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HS Code |
723927 |
| Cas Number | 446-17-3 |
| Molecular Formula | C7H3F3O2 |
| Molar Mass | 176.09 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 131-135 °C |
| Boiling Point | 275 °C (estimated) |
| Density | 1.5 g/cm³ (approximate) |
| Solubility In Water | Slightly soluble |
| Pka | 3.56 (approximate) |
| Smiles | C1=CC(=C(C=C1F)F)C(=O)O |
| Inchi | InChI=1S/C7H3F3O2/c8-4-1-2-5(7(11)12)6(10)3-4/ /h1-3H,(H,11,12) |
| Synonyms | 2,3,5-Trifluorobenzoic acid |
As an accredited 2,3,5-Trifluorobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled “2,3,5-Trifluorobenzoic Acid, 99%,” including hazard warnings. |
| Shipping | 2,3,5-Trifluorobenzoic Acid is typically shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It should be packaged according to relevant hazardous material regulations, labeled clearly, and accompanied by a Safety Data Sheet (SDS). Store and transport in a cool, dry place, away from incompatible substances and direct sunlight. |
| Storage | 2,3,5-Trifluorobenzoic acid should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong bases and oxidizing agents. Keep out of direct sunlight and moisture. Ensure proper labeling and segregation from food and drink. Use chemical-resistant shelving and follow all relevant safety regulations. |
Applications of 2,3,5-Trifluorobenzoic Acid in Industrial ManufacturingAs a specialized manufacturer of 2,3,5-Trifluorobenzoic Acid, we supply this finely tuned intermediate to industries requiring precision and compliance in downstream synthesis. The following sectors demonstrate authentic, value-driven integration of our material in advanced manufacturing pipelines. 1. Pharmaceutical Intermediate for Fluorinated Drug SynthesisMajor pharmaceutical producers utilize 2,3,5-trifluorobenzoic acid as a key fluorinated aromatic building block in multi-step synthesis of active pharmaceutical ingredients (APIs). The electron-withdrawing trifluoromethyl motif introduces significant metabolic stability to drug candidates. Process chemists employ this material during core benzene ring construction, typically performing selective coupling, amidation, or esterification reactions to elaborate more complex intermediates. Robust analytical QC at every stage ensures traceability and compliance with regulatory authorities. Choice of incorporation point and dosage reflects the target compound’s design and scale. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide and Fungicide FormulationsAgrochemical formulators select this trifluorinated benzoic acid for the preparation of proprietary herbicide and fungicide actives featuring high bioactivity and environmental persistence. Synthetic teams deploy it in controlled acylation, halogenation, or ester conversion steps, targeting molecules that interfere with plant enzymatic pathways. Its unique substitution pattern allows tight control of molecular reactivity and environmental breakdown, meeting both efficacy and regulatory demands. Finished actives support the production of stable, field-ready emulsifiable concentrates and granules. Industry compliance standards
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3. Specialty Polymer Monomer for High-Performance CoatingsCoatings developers rely on 2,3,5-trifluorobenzoic acid to introduce controlled fluorination at key sites in specialty polymers, enabling low surface energy and superior weather resistance in end-use applications. During polymerization, the acid undergoes esterification or amidation, forming monomers that integrate directly into polyarylates, polyesters, or copolymer chains. This results in high-performance coating resins for critical end-markets such as electronics, aerospace, and industrial protection, each demanding rigorous characterization and trace material management. Industry compliance standards
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4. Fine Chemicals for Liquid Crystal Material SynthesisManufacturers producing advanced liquid crystal materials for display technology and optoelectronics incorporate this trifluorinated benzoic acid in multi-step organic synthesis. Its unique fluorination pattern imparts anisotropic electronic and dielectric properties to final liquid crystal compounds. Chemists use this material as the aromatic acid precursor in condensation and substitution reactions, often working under strictly controlled moisture and temperature regimes to assure purity and phase behavior. Every lot receives full analytical documentation to support process reproducibility at scale. Industry compliance standards
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