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1,2-Cyclohexanediamine

    • Product Name 1,2-Cyclohexanediamine
    • Alias 1,2-Diaminocyclohexane
    • Einecs 208-521-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    107908

    Cas Number 694-83-7
    Molecular Formula C6H14N2
    Molecular Weight 114.19 g/mol
    Appearance Colorless to pale yellow liquid or crystalline solid
    Boiling Point 221 °C
    Melting Point 36-40 °C
    Density 0.97 g/cm³
    Solubility In Water Soluble
    Refractive Index 1.512
    Flash Point 108 °C
    Pka 10.51 (for the amino group)
    Odor Ammonia-like
    Synonyms 1,2-Diaminocyclohexane; DACH

    As an accredited 1,2-Cyclohexanediamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,2-Cyclohexanediamine is packaged in a 500 mL amber glass bottle with a secure screw cap and chemical safety labeling.
    Shipping 1,2-Cyclohexanediamine is typically shipped in sealed, corrosion-resistant containers under ambient conditions. It should be handled with care, kept away from strong oxidizers, and stored in a cool, dry, well-ventilated area. Ensure containers are properly labeled and comply with all relevant transport regulations for hazardous chemicals.
    Storage 1,2-Cyclohexanediamine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store at room temperature and ensure proper labeling. Use secondary containment if possible to prevent leaks or spills, and keep away from sources of ignition.
    Application of 1,2-Cyclohexanediamine

    Applications of 1,2-Cyclohexanediamine in Industrial Manufacturing

    1,2-Cyclohexanediamine serves as a vital intermediate in multiple sectors of chemical production. Its regioselective reactivity supports custom polymer synthesis, advanced coatings formulation, and specialized chemical modification processes. Below, we summarize core downstream application scenarios based on our manufacturing expertise.

    1. Epoxy Resin Curing Agents for High-Performance Coatings

    Manufacturers widely prefer 1,2-cyclohexanediamine as a curing agent for high-solids epoxy coatings. Its cyclic diamine structure enhances cross-link density and mechanical performance in protective layers for industrial flooring, automotive parts, and corrosion-control applications. The raw material directly participates in amine-epoxy reactions, enabling rapid curing even at ambient temperature. Our QC teams verify amine content and purity to ensure batch compliance.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006)
    • RoHS Directive (2011/65/EU) for electronics coatings
    • ISO 12944-5 for corrosion protection systems
    • ASTM D3271 for epoxy resin compound evaluation

    Typical usage ratio

    • 10-18 wt% of the total polymer mix; dosage varies with epoxy equivalent weight and desired final film properties

    Downstream process integration

    • Incorporated during resin formulation, just prior to application and curing step
    • Dispersion via mechanical mixing at controlled temperature (15-25°C)
    • Amine hardener and base resin measured separately for precision

    Final product types

    • High-build anticorrosive coatings
    • Industrial self-leveling floors
    • Automotive OEM epoxy primers
    • Electrical insulation coatings

    2. Polyamide Synthesis for Engineering Plastics

    1,2-Cyclohexanediamine acts as a key monomer in the production of specialty polyamides, particularly those requiring flexibility and chemical resistance. Its use in polymer chains imparts improved thermal and hydrolytic stability, making it valuable in automotive, electronics, and oilfield equipment plastics. Polymerization typically occurs via condensation with dicarboxylic acids, using high-purity feedstock to meet strict viscosity and intrinsic strength parameters.

    Industry compliance standards

    • ISO 1874-1 for polyamide materials
    • UL 94 for flammability in plastics
    • RoHS Directive (2011/65/EU) for plastics in electronics
    • Automotive OEM material specifications (e.g., VW TL 52674 for polyamide parts)

    Typical usage ratio

    • 12-20 mol% of total diamine fraction, adjusted based on desired glass transition temperature and flexibility

    Downstream process integration

    • Used as co-monomer during melt polycondensation with adipic, sebacic, or terephthalic acids
    • Pre-compounded under nitrogen to avoid oxidative degradation
    • Post-polymerization blending for tailored mechanical properties

    Final product types

    • Heat-resistant engineering plastics
    • Flexible cabling polymers
    • Automotive air intake manifolds
    • Electrical connectors and switches

    3. Chemical Intermediate for Agrochemical Active Ingredient Synthesis

    Several agrochemical producers utilize 1,2-cyclohexanediamine as a molecular building block in synthesizing selective herbicides and fungicides. Its diamine functionality allows for robust amide bond formation during the creation of bioactive compounds with targeted activity and environmental persistence profiles. Consistent reactivity and purity level are essential to meet regulatory registration requirements for crop protection products.

    Industry compliance standards

    • FAO/WHO Technical Specifications for agricultural chemicals
    • OECD Good Manufacturing Practices (GMP) for crop protection synthesis
    • EU Regulation (EC) No 1107/2009 for plant protection product approval
    • US EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)

    Typical usage ratio

    • Stoichiometric molar ratios; adjusted on scale-up based on downstream process yield and impurity removal

    Downstream process integration

    • Used in amidation step post-chlorination or nitration of aromatic intermediates
    • Requires controlled pH and solvent selection to favor selective conversion
    • Batchwise reaction under inert gas for sensitive intermediates

    Final product types

    • Selective pre- and post-emergence herbicides
    • Systemic fungicides for cereal crops
    • Seed treatment formulations
    • Pesticide intermediates

    4. Curing Component in Polyurea and Specialty Polyurethane Systems

    The use of 1,2-cyclohexanediamine in polyurea and two-component polyurethane formulations provides manufacturers with fast gel and tack-free times, essential for protective linings and construction sealants. Its secondary amine groups act as unique chain extenders, promoting robust material properties under variable ambient or low-temperature environments. Strict raw material specifications control viscosity, reactivity index, and shelf stability.

    Industry compliance standards

    • EN 1504-2 for concrete surface protection
    • ASTM D790 for flexural properties of plastics
    • ISO 9001:2015 for quality management systems in polyurethane production
    • Regulation (EU) 2019/1021 (POP Regulation) for end-use in construction

    Typical usage ratio

    • 3-14 wt% as chain extender, depending on required crosslinking density and flexibility of end product

    Downstream process integration

    • Added directly to isocyanate prepolymer stream during mixing
    • Reactivity calibrated to pot life and application method (spray, pour, brush)
    • Component metering carefully controlled on automated production lines

    Final product types

    • Polyurea spray coatings for waterproofing
    • Elastomeric expansion joint sealants
    • Industrial pipe and tank linings
    • Construction adhesives

    5. Chelating Agent Precursor for Water Treatment Chemicals

    Water treatment chemical producers leverage the diamine structure of 1,2-cyclohexanediamine to manufacture chelating agents with superior binding efficiency for transition metal ions. Through selective functionalization, it forms the backbone for specialty ligands used in industrial water circuits, boilers, and cooling towers. Compliance with environmental discharge standards mandates high-purity raw materials.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management in chemical production
    • EN 12124 for water treatment chemical requirements
    • EU REACH registration for process chemicals
    • US EPA Clean Water Act effluent guidelines

    Typical usage ratio

    • Intermediate input at equimolar ratios with aldehyde and carboxyl agents; dosage adapted to formulation design

    Downstream process integration

    • Reacted in aqueous or mixed solvent systems for selective chelate formation
    • Followed by purification (filtration, crystallization) to meet chelant product grade
    • QC monitored for residual amine content and heavy metal impurities

    Final product types

    • Scale inhibitors for boiler feedwater
    • Iron and copper chelating agents
    • Industrial cooling water stabilizers
    • Process water cleaners

    6. Intermediate for Pharmaceutical Bulk API Synthesis

    Pharmaceutical manufacturers employ 1,2-cyclohexanediamine as an essential building block in the synthesis pathway of certain active pharmaceutical ingredients, particularly where a rigid cyclic diamine framework is necessary for molecular activity. The raw material enters protected amination or acylation steps, and strict GMP controls govern both input and process. We guarantee tight specification control and traceability to ensure medicinal end-use compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF Monographs (where applicable in synthesis route)
    • EU GMP Part II for API synthesis
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Predominantly stoichiometric, determined by target API synthesis scheme and impurity profile requirements

    Downstream process integration

    • Amine component added in first or second step of multi-step organic synthesis
    • May require protection/deprotection cycles depending on neighboring functional groups
    • QC sampling at each checkpoint for identity and purity confirmation

    Final product types

    • API intermediates for antiviral medications
    • Certain antihypertensive bulk APIs
    • Pharmaceutical-grade intermediates with diamine motifs
    • Small-molecule bioactive compounds
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