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3-Fluoro-4-Methylbenzoic Acid

    • Product Name 3-Fluoro-4-Methylbenzoic Acid
    • Alias 3-Fluoro-p-toluic acid
    • Einecs 609-981-4
    • 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
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    Specifications

    HS Code

    707515

    Product Name 3-Fluoro-4-Methylbenzoic Acid
    Cas Number 403-12-5
    Molecular Formula C8H7FO2
    Molecular Weight 154.14
    Appearance White to off-white solid
    Melting Point 107-110°C
    Boiling Point 287°C
    Purity ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Density 1.29 g/cm3
    Smiles CC1=CC(=CC(=C1)F)C(=O)O
    Inchi InChI=1S/C8H7FO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)
    Synonyms 3-Fluoro-4-methylbenzoic acid; 4-Methyl-3-fluorobenzoic acid
    Storage Conditions Store at room temperature in a tightly closed container
    Hazard Statements Irritant to eyes, skin and respiratory system

    As an accredited 3-Fluoro-4-Methylbenzoic 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, 100 grams, white screw cap, hazard label, chemical name and CAS number, manufacturer’s logo, tamper-evident seal.
    Shipping 3-Fluoro-4-Methylbenzoic Acid ships as a solid, typically in sealed, labeled containers to prevent contamination and moisture absorption. It is classified as non-hazardous for transport, but should be handled with care. Ensure compliance with local regulations, and keep material away from incompatible substances during shipping and storage.
    Storage 3-Fluoro-4-Methylbenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of moisture, heat, and ignition. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature and protect from direct sunlight. Ensure proper labeling and use secondary containment to prevent accidental spillage.
    Application of 3-Fluoro-4-Methylbenzoic Acid

    Applications of 3-Fluoro-4-Methylbenzoic Acid in Industrial Manufacturing

    3-Fluoro-4-Methylbenzoic Acid serves as a specialized intermediate in a range of advanced industrial sectors. Our direct synthesis and rigorous quality controls enable precise integration into intricate downstream processes. Here we detail real applications across genuine industry segments, covering compliance, technical usage, process flow, and finished goods.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use this acid as a building block in the production of complex APIs, particularly fluorinated drug candidates for oncology and CNS therapies. Our material exhibits high purity and low residual solvents, which supports multistep syntheses under stringent regulatory oversight. Process chemists deploy the compound in early-stage amidation or esterification, allowing selective fluorine introduction that enhances metabolic stability and bioavailability in the API structure. Formulators monitor trace impurities and scale up under validated conditions according to regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA regulations for finished pharmaceuticals)
    • EU GMP Guidelines for APIs
    • Relevant monographs in USP/Ph. Eur. for intermediate control

    Typical usage ratio

    • 0.5–3.5 molar equivalents per API molecule, depending on process stage and desired fluorination degree; process chemists adjust based on targeted yield and impurity profile.

    Downstream process integration

    • Introduced during advanced intermediate formation—often via palladium-catalyzed coupling, amide bond formation, or ring closure reactions in multi-step API syntheses; integrated under GMP-compliant, traceable batch records.

    Final product types

    • Anticancer small-molecule APIs
    • CNS-targeted fluorinated pharmaceutical active substances
    • Custom contract-manufactured intermediates for drug R&D projects
    • Reference standards for impurity profiling

    2. Agrochemical Synthesis for Herbicide Intermediates

    Major agrochemical groups utilize this compound during synthesis of selective fluorinated herbicides. Process teams value its reactivity and compatibility with various coupling agents, which allows efficient integration into complex aromatic heterocycles used for high-selectivity weed control. Quality teams analyze each lot for halide content, moisture, and trace organofluorine byproducts to meet stewardship guidelines.

    Industry compliance standards

    • ISO 9001:2015 for quality management during synthesis
    • FAO/WHO specification for pesticide technical requirements
    • REACH Regulation (EC 1907/2006) for registration and stewardship
    • Globally Harmonized System (GHS) for labeling and SDS documentation

    Typical usage ratio

    • 5–10% by mass of total precursor formulation, adjusted based on reaction route and targeted fluorination; batch chemists optimize based on desired yield and byproduct minimization.

    Downstream process integration

    • Entry point: nucleophilic aromatic substitution or condensation with activated heterocycles; usually performed in basic or polar aprotic media under controlled temperature profiles.

    Final product types

    • Selective herbicide technical grade products
    • Intermediate concentrates for downstream formulation blending
    • Reference impurity standards for analytical support
    • Custom fluorinated agrochemical candidates for regulatory submission

    3. Fine Chemical Intermediate for Specialty Polymers

    Producers in the specialty polymer field deploy this compound as a functionalized aromatic acid monomer. The fluorinated and methylated aromatic ring imparts enhanced hydrophobicity and chemical resistance to end-stage polymers. Engineers optimize batch incorporation to enable controlled molecular weight and thermal stability in high-performance film or coating materials. Stringent in-process analysis verifies purity before polycondensation or chain extension.

    Industry compliance standards

    • ISO 14001:2015 (environmental management for polymer facilities)
    • ASTM D638 for plastics tensile properties (for end-user QC)
    • REACH compliance for monomer import and handling
    • IEC 60296 (for insulating varnish compatibility where relevant)

    Typical usage ratio

    • 2–8% molar content relative to total acid monomer pool, customized per polymer architecture and target film properties.

    Downstream process integration

    • Reacted during polycondensation (with diamines or diols) in melt or solution phase; incorporation precedes catalyst addition for controlled branching and end-group formation.

    Final product types

    • High-durability fluorinated polyesters and polyamides
    • Specialty coatings with chemical and weather resistance
    • Insulating films for electronics and capacitors
    • Custom-engineered plastics for automotive or aerospace components

    4. Chemical Synthesis of Liquid Crystals for Display Technologies

    Manufacturers in the display sector use this material in the preparation of advanced liquid crystal compounds. These molecules require precise aromatic substitution for fine-tuned transition temperatures and dielectric properties. Synthesis teams integrate the compound early in serial esterification and halogen-exchange reactions, supporting patterned alignment and high contrast for LCD and OLED technologies. Oriented crystal assemblies benefit from the reproducibility and purity levels our plant achieves.

    Industry compliance standards

    • ISO 9001:2015 for quality and traceability in electronic chemicals
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • IPC-4553 for organic solderability and cleanliness standards
    • JIS C0950 (Japanese electronic chemical standards)

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to liquid crystal compound backbones; digital manufacturing teams control ratios for target melting point and alignment behavior.

    Downstream process integration

    • Material enters as an aromatic acid precursor in multistep organofluorine synthesis; after methyl esterification and halogen substitution, engineers purify via column or recrystallization before final blending.

    Final product types

    • Twisted-nematic liquid crystals for LCD panels
    • Fluorinated mesogenic compounds for advanced display modules
    • High-stability liquid crystal mixtures for touch screens and e-paper
    • Intermediate building blocks for R&D in photonic applications
    Free Quote

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