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3'-Fluoro-Biphenyl-4-Carboxylic Acid

    • Product Name 3'-Fluoro-Biphenyl-4-Carboxylic Acid
    • Alias 3-Fluoro-4-biphenylcarboxylic acid
    • Einecs 819-029-8
    • 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

    656160

    Productname 3'-Fluoro-Biphenyl-4-Carboxylic Acid
    Molecularformula C13H9FO2
    Molecularweight 216.21 g/mol
    Casnumber 241153-75-7
    Appearance White to off-white solid
    Meltingpoint 175-178°C
    Purity Typically ≥98%
    Smiles C1=CC=C(C=C1)C2=CC(=CC=C2F)C(=O)O
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 3'-Fluoro-4-biphenylcarboxylic acid
    Storagetemperature 2-8°C
    Pka Approx. 4-5 (estimate based on carboxylic acid group)

    As an accredited 3'-Fluoro-Biphenyl-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed 10g HDPE bottle with tamper-evident cap, labeled with "3'-Fluoro-Biphenyl-4-Carboxylic Acid, 99% purity, CAS, and hazard warnings."
    Shipping 3'-Fluoro-Biphenyl-4-Carboxylic Acid is securely packaged in sealed containers to prevent contamination and degradation. The shipment complies with all relevant chemical transport regulations, including appropriate labeling and documentation. It is shipped at ambient temperature, unless otherwise specified, ensuring safe and reliable delivery to laboratories and research facilities.
    Storage Store 3'-Fluoro-Biphenyl-4-Carboxylic Acid in a cool, dry, well-ventilated area away from direct sunlight and sources of heat or ignition. Keep the container tightly closed and clearly labeled. Avoid contact with incompatible materials such as strong oxidizers. Store in a corrosive-resistant container with appropriate chemical labels and ensure good ventilation in the storage area. Handle under appropriate safety protocols.
    Application of 3'-Fluoro-Biphenyl-4-Carboxylic Acid

    Applications of 3'-Fluoro-Biphenyl-4-Carboxylic Acid in Industrial Manufacturing

    3'-Fluoro-Biphenyl-4-Carboxylic Acid serves as a key intermediate in several high-value chemical manufacturing sectors. Its structural features make it critical for synthesis processes that demand precise molecular orientation, reliable reactivity, and targeted electronic properties.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    Manufacturers integrate this compound during the synthesis of fluorinated pharmaceutical intermediates, especially in the production of anti-inflammatory and anticancer APIs. Its presence enables medicinal chemists to introduce fluorine at specific locations in complex molecules, increasing metabolic stability and modulating bioactivity. Production operates under stringent validation within GMP-certified facilities, with molecular purity and traceability recorded for every batch. Downstream chemical engineers control temperature, solvent polarity, and reaction time to achieve high yields during Suzuki or Buchwald-Hartwig coupling reactions. The final APIs benefit from this integration by exhibiting improved absorption or target specificity.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient production
    • USP monograph standards for intermediate purity
    • EU EudraLex Volume 4 GMP guidelines
    • FDA 21 CFR Part 211 for manufacturing process controls

    Typical usage ratio

    • 10–30 mol% relative to core scaffold, adjustable based on target fluorination level and process efficiency

    Downstream process integration

    • Introduced in early to mid-stage synthetic routes prior to ring closure or amide bond formation
    • Frequently enters during cross-coupling chemistry as a fluoroaryl donor
    • Ensures positional selectivity during aromatic substitution steps
    • Handled in contained reaction vessels with in-process QC for residual solvent and byproduct profiling

    Final product types

    • Non-steroidal anti-inflammatory drug intermediates
    • Targeted kinase inhibitor scaffolds
    • Novel small molecule oncology compounds
    • Specialty CNS drug basic structures

    2. Advanced Liquid Crystal Materials

    Developers of high-end liquid crystal mixtures select this compound for its biphenyl core and fluorine substituent, both known to impart high birefringence, thermal stability, and controlled dielectric properties. It is dissolved and reacted with other mesogenic units under nitrogen and controlled temperature to ensure purity and prevent oxidation. QC teams run HPLC and NMR to verify residual acidity and isomer purity, following industry-standard mixture optimization. Integration takes place in the blending or pre-polymerization steps, with close monitoring of the effect on phase transition temperatures critical for downstream LCD manufacturers.

    Industry compliance standards

    • IEC 61249: guideline for base materials for electronic and LCD applications
    • REACH SVHC compliance for raw materials
    • RoHS Directive for restricted substances in electronics
    • ISO 9001: Quality management systems for specialty chemical processing

    Typical usage ratio

    • 1–5% as a component within liquid crystal mixture, finely tuned in pilot scale blending trials

    Downstream process integration

    • Added to the nematic or smectic phase mixture prior to injection into glass substrates
    • Mixed with other diphenyl or phenyl-cyclohexane derivatives to achieve desired optical switching properties
    • Process requires anhydrous solvents and nitrogen blanket to prevent decomposition
    • Tested under simulated operational temperature gradients to validate mixture stability

    Final product types

    • TFT-LCD display modules
    • Liquid crystal alignment layers
    • High-contrast display panels for industrial instrumentation
    • Wearable device display units

    3. Monomer for High-Performance Polymers

    In specialty polymer synthesis, this compound functions as a fluorinated aromatic monomer, participating directly in polycondensation and copolymerization reactions. Polymer engineers use it to build rigid-rod main chains for polyesters or polyamides aiming for high glass transition temperatures, predictable solubility profiles, and enhanced chemical resistance. Its integration occurs within controlled reactors where monomer feed ratios, catalyst loading, and thermal profiles receive strict procedural oversight. In-process FTIR confirms reaction endpoints. The resulting polymers often enter further downstream compounding or film-casting operations, with batch records linking monomer lot numbers for traceability.

    Industry compliance standards

    • ISO 10993-5 for polymer biocompatibility (for select applications)
    • ASTM D638 for tensile property testing
    • REACH Annex XVII for restricted aromatic compounds
    • UL 94 for polymer flammability classification

    Typical usage ratio

    • 10–50 mol% of total aromatic monomer content, optimized by mechanical and thermal performance targets

    Downstream process integration

    • Introduced at the start of melt or solution polymerization cycles
    • Subjected to end-capping or chain extension stages for property adjustment
    • Monitored for unreacted carboxyl or fluoro functionalities in pre-polymer purification
    • Resin processed into films, rods, or injection-molded geometries

    Final product types

    • Electrical and electronic substrate films
    • Membrane materials for fuel cells or batteries
    • Precision-molded structural polymer parts
    • Specialty wire and cable coatings with extended thermal life

    4. Organic Electronic Material Synthesis

    Organic electronics manufacturers rely on this biphenyl derivative for constructing low-bandgap, highly ordered molecular frameworks, necessary in developing organic semiconductors and advanced charge-transport layers. It is introduced during the synthesis of extended π-conjugated systems where the fluorine position modulates LUMO/HOMO energy levels. Technicians ensure solvent and reactant purity at every stage, using glovebox procedures when moisture or oxygen sensitivity arises. Material scientists further characterize synthesized intermediate performance via UV-Vis, cyclic voltammetry, and thin-film transistor measurements. Consistent sourcing and extensive batch analysis ensure fit-for-purpose integration into functional device fabrication.

    Industry compliance standards

    • IPC-4101 for base materials in electronic circuits
    • REACH registration for precursor commercialization
    • ISO 14001 environmental management for electronic material plants
    • Internal SOPs for trace metal and halogen content control

    Typical usage ratio

    • 2–12% by mass in precursor blend, tailored for each semiconductor architecture

    Downstream process integration

    • Used in precursor feeds for solution-processable semiconductor inks
    • Integrated during synthesis of photoactive dyes or electron-transport layers
    • Subjected to high-purity filtration and zone refining before device prototyping
    • Closely monitored for batch-to-batch consistency in electronic property delivery

    Final product types

    • Organic thin-film transistors (OTFTs)
    • OLED backplanes and emission layers
    • Flexible sensors for industrial process controls
    • Organic photovoltaic device stacks
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