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2,6-Dimethylcyclohexanol

    • Product Name 2,6-Dimethylcyclohexanol
    • Alias 2,6-Dimethyl-1-cyclohexanol
    • Einecs 211-011-9
    • 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
    VTB
    Specifications

    HS Code

    665077

    Chemical Name 2,6-Dimethylcyclohexanol
    Molecular Formula C8H16O
    Molar Mass 128.21 g/mol
    Appearance Colorless liquid or solid
    Melting Point 35-38 °C
    Boiling Point 192-194 °C
    Density 0.93 g/cm3
    Refractive Index 1.466
    Solubility In Water Slightly soluble
    Flash Point 82 °C
    Cas Number 1193-47-1

    As an accredited 2,6-Dimethylcyclohexanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,6-Dimethylcyclohexanol is supplied in a 100-gram amber glass bottle with a secure screw cap and proper hazard labeling.
    Shipping 2,6-Dimethylcyclohexanol is shipped in tightly sealed containers, typically made of polyethylene or glass, to prevent leakage and contamination. The chemical should be kept in a cool, dry, and well-ventilated area away from heat sources and incompatible substances. All packages are clearly labeled, following regulatory guidelines for safe transportation.
    Storage 2,6-Dimethylcyclohexanol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect from moisture and direct sunlight. Store at room temperature and ensure spill containment measures are in place to prevent environmental contamination.
    Application of 2,6-Dimethylcyclohexanol

    Applications of 2,6-Dimethylcyclohexanol in Industrial Manufacturing

    As a specialty chemical manufacturer, we supply 2,6-Dimethylcyclohexanol for key roles in established value chains. This advanced intermediate sees consistent demand from major segments across the coatings, fragrance, polymer, and agrochemical fields. The following details real-world use cases, integrated at scale by global industry leaders, with special focus on application standards, technical incorporation, and downstream impacts.

    1. High-Performance Coating Resin Monomer Synthesis

    Leading formulators specify this cycloaliphatic alcohol for the synthesis of specialty polyester and acrylic resins where molecular branching and glass transition temperature control are critical. The unique di-substituted structure facilitates the creation of resins for demanding industrial coatings, improving hardness, flexibility, and chemical resistance for automotive and protective finishes. Integration takes place during polycondensation or radical polymerization, where precise dosing supports repeatable process control under audited ISO and REACH frameworks.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for resin production)
    • REACH Regulation (EC) No 1907/2006 (Substance Registration and Use)
    • Automotive OEM approval protocols (e.g., Volkswagen TL226, GM GMW3044)
    • EN 13501 Parts 1–5 (Fire performance of construction products)

    Typical usage ratio

    • 5–15% wt in polyol or monomer blend, adjusted per target molecular weight and desired mechanical property profile

    Downstream process integration

    • Alcohol component charged during pre-polymer preparation or direct monomer mix; introduced prior to condensation or acrylic polymerization stage, monitored under in-line FTIR/viscometry for homogeneity

    Final product types

    • Automotive topcoats and clearcoats
    • High-durability floor and industrial maintenance coatings
    • Protective marine and pipeline coatings
    • Electrical insulation enamel resins

    2. Synthetic Fragrance Intermediate for Fine and Functional Fragrances

    Major fragrance houses use this alcohol as a building block for esterification into musk-like and green-woody aromatic molecules. Its controlled reactivity enables targeted selectivity for high-purity esters, such as in the synthesis of 2,6-dimethylcyclohexylacetate, valued for stable, fresh top notes. Batch processes run under IFRA and IFRA-certified GMP, with purity and residual solvents monitored for compliance with international fragrance safety requirements.

    Industry compliance standards

    • IFRA Standards (latest Amendment)
    • Good Manufacturing Practice (GMP) for Fragrance Ingredients
    • EU Regulation (EC) No 1223/2009 (Cosmetic Products Regulation for personal care aroma compounds)
    • RIFM safety guidelines (Research Institute for Fragrance Materials)

    Typical usage ratio

    • 20–50% molar basis in aromatic esterification step for targeted synthetic notes; actual usage determined by olfactory loading and performance in base oil or solvent matrix

    Downstream process integration

    • Charged into reaction with activated acid chlorides or anhydrides to obtain the desired ester intermediate; inline GC–MS/QC for byproduct removal before blending into master fragrance compounds

    Final product types

    • Fine fragrances (parfum/de toilette)
    • Fabric and air care formulations
    • Personal care (shampoos, body washes, creams)
    • Industrial odor masking agents

    3. Cyclohexyl-Based Agrochemical Intermediates

    Global agrochemical manufacturers, especially in herbicide and plant growth regulator spaces, employ this compound in the synthesis of specialty cyclohexyl derivatives. Selective reactivity with acylating agents and halogenation steps allows formulation of actives with desired lipophilic balance for targeted crop application. Controlled production environments meet responsible care standards, and traceability supports regular audits under leading crop protection guidelines.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specification
    • ISO 9001:2015 (Process and Quality Control)
    • OECD Environmental Safety and Toxicology Protocols
    • China GB 2763–2021 (MRLs for pesticides / raw material purity for export)

    Typical usage ratio

    • 10–25% molar in intermediate synthesis steps, fine-tuned to optimize downstream yield and minimize waste streams; adjusted based on type of pesticide or PGR target molecule

    Downstream process integration

    • Reacted at defined temperature/time in closed vessels with acyl chlorides, sulfonyl chlorides, or haloalkanes; final conversion subjected to controlled crystallization or solvent extraction before onward formulation

    Final product types

    • Selective herbicide actives
    • Fungicidal intermediates
    • Plant growth regulators
    • Seed treatment agents

    4. Cycloaliphatic Polyurethane Prepolymer Manufacture

    Polyurethane manufacturers employ this raw material for production of specialized cycloaliphatic diol prepolymers, providing targeted flexibility, UV stability, and chemical inertness in the finished matrix. Added to the polyol blend before reaction with isocyanates, it allows formulation of systems suitable for optical instrument housings, high-performance elastomers, and light-stable sealants. End users require conformance with automotive, aerospace, and electronics quality audits, with residual monomer and reaction byproduct levels stringently monitored.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for chemical process)
    • ASTM D7707–15 (Polyurethane elastomer raw material specification)
    • UL 94 (Flammability for polymeric components)
    • OEM-specific restricted substances and low VOC requirements

    Typical usage ratio

    • 5–12% by weight in polyol formulation, tailored based on modulus/elasticity requirements and UV resistance parameters

    Downstream process integration

    • Charged into reactor in blend with other cycloaliphatic or linear diols prior to controlled NCO-terminated prepolymer formation; blending monitored for moisture and hydroxyl value consistency

    Final product types

    • UV-stable automotive and aerospace gaskets
    • Extruded polyurethane profiles
    • Precision sealing foams
    • Optical device protection housings

    5. Plasticizer Modifier in Specialty Polymer Processing

    This compound functions as a polar, low-viscosity co-plasticizer in vinyl compounds and engineering polymer blends. It refines processability, flexibility, and plasticizer migration resistance in sensitive technical parts. Plasticizer systems are formulated under direct additive incorporation protocols, and finished blends are batch tested for compliance with end-use mechanical, migration, and emission limits required by the automotive, consumer, and wire & cable sectors.

    Industry compliance standards

    • EN 71-3 (Safety of toys — Migration of certain elements)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electrical/electronic equipment)
    • UL 746C (Polymeric Materials – Use in Electrical Equipment Evaluations)
    • OEM automotive and electronics industry restricted substances lists

    Typical usage ratio

    • 3–8 phr (parts per hundred resin) in PVC and engineering thermoplastic blends; typically adjusted to meet balance of hardness and migration test results

    Downstream process integration

    • Added to polymer melt along with primary plasticizers and stabilizers; disperses via high-shear mixing prior to extrusion, calendaring, or molding, with in-process rheology and volatility testing

    Final product types

    • Wire and cable sheathing materials
    • Automotive dash and trim components
    • Flexible consumer goods casings
    • Medical device housing polymers (non-patient contact)
    Free Quote

    Competitive 2,6-Dimethylcyclohexanol prices that fit your budget—flexible terms and customized quotes for every order.

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