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3,5-Difluorobenzenesulfonyl Chloride

    • Product Name 3,5-Difluorobenzenesulfonyl Chloride
    • Alias DFBSC
    • Einecs 249-988-7
    • 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

    944859

    Product Name 3,5-Difluorobenzenesulfonyl Chloride
    Cas Number 67128-55-2
    Molecular Formula C6H3ClF2O2S
    Molecular Weight 212.6 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 255-257°C
    Density 1.55 g/cm³
    Purity Typically ≥97%
    Solubility Reacts with water; soluble in common organic solvents
    Synonyms 3,5-Difluoro-benzenesulfonyl chloride
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Hazard Statements Causes burns; corrosive

    As an accredited 3,5-Difluorobenzenesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle containing 3,5-Difluorobenzenesulfonyl Chloride, sealed with a red cap and labeled with hazard warnings.
    Shipping 3,5-Difluorobenzenesulfonyl chloride is shipped in tightly sealed containers under cool, dry conditions, away from incompatible substances such as water and strong bases. It is classified as a corrosive substance, so proper labeling and protective packaging are required according to DOT and IATA regulations. Handle with care and use personal protective equipment.
    Storage 3,5-Difluorobenzenesulfonyl chloride should be stored in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as water, alcohols, and strong bases. Keep the container tightly closed and properly labeled. Store at room temperature in a corrosion-resistant area, and avoid exposure to moisture, as the compound reacts with water and may release hazardous gases.
    Application of 3,5-Difluorobenzenesulfonyl Chloride

    Applications of 3,5-Difluorobenzenesulfonyl Chloride in Industrial Manufacturing

    3,5-Difluorobenzenesulfonyl chloride serves as a critical intermediate in specialized chemical synthesis. Our manufacturing customers rely on its unique reactivity for several well-established downstream applications. As a direct producer, we ensure its purity aligns with demanding process integration, compliance, and end-use requirements in regulated industries.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers incorporate this specialty sulfonyl chloride into multi-step reactions to introduce sulfonyl fluoride motifs into small-molecule APIs. Its electron-withdrawing fluorine pattern supports formation of advanced building blocks for kinase inhibitors and anti-infective drugs, particularly in patented synthesis routes. Consistent batch quality enables precise control over reaction yields and impurity profiles at manufacturing scale.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Part II (APIs)
    • USP/NF and EP monograph references for intermediates
    • FDA 21 CFR Part 210/211 (if producing on U.S. territory for regulated APIs)

    Typical usage ratio

    • 0.2–1.5 molar equivalents per step, adjusted for stoichiometry; exact loading depends on target API structure and scale of transformation

    Downstream process integration

    • Charged in the secondary functionalization phase, after aromatic core assembly, typically via nucleophilic aromatic substitution or coupling with protected amines/alcohols under controlled temperatures

    Final product types

    • Kinase inhibitor pharmaceuticals (e.g., anti-cancer agents)
    • Sulfonamide-based anti-bacterials
    • Specialty API intermediates for custom synthesis

    2. Agrochemical Intermediate Formation

    Cropprotection compound manufacturers deploy this difluorinated chlorosulfonate in downstream sulfonamide and sulfonylurea synthesis, providing thermal stability and enhanced biological selectivity to herbicide and fungicide active ingredients. Producers value its high assay consistency to maintain agroactive product yields and support compliance in regulated market registrations.

    Industry compliance standards

    • ISO 9001 (Quality Management for Crop Protection Raw Materials)
    • FAO/WHO specifications for active pesticide ingredients
    • REACH (Regulation EC No 1907/2006 for Registration, Evaluation and Authorization of Chemicals in EU)
    • SCCS/EFSA reports for metabolite evaluation (when applicable)

    Typical usage ratio

    • 0.8–1.2 equivalents relative to backbone amine or urea moiety; usage optimized during scale-up and pilot trials

    Downstream process integration

    • Introduced in late-stage derivatization prior to crystallization of technical-grade agrochemical active ingredients; often under inert atmosphere with phase-transfer conditions

    Final product types

    • Sulfonylurea herbicides (e.g., for cereal crop protection)
    • Fluorinated sulfonamide fungicides
    • Precursor intermediates for seed-coating actives

    3. Fluorinated Polymer Additive Synthesis

    Specialty polymer and resin manufacturers integrate this difluorinated sulfonyl chloride in the synthesis of pendant aryl sulfonyl fluoride monomers. This allows the production of functionalized copolymers with enhanced chemical resistance and dielectric properties, crucial for electronics encapsulants and high-performance coatings. Producers rely on batch-to-batch reproducibility to maintain downstream polymerization efficiency and finished material consistency.

    Industry compliance standards

    • ISO 14001 (Environmental Management for Chemical Processing)
    • RoHS Directive 2011/65/EU (on hazardous substances in electronics applications)
    • UL 94 (Flame Classification for Plastics and Polymers)
    • Customer-specific QC protocols for electronics resin inputs

    Typical usage ratio

    • 0.5–2% monomer feedstock by weight in copolymer blends; ratio determined by target dielectric and chemical resistance properties

    Downstream process integration

    • Undergoes sulfonylation reaction in monomer feed step; followed by controlled addition during batch or continuous copolymerization for structure-property tuning

    Final product types

    • Electronics-grade encapsulating resins
    • Fluorinated high-resistance coatings for industrial equipment
    • Specialty adhesive films with improved chemical resistance

    4. Specialty Dye Intermediate Manufacturing

    Dye and pigment producers employ this difluorobenzenesulfonyl chloride to introduce sulfonated and fluorinated functional groups onto aromatic scaffolds, yielding chromophores with altered solubility, bathochromic shifts, and wash-fast characteristics. Dye houses utilize it in controlled synthesis for advanced reactive dyes targeted at synthetic fiber coloration with improved resistance profiles.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for dyes in textiles)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • REACH Annex XVII (Restrictions on azo dyes for textile usage within EU)
    • GOTS V6.0 (Global Organic Textile Standard for dye intermediates)

    Typical usage ratio

    • 1.0–1.3 molar equivalents per dye precursor; ratio refined based on target chromophore reactivity and bath performance

    Downstream process integration

    • Fed into sulfonation-modification stage post-coupling of aromatic amines or phenol scaffolds; followed by purification and formulation for textile or ink applications

    Final product types

    • Disperse dyes for polyester fibers
    • Reactive dyes for polyamide and synthetic blends
    • High-resistance printing inks
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    Competitive 3,5-Difluorobenzenesulfonyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.

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