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3,5-Dichloro-4-Methylbenzoic Acid

    • Product Name 3,5-Dichloro-4-Methylbenzoic Acid
    • Alias Benzoic acid, 3,5-dichloro-4-methyl-
    • Einecs 221-263-5
    • 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

    612919

    Productname 3,5-Dichloro-4-Methylbenzoic Acid
    Casnumber 2905-62-6
    Molecularformula C8H6Cl2O2
    Molecularweight 205.04 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 165-169°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in ethanol and methanol
    Density 1.47 g/cm³
    Smiles CC1=C(C=C(C=C1Cl)Cl)C(=O)O
    Inchi InChI=1S/C8H6Cl2O2/c1-4-6(9)2-5(8(11)12)3-7(4)10/h2-3H,1H3,(H,11,12)
    Synonyms 4-Methyl-3,5-dichlorobenzoic acid

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

    Packing & Storage
    Packing A 100-gram amber glass bottle with a secure screw cap, clearly labeled with "3,5-Dichloro-4-Methylbenzoic Acid" and safety information.
    Shipping 3,5-Dichloro-4-Methylbenzoic Acid is shipped in tightly sealed, chemically resistant containers, clearly labeled with hazard information. The package should be protected from moisture and direct sunlight, and comply with local and international regulations for shipping hazardous materials. Appropriate documentation, including safety data sheets (SDS), accompanies each shipment for safe handling and transport.
    Storage Store 3,5-Dichloro-4-Methylbenzoic Acid in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Clearly label the container, and ensure appropriate chemical spill containment and proper access to safety equipment such as eyewash and safety showers.
    Application of 3,5-Dichloro-4-Methylbenzoic Acid

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

    As a direct manufacturer, we supply 3,5-Dichloro-4-Methylbenzoic Acid for specialized use in advanced chemical industries where fine control over synthesis and compliance is essential. Below we detail key downstream applications and the technical context required for productive integration into manufacturing processes.

    1. Agrochemical Synthesis for Wheat Herbicides

    Agrochemical manufacturers utilize this material as an essential intermediate in the multi-step synthesis of post-emergence herbicides targeting broadleaf weeds in wheat fields. The compound participates in specific condensation and chlorination reactions unique to phenoxyacetic acid-type herbicide production, demanding strict feedstock purity controls and traceability to comply with regulatory limits on secondary contaminants. Industrial users optimize the input ratio based on reaction efficiency and downstream purification, adapting process parameters to crop protection regulatory requirements in export markets.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 for plant protection products
    • EPA 40 CFR Part 180 – Tolerance for residues
    • ISO 9001:2015 certified quality management systems for agrochemical intermediates
    • REACH Annex XVII for use restrictions and supply chain documentation

    Typical usage ratio

    • Batch processes typically incorporate 8–15% by weight relative to total active ingredient precursors, with adjustments based on target herbicide formulation and process yield.

    Downstream process integration

    • Charged to the condensation reaction vessel immediately after initial solvent charging; reacts with aminobenzoic acid derivatives under controlled pH and temperature before extraction and downstream formulation.

    Final product types

    • Selective wheat herbicides (granules, wet dispersible powders)
    • Formulated agrochemical concentrates for field application

    2. Synthesis of Pharmaceutical Intermediates

    Within API manufacturing, process chemists employ this acid as a specialized carboxylic precursor in assembling complex molecular scaffolds for certain non-steroidal anti-inflammatory drug intermediates. Regulatory agencies require traceable use of such benzoic acid derivatives due to potential carry-over of chlorinated impurities. Production processes stipulate tight input controls and batch record documentation, with active ingredient manufacturers scaling the inclusion rate based on reaction stoichiometry and final process validation results.

    Industry compliance standards

    • cGMP systems per ICH Q7 guidelines
    • Pharmacopeia monographs (USP, EP, JP for related compounds)
    • FDA 21 CFR Part 211: Finished pharmaceuticals
    • Directive 2001/83/EC (EU marketing authorization for medicinal products)

    Typical usage ratio

    • Feedstock input ranges from 3–7% by weight in targeted reaction steps, scaled by batch size and controlled by in-process chromatographic monitoring.

    Downstream process integration

    • Introduced into ring-closing or coupling reactions following initial aryl amination; incorporated under inert conditions in stainless steel reactors, then subjected to purification steps using preparative HPLC.

    Final product types

    • Pharmaceutical intermediates for NSAIDs and anti-inflammatory APIs
    • Final bulk APIs for further formulation

    3. Specialty Polymer Processing for High-Performance Coatings

    Manufacturers of specialty polymers integrate this benzoic acid derivative in the synthesis of high-molecular-weight polyesters and modified polyamides used in protective industrial coatings. The chlorine substitution and methyl group guide polymer structure toward chemical resistance and controlled surface reactivity. Operators dose the additive based on polymer chain growth rate and desired end-use mechanical characteristics, verifying raw material quality under industry-specific standards for polymers intended for industrial equipment and machinery.

    Industry compliance standards

    • ASTM D256, D638 for mechanical testing of polymer materials
    • ISO 9001:2015 for raw material traceability in polymer production
    • RoHS Directive 2011/65/EU on hazardous substances in electrical and electronic coatings

    Typical usage ratio

    • In polymer synthesis, this material represents 2–6% by mass, adjusted per monomer blend and polymerization method, verified in pilot-scale runs before industrial scale-up.

    Downstream process integration

    • Fed directly to melt polycondensation vessels after drying and mixing with other monomers; reaction progress monitored for molecular weight control before extrusion and coating formulation.

    Final product types

    • Chemical-resistant powder coatings
    • High-durability industrial floor paints
    • Protective lacquer formulations for equipment components

    4. Advanced Dye and Pigment Manufacturing

    Producers of specialty colorants use this compound as a building block in the design of halogenated azo and anthraquinone dyes. The unique substitution pattern affects electronic delocalization, enabling color tuning for specific textile and leather applications. Batch chemists carefully regulate the addition rate during the diazotization and coupling phases, considering downstream application regulations for exported dye goods.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted substances in textiles
    • EN 71-3 (Safety of Toys – Migration of certain elements) if dyes are used in relevant applications
    • ZDHC MRSL v3.1 for input chemical management
    • ISO 14001:2015 for environmental management in dye production

    Typical usage ratio

    • 5–12% by weight of total reactive intermediates, adjusted for target chromophore group and final dye purity after coupling reactions and crystallization.

    Downstream process integration

    • Added during azo/anthraquinone coupling with stringent in-process monitoring; purification follows to eliminate unreacted acid before product isolation, followed by blending with dispersants or carriers for downstream application.

    Final product types

    • Reactive dyes for cotton and synthetic fibers
    • Leather pigments for shoe and upholstery finishing
    • Industrial inkjet dyes for high-performance printing
    Free Quote

    Competitive 3,5-Dichloro-4-Methylbenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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