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HS Code |
407765 |
| Cas Number | 591-23-1 |
| Molecular Formula | C7H14O |
| Molar Mass | 114.19 g/mol |
| Appearance | Colorless liquid |
| Odor | Camphor-like |
| Melting Point | 36-38 °C |
| Boiling Point | 171-174 °C |
| Density | 0.926 g/cm3 at 25 °C |
| Solubility In Water | Moderately soluble |
| Refractive Index | 1.456 at 20 °C |
| Flash Point | 66 °C (closed cup) |
| Vapor Pressure | 1.2 mmHg at 25 °C |
As an accredited 3-Methylcyclohexanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Methylcyclohexanol is packaged in a sealed 500 mL amber glass bottle, labeled with hazard symbols, chemical name, and CAS number. |
| Shipping | 3-Methylcyclohexanol is shipped in tightly sealed containers, protected from light, moisture, and heat. It should be stored in a cool, dry, well-ventilated area, away from incompatible substances. During transport, appropriate labeling for hazardous materials is required, and spill containment measures should be in place to prevent environmental contamination. |
| Storage | 3-Methylcyclohexanol should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from heat sources and incompatible substances such as strong oxidizing agents. The storage area should be clearly labeled and protected from direct sunlight and moisture. Ensure containers are made of compatible material and equipped to prevent leaks or spills to minimize health and environmental risks. |
Applications of 3-Methylcyclohexanol in Industrial ManufacturingWe supply 3-Methylcyclohexanol for critical applications in various chemical processing and advanced materials sectors. The following describes key industrial uses, with reference to actual manufacturing flows, regulatory strictness, and market-end product types. 1. Pharmaceutical Intermediate in Antihistamine SynthesisMany pharmaceutical manufacturers use 3-Methylcyclohexanol as a core intermediate during multi-step synthesis of certain first and second-generation antihistamines. Its controlled reactivity and chiral properties allow for selective functionalization in cyclohexyl ring precursors during active pharmaceutical ingredient (API) production. Batch-specific QC ensures very low residual solvents and complies with traceability protocols required in regulated drug synthesis. Material entry typically occurs after initial ring functionalization and prior to amide bond formation, supporting high-value molecule assembly with strict impurity limits. Industry compliance standards
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2. Precursor for Cyclohexylamine Derivatives in Rubber Additive Manufacturing3-Methylcyclohexanol enters the synthesis of specialty amines utilized as accelerators and antioxidants in synthetic rubber compounding. Manufacturers benefit from its reproducible purity and low water content, which are crucial for forming cyclohexylamine derivatives with consistent amination and reduction yields. Process engineers dose the material into catalytic hydrogenation reactors, ensuring correct amine functionalization for subsequent formulation with rubber latex or masterbatch systems. This approach helps meet high-precision additive performance for tire, hose, and sealant production. Industry compliance standards
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3. Intermediate in Fragrance and Flavor Compound SynthesisOur manufacturing partners use this raw material to prepare key cyclohexyl moieties in aroma chemical synthesis, including stable alcohols and downstream lactones. In flavor and fragrance ingredient flows, it acts as an initial core for ring-opening, oxidation, or selective hydrogenation steps, producing signature green, woody, or floral odor notes. Strict attention to residuals ensures food-grade and fine fragrance standards, particularly for IFRA-certified applications. Material dosing is tightly controlled through in-line blending with aldehyde and etheric intermediates. Industry compliance standards
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4. Solvent and Carrier in Agrochemical FormulationIn agrochemical production, the material is employed as a specialty solvent and carrier for specific classes of herbicidal or insecticidal actives. It supports formulations requiring controlled polarity and volatility, promoting dispersion and uptake in crop-spray concentrates. Producers monitor water and impurity levels to optimize emulsification, wetting, and shelf-stability. Addition typically follows active ingredient synthesis and precedes microencapsulation or bulk blending processes, allowing precision integration for agricultural spraying systems. Industry compliance standards
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5. Monomer Modifier in Specialty Polyamide and Polyurethane ProductionAdvanced polymer manufacturers utilize this material to introduce methyl-cyclohexyl units into polyamide and polyurethane chains, influencing mechanical, thermal, and flexibility properties of final resins. Its introduction improves low-temperature toughness and alters crystallinity in target formulations, supporting applications in precision engineering plastics and high-durability coatings. Chemical engineers meter the compound into prepolymerization tanks to ensure accurate incorporation through transamidation or polyaddition, optimizing reaction profiles and minimizing undesired crosslinking effects. Industry compliance standards
Typical usage ratio
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