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4-Amino-4'-Fluorobiphenyl

    • Product Name 4-Amino-4'-Fluorobiphenyl
    • Alias 4-Fluoro-4-aminobiphenyl
    • Einecs 217-421-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    755648

    Chemical Name 4-Amino-4'-Fluorobiphenyl
    Cas Number 3867-15-4
    Molecular Formula C12H10FN
    Molecular Weight 187.21 g/mol
    Appearance Off-white to light brown solid
    Melting Point 98-102 °C
    Solubility In Water Insoluble
    Density Approximately 1.2 g/cm³
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Smiles Nc1ccc(cc1)-c2ccc(F)cc2
    Synonyms 4-Fluoro-4'-aminobiphenyl
    Hazard Statements May cause skin and eye irritation

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

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 25 grams of 4-Amino-4'-Fluorobiphenyl, labeled with hazard and handling information.
    Shipping **Shipping Description:** 4-Amino-4'-Fluorobiphenyl should be shipped in airtight, sealed containers clearly labeled according to regulatory guidelines. It must be handled with care as a laboratory chemical, avoiding exposure to heat, moisture, or direct sunlight. Ensure transportation complies with relevant hazardous material regulations and includes all necessary safety documentation.
    Storage 4-Amino-4'-Fluorobiphenyl 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 oxidizers. Keep it away from direct sunlight and moisture. Store under inert gas if possible. Proper labeling and containment are essential due to its potential toxicity and harmful effects.
    Application of 4-Amino-4'-Fluorobiphenyl

    Applications of 4-Amino-4'-Fluorobiphenyl in Industrial Manufacturing

    As a primary manufacturer of 4-Amino-4'-Fluorobiphenyl, we supply this advanced aromatic amine derivative directly to industries engaged in pharmaceutical intermediates, specialty chemical synthesis, organic electronics, and advanced pigment manufacture. Our material undergoes rigorous batch control and meets the quality expectations of global leaders operating in downstream application scenarios where structural purity, consistency in amination, and precise fluorine substitution are critical to process outcomes.

    1. Pharmaceutical Intermediate Synthesis for Custom Oncology Agents

    Pharmaceutical manufacturers incorporate our material as a core intermediate in the development of targeted kinase inhibitors and related anti-cancer investigational APIs. Its unique biphenyl scaffold, combined with precise amino and fluorine positioning, allows for structural variation in lead compound synthesis. Medicinal chemists rely on the purity and reactivity profile to proceed with Buchwald–Hartwig amination, Suzuki-Miyaura coupling, and regioselective N-acylation, forming the foundational aromatic units of several patent challenge and specialty oncology candidates.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs—pharmaceutical intermediates)
    • US FDA 21 CFR 211 (where used in regulated drug synthesis)
    • ISO 9001 (chemical quality management as relevant to pharma supply chains)

    Typical usage ratio

    • Standard integration at 0.1–1.2 molar equivalents per core heterocycle structural step, adjusted for desired derived analog yield and process route

    Downstream process integration

    • Introduced during pre-final intermediate stage for direct aromatic amine coupling or N-alkylation, prior to API purification and crystallization

    Final product types

    • Investigational kinase inhibitors
    • Biphenylamine-derived proprietary oncology research APIs
    • Advanced intermediates for phase I/II clinical candidates

    2. Advanced OLED and Organic Electronic Material Systems

    Producers of functional organic electronic materials utilize our biphenyl derivative as an electron-donating or functionalizing monomer for high-performance OLED emitter and transport layer precursors. The para-amino and para-fluoro substitution pattern enhances electron transport features, chemical stability, and fine-tunes photoluminescence wavelength when copolymerized or further derivatized into arylamines or fluorinated polyarylene matrices. The precise molecular structure supports batch-to-batch reproducibility in pilot and commercial-scale thin-film device processing.

    Industry compliance standards

    • RoHS 3 Directive (2015/863/EU, limits on hazardous substance content)
    • JEITA/IEC 60068-2-20 (soldering and thermal cycling for electronic materials)
    • ISO 14644-1 (cleanroom standards for organic device fabrication)
    • Customer-specific OLED QC protocols (material purity ≥99.5%, organometallic trace limits)

    Typical usage ratio

    • 0.2–5 wt% as a core comonomer or nucleophilic substituent, adjusted for desired charge balance and emission color in emitting/transport material synthesis

    Downstream process integration

    • Enter stage as reacting amine during arylamine formation or as a monomeric pre-cursor prior to film-forming polymerization and vacuum deposition

    Final product types

    • Emitter and transporter layers for OLED panels (displays/lighting)
    • Organic field-effect transistor (OFET) base layers
    • Semiconducting films for flexible displays

    3. Specialty Dye and Pigment Precursor Manufacturing

    Colorant manufacturers select our amino-fluorinated biphenyl for use as a color base in premium vat dyes and as a coupling intermediate in azo pigment development where both halogen tolerance and amine reactivity impact hue and stability. Used directly in diazotization or condensation reactions, it helps achieve strong, lightfast colors for plastics and specialty printing inks, especially those required to be halogenated for high weather resistance or specific spectral absorption properties.

    Industry compliance standards

    • EN 71-3 (Toy safety—migration of certain elements)
    • REACH Regulation (EC) No 1907/2006 for pigment substance registration
    • ISO 105 series (requirements for dye fastness)
    • OEKO-TEX® Standard 100 (restricted substances in dye applications)

    Typical usage ratio

    • 0.5–3.5 wt% as an amino reagent or diazo base per pigment batch, modulated for target concentration and tinting strength

    Downstream process integration

    • Undergoes diazotization or direct coupling at color intermediate synthesis stage, preceding insolubilization or salt formation

    Final product types

    • Specialty vat dyes for textile and plastics processing
    • Azo pigments with halogenated biphenyl nuclei
    • Heat-resistant coloration agents for specialty polymer masterbatches

    4. Performance Additives for High-End Polymeric Materials

    Manufacturers of specialty polymers integrate this fluorinated aromatic amine as a performance additive or chain modifier in advanced engineering plastic and thermoset formulations. The compound’s para-amino and fluoro functional groups participate in curing reactions or as co-monomers for resins, promoting increased thermal stability, chemical resistance, and adjusted dielectric properties for electronics encapsulation or automotive high-performance composites.

    Industry compliance standards

    • UL 94 (flammability of plastic materials for parts in devices)
    • RoHS 3 (2015/863/EU, relevant for electronics applications)
    • ASTM D638 (tensile properties of plastics, when benchmarking effect)
    • ISO 9001 (additive and resin manufacturing quality management)

    Typical usage ratio

    • 0.1–1.0 phr (parts per hundred resin), dosage adjusted based on thermal and dielectric property targets

    Downstream process integration

    • Added during resin compounding or pre-polymerization alongside other chain extenders, then processed via injection molding, compression molding, or resin casting

    Final product types

    • High-temperature thermoset composites for electronics or automotive
    • Advanced engineering plastics with modified dielectric properties
    • Encapsulation and insulating resins for high-performance applications
    Free Quote

    Competitive 4-Amino-4'-Fluorobiphenyl prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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