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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 | 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. |
Applications of 3'-Fluoro-Biphenyl-4-Carboxylic Acid in Industrial Manufacturing3'-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
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2. Advanced Liquid Crystal MaterialsDevelopers 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
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3. Monomer for High-Performance PolymersIn 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
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4. Organic Electronic Material SynthesisOrganic 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
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