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3-Chloro-4-Methylbenzoic Acid

    • Product Name 3-Chloro-4-Methylbenzoic Acid
    • Alias 3-Chloro-p-toluic acid
    • Einecs 223-508-9
    • 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

    914074

    Product Name 3-Chloro-4-Methylbenzoic Acid
    Synonyms 3-Chloro-p-toluic acid
    Molecular Formula C8H7ClO2
    Molar Mass 170.60 g/mol
    Cas Number 17833-43-7
    Appearance White to off-white crystalline powder
    Melting Point 167-171°C
    Solubility In Water Slightly soluble
    Density 1.37 g/cm³
    Pka 3.98
    Smiles CC1=CC(=C(C=C1)Cl)C(=O)O

    As an accredited 3-Chloro-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 100g amber glass bottle, tightly sealed, labeled "3-Chloro-4-Methylbenzoic Acid," with hazard warnings and lot number displayed.
    Shipping 3-Chloro-4-Methylbenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. It is handled according to standard chemical shipping regulations, with clear hazard labeling. Packages are cushioned to prevent breakage, and a safety data sheet (SDS) accompanies each shipment to ensure safe handling during transport and delivery.
    Storage 3-Chloro-4-Methylbenzoic Acid should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid extremes of heat. Use appropriate chemical storage cabinets if available, and clearly label the container for safety and easy identification.
    Application of 3-Chloro-4-Methylbenzoic Acid

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

    As a direct manufacturer of 3-Chloro-4-Methylbenzoic Acid, we provide this specialty aromatic carboxylic acid for several advanced downstream industries. Our technical grade meets the demands of differentiated production scenarios, with each sector having specific process requirements, compliance considerations, and performance criteria. The following sections outline how this material integrates into four major application chains, detailing practical deployment in industrial environments.

    1. Agrochemical Active Ingredient Synthesis

    Manufacturers of pre-emergent and post-emergent herbicide actives rely on this intermediate in the synthesis pathway for targeted benzoyl derivatives used in selective weed control. The compound is directly incorporated in multi-step organic synthesis, often via acylation or halogenation reactions, to construct key agrochemical cores while maintaining regulatory-compliant impurity profiles. Downstream players adjust the charge to match the conversion rate in batch or continuous reactors, factoring in catalyst compatibility and residual solvent control for regulatory approval.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • FAO/WHO Specifications for Pesticide Technical Materials
    • REACH Registration (EC) No 1907/2006
    • China ICAMA pesticide registration where locally produced

    Typical usage ratio

    • 10–25% by mass in targeted organic syntheses; ratio varies according to the specific herbicidal active pathway and required stoichiometry

    Downstream process integration

    • Added at the primary condensation or acylation step for building benzoyl frameworks, typically under controlled temperature and solvent conditions with in-line HPLC monitoring

    Final product types

    • Benzoyl-containing herbicide actives for broadleaf and grassy weed management
    • Plant protection intermediates for further formulation in water-dispersible granules or EC (emulsifiable concentrate) products

    2. Pharmaceutical Intermediate Production

    Specialty API manufacturers utilize this material as a key benzoic acid derivative for producing advanced pharmaceutical intermediates, especially for non-steroidal anti-inflammatory APIs and select cardiovascular drug syntheses. It typically supports side-chain modification reactions and facilitates halogen-substituted scaffold development. Process engineers calibrate addition volumes based on route selectivity, monitoring residuals to meet ICH Q3A impurity thresholds.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF Monograph specifications (where applicable intermediates are listed)
    • EDQM Certification of Suitability (CEP) requirements
    • Local pharmacopoeial standards in finished API export markets

    Typical usage ratio

    • 5–18% by weight in stage-specific synthetic blocks; adjusted based on desired substitution pattern and final yield optimization

    Downstream process integration

    • Charged at the derivatization stage (e.g., Friedel-Crafts, Suzuki coupling), with in-process GC-MS/LC-MS confirmation of intermediate purity

    Final product types

    • Halogenated benzoic acid pharmaceutical intermediates
    • APIs for NSAID, antifungal, or antiarrhythmic formulations (intermediate level)

    3. Polymer Additives and Monomer Synthesis

    Producers of functional polymers and specialty resin systems incorporate this compound as an intermediate for synthesizing custom monomers or chain modifiers, where its aromatic and halogenated functionalities provide desired compatibility and reactivity. It enters condensation reactions with diols and diamines, contributing to tailored thermal and physical properties in resins used for advanced coatings and engineering plastics, especially where controlled halogen content is specified for insulation or flame resistance.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical processing
    • UL 94 Flammability Certification for final polymer applications
    • RoHS Directive 2011/65/EU for halogenated materials
    • REACH SVHC screening for polymer raw materials

    Typical usage ratio

    • Typically 2–12% in monomer reaction feeds; ratio depends on targeted molecular weight and specified end-use performance (adjustable for resin hardness or flame resistance)

    Downstream process integration

    • Reacted in esterification, amidation, or direct copolymerization stages to yield halogenated aromatic monomers or polymer resins

    Final product types

    • Halogen-modified epoxy resins and polyesters
    • Polymeric coatings for electronics or wire insulation with specific UL 94 ratings
    • Engineering plastic blends requiring controlled aromatic structure

    4. Dyes and Pigment Intermediate Manufacturing

    Specialty dye and pigment formulators use this compound to build precise halogenated aromatic structures in high-performance organic pigment molecules. The acid group serves as a reactive handle for azo coupling and other arylation chemistries, while chlorinated and methyl substituents regulate hue and stability. The formulation chemist specifies the charge based on required chromophore intensity and end-use application, whether for technical inks or specialty plastics coloration.

    Industry compliance standards

    • OEKO-TEX® Standard 100 compliance for textile dye substances
    • EN 71-3 Safety of Toys regulations for migration of pigment components
    • ISO 9001:2015 for pigment and dye manufacturing
    • REACH Annex XVII restrictions applicable to aromatic intermediates

    Typical usage ratio

    • 4–15% in pigment intermediates synthesis, with dosing adjusted according to chromophoric group structure and performance requirements for lightfastness and color strength

    Downstream process integration

    • Utilized at the initial coupling or diazotization stages for construction of pigment scaffolds, supported by in-process HPLC/PXRD monitoring; subsequent processing includes milling or dispersion

    Final product types

    • Organic pigments for plastics, printing inks, and technical coatings
    • High-stability dyes for synthetic fibers and specialty colorants
    Free Quote

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