Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,4,5-Trifluoro-3-Methylbenzoic Acid

    • Product Name 2,4,5-Trifluoro-3-Methylbenzoic Acid
    • Alias 2,4,5-Trifluoro-m-toluic acid
    • Einecs 242-673-5
    • 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

    812922

    Product Name 2,4,5-Trifluoro-3-Methylbenzoic Acid
    Cas Number 881674-61-9
    Molecular Formula C8H5F3O2
    Molecular Weight 190.12 g/mol
    Appearance White to off-white solid
    Melting Point Approximately 115-120°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC1=C(C(=C(C=C1F)F)C(=O)O)F
    Inchi InChI=1S/C8H5F3O2/c1-4-5(9)2-3(10)6(7(4)11)8(12)13/h2H,1H3,(H,12,13)
    Synonyms 3-Methyl-2,4,5-trifluorobenzoic acid
    Storage Temperature Store at 2-8°C

    As an accredited 2,4,5-Trifluoro-3-Methylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,4,5-Trifluoro-3-Methylbenzoic Acid is supplied in a 25g amber glass bottle with a secure screw cap.
    Shipping 2,4,5-Trifluoro-3-Methylbenzoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package includes clear hazard labeling and complies with local and international transport regulations. It is protected from moisture, extreme temperatures, and direct sunlight during transit to ensure chemical stability and safety.
    Storage 2,4,5-Trifluoro-3-Methylbenzoic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong bases or oxidizing agents. Ensure the storage area is clearly labeled and compliant with chemical safety guidelines. Protect the chemical from moisture and physical damage. Store at ambient temperature unless otherwise specified.
    Application of 2,4,5-Trifluoro-3-Methylbenzoic Acid

    Applications of 2,4,5-Trifluoro-3-Methylbenzoic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 2,4,5-Trifluoro-3-Methylbenzoic Acid (TFMBA) to downstream processors who integrate this advanced fluorinated aromatic acid into several high-value chemical manufacturing routes. TFMBA's unique substituent profile provides performance advantages for specialty chemicals, pharmaceutical intermediates, agricultural actives, and material science precursors. Below, we detail actual industrial segments and processing frameworks where our material delivers consistent, specification-driven functionality.

    1. Pharmaceutical Intermediate for Fluorinated Active Pharmaceutical Ingredients (APIs)

    Multinational and regional pharmaceutical manufacturers employ TFMBA as a building block in the synthesis of advanced fluorinated intermediates, which are further transformed into central nervous system therapeutics and anti-infective agents. Fluorination at the aromatic ring increases the metabolic stability and membrane permeability of API candidates, making TFMBA an essential input in early-stage and commercial-scale pharmaceutical production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia–National Formulary)
    • European Pharmacopoeia (Ph. Eur.)
    • REACH Registration (EU) for chemical safety

    Typical usage ratio

    • As a raw intermediate, typically introduced at 1–8% molar ratio relative to final API batch mass, with adjustments depending on the target compound’s molecular structure and desired fluoro-substitution level.

    Downstream process integration

    • TFMBA is charged as a key substrate during the aromatic substitution or amidation stage of API intermediate synthesis, following initial block coupling or halogen exchange. It is closely monitored for purity and residual solvent prior to scale-up. The intermediate is subsequently isolated prior to further transformations such as reduction, acylation, or cyclization.

    Final product types

    • Mainly fluorine-containing APIs for CNS drugs, anti-psychotics, and anti-infective agents.
    • Advanced intermediates for licensed pharmaceutical manufacturing (private label and new chemical entities).

    2. Advanced Agrochemical Synthesis (Herbicide Precursors)

    Key agrochemical manufacturers incorporate TFMBA as a fluorinated aromatic precursor during development and mass production of specialty herbicides. Its structural motif is especially important in the construction of trifluoromethyl-derivatized benzoic acids, which exhibit enhanced crop selectivity and persistence profiles, supporting highly specific field application products.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization specifications for agrochemical actives
    • EU Plant Protection Products Regulation (EC) No 1107/2009
    • ISO 9001:2015 certified quality management systems for pesticide raw materials

    Typical usage ratio

    • Used at 2–10% by mass within the reaction charge, depending on targeted derivative synthesis and crop safety screening data. Ratios may shift according to the seasonality or regional toxicology requirements.

    Downstream process integration

    • Introduced during the benzoylation or etherification stages of herbicide precursor synthesis, typically following chlorination or sulfonation. Producers optimize reactor charging order to control exothermicity and byproduct minimization, supported by in-line HPLC purity checks.

    Final product types

    • Trifluoromethyl-substituted benzoic acid herbicides (e.g., dicamba analogs)
    • Pre-mix and technical grade crop protection agents for row crop and horticultural use

    3. Specialty Polymer Monomer for Fluorinated Coatings

    Leading manufacturers in advanced materials leverage TFMBA as a specialty monomeric unit for synthesizing fluorinated aromatic resins and copolymers. Its substitution pattern imparts high chemical resistance and weatherability to the final polymer chains, supporting demanding applications for architectural, automotive, and electronic component surface coatings.

    Industry compliance standards

    • RoHS 2 (Directive 2011/65/EU) for electronic and automotive coatings
    • ASTM D5402 and D6578 for solvent resistance and stain removal
    • EPA Toxic Substances Control Act (TSCA) chemical inventory

    Typical usage ratio

    • Typically loaded at 0.2–3% novel monomer content in the total monomer feed, balancing cost-performance requirements and crosslinking degree to specific coating end-uses.

    Downstream process integration

    • Dosed during monomer feed preparation for solution or emulsion polymerization. TFMBA reacts with acrylate or epoxy-functional comonomers under controlled initiation and temperature programs, producing copolymers subsequently formulated with additives and crosslinkers.

    Final product types

    • High-performance fluororesin surface coatings
    • Electronics-grade conformal coatings and automotive clear coats

    4. Fine Chemical Intermediate for Specialty Dyes and Pigments

    TFMBA functions as a molecular building block for select colorant and pigment manufacturers seeking robust color fastness and increased solvent stability in specialty dyes for plastics and industrial inks. Its multi-fluoro substitution supports high-purity fine chemicals crucial for pigment performance in aggressive processing environments.

    Industry compliance standards

    • EN 71-3 safety standards (colorants in toys and plastics)
    • REACH Annex XVII (restrictions on hazardous colorant substances)
    • ISO 787/2 general methods for colorant chemical testing

    Typical usage ratio

    • Dosed at 1–6% by mass in the precursor batch, with precise control adjusted based on target hue, shade purity, and polymer compatibility requirements.

    Downstream process integration

    • TFMBA enters the synthetic dye pathway during early condensation or diazotization steps. Manufacturers monitor for trace metal and halogen content prior to downstream oxidative coupling or metal complexation.

    Final product types

    • Fluorinated azo and anthraquinone dyes for technical plastics and masterbatches
    • Industrial pigment dispersions for fiber and ink applications

    5. Building Block in Advanced Organic Electronic Materials

    Producers in the organic electronics sector employ TFMBA as an input for synthesizing functionalized monomers and oligomers, intended for next-generation organic semiconductors and optoelectronic materials. Its trifluoromethyl and methyl groups aid in tuning energy levels and charge-carrier mobility in organic devices.

    Industry compliance standards

    • IEC 62899-202:2016 (Printed Electronics)
    • IPC-4101 for base materials for printed circuit boards
    • ISO 9001:2015 for quality management in electronic material production

    Typical usage ratio

    • Integrated at 0.5–2.5 mol% in the monomer synthesis charge, optimized for finalized device performance based on electronic bandgap requirements and film-forming properties.

    Downstream process integration

    • Charged during the construction of the building block precursor for molecular wires and semiconductive oligomers prior to cross-coupling or Suzuki–Miyaura reactions. Stringent traceability and impurity control are maintained to meet electronic device specifications.

    Final product types

    • Organic field-effect transistor (OFET) active layers
    • OLED emitting layer monomers
    • Printable functional inks for flexible electronics
    Free Quote

    Competitive 2,4,5-Trifluoro-3-Methylbenzoic 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance