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2,4-Dichlorobenzenesulfonyl Chloride

    • Product Name 2,4-Dichlorobenzenesulfonyl Chloride
    • Alias 2,4-DCBSC
    • Einecs 221-116-0
    • 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

    155285

    Cas Number 2097-20-9
    Molecular Formula C6H3Cl2O2SCl
    Molecular Weight 243.52 g/mol
    Appearance White to off-white solid
    Melting Point 43-46°C
    Boiling Point ~335°C (decomposes)
    Density 1.6 g/cm³
    Solubility In Water Reacts with water
    Purity Typically ≥ 98%
    Synonyms 2,4-DCBSC, 2,4-dichlorobenzenesulphonyl chloride
    Storage Temperature Store at 2-8°C in a dry place

    As an accredited 2,4-Dichlorobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,4-Dichlorobenzenesulfonyl Chloride, 100g: Supplied in a sealed amber glass bottle with hazard labels and tamper-evident cap for chemical safety.
    Shipping 2,4-Dichlorobenzenesulfonyl chloride should be shipped in tightly sealed containers, clearly labeled with hazard warnings. Store and transport in a cool, dry place, away from incompatible substances such as water and bases. Handle as a corrosive and potentially toxic chemical, following all local, national, and international shipping regulations for hazardous materials.
    Storage **2,4-Dichlorobenzenesulfonyl chloride** should be stored in a tightly closed, corrosion-resistant container in a cool, dry, well-ventilated area, away from moisture, heat, and incompatible substances such as strong bases, oxidizers, and water. Protect from physical damage and direct sunlight. Proper labeling and secondary containment are recommended to prevent accidental exposure or leaks. Use appropriate personal protective equipment when handling.
    Application of 2,4-Dichlorobenzenesulfonyl Chloride

    Applications of 2,4-Dichlorobenzenesulfonyl Chloride in Industrial Manufacturing

    2,4-Dichlorobenzenesulfonyl chloride is a specialty intermediate widely utilized by industrial manufacturers for the synthesis of advanced chemical products in regulated markets. As the direct producer, we engage with formulation plants and process integrators who require stringent batch-to-batch consistency, traceability, and clear input-to-product mapping in downstream sectors.

    1. Crop Protection Actives Synthesis

    Major players in the agrochemical sector incorporate this molecule as a sulfonylation agent in the creation of specific sulfonylurea and triazine herbicides. Technical managers closely monitor compliance with international agrochemical residue limits and control input ratios to meet targeted biological activity while avoiding excess reagent contamination in the final technical concentrate. Our technical service includes batch records suitable for regulatory review and support on in-plant quenching or waste minimization to control hydrochloric acid byproduct management.

    Industry compliance standards

    • FAO/WHO Specification Guidelines (Manual on the Development and Use of FAO and WHO Specifications for Chemical Pesticides)
    • ISO 9001:2015 for Quality Management in agrochemical intermediates
    • European Crop Protection Association manufacturing standards
    • United States EPA Registration 40 CFR Part 158 (Pesticide Data Requirements)

    Typical usage ratio

    • Input ranges from 0.95 to 1.10 equivalents relative to aminobenzene core, with adjustment to ensure complete sulfonylation while minimizing waste; optimized via in-line NMR or titration during development trials.

    Downstream process integration

    • Direct addition at the initial condensation stage in the synthesis of sulfonylurea herbicide cores, followed by controlled neutralization and purification before formulation blending.

    Final product types

    • Sulfonylurea-based herbicides (metsulfuron-methyl, chlorimuron-ethyl)
    • Chlorotriazine pesticides
    • Technical concentrates for bulk agricultural chemical supply
    • Formulated ready-mix foliar spray products

    2. Pharmaceutical Intermediate Production

    Research-based pharmaceutical plants employ this raw material for targeted sulfonylation steps in the synthesis of certain APIs, particularly sulfonamide derivatives and select oncology compounds. Plant management relies on robust documentation and impurity control to align with Good Manufacturing Practice (GMP) and region-specific monographs. The sulfonylating agent joins multistep, often cGMP-audited flow lines which demand total traceability of input, validated cleaning, and disposal of corrosive off-gas byproducts in secure closed systems.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia Monographs
    • FDA 21 CFR Parts 210/211 (cGMP for Finished Pharmaceuticals)
    • ISO 14001:2015 for Environmental Management in pharma production

    Typical usage ratio

    • Used at 1.00–1.05 molar equivalents versus substrate, with excess minimized according to process validation studies and impurity profiles tailored to monograph requirements.

    Downstream process integration

    • Charged as a key reagent during active intermediate coupling stages; integration in fully contained reaction vessels with real-time neutralization, followed by phased quality sampling of each batch.

    Final product types

    • Sulfonamide antibiotic intermediates
    • Sulfonylated cytostatic raw materials (e.g., for anti-cancer APIs)
    • Pharmaceutical-grade fine chemicals
    • High-purity API building blocks for GMP production

    3. Dyestuff and Pigment Manufacturing

    Specialty dye producers adopt this compound as a functional sulfonating reagent, especially in the production of certain azo, anthraquinone, and phthalocyanine pigments. Colorant manufacturers require batch testing for color consistency, low inorganic residue, and residual chloride within strict BfR and REACH limits. The raw material is introduced during specific aromatic substitution steps in reaction kettles equipped with corrosion-resilient linings and advanced fume treatment units.

    Industry compliance standards

    • REACH Regulation (EU) No 1907/2006 registration for downstream use
    • EN 71-3:2019 (Safety of Toys - Migration of Certain Elements)
    • BfR IX Guidelines for Food Contact Colorants (Germany)
    • ISO 1248:2015 for Pigment Testing and Identification

    Typical usage ratio

    • Applied at 0.8–1.2 molar ratio to the target aromatic substrate; operators customize input quantity and residence time based on color index specification and waste stream chemical oxygen demand (COD) management.

    Downstream process integration

    • Side-chain introduction at sulfonation stages, followed by isolation and washing; pigment processing lines adapt agitation and cooling to minimize thermal degradation during exothermic sulfonylations.

    Final product types

    • Reactive azo dyes
    • Anthraquinone-based textile colorants
    • Phthalocyanine pigments for coatings
    • High-fastness organic pigments for plastics and inks

    4. Polymer Cross-Linking and Modification

    Advanced plastic and elastomer producers apply this molecule to introduce cross-linkable sulfonyl groups into engineering resins and specialty rubbers. Technical formulation teams work within industry-specific purity and reactivity parameters, adjusting sulfonylation levels to engineer chemical resistance, thermal performance, or processability. Polymer plants integrate real-time analytics to check degree of modification and monitor emissions compliance under national chemical safety directives.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for restricted substances in plastics)
    • ISO 9001:2015 for Quality Assurance in Polymer Manufacturing
    • US EPA TSCA reporting rules for chemical usage
    • REACH registration for modified monomers

    Typical usage ratio

    • Input levels between 0.5%–5% by weight of resin, precisely controlled based on target cross-link density and downstream mechanical property testing.

    Downstream process integration

    • Inline introduction at extrusion or reaction kettle stage, followed by neutralization and compounding, with controlled removal of trace acid chlorides under vacuum or inert sweep gas.

    Final product types

    • Sulfonated engineering plastics
    • Cross-linked synthetic rubbers
    • Modified thermosets for electronic insulation
    • High-performance membranes for filtration or fuel cell applications
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