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4-Biphenylmethanol

    • Product Name 4-Biphenylmethanol
    • Alias benzhydrol
    • Einecs 202-300-9
    • 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

    872348

    Chemicalname 4-Biphenylmethanol
    Synonyms p-Biphenylmethanol, 4-Phenylbenzyl alcohol
    Casnumber 3528-27-8
    Molecularformula C13H12O
    Molecularweight 184.23 g/mol
    Appearance White to off-white solid
    Meltingpoint 72-75°C
    Boilingpoint 368°C
    Density 1.15 g/cm3
    Solubilityinwater Insoluble
    Pubchemcid 17460
    Smiles C1=CC=C(C=C1)CC2=CC=CC=C2O
    Inchi InChI=1S/C13H12O/c14-13-10-8-12(9-11-13)11-6-4-2-1-3-5-7-11/h1-10,14H
    Refractiveindex 1.625
    Storagetemperature Store at room temperature

    As an accredited 4-Biphenylmethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Biphenylmethanol is packaged in a 25g amber glass bottle with a secure screw cap and detailed hazard labeling.
    Shipping 4-Biphenylmethanol is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be transported according to local, national, and international regulations for chemicals. Proper labeling and documentation are required to ensure safe handling, and the package must prevent leaks or spills during transit.
    Storage 4-Biphenylmethanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from direct sunlight and moisture. Keep the container clearly labeled and securely sealed when not in use, and follow all relevant chemical safety protocols during storage.
    Application of 4-Biphenylmethanol

    Applications of 4-Biphenylmethanol in Industrial Manufacturing

    4-Biphenylmethanol serves as a key intermediate in several precision-driven manufacturing sectors. As a producer, we work directly with specialty chemicals formulators, pharmaceutical manufacturers, polymer pioneers, and electronics solution providers. Below, we detail its vital applications, compliance standards, standard concentrations, position in process flows, and the resulting end products across multiple real-world industrial segments.

    1. Pharmaceutical Intermediate for Antihistamines and Antipsychotics

    Pharmaceutical manufacturers incorporate this material at the synthesis stage for various active pharmaceutical ingredients (APIs). It acts as a benzylating agent in multistep routes for drug compounds such as cetirizine and certain derivatives of diphenhydramine. Integrated under cGMP conditions, customers ensure compliance from raw material receipt through to synthesis, purification, and packaging. QC labs monitor impurity profiles according to stringent guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs for registered APIs
    • FDA 21 CFR 210/211 for finished pharmaceuticals
    • EMEA Guideline on Starting Materials

    Typical usage ratio

    • 0.8–1.2 mol equivalents per target intermediate, adjusted based on substrate reactivity in the custom route

    Downstream process integration

    • Utilized at Stage II or III in multistep synthesis for alkylation or benzylation reactions
    • Added post-activation step, prior to workup and intermediate purification
    • Solvent compatibility: Toluene, dichloromethane, or THF under inert atmosphere
    • Isolated by extraction, followed by chromatography or crystallization

    Final product types

    • Antihistamine tablet and syrup formulations (e.g., cetirizine HCl)
    • Antipsychotic bulk APIs (e.g., quetiapine intermediates)
    • Allergy relief OTC drugs
    • R&D pharmaceutical intermediates supplied to contract research organizations

    2. Fine Chemicals Synthesis: Liquid Crystal Monomers

    Manufacturers in advanced electronics utilize this compound as a core precursor for biphenyl-based monomers critical to liquid crystal display (LCD) applications. The aromatic structure provides backbone rigidity, giving rise to key performance metrics such as clearing point and viscosity in the finished mesogenic materials. Material traceability is managed through batch control, spectral identity, and impurity trace records aligned with electronics QC protocols.

    Industry compliance standards

    • JEITA EM-3508 safety and purity guidelines
    • RoHS Directive (EU) 2015/863
    • REACH EC 1907/2006 Registration
    • IEC 61249-2-21 for flame retardant-free materials

    Typical usage ratio

    • Typically 4-12% (w/w) as a precursor, calculated relative to final mesogen batch size; adjustment made per manufacturer’s molecular design

    Downstream process integration

    • Initial monomer synthesis through direct etherification or esterification reactions
    • Followed by oligomerization or copolymerization with acrylates, cinnamates, or cyano-biphenyls
    • Strict temperature and moisture controls maintained to preserve monomer purity
    • Final blend is filtered and solvent-stripped before LCD formulation

    Final product types

    • Liquid crystal panels for displays
    • Specialty films for flexible OLEDs
    • Advanced optical retardation sheets
    • Active matrix backplanes (TFT-LCD)

    3. Polymer Additive for High-Performance Resin Synthesis

    4-Biphenylmethanol is engaged as a chain-stopping or branching monomer in the production of high-glass transition temperature (Tg) polyesters and polycarbonates. Resin chemists exploit its rigid biphenyl group to enhance high-temperature performance, solvent resistance, and dimensional stability, especially in specialty coatings and technically advanced composites for automotive and electrical parts. Adherence to quality frameworks ensures raw material traceability and consistent functional group conversion.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • UL 94 flammability certification (for resin composites)
    • ISO 14001:2015 Environmental Management (where required)
    • EPA TSCA inventory and reporting

    Typical usage ratio

    • 1–5% (w/w) chain stopper or brancher based on total polyol or polycarbonate monomer batch; rate modified for end-use stiffness or heat resistance targets

    Downstream process integration

    • Introduced during polycondensation/polycarbonate formation in reactor charge
    • In-line monitoring of molecular weight and functional group termination
    • Finished resin is pelletized or solution-cast as per customer spec
    • QC releases based on spectral match and heat resistance

    Final product types

    • High-Tg structural polyesters for electronics housing
    • Specialty automotive under-the-hood composites
    • Flame-resistant enclosures
    • Polycarbonate-based optical films and sheets

    4. Fragrance Ingredient for Fine Perfume and Aroma Compound Synthesis

    Downstream aroma and fragrance manufacturers rely on this intermediate as a key building block for alkylated biphenyl derivatives, widely applied in fine fragrance and flavorant formulation. Its aromatic-alcohol structure allows targeted conversion to specialty aldehydes and esters, imparting complex woody or musky notes. Raw material traceability aligns with IFRA and food regulation mandates, ensuring safety and compliance in both perfumery and food-use settings.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • EU Regulation (EC) No 1223/2009 for cosmetics
    • FDA 21 CFR 172.515 for flavoring substances in food
    • ISO 9235:2013 for classification of aroma substances

    Typical usage ratio

    • Typically 2–10% (w/w) for intermediate synthesis in fragrance bases; adjusted depending on the desired olfactory intensity

    Downstream process integration

    • Utilized in Grignard or Friedel-Crafts alkylation to build core aroma molecules
    • Subsequent oxidation or esterification step to deliver target odorant
    • Batch-by-batch aroma panel and GC-MS evaluation before final blending
    • Handled under food-grade or cosmetic-grade hygiene controls

    Final product types

    • Fine perfume concentrate stocks
    • Cosmetic fragrance formulations (soaps, lotions)
    • Flavorants for beverages and confectionery (where permitted)
    • Personal care aroma bases

    5. Research Intermediate in Agrochemical Discovery

    Leading agrochemical R&D teams apply this specialty alcohol for structure-activity relationship (SAR) studies, enabling targeted synthesis of biphenyl-based herbicide and fungicide candidates. Its unique scaffold provides a handle for introducing bioactive functional groups through precision coupling or functionalization. All exploratory development complies with established agricultural chemical quality and safety protocols, targeting rapid response for pilot trials and regulatory submission batches.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • EPA 40 CFR Part 169 for pesticide records
    • Japan Agricultural Chemicals Inspection Station (JACIS) requirements
    • ISO 17025 for analytical laboratory competence

    Typical usage ratio

    • 1–3 molar equivalents in coupling reactions for lead compound synthesis; adjusted based on target molecule and expected yield

    Downstream process integration

    • Deployed during SAR intermediate synthesis at early-stage discovery
    • Paired with aryl halides or acyl chlorides for biphenyl coupling
    • Material fed directly into chlorination, nitration, or alkylation vessels
    • Final compounds purified and tested for field trials

    Final product types

    • Lead agrochemical active ingredients (AIs) for herbicide/fungicide pipeline
    • Experimental trial samples for regulatory field test
    • Reference substances for analytical method development
    • Biphenyl-based SAR libraries for patent filings
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