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4-Chloro-3-Methylbenzoic Acid

    • Product Name 4-Chloro-3-Methylbenzoic Acid
    • Alias 4-Chloro-m-toluic acid
    • Einecs 211-795-2
    • 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

    315197

    Productname 4-Chloro-3-Methylbenzoic Acid
    Casnumber 619-36-1
    Molecularformula C8H7ClO2
    Molecularweight 170.59
    Appearance White to off-white solid
    Meltingpoint 186-189°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.37 g/cm3 (approximate)
    Purity Typically ≥98%
    Smiles CC1=C(C=CC(=C1)Cl)C(=O)O
    Inchi InChI=1S/C8H7ClO2/c1-5-6(8(10)11)3-2-4-7(5)9/h2-4H,1H3,(H,10,11)
    Synonyms 4-Chloro-m-toluic acid; 3-Methyl-4-chlorobenzoic acid
    Storageconditions Store at room temperature, keep container tightly closed

    As an accredited 4-Chloro-3-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 labeled “4-Chloro-3-Methylbenzoic Acid, 100g, for laboratory use only.” Tamper-evident seal, with hazard pictograms.
    Shipping `4-Chloro-3-Methylbenzoic Acid` is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled as a non-hazardous solid under standard shipping regulations, kept away from incompatible substances, and stored in a cool, dry place. Proper labeling and documentation accompany all shipments to ensure safe delivery.
    Storage 4-Chloro-3-Methylbenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from direct sunlight and moisture. Store at room temperature and avoid sources of ignition. Properly label the container and handle with appropriate personal protective equipment to prevent exposure.
    Application of 4-Chloro-3-Methylbenzoic Acid

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

    As an established producer, we supply 4-Chloro-3-Methylbenzoic Acid to specialty chemical manufacturers in several advanced sectors. Below are industrial application scenarios supported by established technical routes and regulatory frameworks.

    1. Pharmaceutical Intermediates for Active Compound Synthesis

    Research-driven pharmaceutical producers use this benzoic acid derivative in the custom synthesis of specific nonsteroidal anti-inflammatory drugs (NSAIDs) and angiotensin receptor antagonists. This material serves in acylation reactions forming molecular cores critical for final API assembly, with careful impurity control in each batch. Chemists incorporate it at optimized stages during multi-step processes, maintaining traceability and compliance from raw input through API crystallization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Pharmacopoeias: USP, Ph. Eur. – analytical and purity requirements
    • 21 CFR Part 211, FDA process documentation requirements
    • EudraLex Volume 4, Annex 1 batch record traceability

    Typical usage ratio

    • 0.9–1.2 molar equivalents relative to coupling amines; adjusted for desired yield and impurity profile

    Downstream process integration

    • Acid chloride preparation precedes amidation (step 2 or 3 of multi-step API synthesis)
    • Final inclusion in recrystallization or salt formation before QC and packaging

    Final product types

    • Bulk APIs such as certain ARBs and NSAID key intermediates
    • Isolated medicinal precursors for contract manufacturing
    • Research-grade compounds for formulation studies
    • Preclinical trial batches distributed to CROs

    2. Agrochemical Intermediate—Herbicide and Insecticide Synthesis

    Manufacturers of specialty agrochemicals employ our product as a strategic key starting material, essential for synthesizing pyrazole-based herbicides and select benzoic acid-derived insecticides. Integrated process lines use this acid in condensation steps with proprietary amines or hydrazines. Regulatory compliance is maintained through residue management protocols and batch validation, enabling safe launch of new pesticide actives.

    Industry compliance standards

    • ISO 9001:2015 (QMS for technical-grade intermediates)
    • FAO/WHO Specifications for Pesticide Technical Concentrates
    • REACH (EC) No 1907/2006—registration and safety data requirements
    • China ICAMA documentation for pesticide registration

    Typical usage ratio

    • 5–12% by total mass of herbicide technical concentrate, depending on the molecular target and subsequent derivatization route

    Downstream process integration

    • Mixed in initial charge for N-arylation or condensation reactor
    • Key reactant in step 1 of multi-component synthesis prior to formulation and granulation

    Final product types

    • Active technical-grade herbicides based on benzoic core
    • Insecticide intermediates for custom synthesis of environment-specific actives
    • Precursor compounds for field trial batch production
    • Specialty agro intermediates supplied to toll formulation facilities

    3. Polymer Additive Manufacturing—Specialty Resin Modifiers

    Leading resin and additive formulators use 4-Chloro-3-Methylbenzoic Acid to tailor-chain aromatic polyesters and engineering plastics. The compound is critical during controlled polycondensation for modifying molecular architecture and imparting chemical resistance or thermal stability. Real-time monitoring assures stoichiometric precision, while process records ensure traceability through master batch creation.

    Industry compliance standards

    • ISO 14001 environmental compliance for polymer plants
    • RoHS Directive (2011/65/EU) for additive component quality
    • EN 10204 traceability documentation for resin supply
    • REACH SVHC assessment for raw material handling

    Typical usage ratio

    • 0.2–1.5% weight-to-weight basis in modified polyester production; adjusted for pigment compatibility and heat performance

    Downstream process integration

    • Dosed during feed stage of continuous polycondensation reactors
    • Homogenized in pre-polymer mixture for high-consistency master batches

    Final product types

    • Specialty resins for automotive and electrical applications
    • High-performance plasticizers for polyesters
    • Polymer modifiers improving solvent resistance
    • Custom master batches for downstream pelletizing

    4. Fine Chemical Synthesis—Dye and Pigment Intermediates

    Dye and pigment manufacturers integrate this aromatic acid to synthesize specific azo and anthraquinone pigments. The material participates in esterification and coupling steps, facilitating chromophore assembly. Batch records capture reagent tracking for compliance audits, and downstream customers value the color strength and thermal durability driven by these precursors.

    Industry compliance standards

    • OEKO-TEX® Standard 100 chemical usage verification
    • EN 71-3 (Safety of Toys – Migration of Certain Elements) for pigment use
    • ISO 9001 process documentation requirements
    • REACH Registration for pigment intermediate safety

    Typical usage ratio

    • 3–7% of pigment intermediate synthesis; percentage adjusted per shade and solubility targets

    Downstream process integration

    • First-step condensate in pigment intermediate production
    • Direct coupling reactant for azo/anthraquinone chromophore formation

    Final product types

    • Resistant azo dyes for plastics and synthetic textiles
    • High-purity pigments for industrial coatings
    • Commercial concentrates for printing ink manufacturing
    • Colorant intermediates distributed to global pigment houses

    5. Specialty Chemical Synthesis—Photoresist Precursors

    Producers of advanced photoresist materials utilize this aromatic acid as a functional group source in synthesizing high-purity blocking and developer agents. Advanced lithography formulations demand strict impurity control, achieved through phase transfer catalysis or continuous-flow synthesis lines. Our material integrates as a functional group donor for photoreactive units in microelectronics manufacturing.

    Industry compliance standards

    • SEMI S2 (Safety Guidelines for Semiconductor Manufacturing)
    • ISO 14644-1 cleanroom process management
    • IATF 16949 for microelectronics chemical supply
    • JEDEC JESD625 material traceability

    Typical usage ratio

    • 0.1–0.8% in developer component blending; formula specifics depend on resolution and coating thickness requirements

    Downstream process integration

    • Direct feed to microreactor for photolabile group synthesis
    • Batch addition prior to final filtration and drum packing for fab customer dispatch

    Final product types

    • Photoresist developer blends for integrated circuit production
    • Microlithography coating precursors
    • Photoreactive intermediates for advanced wafer patterning
    • High-purity additive packages for semiconductor fabs
    Free Quote

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    Tel: +8615371019725

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