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Cyclohexanemethanol

    • Product Name Cyclohexanemethanol
    • Alias CHM
    • Einecs 202-682-8
    • 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
    VTB
    Specifications

    HS Code

    524965

    Cas Number 100-49-2
    Molecular Formula C7H14O
    Molar Mass 114.19 g/mol
    Appearance Colorless liquid
    Boiling Point 161-163 °C
    Melting Point -60 °C
    Density 0.948 g/cm3 at 20 °C
    Solubility In Water Slightly soluble
    Flash Point 73 °C (closed cup)
    Refractive Index 1.463 at 20 °C
    Pubchem Cid 7516
    Odor Weak, characteristic

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

    Packing & Storage
    Packing Cyclohexanemethanol is supplied in a 500 mL amber glass bottle with a secure screw cap, labeled with product and hazard information.
    Shipping Cyclohexanemethanol should be shipped in tightly sealed containers, protected from physical damage. Store and transport in a cool, well-ventilated area away from incompatible substances and ignition sources. It is classified as a hazardous chemical, so compliance with local, national, and international regulations for handling and transportation is required.
    Storage Cyclohexanemethanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition. Keep it away from heat, strong oxidizing agents, and direct sunlight. Ensure proper labeling and use chemical-resistant shelving. Store at room temperature and avoid incompatible substances to prevent hazardous reactions. Handle with appropriate personal protective equipment.
    Application of Cyclohexanemethanol

    Applications of Cyclohexanemethanol in Industrial Manufacturing

    As a dedicated chemical raw material producer, we focus on supplying high-quality cyclohexanemethanol for specialized usage in globally established downstream sectors. This section details precisely how industrial practitioners integrate our material into production environments, reflecting real formulation experience, compliance criteria, and finished-goods deliverables.

    1. Plasticizer Intermediate for Specialty Plastic Production

    Plasticizer manufacturers use cyclohexanemethanol as an intermediate during the synthesis of high-molecular esters for flexible vinyl, polyurethane, and engineering plastics. Its primary hydroxyl group reacts efficiently with dicarboxylic acids, improving performance characteristics such as plasticity and low-temperature flexibility in niche compounding blends where phthalate alternatives are required. QC teams monitor residual alcohol content to ensure downstream polymer compliance and stability during melt processing.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • US FDA 21 CFR 177.2600 (elastomeric materials in contact with food)
    • EU Plastics Regulation (EU) No 10/2011
    • ISO 9001:2015 quality management for polymer additives

    Typical usage ratio

    • Generates esters at 0.7–1.0 molar ratio with acids; resulting plasticizer content in final polymer blends ranges 15–30% by weight, fine-tuned per application hardness and migration requirements.

    Downstream process integration

    • Direct feed to esterification reactors, followed by vacuum stripping and purification prior to plasticizer blending in compounding/extrusion lines.

    Final product types

    • Flexible cable coatings
    • Automotive underbody sealants
    • High-durability synthetic leather
    • Custom-engineered polyurethane elastomers

    2. Solvent Component in Industrial Coatings Formulation

    Manufacturers of industrial solvent-borne coatings adopt cyclohexanemethanol as a co-solvent to modulate evaporation profile, viscosity, and application characteristics. Its intermediate polarity helps optimize paint film formation without contributing excessive volatile organic compounds, especially in aliphatic polyurethane and epoxy systems that require balanced open time and atomization control during spray or roll-on processes.

    Industry compliance standards

    • US EPA 40 CFR Part 59 (VOC limits for paints and coatings)
    • EU Directive 2004/42/EC (limitation of emissions of VOCs)
    • China GB 24408-2020 (limits for VOCs in architectural coatings)
    • ASTM D5403: Solvent emission levels

    Typical usage ratio

    • Added at 2–8% w/w of total solvent composition; adjustment is based on resin type, film thickness target, and cure schedule.

    Downstream process integration

    • Weighing and blending in solvent tank farm with other cosolvents, followed by inline transfer to high-shear mixers during pigment and resin dispersion steps.

    Final product types

    • Polyurethane automotive topcoats
    • Heavy-duty industrial floor paints
    • Chemical-resistant tank linings
    • Epoxy-based machinery coatings

    3. Building Block in Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies incorporate cyclohexanemethanol into complex synthetic routes where it functions as a selective nucleophile, particularly for constructing intermediates needed in cardiovascular and CNS agent synthesis. Its high chemical purity limits potential impurities that could affect batch reproducibility during multistep reactions or hinder downstream purification of APIs.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • United States Pharmacopeia (USP General Chapter <797>)
    • European Pharmacopoeia (Ph. Eur. 9.0)
    • FDA Drug Master File (DMF) regulations

    Typical usage ratio

    • Used as a synthetic intermediate at reaction-specific dosages, typically 0.2–2.0 equivalents relative to starting halogenated substrates; exact molar excess determined via process validation and pilot runs.

    Downstream process integration

    • Charge to batch reactor during nucleophilic substitution or reduction steps, often followed by in-process control for residual alcohol and side products prior to intermediate workup and refinement.

    Final product types

    • Piperidine-based drug intermediates
    • Sartans (angiotensin receptor blockers) building blocks
    • Antidepressant precursor chemicals

    4. Raw Material for Fragrance Ester Synthesis in Fine Chemicals

    Fragrance and aroma chemical producers react cyclohexanemethanol with aliphatic or aromatic acids to synthesize esters valued for their mild, musky scent profiles in high-end perfumery and consumer product fragrances. The alcohol’s controlled reactivity results in clean esterification, ensuring minimal byproduct development—a critical parameter for supply to customers requiring stable aroma profiles over long storage periods.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Cosmetics Regulation EC No 1223/2009
    • US Food, Drug and Cosmetic Act (FD&C Act – fragrance use)
    • ISO 9235: Fragrance ingredients

    Typical usage ratio

    • Used in esterification at close to 1:1 molar ratio with target acid; the resulting fragrance esters typically make up 0.05–0.20% of total fragrance oil formulation for finished products, subject to olfactory intensity requirements.

    Downstream process integration

    • Reaction with specific acids in stainless reactors under acid catalysis, followed by phase separation, distillation, and QC for olfactory purity prior to incorporation in fragrance blending lines.

    Final product types

    • Luxury fine fragrance oils
    • Air care and home fragrance diffusers
    • Personal care perfumes and eau-de-toilettes
    • Specialty deodorizer bases

    5. Functional Monomer in Reactive Resin Formulations for Adhesives

    Producers of high-performance industrial adhesives integrate cyclohexanemethanol as a monomeric alcohol segment in the design of isocyanate-terminated prepolymers. Its unique hydrophobic cyclohexyl ring improves flexibility and moisture resistance in one- and two-component reactive adhesive systems, enhancing bond retention to metal, composite, and flexible substrates. Formulation chemists monitor molecular incorporation by NMR and FTIR to guide scale-up decisions.

    Industry compliance standards

    • ISO 10993-5 for biocompatibility of adhesives (where relevant)
    • ANSI/UL 746C for chemical resistance in electrical component adhesives
    • ASTM C557 for adhesive shear strength
    • RoHS Directive 2011/65/EU for lead-free formulations

    Typical usage ratio

    • Forms 5–25% of the polyol component by weight in prepolymer synthesis, with precise percentage set based on target flexibility and moisture cure speed.

    Downstream process integration

    • Charged to prepolymer reactor during polyol-isocyanate blending, followed by controlled moisture addition to start partial crosslinking, then downstream transfer to filling and packaging lines.

    Final product types

    • Structural adhesives for automotive assembly
    • Flexible bonding agents in building panel lamination
    • Sealant systems for electronics enclosures

    6. Synthesis Intermediate in Specialty Agrochemical Production

    Agrochemical formulators engage cyclohexanemethanol in syntheses of certain herbicide and pesticide intermediates, particularly those requiring alicyclic alcohols for ring-closed active ingredient structures. Manufacturers focus on traceability and project-specific impurity profiles, as downstream performance depends on input alcohol purity and functionality during condensation or oxidation steps.

    Industry compliance standards

    • FAO/WHO Specifications for plant protection products
    • US EPA 40 CFR Part 180 (residues of pesticides)
    • ISO 9001:2015 in pesticide active ingredient production
    • China GB 20813-2006 (safety requirements for pesticide ingredients)

    Typical usage ratio

    • Utilized at 0.8–1.2 molar equivalents in intermediate steps, with scale adjusted to downstream demand forecasts and process yield optimizations.

    Downstream process integration

    • Fed to batch or continuous reactors for nucleophilic substitution or oxidation, followed by extraction and further derivatization prior to formulation working solution or active ingredient isolation.

    Final product types

    • Substituted cycloalkyl herbicide precursors
    • Custom insecticide intermediates
    • Building blocks for selective growth regulators
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