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2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid

    • Product Name 2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid
    • Alias 2-Hydroxy-5-(trifluoromethoxy)salicylic acid
    • Einecs 249-497-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    921284

    Iupac Name 2-Hydroxy-5-(trifluoromethoxy)benzoic acid
    Cas Number 115029-67-1
    Molecular Formula C8H5F3O4
    Molar Mass 222.12 g/mol
    Appearance White to off-white solid
    Melting Point 162-165 °C
    Solubility In Water Slightly soluble
    Smiles C1=CC(=C(C=C1OC(F)(F)F)O)C(=O)O
    Inchi InChI=1S/C8H5F3O4/c9-8(10,11)15-5-2-1-4(7(14)13)6(12)3-5/h1-3,12H,(H,13,14)
    Pubchem Cid 11764643
    Storage Temperature Room temperature

    As an accredited 2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, white printed label, 25 grams net weight, marked with chemical name, CAS number, and safety warnings.
    Shipping 2-Hydroxy-5-(Trifluoromethoxy)benzoic acid is securely packaged in tightly sealed containers to prevent moisture and contamination. Shipping complies with relevant chemical transport regulations, including labeling and handling as required. During transit, the product is protected from excessive heat and direct sunlight to maintain purity and integrity. Safety data accompanies each shipment.
    Storage 2-Hydroxy-5-(Trifluoromethoxy)benzoic acid should be stored in a tightly closed container, in a cool, dry, well-ventilated area. Protect from light, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature, away from heat sources and direct sunlight. Ensure labeling is clear and secure. Use proper personal protective equipment when handling the chemical.
    Application of 2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid

    Applications of 2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid in Industrial Manufacturing

    As a specialized manufacturer of 2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid, we support industrial partners in fields requiring strict quality and process control. This highly functional intermediate achieves consistent performance in pharmaceutical synthesis, crop protection chemistry, specialty coatings, advanced polymer modification, and electronic chemical applications. Below are the core downstream use cases supported by our material.

    1. Pharmaceutical Intermediate for Nonsteroidal Anti-Inflammatory Drug Synthesis

    Major pharmaceutical manufacturers use our raw material as a key intermediate when synthesizing select NSAIDs, requiring precise control of functional group integrity. These processes demand consistent purity and traceability, as the compound contributes critical benzoic acid derivatives within a tightly regulated cGMP workflow. Production lines leverage the unique trifluoromethoxy substitution to strategically influence drug molecule polarity and metabolic stability, optimizing bioavailability in final oral or injectable formulations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210/211, US FDA)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) requirements for relevant API synthesis
    • REACH and TSCA substance registration for onward pharmaceutical use

    Typical usage ratio

    • 5–15% of total reaction mass in final step to introduce benzoic acid core; precise input determined by stoichiometry of target NSAID structure

    Downstream process integration

    • Charged at condensation or acylation stage along with reactants; batch addition post-qualification; followed by purification, crystallization, and subsequent conversion to active API

    Final product types

    • Finished NSAID tablets, capsules, injectable solutions containing fluorinated benzoic acid moieties

    2. Selective Herbicide Intermediate in Agrochemical Formulation

    Global agrochemical companies incorporate this compound as a fluorinated building block in the synthesis of targeted herbicide actives. The strong electron-withdrawing trifluoromethoxy group improves the environmental stability and biological selectivity of the end products, supporting increased crop safety and weed resistance management while maintaining regulatory traceability throughout agrochemical supply chains.

    Industry compliance standards

    • ISO 9001 Quality Management System certification for pesticide intermediates
    • Regulation (EC) No 1107/2009 (EU) for plant protection product ingredients
    • Food and Agriculture Organization (FAO) technical specification (for actives and impurities)
    • U.S. EPA FIFRA registration—material traceability for herbicidal actives

    Typical usage ratio

    • 3–10% of batch composition when forming key phenoxyacetic acid or benzoic herbicides; subject to structure-activity relationship and downstream modification path

    Downstream process integration

    • Introduced at ring functionalization or coupling reaction step within multi-stage herbicide synthesis, followed by chlorination, esterification or formulation for granule/liquid concentrates

    Final product types

    • Selective pre- and post-emergent herbicide formulations such as liquid concentrates, SC, WG, and EC finished products

    3. Specialty Monomer for Fluorinated Polymer Additives

    Our material serves as a high-purity specialty monomer for the production of advanced fluorinated polymers, favorably altering surface energy, chemical resistance, and hydrophobicity in finished plastics. Downstream processors employ it during the functional co-polymerization stage to engineer niche resins for demanding coatings and engineered plastics, where strong performance under thermal and chemical exposure is essential.

    Industry compliance standards

    • ISO 14001 Environmental Management System during polymer processing
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) for polymers in the European market
    • RoHS Directive (2011/65/EU) for additive use in electronics or automotive supply chains
    • ASTM D2564-17 for plasticizer compatibility (if applicable in downstream blends)

    Typical usage ratio

    • 0.5–3% by weight in resin mass during co-polymerization; actual dosage determined by targeted polymer property modification and end-use physicochemical requirements

    Downstream process integration

    • Blended during pre-polymerization, chain extension, or post-grafting phase; fully incorporated before extrusion, pelletizing, or final article molding

    Final product types

    • Fluoropolymer-modified industrial coatings, high-resilience engineering plastics, automotive under-hood parts, electronic device housings

    4. Functional Additive in Electronic Chemical Processing

    Electronics and semiconductor fabrication facilities utilize this intermediate during the synthesis of advanced resist materials, particularly for photolithography in high-resolution applications. The trifluoromethoxy group imparts enhanced solubility and patterning accuracy, meeting the extreme purity and particle control requirements essential for next-generation integrated circuit production and flat-panel display manufacturing.

    Industry compliance standards

    • SEMI C93 standard for chemical purity and contamination control in photolithography
    • ISO 14644 Cleanroom Standard for production and packaging
    • IPC-4101 standard for electronic base materials (for end-use compatibility)
    • Local RoHS/REACH compliance for chemical handling in microelectronics

    Typical usage ratio

    • 0.2–1.5% loading in photoresist or ancillary formulations; dosage adjusted based on process resolution targets and substrate compatibility

    Downstream process integration

    • Incorporated into resist or etchant formulation tanks during blending; introduced pre-filtration and transferred through closed delivery to coating or wafer processing lines

    Final product types

    • Photolithographic resists, micro-patterned etchants, fine-line circuit substrates, OLED display panel coatings

    5. High-Performance Corrosion-Inhibitor in Industrial Coating Systems

    Coating industry formulators exploit the fluorinated benzoic acid structure when developing advanced anti-corrosive primers and topcoats for metal substrate protection. The trifluoromethoxy moiety supports superior barrier properties against water ingress and aggressive chemicals, which extends service life in offshore infrastructure, chemical tanks, and specialized industrial plant equipment.

    Industry compliance standards

    • ISO 12944 for corrosion protection of steel structures
    • ASTM D3359 Adhesion Testing for Coating Systems
    • SSPC Paint Application Standards for industrial equipment
    • VOC content compliance: EU Directive 2004/42/EC

    Typical usage ratio

    • 0.1–1% by total paint weight in anti-corrosion primer and topcoat formulations, established via accelerated weathering and electrochemical testing

    Downstream process integration

    • Dissolved in primary polymer and additive pre-mix before dispersion milling; final coating undergoes quality assurance for homogeneity and corrosion resistance

    Final product types

    • Industrial metal primers, heavy-duty maintenance coatings, offshore and marine topcoats, chemical storage tank linings
    Free Quote

    Competitive 2-Hydroxy-5-(Trifluoromethoxy)Benzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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