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2-Methylbenzhydrol

    • Product Name 2-Methylbenzhydrol
    • Alias 2-Methyl-1,1-diphenylmethanol
    • Einecs 214-682-8
    • 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

    285325

    Chemicalname 2-Methylbenzhydrol
    Casnumber 613-71-0
    Molecularformula C14H14O
    Molecularweight 198.26 g/mol
    Appearance White to off-white solid
    Meltingpoint 54-56 °C
    Boilingpoint 345 °C at 760 mmHg
    Density 1.092 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Iupacname 2-methyl-1,1-diphenylmethanol
    Smiles CC1=CC=CC=C1C(O)(C2=CC=CC=C2)

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

    Packing & Storage
    Packing 2-Methylbenzhydrol, 25g, is packaged in a sealed amber glass bottle with a secure screw cap and clear hazard labeling.
    Shipping 2-Methylbenzhydrol is shipped in tightly sealed containers made of compatible materials, protected from light and moisture. It should be handled as a combustible solid. During transport, it is labeled per applicable regulations, kept away from oxidizers, and stored at controlled temperatures to ensure stability and prevent degradation or accidental release.
    Storage 2-Methylbenzhydrol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizing agents. Store at room temperature and label clearly. Prevent moisture ingress and avoid handling near open flames or ignition sources. Use appropriate secondary containment to prevent spills.
    Application of 2-Methylbenzhydrol

    Applications of 2-Methylbenzhydrol in Industrial Manufacturing

    Our 2-Methylbenzhydrol, produced with strict quality control in our own facilities, supports downstream manufacturers across multiple specialized sectors. Below, we outline precise applications, standards, process routes, and finished goods where our material has established industrial relevance.

    1. Pharmaceutical Intermediate for Antihistamine Synthesis

    Pharmaceutical manufacturers use 2-Methylbenzhydrol as a critical intermediate in multiple synthesis pathways, especially for certain first-generation antihistamine drugs. Its structure facilitates key Grignard reactions for producing diphenhydramine derivatives, and its purity has a direct impact on downstream yield and impurity profiles. Our material undergoes full batch traceability and meets the stringent regulatory demands of active pharmaceutical ingredient (API) manufacturers integrating it into validated production schemes.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP–NF monograph reference (pertaining to finished antihistamines)
    • 21 CFR Part 210/211 (cGMP for Drug Products, FDA)
    • EDQM Guidelines for Intermediates

    Typical usage ratio

    • Batch molar equivalent of 0.95–1.05 relative to targeted phenyl ring insertions (adjusted to minimize by-products in Grignard couplings)

    Downstream process integration

    • Material enters after aromatic halide preparation, used directly in Grignard reaction vessels, followed by isolation and purification before further condensation and salt formation

    Final product types

    • Bulk diphenhydramine hydrochloride
    • Finished oral tablet and syrup dosage forms
    • Injectable antihistamine ampoules
    • Pharmaceutical intermediates for OTC allergy drugs

    2. UV Stabilizer Intermediate in Polymer Manufacturing

    Producers of polymer additives use 2-Methylbenzhydrol as a core structural unit in the manufacture of benzophenone-based UV stabilizers. The compound feeds directly into acylation reactions, providing the methyl-substituted diphenylmethanol structure necessary for certain high-performance stabilizers used in automotive and outdoor plastics. Accurate addition and impurity control at this stage are fundamental for photochemical activity in finished UV absorber grades.

    Industry compliance standards

    • ISO 9001:2015 certified QC protocols
    • EU Regulation (EC) No 1907/2006 (REACH)
    • EN 71-3 (for plastics in toys)
    • ASTM D3424 (UV stabilizer performance for plastics)

    Typical usage ratio

    • Feed stock at 1.2–1.4 molar equivalents relative to acyl acceptor, ratio optimized for maximum UV absorbance and polymer compatibility

    Downstream process integration

    • Charged to specialty reactor lines as the alcohol source for benzophenone UV-stabilizer synthesis; subsequent blending with polyolefin and PVC masterbatch lines

    Final product types

    • UV-absorber additives for automotive plastics
    • Outdoor equipment polyolefin sheets
    • Weatherable consumer packaging films
    • Specialty coatings for solar protection panels

    3. Fine Fragrance and Aroma Chemical Intermediacy

    In the aroma chemicals industry, 2-Methylbenzhydrol is important as a building block for the manufacture of specialty musks and benzyl-type fragrance molecules. Perfumery chemical manufacturers carry out dehydration and rearrangement steps using this raw material to produce alcohols and esters essential to fragrance house bases. Tight control over side product formation and odor profile begins at the raw material stage, with batch QA linked directly to olfactory performance testing in finished perfumery accords.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • ISO 9001 for fragrance ingredient manufacturing
    • EU Regulation (EC) No 1223/2009 (Cosmetics Rules)
    • RIFM Safety & Toxicology Guidelines

    Typical usage ratio

    • 0.3–0.8% by weight in precursor distillation fractions, adjusted to target specific aromatic intensity and volatility in end molecule design

    Downstream process integration

    • Enters dehydration or esterification sections of aroma intermediate production, followed by vacuum distillation, headspace analysis, and blending for bulk perfumery ingredient lots

    Final product types

    • Musky aromatic bases for fine fragrance concentrates
    • High-purity intermediates for synthetic musk ketones
    • Cosmetic-grade aromatic esters for lotions and body sprays
    • Household fragrance blends

    4. Organic Electronic Materials Synthesis

    Suppliers to the electronics chemicals sector use 2-Methylbenzhydrol in the synthesis of diarylmethane derivatives for organic light-emitting diode (OLED) and other advanced material applications. The compound serves as a tailored precursor where methyl substitution modulates electronic and photophysical properties for improved charge transport. Consistent crystal form, purity, and moisture control are key to downstream device reliability and performance.

    Industry compliance standards

    • RoHS Directive (2011/65/EU)
    • IEC 61249-2-21 (halogen-free materials)
    • ISO 14001 (Environmental Management Systems for electronic chemicals)
    • REACH Annex XVII for hazardous substances

    Typical usage ratio

    • 0.9–1.1 equivalents in functional group activation steps, calibrated to minimize excess reagent and control electronic doping in downstream layers

    Downstream process integration

    • Main input in C–C coupling or cross-coupling for diarylmethane semiconductors; subsequent high-vacuum sublimation and purity checks before incorporation into thin-film deposition lines

    Final product types

    • OLED emissive layer materials
    • Semi-conducting organic films for display technology
    • Photonic material intermediates
    • Customized charge transport layers for organic electronics

    5. Specialty Dye and Pigment Synthesis

    Chemical formulators of specialty dyes apply 2-Methylbenzhydrol in the creation of targeted anthraquinone and benzil-based colorants, exploiting its reactivity in condensation and ring-extension reactions. The methyl group enhances shade intensity and fastness properties, making it valuable for niche coloration systems in high-performance textile and industrial coating applications. Each stage—dye synthesis, product isolation, and formulation—is closely monitored for purity, color strength, and compliance with downstream industry requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • ISO 105 (Color Fastness Test Methods)
    • EU Regulation (EC) No 1907/2006 (REACH) for dye substances
    • GHS (Globally Harmonized System) safety labeling

    Typical usage ratio

    • Typically 0.7–1.2 moles per target dye molecule, modulated for tinting strength and bath exhaustion characteristics in dye house recipes

    Downstream process integration

    • Added in initial condensation reactor for dye synthesis, followed by multi-stage purification, then blended into granulated or liquid dye formulations

    Final product types

    • Textile dyes for synthetic and natural fibers
    • Industrial coatings pigments
    • Printing ink bases for high-speed presses
    • Plastisol coloration agents
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