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2,3,5-Trifluorobenzoic Acid

    • Product Name 2,3,5-Trifluorobenzoic Acid
    • Alias 2,3,5-TFBA
    • Einecs 219-468-7
    • 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

    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 & Storage
    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.
    Application of 2,3,5-Trifluorobenzoic Acid

    Applications of 2,3,5-Trifluorobenzoic Acid in Industrial Manufacturing

    As 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 Synthesis

    Major 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

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.); United States Pharmacopeia (USP)
    • FDA 21 CFR Parts 210/211 for pharmaceutical manufacturing
    • REACH registration for industrial chemical intermediates

    Typical usage ratio

    • 5–20 mol% of total synthesis batch, depending on target compound’s structural requirements; ratio adjusted per synthetic route and final yield optimization

    Downstream process integration

    • Added during stepwise aromatic ring functionalization, through direct amidation or esterification with amines/alcohols, followed by coupling or reduction in API synthesis

    Final product types

    • Small molecule APIs containing fluorinated benzene rings
    • Analytical reference standards for pharmaceutical research
    • Precursors for oncology, anti-viral, and CNS drug candidates
    • Contract synthesis intermediates for branded generic formulations

    2. Agrochemical Intermediate for Herbicide and Fungicide Formulations

    Agrochemical 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

    • OECD Guidelines for the Testing of Chemicals (agrochemical registration dossiers)
    • FAO/WHO Codex Alimentarius pesticide residue regulations
    • ISO 9001:2015 for agrochemical manufacturing facilities
    • REACH Annex II requirements for intermediates

    Typical usage ratio

    • 3–12 wt% of reaction mass; selected per target molecule’s synthetic pathway and desired biological activity, fine-tuned based on crop-specific efficacy analysis

    Downstream process integration

    • Enters as the aromatic acid core for chlorination, methylation, or etherification prior to downstream formulation into technical concentrate

    Final product types

    • Active ingredients for post-emergent herbicides
    • Systemic and contact fungicide components
    • Technical concentrates for emulsion or granule formulations
    • Custom crop protection agents for proprietary product portfolios

    3. Specialty Polymer Monomer for High-Performance Coatings

    Coatings 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

    • ASTM D5201 and D3029 for polymer raw material properties
    • ISO 9001:2015 for materials traceability in specialty polymers
    • Restriction of Hazardous Substances (RoHS, for electronics coatings)
    • REACH SVHC (Substances of Very High Concern) compliance

    Typical usage ratio

    • 0.5–8 mol% of total monomer blend; adjusted based on target hydrophobicity/hardness in cured polymer film, as determined by functional testing

    Downstream process integration

    • Incorporated via direct monomer synthesis—esterification with glycols or conversion to acid chlorides for subsequent condensation polymerization

    Final product types

    • Anti-corrosive coatings for electronics and PCBs
    • High-durability clear coats for aerospace and automotive use
    • Engineered films for industrial barrier applications
    • UV- and chemical-resistant architectural coatings

    4. Fine Chemicals for Liquid Crystal Material Synthesis

    Manufacturers 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

    • ISO 9001:2015 for specialty organic chemical production
    • IEC 61340 (static control for electronic chemicals)
    • REACH registration for liquid crystal precursors
    • RoHS compliance for indirect use in display components

    Typical usage ratio

    • 1–5 mol% of initial reactant mass in the mixture, balanced per liquid crystal chain design and desired mesophase properties

    Downstream process integration

    • Condensation with alkyl/alkoxy amines and halogenated aromatics during custom liquid crystal molecule synthesis by stepwise functionalization

    Final product types

    • Twisted nematic and in-plane switching (IPS) liquid crystal mixtures
    • LC materials for TFT-LCD/OLED display panels
    • Non-linear optical compounds for photonics
    • Precision-engineered organic intermediates for imaging and sensors
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