecs 211-608-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    812461

    Chemical Name 4-Aminocyclohexanecarboxylic Acid
    Cas Number 6563-07-9
    Molecular Formula C7H13NO2
    Molecular Weight 143.18 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 225-230 °C (dec.)
    Solubility In Water Slightly soluble
    Density 1.17 g/cm3
    Pka 4.2 (carboxylic acid), 10.4 (amino group)
    Smiles C1CC(CCC1(N)C(=O)O)
    Inchi InChI=1S/C7H13NO2/c8-6-3-1-2-5(4-6)7(9)10/h5-6H,1-4,8H2,(H,9,10)
    Storage Temperature 2-8 °C

    As an accredited 4-Aminocyclohexanecarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package of 4-Aminocyclohexanecarboxylic Acid comes in a sealed, light-resistant amber glass bottle with a secure screw cap.
    Shipping 4-Aminocyclohexanecarboxylic Acid should be shipped in tightly sealed containers, protected from moisture and physical damage. Store and transport it at room temperature in compliance with local and international chemical shipping regulations. Proper labeling and documentation are required, and the package must be handled by trained personnel using appropriate safety precautions.
    Storage 4-Aminocyclohexanecarboxylic acid should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Clearly label the storage container and ensure access is limited to trained personnel. Follow all relevant safety guidelines and local regulatory requirements for storage.
    Application of 4-Aminocyclohexanecarboxylic Acid

    Applications of 4-Aminocyclohexanecarboxylic Acid in Industrial Manufacturing

    Our facility produces high-purity 4-Aminocyclohexanecarboxylic Acid (ACHC), addressing key downstream industrial applications with strict quality control and compliance throughout our manufacturing chain. The following application scenarios reflect established, real-world uses of ACHC, supported by validated formulation protocols, internationally recognized industry standards, and integration into well-defined industrial process steps.

    1. Active Pharmaceutical Ingredient Synthesis (Anti-fibrinolytic Agents)

    Pharmaceutical manufacturers use ACHC as a core intermediate in the synthesis of tranexamic acid and related antifibrinolytic substances. The controlled purity and traceability of our material ensure reliable performance during esterification and amide coupling processes in commercial-scale API production. Accurate dosing supports both cost efficiency and regulatory requirements across large-batch synthesis lines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph for Tranexamic Acid synthesis intermediates
    • U.S. FDA CFR 21 Parts 210 & 211 (Drug manufacturing compliance)
    • China Pharmacopoeia (ChP) API intermediate standards

    Typical usage ratio

    • Typically 0.95–1.10 molar equivalents per reaction batch, adjusted based on target yield and downstream impurity profile; fine-tuned by in-process analytical feedback.

    Downstream process integration

    • Charged into initial reactor during amidation step, followed by hydrogenation and crystallization for finished API isolation.
    • Used in continuous feed or fed-batch reactors, depending on the manufacturing site's process scale and regulatory batch size limits.

    Final product types

    • Tranexamic acid API (bulk powder)
    • Tablet-grade and injectable-grade tranexamic acid for finished dose manufacturing
    • Specialty antifibrinolytic API derivatives for niche pharmaceutical preparations

    2. Specialty Coating Additives (Corrosion Inhibitor Synthesis Pathways)

    Coating formulators integrate ACHC as a building block for amine-functionalized corrosion inhibitors deployed in automotive, marine, and heavy equipment paints. Its cycloaliphatic backbone provides resistance against hydrolytic degradation, protecting steel substrates in harsh operating regimes, especially where long-term exposure to moisture and salt occurs. Manufacturing facilities blend ACHC-based intermediates during pigment dispersion to improve bath stability and pigment adhesion attributes.

    Industry compliance standards

    • ISO 12944-5 (Performance requirements for corrosion protection coatings)
    • GHS/REACH Registered Substances—Annex XVII Restrictions
    • ASTM D7087 (Environmental performance of coatings)
    • Automotive OEM approval protocols (e.g., VW TL226, GM 9985949)

    Typical usage ratio

    • 0.2–1.3% by total coating solids weight, depending on the metal surface exposure class and primer system chemistry; dosage reduction possible with optimized dispersants.

    Downstream process integration

    • Reacted with polyisocyanates or epoxy oligomers in blending tanks to synthesize proprietary amide-functional dispersants.
    • Post-addition to aqueous or solvent-based primer systems during pigment mill base preparation for enhanced anticorrosive protection.

    Final product types

    • Industrial epoxy primers for ship hulls and offshore platforms
    • Automotive underbody coatings and anti-rust primers
    • Heavy machinery maintenance paints
    • High-durability architectural anti-corrosion topcoats

    3. Biomedical Polymer Synthesis (Controlled-Release Matrix Formation)

    Medical device manufacturers and pharmaceutical excipient suppliers use ACHC in the preparation of polyamino acid matrices for biomedical polymers. Its secondary amine group facilitates bespoke polycondensation reactions, generating drug-incorporating hydrogels or implantable scaffolds. These materials control the release profile of embedded therapeutic agents, meeting design criteria for absorption and biocompatibility in surgical and wound care applications.

    Industry compliance standards

    • ISO 10993-1 (Biological evaluation of medical devices—Part 1)
    • USP General Chapter <87> (Biological Reactivity Tests, In Vitro)
    • ISO 13485 (Medical devices—Quality management systems)
    • EU Medical Devices Regulation (MDR 2017/745 Annex I General Safety and Performance Requirements)

    Typical usage ratio

    • 5–18% molar fraction relative to other polyamino acid monomers, adjusted to achieve target crosslink density and mechanical properties of the polymer matrix; deviations based on required degradation rate.

    Downstream process integration

    • Pre-reacted in batch reactors or continuous polymerization lines with dicarboxylic acid monomers and multifunctional linkers to form hydrophilic polyamide networks.
    • Solution-cast or extruded as films, microneedles, or 3D-printed medical grade parts.

    Final product types

    • Implantable hemostatic sponges
    • Wound dressing pads with slow-release antibiotics
    • Bioabsorbable surgical films
    • Controlled-release oral or transdermal drug delivery platforms

    4. Dye and Pigment Intermediates (Reactive Dye Modifier Manufacturing)

    ACHC enters the dye and pigment industry as a unique cycloaliphatic amino acid used to synthesize reactive dye modifiers, especially for high-performance textile dye molecules. Dye producers utilize its amine and carboxylic moieties to introduce hydrophilic handles or steric bulk, thereby enhancing washfastness and shade retention in cellulosic fiber applications. Custom molecular modifications via ACHC streamline patentable dye series for performance apparel and home textiles.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Harmful substances in textiles)
    • ZDHC MRSL 2.0 (Zero Discharge of Hazardous Chemicals)
    • EU REACH Annex XIV Authorisation List (intermediate substance status)
    • GB/T 17592 (Testing for banned azo dyes)

    Typical usage ratio

    • 0.5–1.8 molar equivalents per dye molecule, depending on required solubility and functional group orientation; application technician determines precise ratio for target color strength and compatibility.

    Downstream process integration

    • Condensed onto anthraquinone or azo dye intermediates via amidation in glass-lined synthesis reactors prior to diazotization, sulfonation, or further coupling steps.
    • End products isolated via spray-drying and micronized for homogeneous textile printing or dyeing lot consistency.

    Final product types

    • Reactive dyes for cotton and rayon
    • Washfast pigment dispersions for technical textiles
    • Custom colorants for high-performance synthetic apparel
    • Low-toxicity dye formulations for babywear and home linens

    5. Electronic Chemicals (Photoresist Monomer Synthesis in Microelectronics)

    ACHC is incorporated into specialty photoresist monomer synthesis lines within semiconductor and PCB fabrication sectors. The unique cyclic amine structure allows creation of solubility-modifying blocks that enhance developer contrast and pattern resolution during wafer lithography. Cleanroom-based manufacturers integrate ACHC-derived intermediates in early stage monomer production to achieve precise chemical structure and minimal ionic contamination, vital for 22 nm or smaller process nodes.

    Industry compliance standards

    • SEMI C1 (Specifications for Electronic Grade Chemicals)
    • IATF 16949 (Electronic component manufacturing quality system)
    • IPC-4101 (PCB base materials qualification)
    • RoHS Directive 2011/65/EU Substance Restrictions

    Typical usage ratio

    • 1–4% by weight in monomer synthesis blends, altered based on desired photoresist sensitivity, solubility in alkaline developer, and process compatibility with 193 nm immersion lithography.

    Downstream process integration

    • Introduced at pre-polymerization stage in photoactive resin manufacture; ensures precise backbone flexibility and prevents microcracking during spin-coating of resist films.
    • Final resist solutions filtered and transported under nitrogen to integrated circuit fabs for direct application onto silicon wafers.

    Final product types

    • Photoresist formulations for advanced CMOS and DRAM devices
    • High-resolution soldermask layers
    • Patterned dielectric films for high-density printed circuit boards
    • Micro-lithographic coatings for MEMS and sensor chip production
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