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2-Chloro-3-Methylbenzoic Acid

    • Product Name 2-Chloro-3-Methylbenzoic Acid
    • Alias 2-Chloro-m-toluic acid
    • Einecs 221-817-8
    • 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

    575564

    Productname 2-Chloro-3-Methylbenzoic Acid
    Casnumber 118-91-2
    Molecularformula C8H7ClO2
    Molecularweight 170.59 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 152-156 °C
    Solubilityinwater Slightly soluble
    Density 1.36 g/cm3
    Purity Typically ≥98%
    Synonyms 2-Chloro-m-toluic acid
    Smiles CC1=C(C=CC=C1Cl)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)
    Storagetemperature Store at room temperature

    As an accredited 2-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 "2-Chloro-3-Methylbenzoic Acid, 100g" with hazard symbols, batch number, and tightly sealed cap for protection.
    Shipping 2-Chloro-3-Methylbenzoic Acid ships in tightly sealed containers, away from incompatible substances and moisture. It is classified as a hazardous chemical, requiring proper labeling and documentation. The package must be handled with care, complying with relevant transport regulations to ensure safety during storage and transit.
    Storage Store 2-Chloro-3-Methylbenzoic Acid in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Store at room temperature and use corrosion-resistant shelving. Avoid inhalation and contact with skin or eyes; ensure appropriate labeling and access to safety data sheets (SDS).
    Application of 2-Chloro-3-Methylbenzoic Acid

    Applications of 2-Chloro-3-Methylbenzoic Acid in Industrial Manufacturing

    Our 2-Chloro-3-Methylbenzoic Acid is produced to the highest industrial specifications, serving as a critical intermediate in multiple high-value chemical sectors. Its refined synthesis and controlled quality enable integration into strictly regulated manufacturing lines. Below we outline verified application fields, highlighting regulatory integration, process specifics, and the precise role in commercial-scale production.

    1. Agrochemical Synthesis – Herbicide Intermediate Manufacturing

    In commercial herbicide production, this compound serves as a vital carboxylic acid intermediate for the synthesis of pyridine- and triazine-based active ingredients. Fine control in batch reactions ensures reliable conversion within multi-stage synthetic routes, supporting large-scale demand for targeted weed control agents. Addition rates depend on the specific downstream molecule but adhere to pre-determined stoichiometric ratios for minimized waste and maximum yield. Finished products target both broad-acre and specialty agricultural markets under rigorous governmental oversight.

    Industry compliance standards

    • ISO 9001:2015-certified Quality Management System
    • REACH Regulation (EC No 1907/2006)
    • China GB 38502-2020: Chemical Pesticide Technical Specifications
    • Good Laboratory Practice (GLP) for pesticide substance testing

    Typical usage ratio

    • 0.7–1.1 molar equivalent relative to the primary amine or heterocycle substrate, adjusted to reaction pathway and desired throughput

    Downstream process integration

    • Charged into the condensation or cyclization reactor during active ingredient core assembly
    • Neutralization and crystallization follow to purify intermediate before formulation steps

    Final product types

    • Phenoxyalkanoic acid herbicides (e.g., MCPA analogues)
    • Triazine herbicides (e.g., simazine derivatives)
    • Pyridine-based selective weed control agents
    • Technical grade pesticide intermediates

    2. Pharmaceutical Intermediate – Non-Steroidal Anti-Inflammatory Drug (NSAID) Precursors

    Within contract and proprietary API synthesis operations, this acid provides a key building block for the formation of structurally modified benzoic acid derivatives employed in analgesic and anti-inflammatory APIs. The compound is dosed according to stringent GMP batch protocols, partnering with N-alkylation or halogenation steps downstream. Its reactivity and purity underpin both pilot and validated scale production for international generic markets, where documentation and traceability are strictly enforced.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) API requirements
    • FDA 21 CFR Part 211: Current Good Manufacturing Practices
    • EDQM Certificate of Suitability (CEP) for starting materials

    Typical usage ratio

    • Typically 1.0–1.3 molar equivalent in condensation or substitution reactions, calculated per validated synthesis protocol

    Downstream process integration

    • Introduced during the arylation step for API precursor construction
    • Subjected to hydrogenation, halogen exchange, or amidation in accordance with established cGMP routes

    Final product types

    • Bulk NSAID intermediates (e.g., mefenamic acid analogues)
    • API key starting materials (KSMs)
    • Custom analgesic compound series (contract synthesis)
    • API regulatory documentation packages

    3. Dyes and Pigments – High-Performance Dye Intermediate

    Producers of specialty dyes use this benzoic acid derivative to construct azo and anthraquinone intermediates. Manufacturers integrate the compound through diazotization or coupling steps, allowing for chromophore fine-tuning and improved dye stability. Compliance with industrial and environmental regulations is critical to support product traceability, especially for textile and leather dye applications. Dosing levels correspond to output shade intensity and yield coefficients for each product line.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • ECHA REACH Annex XVII: Restrictions on certain hazardous substances
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 14001: Environmental Management Systems

    Typical usage ratio

    • 0.8–1.0 molar equivalent relative to diazo precursor; adjusted for color depth and reaction efficiency

    Downstream process integration

    • Added in the early phase of diazotization or coupling reactions to build extended chromophores
    • Undergoes purification and isolation before formulation into dye pastes or powders

    Final product types

    • Textile acid dyes
    • Leather finishing pigments
    • High-stability printing inks
    • Specialty colorants for automotive and plastic industries

    4. Plasticizer and Resin Additives – Modified Polyester Systems

    Leading resin manufacturers introduce this acid as a co-monomer to adjust thermal and mechanical properties in custom polyester resins. The material enters direct esterification or transesterification steps, enhancing the flexibility, adhesion, and resistance characteristics of the cured resin. Dosage precision depends on the specific performance target and compatibility with other additives, aligning with evolving health and safety legislation for industrial polymers.

    Industry compliance standards

    • FDA 21 CFR 177.2420: Polyester resins for food-contact coatings
    • EU Regulation (EC) No 10/2011: Plastic materials and articles intended to come into contact with food
    • UL 94: Flammability Standard for Plastic Materials
    • ISO 9001:2015 for manufacturing process control

    Typical usage ratio

    • 0.5–2.5 wt% of total polymer matrix, varied to achieve target flexibility and thermal resistance

    Downstream process integration

    • Metered addition to esterification reactor during polyester resin pre-polymer formation
    • Integrated with multifunctional alcohols and phthalic derivatives for performance balance

    Final product types

    • High-flexibility polyester coatings
    • Adhesion promoters in industrial films
    • Modified plasticizers for wire and cable
    • High-durability composites for automotive interiors
    Free Quote

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