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2-Biphenylmethanol

    • Product Name 2-Biphenylmethanol
    • Alias Benzhydrol
    • Einecs 202-904-2
    • 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

    605427

    Cas Number 91-01-0
    Molecular Formula C13H12O
    Molar Mass 184.23 g/mol
    Iupac Name biphenyl-2-ylmethanol
    Appearance White solid
    Melting Point 54-57 °C
    Boiling Point 192-194 °C at 17 mmHg
    Density 1.14 g/cm³
    Solubility In Water Slightly soluble
    Smiles C1=CC=C(C=C1)C2=CC=CC=C2CO
    Refractive Index 1.625
    Pubchem Cid 7133

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

    Packing & Storage
    Packing The 2-Biphenylmethanol is packaged in a 100g amber glass bottle with a tamper-evident cap and hazard labeling for safe handling.
    Shipping 2-Biphenylmethanol should be shipped in tightly sealed containers, protected from light and moisture. It must comply with applicable local, national, and international regulations. Ensure packaging prevents leaks or spills. Typically transported as a non-hazardous substance, but appropriate safety documentation and labeling should accompany all shipments. Store and ship at room temperature.
    Storage 2-Biphenylmethanol should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, preferably in a designated chemical storage cabinet. Avoid excessive heat or sources of ignition. Proper labeling and adherence to safety data sheet (SDS) recommendations are essential for safe storage.
    Application of 2-Biphenylmethanol

    Applications of 2-Biphenylmethanol in Industrial Manufacturing

    As a specialty manufacturer, we support the industrial integration of 2-Biphenylmethanol into regulated sectors where this material delivers distinctive chemical performance. We prioritize applications verified by market adoption, established formulation practices, and statutory compliance across downstream value chains. The following scenarios highlight real, focused areas of usage, including compliance standards, adjustment and control of addition ratios, manufacturing stage integration, and associated finished goods.

    1. Pharmaceutical Intermediate Synthesis for Antihistamines

    Research-driven pharmaceutical producers utilize 2-Biphenylmethanol as an essential intermediate during the synthesis of key antihistamine active pharmaceutical ingredients (APIs), serving primarily in the manufacture of first-generation H1 receptor antagonists. Integrated under GMP environments, its phenyl-rich structure supports precise benzylation and derivatization steps, forming the core pharmacophore in products like diphenylhydramine derivatives. Downstream, this supports large-scale synthesis and subsequent purification, ensuring low trace contaminants throughout the API chain.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.), United States Pharmacopeia (USP) API precursor standards
    • 21 CFR Part 211 (US FDA) cGMP for Finished Pharmaceuticals
    • REACH Annex IV/VI (EU) for intermediate chemical registration and traceability

    Typical usage ratio

    • Applied at 0.13–0.21 molar equivalents relative to targeted amine precursor, adjusted for molecular yield and process throughput; step yields monitored to minimize unreacted residue

    Downstream process integration

    • Implemented during the initial alkylation and benzyl ether protection steps of antihistamine backbone construction; enters batch reactors after solvent charging
    • Sequential neutralization and crystallization follow to ensure product purity

    Final product types

    • Bulk pharmaceutical intermediates for first-generation antihistamine APIs (e.g., diphenhydramine, orphenadrine)
    • Purified API forms for tablet, capsule, and injectable antihistamine drugs

    2. Fine Fragrance and Aroma Chemical Manufacture

    Manufacturers focused on aroma chemicals apply 2-Biphenylmethanol in specialized esterification, yielding aromatic ethers and esters with high stability, persistence, and musk character. Regulated for indirect flavor and fragrance contact, this ingredient functions as a key building block for floral–woody note modulations and serves niche applications in luxury perfume bases and high-end household air freshener formulations. During downstream blending, ingredient purity and traceability must meet IFRA limits and customer sensory specifications.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards – Prohibited & Restricted Substances
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products Annex III–VI
    • ISO 9235: Aromatic Natural and Synthetic Raw Materials in Perfumery
    • Global Food Safety Initiative (GFSI) for aroma ingredients in food-related applications

    Typical usage ratio

    • Integrated at 0.5–3.0% w/w within aroma chemical concentrate formulas; batch size and target odor strength dictate upper limit

    Downstream process integration

    • Introduced at the initial esterification/methylation phase to synthesize constituent aromatic esters (e.g., biphenylmethyl acetate), prior to final distillation and organoleptic QC
    • Subsequently dosed into perfumer’s base blend or finished consumer product concentrate

    Final product types

    • Musk and woody-note aroma chemicals for fine fragrances
    • Specialty air care bases for luxury diffusers and candles
    • Concentrated compounds for premium laundry care and cosmetic scents

    3. UV-Curable Resin Photoinitiator Synthesis

    Specialty resin producers employ 2-Biphenylmethanol as a foundational alcohol donor for the synthesis of high-performance photoinitiator compounds used in UV-curable industrial inks, coatings, and adhesives. Its structure enables precise etherification and ester linkage reactions during photoinitiator core assembly, ensuring efficient initiation rates during polymerization of acrylate or epoxy matrices, with controlled residue and impurity profiles required for electronic-grade coatings and microelectronics packaging.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical synthesis
    • Restriction of Hazardous Substances (RoHS) Directive 2011/65/EU (for electronics applications)
    • EN 71-3 Toy Safety Standard (for coatings in toys and children’s products applications)
    • Global Harmonized System (GHS/CLP) chemical hazard labeling

    Typical usage ratio

    • Charged at 1.5–7.5% w/w in photoinitiator synthesis batch, considering light absorption spectrum and molecular weight requirements of target initiator

    Downstream process integration

    • Incorporated at the hydroxylation/alkoxylation stage in photoinitiator manufacturing, followed by condensation and purification before product isolation
    • Post-synthesis, filtered photoinitiator resins are dosed directly into UV-curable ink or varnish concentrates as functional additives

    Final product types

    • UV-curable ink and coating photoinitiator masterbatches
    • Clear and pigmented UV adhesives for electronic device assembly
    • Protective overcoats for printed circuit boards, fiber optics, and high-value plastic substrates

    4. Specialty Polymer Additive for High-Temperature Plastics

    2-Biphenylmethanol supports specialty plastics manufacturers as a reactive modifier in the synthesis of high-performance polymers requiring increased glass transition temperatures and dimensional stability. It typically functions as a co-monomer or chain extender in the production of polyesters and polycarbonates destined for engineering and electrical applications, where aromatic content and controlled reactivity yield materials capable of withstanding rigorous mechanical and thermal stress.

    Industry compliance standards

    • UL 94 Flame Retardancy Standard for Plastic Materials
    • ISO 26000:2010 Guidance on Social Responsibility (applies to sourcing and processing)
    • IEC 60695 Fire Hazard Testing (applicable for electrical insulation materials)
    • REACH SVHC (Substances of Very High Concern) candidate list compliance for aromatic monomers

    Typical usage ratio

    • Used at 0.2–1.2% molar equivalents relative to primary diol components in polycondensation recipes; precise level set by desired polymer molecular weight and target physical properties

    Downstream process integration

    • Added during polycondensation reactor charging, immediately prior to vacuum application and catalyst introduction, ensuring uniform distribution and chain extension effect
    • Blended with additional heat stabilizers and processing aids prior to extrusion

    Final product types

    • High-temperature polyesters for automotive connectors
    • Rigid polycarbonate blends for electrical housings and appliance enclosures
    • Advanced polymer composites for industrial 3D printing and lightweight structural components

    5. Agricultural Fungicide Intermediate Production

    Major agrochemical manufacturers integrate 2-Biphenylmethanol into the synthesis of strobilurin and biphenyl-based fungicides, leveraging its aromatic alcohol framework to facilitate selective etherification and downstream chlorination reactions necessary for active ingredient construction. Consistent impurity control and adherence to crop protection chemical guidelines remain critical, given stringent tolerances enforced during large-scale synthesis of actives used in regulated agrochemical formulations.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Agricultural Pesticides
    • ISO 9001:2015 Quality Management for agrochemical manufacturing
    • European Regulation (EC) No 1107/2009 for Plant Protection Products
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)

    Typical usage ratio

    • Dosed at 0.05–0.25 molar equivalents in active compound synthesis, depending on fungicide class and targeted conversion rates; levels optimized for downstream active content

    Downstream process integration

    • Enters at the alkylation/etherification step of active ingredient synthesis, prior to final chlorination and crystallization; followed by continuous filtration and solvent stripping

    Final product types

    • Active fungicidal ingredients for systemic and contact fungicide products
    • Bulk technical-grade actives for agricultural suspension concentrates and wettable powders
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