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3-Methoxy-2,4,5-Trifluorobenzoic Acid

    • Product Name 3-Methoxy-2,4,5-Trifluorobenzoic Acid
    • Alias 3-Methoxy-2,4,5-trifluorobenzoic acid
    • Einecs 846-070-7
    • 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

    106651

    Productname 3-Methoxy-2,4,5-Trifluorobenzoic Acid
    Casnumber 886762-98-7
    Molecularformula C8H5F3O3
    Molecularweight 206.12
    Appearance White to off-white solid
    Meltingpoint 107-112°C
    Solubility Soluble in organic solvents like DMSO, methanol
    Purity Typically ≥97%
    Smiles COC1=C(C=C(C(=C1F)C(=O)O)F)F
    Inchi InChI=1S/C8H5F3O3/c1-14-5-2-4(10)7(8(12)13)6(11)3-5/h2-3H,1H3,(H,12,13)
    Synonyms 3-Methoxy-2,4,5-trifluorobenzoic acid

    As an accredited 3-Methoxy-2,4,5-Trifluorobenzoic 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 containing 25 grams of 3-Methoxy-2,4,5-Trifluorobenzoic Acid, securely sealed, labeled with hazard and identification information.
    Shipping **Shipping Description:** 3-Methoxy-2,4,5-Trifluorobenzoic Acid is shipped in tightly sealed, chemically compatible containers to prevent moisture and contamination. The package is clearly labeled with product and hazard information, and is transported according to local, national, and international regulations for chemicals, including all safety and environmental guidelines.
    Storage 3-Methoxy-2,4,5-trifluorobenzoic acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably in a designated corrosive or chemical storage cabinet. Ensure it is properly labeled, and segregate it from incompatible substances such as strong oxidizers and bases.
    Application of 3-Methoxy-2,4,5-Trifluorobenzoic Acid

    Applications of 3-Methoxy-2,4,5-Trifluorobenzoic Acid in Industrial Manufacturing

    3-Methoxy-2,4,5-Trifluorobenzoic Acid functions as a specialized aromatic intermediate in multiple advanced chemical manufacturing sectors. As the original producer, we supply this compound to qualified manufacturers spanning pharmaceutical, agrochemical, electronics, and specialty polymer markets, consistently supporting precise formulation, process reliability, and regulatory compliance throughout demanding downstream processes.

    1. Pharmaceutical Active Ingredient Synthesis

    Our material finds targeted use as a key building block in active pharmaceutical ingredient (API) synthesis for innovative oral and injectable drugs. It introduces multiple electron-withdrawing fluorine substituents into molecular scaffolds, enabling improved bioavailability, stability, and metabolic profile of drug candidates. In these reactions, this benzoic acid derivative undergoes acylation, amidation, and halogen-lithiation to yield intermediates for anti-inflammatory, antiviral, and CNS acting molecules, in accordance with the latest GMP and pharmacopeial requirements for process impurities and residual solvents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia monographs for fluorinated API intermediates
    • U.S. FDA cGMP 21 CFR Part 210/211
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 5%–18% molar equivalent relative to the pharmaceutical core structure being functionalized; precise ratio adjusted according to target final product purity, impurity profile, and route efficiency.

    Downstream process integration

    • Stepwise introduction via acid chloride formation, Suzuki or Buchwald coupling, or direct amidation in early or mid-stage API intermediate synthesis routes.

    Final product types

    • Fluorinated pharmaceutical actives (small molecule APIs)
    • CNS and anti-infective intermediates
    • Stabilized drug candidates for development pipelines
    • Pharmaceutical reference standards with enhanced stability

    2. Agrochemical Herbicide and Fungicide Intermediate Production

    Leading agrochemical synthesis utilizes this material to introduce highly stable fluorine-bearing motifs into new-generation herbicide and fungicide actives. Its distinct substitution pattern supports synthesis of carboxamide and oxadiazole-type intermediates with strong crop selectivity and weather resistance. Formulators select and dose this acid according to downstream cyclization and acylation reaction efficiencies, considering EU REACH and global pesticide MRL residue expectations.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006
    • U.S. EPA pesticide registration and tolerance requirements
    • OECD Guidelines for the Testing of Chemicals
    • ISO 14001 Environmental Management System (site process)

    Typical usage ratio

    • 3%–10% by weight in pre-condensation batches depending on the complexity and targeted active ingredient yield.

    Downstream process integration

    • Condensation and ring closure in the synthesis of N-heterocyclic pesticides; acid group converted in the presence of activating agents or dehydrating condensors.

    Final product types

    • Selective post-emergence herbicides
    • Systemic agricultural fungicides
    • Pesticide intermediates for global crop protection formulations
    • Tested reference standards for regulatory submissions

    3. Liquid Crystal Display (LCD) Intermediate Manufacture

    Specialty electronics manufacturers employ this molecule for synthesis of key mesogenic intermediates in high-performance liquid crystal materials. The tri-fluorinated system imparts high dielectric anisotropy and chemical durability to commercial display films. Integration into these proprietary routes adheres to specific electronics-sector protocols on ultra-trace metal and halide impurity control, with batchwise addition based on precise phase transition requirements for the targeted nematic mixtures.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic material inputs
    • ISO 9001:2015 for electronic chemicals
    • IECQ QC 080000:2017 (Hazardous Substance Process Management)
    • Proprietary OEM qualification protocols for display material purity

    Typical usage ratio

    • 1.5%–7% by mole for mesogen ring construction; adjusted as required for chain length and substitution pattern of downstream liquid crystal precursors.

    Downstream process integration

    • Inserted at the aryl coupling or etherification stage in the core synthesis of high-purity mesogenic compounds for LCD mixing.

    Final product types

    • Fine pitch and large-format LCD display mixtures
    • Temperature-stable liquid crystal films
    • Materials for OLED display sealing and alignment
    • Process validation standards for electronics QC

    4. Fluorinated Polymer Manufacturing

    The specialty polymer sector incorporates this acid as a functional monomer precursor for engineering polymers requiring precise control of chemical resistance and mechanical properties. Through direct copolymerization or pre-condensation with diols and diamines, processors achieve highly-defined molecular weights and controlled distribution of fluorinated units. Manufacturers comply with exhaustive regulatory and customer-specific analytical protocols for extractables and leachables, with dosing set to meet proprietary film or resin performance targets.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001 for chemical process management
    • FDA Title 21 CFR 177.1550 (if entering food contact applications)
    • Automotive OEM materials qualification (e.g., VW TL/GM GMW standards, as required by end-use)
    • Polymer industry REACH registration/exemption requirements

    Typical usage ratio

    • 2%–8% by monomer feed weight; adjusted to match targeted fluorine-content for resilience, chemical inertness, and processabiliy of the final polymer matrix.

    Downstream process integration

    • Direct monomer addition prior to condensation or addition polymerization; acid functionality activated via DCC, carbodiimide, or acid chloride for in-situ copolymer formation.

    Final product types

    • Specialty fluorinated polyesters and polyamides
    • High-performance engineering films
    • Chemical-resistant tubings and membranes
    • Surface-coating precursors for anti-fouling and electrical insulation
    Free Quote

    Competitive 3-Methoxy-2,4,5-Trifluorobenzoic 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 admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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