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3,3'-Difluorobiphenyl

    • Product Name 3,3'-Difluorobiphenyl
    • Alias 3,3'-Biphenyldifluoride
    • Einecs 629-296-8
    • 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
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    Specifications

    HS Code

    275460

    Chemicalname 3,3'-Difluorobiphenyl
    Molecularformula C12H8F2
    Molecularweight 190.19 g/mol
    Casnumber 348-80-5
    Appearance White to off-white solid
    Meltingpoint 62-66 °C
    Boilingpoint 280-282 °C
    Density 1.15 g/cm³
    Solubility Insoluble in water; soluble in organic solvents
    Smiles Fc1cccc(c1)c2cccc(F)c2
    Inchi InChI=1S/C12H8F2/c13-11-6-2-4-9(7-11)8-5-1-3-10(14)12(8)11/h1-8H
    Pubchemcid 10725

    As an accredited 3,3'-Difluorobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram sample of 3,3'-Difluorobiphenyl is packaged in a tightly sealed amber glass bottle with a printed safety label.
    Shipping 3,3'-Difluorobiphenyl is shipped in tightly sealed containers to prevent contamination and moisture exposure. It should be transported according to standard chemical shipment regulations, away from incompatible substances, with appropriate hazard labeling. Ensure compliance with local, national, and international regulations for safe handling and shipping of organic chemicals during transit.
    Storage 3,3'-Difluorobiphenyl should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from light, moisture, and sources of ignition. Keep the container labeled and tightly closed when not in use. Store at room temperature, ensuring access is restricted to trained personnel only.
    Application of 3,3'-Difluorobiphenyl

    Applications of 3,3'-Difluorobiphenyl in Industrial Manufacturing

    3,3'-Difluorobiphenyl contributes to multiple advanced chemical manufacturing processes owing to its unique molecular structure. As a direct manufacturer, we supply this raw material to leading enterprises across specialized downstream sectors that demand strict process control, compliance, and reliable performance in critical formulations.

    1. Liquid Crystal Display (LCD) Intermediate Synthesis

    3,3'-Difluorobiphenyl functions as a critical intermediate in the synthesis of specialized biphenyl-based liquid crystal materials. Its precise fluorine substitution pattern enhances thermal stability and improves torque response in display-active mesogens. Customers integrate this material at controlled points during the organic synthesis phase, ensuring homogeneous incorporation into target LC compounds within production flows for thin film transistor (TFT) and high-definition display panels.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • IEC 61249-2-21 for halogen-free electronic materials
    • QC080000 IECQ HSPM (Hazardous Substance Process Management System)
    • REACH Regulation (EC) No 1907/2006 for registration and assessment of chemicals

    Typical usage ratio

    • Customarily 5–20% of total organic intermediates by mass, adjusted based on desired mesogenic phase characteristics and downstream LC composition requirements

    Downstream process integration

    • Incorporation as a building block during Grignard coupling or Ullmann reaction in LC precursor synthesis
    • Maintained under inert atmospheres to prevent side fluorine loss
    • Batch monitored for impurity profile to meet strict device-grade specifications
    • Use coordinated with solvent-exchange and final purification steps prior to cell assembly

    Final product types

    • TFT-LCD panels
    • OLED alignment layers
    • Specialty high-contrast LC modules
    • Advanced automotive and medical displays

    2. Pharmaceutical Intermediate: Sartan Synthesis

    This difluorinated biphenyl core structure is essential in the production of several angiotensin receptor blocker (ARB) pharmaceuticals, notably the synthesis of biphenyl-tetrazole moieties within sartan-class drugs. Active pharmaceutical ingredient (API) manufacturers leverage its defined structure to reach stringent impurity specifications, batch repeatability, and process validation in cGMP-compliant environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and European Pharmacopoeia Monographs
    • FDA DMF Type II submission requirements
    • GMP inspection by CFDA, EMA, US FDA

    Typical usage ratio

    • Comprises 10–25% of the total reagent input in multi-step syntheses, with ratios optimized for limiting side-product formation and maximizing purity of biphenyl tetrazole intermediates

    Downstream process integration

    • Reacted via cross-coupling (Suzuki, Buchwald-Hartwig) with aryl halides in API key step assembly
    • Input at controlled temperatures with monitoring of fluorine retention
    • Subject to in-process QC for residual solvents and metallic catalysts
    • Cleanroom conditions maintained during isolation and subsequent purification

    Final product types

    • Losartan potassium
    • Valsartan API
    • Irbesartan intermediate
    • Other related hypertensive pharmaceuticals

    3. High-Performance Polyarylene Polymers

    Polymer manufacturers employ 3,3'-Difluorobiphenyl as a comonomer for fabrication of high-performance polyarylene sulfide (PPS), polyetheretherketone (PEEK), and other heat-resistant specialty resins. The difluoro groups ensure desired flame retardance, chemical resilience, and consistent mechanical properties in engineering plastics, crucial for aerospace, industrial electronics, and advanced transportation components production.

    Industry compliance standards

    • UL 94 V-0 flammability classification for plastics
    • RoHS/REACH for polymer additives
    • ISO 9001:2015 Quality Management for manufacturing
    • ASTM D638 for mechanical property testing

    Typical usage ratio

    • Introduced at 2–8 mol% of total aromatic monomer charge, typically controlled to balance melt flow and thermal deflection traits in final polymer matrix

    Downstream process integration

    • Charged in initial polycondensation phase via melt or solution polymerization
    • Integrated with other fluorinated/aromatic dihalides or diols under controlled conditions
    • Monitored for molecular weight distribution and avoided overfeed to prevent brittleness
    • Post-polymerization finishing and pelletizing for molders

    Final product types

    • High-frequency printed circuit board laminates
    • Aerospace-grade thermoplastic structural parts
    • Automotive under-the-hood housings
    • Industrial pump and valve components

    4. Agrochemical Synthesis: Herbicide Building Block

    3,3'-Difluorobiphenyl represents a core scaffold for the development of certain fluorinated biphenyl herbicide active ingredients. Agrochemical formulation plants utilize this intermediate in sequence with chlorination and alkylation reactions, aiming for high selectivity and minimized byproduct waste in final active formulation. Process engineers prioritize batch traceability, intermediate purity, and up-to-date regulatory documentation throughout the supply and synthesis chain.

    Industry compliance standards

    • FAO/WHO Technical Grade Active Ingredient Specifications
    • ISO 9001:2015 for agrochemical manufacturing QMS
    • National Agrochemical Registration (US EPA, EU PPP, China ICAMA)
    • GHS Safety Data Sheet (SDS) compliance

    Typical usage ratio

    • Commonly 8–15% w/w of total reaction charge in multiphase syntheses, optimized in pilot plant scale to balance conversion efficiency and downstream isolation cost

    Downstream process integration

    • Feeding during controlled biphenyl backbone introduction post-methylation or halogen-exchange step
    • Closed-system handling during solvent extraction and crystallization
    • Batch footage provided for traceability in later formulation blends
    • Material verified for isomeric purity to prevent crop phytotoxicity

    Final product types

    • Selective herbicidal actives for rice and corn protection
    • Mixed formulation pre-emergent herbicides
    • Exported technical-grade herbicide intermediates
    • Specialty weed control agents

    5. OLED Material Intermediate

    Manufacturers in the organic light-emitting diode (OLED) sector utilize this raw material in the preparation of novel biphenyl derivative emitter layers and charge transport materials. The difluoro-substitution pattern influences charge balance and color purity, enabling improved quantum efficiency and device longevity. Integration into the OLED material synthesis step follows closely regulated handling to maintain lot uniformity.

    Industry compliance standards

    • ISO 14001 Environmental Management for specialty chemicals
    • RoHS/REACH compliance for display components
    • OHSAS 18001/ISO 45001 for manufacturing safety
    • Confidentiality agreements for proprietary OLED formulations

    Typical usage ratio

    • Added as 3–12% of emitter precursor or transport matrix formulation, tuned based on layer thickness and targeted emission wavelength

    Downstream process integration

    • Input as a monomer/precursor for emitter or host layer molecule synthesis
    • Processed under anhydrous, oxygen-free conditions to preserve functional side groups
    • Purified to electronic-grade standards prior to deposition step
    • QC sampling for residual metal and impurity tracing

    Final product types

    • Blue and green OLED emitter compounds
    • Charge transport matrix for OLED panels
    • Flexible and rigid OLED display substrates
    • Wearable and automotive OLED lighting modules
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