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Chloroacetic Acid

    • Product Name Chloroacetic Acid
    • Alias Monochloroacetic acid
    • Einecs 200-901-0
    • 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

    139039

    Chemicalname Chloroacetic Acid
    Casnumber 79-11-8
    Molecularformula C2H3ClO2
    Molarmass 94.50 g/mol
    Appearance Colorless to white crystalline solid
    Meltingpoint 61°C
    Boilingpoint 189°C
    Density 1.58 g/cm³
    Solubilityinwater 860 g/L (20°C)
    Pka 2.86
    Odor Pungent
    Vaporpressure 0.16 mmHg (20°C)

    As an accredited Chloroacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Chloroacetic Acid is typically packaged in a 25 kg white HDPE drum with a tightly sealed lid and hazard warning labels.
    Shipping Chloroacetic acid should be shipped in tightly sealed containers made of resistant materials, labeled with appropriate hazard warnings. It must be kept away from heat, oxidizers, and incompatible substances. Transport should comply with local and international regulations, such as DOT and IMDG, as it is classified as a corrosive and toxic substance.
    Storage Chloroacetic acid should be stored in a cool, dry, well-ventilated area away from heat, sparks, open flames, and incompatible substances such as strong bases and oxidizing agents. Store in tightly sealed containers made of corrosion-resistant material. Keep away from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent spills and accidental contact.
    Application of Chloroacetic Acid

    Applications of Chloroacetic Acid in Industrial Manufacturing

    As a direct manufacturer with decades of experience in synthesis and bulk production, we supply high-purity chloroacetic acid to diversified chemical sectors worldwide. Our customers apply this essential intermediate across regulated downstream routes, supporting specialized formulations and end-use products in several strategic industries.

    1. Agrochemical Formulation for Herbicide Synthesis

    Producers of herbicides, notably 2,4-D (2,4-dichlorophenoxyacetic acid) and MCPA, incorporate chloroacetic acid as a key building block. The manufacturing process involves monochloroacetic acid reacting with specific phenol derivatives, under controlled alkaline or acid catalysis. Product quality directly impacts purity, reaction efficiency, and downstream environmental compliance. Strict plant controls and batch traceability are required to meet export and domestic agricultural chemical regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • US EPA Reregistration Eligibility Decision (RED) requirements
    • REACH registration for agricultural intermediates

    Typical usage ratio

    • Used as the main acetic acid source at 1.05–1.25 molar equivalents relative to active phenolic substrates; ratio adjusted based on raw substrate reactivity and product purity demand.

    Downstream process integration

    • Added after phenol derivatization, with precise dosing control and temperature regulation in main reactor vessels. Used in batch and continuous production lines for large-volume herbicide synthesis.

    Final product types

    • Technical 2,4-D acid
    • MCPA acid
    • Herbicide salts and esters
    • Concentrated herbicide formulations for agriculture

    2. Carboxymethyl Cellulose (CMC) Manufacturing

    Industrial CMC production requires a consistent supply of high-purity chloroacetic acid for etherification reactions with cellulose. The process takes place in alkaline media, where precise pH and moisture control determine product viscosity grades. End-use applications, such as food additives, paper coatings, or oil drilling fluids, rely on tight molecular substitution levels. Manufacturers must comply with stringent testing of residual impurities and substitution distribution.

    Industry compliance standards

    • FCC (Food Chemicals Codex) for food-grade CMC
    • USP/NF monograph for pharmaceutical CMC
    • GB 29941-2013 for China food additive quality
    • ISO 9001:2015 certified production

    Typical usage ratio

    • Ranges from 0.10–0.23 kg chloroacetic acid per kg dry cellulose. Actual ratio varies by target degree of substitution (DS), typically 0.6–1.2 DS for diverse viscosity grades.

    Downstream process integration

    • Dosed after caustic activation of cellulose fibers, followed by etherification reaction, washing, and neutralization. Continuous QC monitoring to maintain batch uniformity and low DCA (di-chloroacetic acid) residues.

    Final product types

    • Thickening agents for food
    • Pharmaceutical excipients
    • Oilfield fluid additives
    • Paper surface-coating solutions

    3. Surfactant Production: Betaines and Amphoteric Agents

    Specialty surfactant manufacturers utilize chloroacetic acid in synthesis of betaine-type amphoteric surfactants. The process involves nucleophilic substitution with tertiary amines under aqueous or mixed solvent conditions. Finished betaines must meet low residual chloroacetate limits and microbiological specifications. Applications range from personal care products to textile auxiliaries and industrial cleaning agents, with formulation records required for traceability.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • China GB 34896-2017 for cleaning agent ingredients
    • REACH registration for surfactant intermediates
    • ISO 22716:2007 GMP for cosmetic raw manufacturing

    Typical usage ratio

    • Fed at 0.75–1.15 molar equivalents to tertiary amine base, optimized for lowest level of unreacted intermediates and tailored chain length distribution.

    Downstream process integration

    • Introduced post-amination, with pH and temperature adjustment in aqueous synthesis reactors. QA procedures confirm end-point adjustment and salt by-product removal before surfactant refining.

    Final product types

    • Cocamidopropyl betaine
    • Lauryl betaine
    • Industrial and cosmetic surfactant blends
    • Textile wetting and leveling agents

    4. Glycine and Pharmaceutical Intermediate Synthesis

    Chloroacetic acid is a principal intermediate in the synthesis of glycine, which serves as a nutritional and pharmaceutical raw material. The process involves ammonolysis under controlled mixing and reaction temperature, requiring precision dosing to avoid excess chlorinated byproducts. Pharmaceutical glycine production demands adherence to pharmacopeia quality standards and validated removal of residual starting material, with batch documentation supporting API regulatory audits.

    Industry compliance standards

    • USP, EP, JP pharmacopoeias for glycine APIs
    • US FDA cGMP (21 CFR Parts 210/211)
    • EDQM CEP certification for Europe
    • China ChP 2020 for API manufacturing

    Typical usage ratio

    • Used at stoichiometric 1:1 molar ratio with ammonia (NH3), adjusted ±5% depending on reaction efficiency and targeted purity; excess ammonia recycled for economic reasons.

    Downstream process integration

    • Added after aqueous base preparation, with strict reaction time and temperature controls. Neutralization, filtration, and crystallization steps follow to ensure contaminant removal before drying and packaging.

    Final product types

    • Pharmaceutical grade glycine (API, excipient)
    • Food-grade glycine additive
    • Feed-grade glycine for animal nutrition
    • Custom amino acid derivatives for finished pharma synthesis

    5. Thioglycolic Acid Production for Cosmetics and Leather Treatment

    In the synthesis of thioglycolic acid, which is a vital component for hair perming agents and leather processing chemicals, chloroacetic acid reacts with sodium or potassium hydrogen sulfide. Process control ensures minimal byproduct formation and consistent batch purity, which are crucial for further formulation in cosmetic products. Compliance with local and international chemical control laws is mandatory for plant export shipments.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 for cosmetic raw material safety
    • REACH Annex VII-VIII for chemical intermediates
    • GB 7916-87 for industrial thioglycolic acid
    • ISO 14001:2015 environmental management in specialty chemical plants

    Typical usage ratio

    • Typically 1.0–1.2 mol chloroacetic acid per 1.0 mol sodium sulfide, fine-tuned to minimize polythio byproducts and adjusted per application requirements.

    Downstream process integration

    • Reaction executed in closed reactors with controlled gas handling. End product purified via acidification, extraction, and distillation steps before transfer to formulation or export packaging.

    Final product types

    • Thioglycolic acid for depilatory creams
    • Reducing agents in permanent waving lotions
    • Leather processing aids
    • Industrial metal cleaners and scale removers

    6. Indoxyl Acetate Synthesis for Fine Chemical and Dye Manufacturing

    Manufacturers of indigo and other vat dyes employ chloroacetic acid in the synthesis of indoxyl acetate intermediates. Production requires strict management of reaction parameters to achieve the necessary purity and conversion rates, supporting both bulk pigment output and specialty dye derivatives. In-process QC measures validate residual mono- and di-chlorinated byproduct concentrations in each production lot, facilitating compliant discharge protocols and supply chain traceability for textile and pigment industries.

    Industry compliance standards

    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)
    • Oeko-Tex Standard 100 for textile chemicals
    • REACH Annex XIV/XVII for dye intermediates
    • ISO 9001:2015 quality systems in dye production

    Typical usage ratio

    • Used at 1.0–1.2 molar equivalents to 2-nitrophenylacetic acid or precursor amino compounds. Ratio tuned for maximum yield and minimal batch-to-batch pigment variation.

    Downstream process integration

    • Dosed during acetylation stage after initial condensation, followed by cyclization and isomer separation. Residuals monitored prior to dye formation and product stabilization.

    Final product types

    • Indoxyl acetate key intermediate
    • Indigo and indigo derivative vat dyes
    • Special effect textile pigments
    • Oxidation-resistant colorants
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