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4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride

    • Product Name 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride
    • Alias CDS-Cl
    • Einecs 278-027-8
    • 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
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    Specifications

    HS Code

    852583

    Product Name 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride
    Cas Number 42018-52-0
    Molecular Formula C8H8Cl2O2S
    Molecular Weight 239.13 g/mol
    Appearance White to light yellow crystalline powder
    Melting Point 62-65°C
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry, well-ventilated place; keep container tightly closed
    Synonyms Benzenesulfonyl chloride, 4-chloro-2,5-dimethyl-
    Smiles CC1=CC(Cl)=C(C)C=C1S(=O)(=O)Cl

    As an accredited 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, 100 grams, hazard labels (corrosive, irritant), white tamper-evident seal, manufacturer's details, chemical formula.
    Shipping 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride is shipped in tightly sealed, corrosion-resistant containers to prevent moisture and air exposure. Packages are labeled as hazardous material and handled according to chemical shipping regulations. Transport is typically by ground or air, ensuring temperature control and appropriate safety documentation accompanies each shipment for compliance.
    Storage 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, and well-ventilated area, separate from incompatible substances such as water, bases, and strong oxidizing agents. Ensure the storage area is equipped with appropriate spill containment and clearly labeled for hazardous chemicals.
    Application of 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride

    Applications of 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride in Industrial Manufacturing

    As a specialized manufacturer of 4-Chloro-2,5-Dimethylbenzenesulfonyl Chloride, we supply this key intermediate to multiple sectors for advanced synthesis needs. Our technical team partners with compliance-focused downstream producers to integrate this material within regulated processes, ensuring reliable batch performance and reproducibility as required for scalable industrial operations.

    1. Pharmaceutical Sulfonamide Synthesis

    Pharmaceutical companies utilize this sulfonyl chloride derivative as a sulfonation agent in the synthesis of specific sulfonamide drugs, especially those requiring ortho-substituted aromatic backbones. Its selective reactivity suits multi-step active pharmaceutical ingredient (API) manufacturing under tightly controlled environments, allowing production of APIs with precise functional group introduction for targeted drug molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) for raw material traceability
    • European Pharmacopoeia monographs for sulfonamide substances
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.2–0.6 molar equivalents per mole of amine compound; exact ratio adjusted per desired substitution extent and process yield optimization.

    Downstream process integration

    • Introduced during sulfonylation stage after completion of aromatic core synthesis; reaction runs under inert atmosphere to control side reactions; sulfonamides isolated and purified for API standards.

    Final product types

    • Antibacterial sulfonamide drug substances
    • Antidiabetic sulfonylurea intermediates
    • CNS-active aryl sulfonamide APIs
    • Veterinary sulfonamide agents

    2. Agrochemical Intermediate Manufacturing

    In the crop protection sector, formulators employ this compound to synthesize sulfonyl-containing herbicide and fungicide intermediates. Its selectivity enhances purity of the active units, particularly in industrial routes requiring substituted benzenesulfonyl frameworks as coupling partners. Strict controls during its use help downstream processors maintain impurity profiles to meet regulatory residue limits for agrochemicals.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides (JMPS)
    • ISO 9001 for agrochemical manufacturing traceability
    • REACH Registration (EU No 1907/2006) for supply in the European market
    • EPA PRIA regulations on inert ingredient tolerances (United States)

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target nucleophile; proportion selected based on the reactivity of substrate and batch size.

    Downstream process integration

    • Used after ring substitution to introduce sulfonyl chloride group onto aromatic intermediates, followed by coupling or further transformation into target herbicide or fungicide molecules.

    Final product types

    • Sulfonylurea herbicide intermediates
    • Benzimidazole sulfonyl fungicide precursors
    • Crop protection agents for cereals and oilseeds
    • Custom synthesis intermediates for contract development projects

    3. Dyestuff and Pigment Additive Production

    Manufacturers of specialty dyes introduce this reagent at controlled steps to prepare sulfonamide- and sulfonyl-modified pigment precursors which enhance color fastness and water solubility. Its role as a sulfonating agent supports formulation of benzene-based dyes with precise ring-substitution patterns, critical for textile, leather, and printing applications with high-performance specifications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textiles
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines
    • EN 71-3 (Safety of Toys – Migration of Certain Elements) for pigment applications
    • ISO 18451-1:2015 for pigment and colorant quality

    Typical usage ratio

    • 5–15% by weight relative to the mass of core aromatic amine, tailored for desired solubility and absorption properties in final dye formulation.

    Downstream process integration

    • Integrated after primary diazotization and coupling steps; reacts with residual aromatic amino groups to form sulfonyl linkages; resulting intermediates undergo final purification to meet dye or pigment grade specifications.

    Final product types

    • Water-dispersible azo dyes
    • Sulfonamido-anthraquinone pigments for plastics
    • Reactive dye intermediates for cotton fabrics
    • Specialty printing ink colorants

    4. Polymer Modifier and Cross-Linker Manufacturing

    Advanced polymer producers incorporate this sulfonyl chloride as a functional cross-linker in specialty resins, coatings, and engineering plastics. Its aromatic core and reactivity enable introduction of sulfonic acid moieties or cross-linked structures, improving performance in electrical insulation and high-temperature use. The compound is precisely dosed to allow downstream polymerization under controlled FDA- and EU-compliant conditions.

    Industry compliance standards

    • UL 94 (Flammability Tests for Plastics Materials)
    • RoHS Directive 2011/65/EU for restricted hazardous substances
    • REACH Annex XVII for safe industrial use in plastics
    • FDA 21 CFR 177 for indirect food contact polymers (where applicable)

    Typical usage ratio

    • 0.1–2.0 wt% depending on the resin matrix, degree of cross-linking required, and electrical/mechanical properties targeted in the final part.

    Downstream process integration

    • Dosage occurs during resin pre-polymer stage, reacted with diamines or polyols under monitored temperature and mixing rates; subsequent extrusion or casting steps yield compounded polymers with built-in sulfonic or sulfonamide branches.

    Final product types

    • Heat-resistant polyester and polyamide resins
    • Electrical-grade encapsulants and potting compounds
    • Cross-linked coatings for industrial surfaces
    • Hydrophilic polymer films for technical filters
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