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4-Bromo-2,5-Difluorobenzenesulfonamide

    • Product Name 4-Bromo-2,5-Difluorobenzenesulfonamide
    • Alias MFCD11863071
    • Einecs 629-493-0
    • 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
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    Specifications

    HS Code

    210752

    Product Name 4-Bromo-2,5-Difluorobenzenesulfonamide
    Cas Number 886363-42-0
    Molecular Formula C6H4BrF2NO2S
    Molecular Weight 288.07
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Conditions Store at room temperature, away from light and moisture
    Synonyms 4-Bromo-2,5-difluoro-benzenesulfonamide
    Smiles NS(=O)(=O)c1cc(F)cc(F)c1Br
    Inchi InChI=1S/C6H4BrF2NO2S/c7-3-1-4(8)2-5(9)6(3)13(10,11)12/h1-2H,12H2

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

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle labeled "4-Bromo-2,5-Difluorobenzenesulfonamide, 10 grams," with hazard and handling warnings.
    Shipping 4-Bromo-2,5-Difluorobenzenesulfonamide is shipped in tightly sealed containers to prevent moisture and contamination. It is transported as a non-hazardous solid under normal temperature conditions. Packaging complies with chemical safety standards, and material safety data sheets (MSDS) accompany each shipment to ensure proper handling during transit and storage.
    Storage Store 4-Bromo-2,5-difluorobenzenesulfonamide in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizing agents. Protect from moisture, heat, and direct sunlight. Ensure the storage area is equipped with appropriate spill containment. Label the container clearly and restrict access to trained personnel only. Follow all relevant safety guidelines.
    Application of 4-Bromo-2,5-Difluorobenzenesulfonamide

    Applications of 4-Bromo-2,5-Difluorobenzenesulfonamide in Industrial Manufacturing

    As the original manufacturer, we supply 4-Bromo-2,5-Difluorobenzenesulfonamide to specialized sectors that demand precise chemical intermediates for synthesis, especially where regulatory adherence and process control are critical. Below are the principal downstream applications supported by customers worldwide in line with established quality, compliance, and production parameters.

    1. Pharmaceutical Intermediate for Antineoplastic APIs

    Pharmaceutical companies employ this sulfonamide derivative as a key building block in multi-step active pharmaceutical ingredient (API) synthesis, particularly for halogenated small-molecule antitumor agents. Its electron-withdrawing groups enhance stability and reactivity in palladium-catalyzed coupling and nucleophilic substitution steps. Downstream plants focus on tight parameter control and traceability, integrating the material under GMP production conditions. Careful dosage calculations prevent by-product formation and ensure molecular integrity, as demanded by regulatory filings.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA current GMP)
    • European Pharmacopoeia 11th Edition (Ph. Eur.) requirements for intermediates
    • Chinese Pharmacopoeia (ChP) API precursor verification

    Typical usage ratio

    • Employed at 0.15–0.4 molar equivalents relative to target core structure, with precise adaptation based on desired halogen substitution pattern and scale-up batch size

    Downstream process integration

    • Added during amidation, Suzuki-Miyaura coupling, or nucleophilic aromatic substitution (NAS) steps in multi-stage synthesis; typically introduced after preliminary aromatic framework assembly and prior to final purification

    Final product types

    • Targeted antineoplastic APIs with difluorinated sulfonamide motifs (e.g., kinase inhibitors, brominated antitumor drugs)
    • Advanced pharmaceutical intermediates registered in Drug Master Files (DMFs)

    2. Agrochemical Intermediate for Herbicide Synthesis

    The compound sees established use by agrochemical formulation plants producing sulfonylurea-based herbicides. Its substitution pattern introduces specific bioactivity profiles, reducing off-target effects. Integration typically occurs in the advanced synthesis stages via controlled nucleophilic substitutions or sulfonamide formation, with stepwise addition to minimize reactive loss. Engineering controls govern emissions, and analytical methods track residuals to comply with crop safety regulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO)
    • China GB/T 20784 and GB 4839-2009 (Pesticide Technical Material and Formulation Standards)
    • ISO 9001:2015 for quality management in crop protection chemicals
    • REACH (EC) No. 1907/2006 registration for compliant import/export in the EU

    Typical usage ratio

    • 0.08–0.23 weight fractions based on final active ingredient yield; ratio determined by target selectivity, downstream synthetic route (single-pot or stepwise), and desired crop selectivity

    Downstream process integration

    • Incorporated after the diazotization or halogenation stage into ring-closing or condensation steps; in some cases, undergoes direct sulfonation before final crude isolation

    Final product types

    • Sulfonylurea herbicide actives (post-emergence weed control formulations)
    • Fluorinated sulfonamide pesticide intermediates

    3. Advanced Specialty Monomers in Polymeric Material Production

    Engineered polymers benefit from the unique halogen-sulfonamide balance provided by this raw material, which imparts flame retardancy and hydrolytic stability to specialty copolymers. Downstream resin plants introduce the compound as a chain terminator or functional co-monomer during controlled polymerization. Reaction ratios undergo optimization to balance end-use material properties with regulatory requirements for safety-critical applications, such as electronics and transportation.

    Industry compliance standards

    • UL 94: Fire Safety Standard for Polymer Materials
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • ISO 9001:2015 for quality consistency in polymer manufacturing
    • EN 45545-2:2013 (Fire protection on railway vehicles)

    Typical usage ratio

    • Introduced at 0.5–5% by weight relative to total monomer content, tuned to achieve target flame-retardant rating and physical performance indices

    Downstream process integration

    • Added together with other halogenated or nitrogen-based monomers at the start of batch or continuous polymerization; post-polymerization work-up ensures purity and minimization of unreacted sulfonamide content

    Final product types

    • High-performance polymer blends for electronics insulation
    • Flame-retardant resins for automotive connectors and transport interior fittings

    4. Electronic Fine Chemical Synthesis for Semiconductor Processing Aids

    Producers of microelectronic process chemicals incorporate this difluorinated, brominated sulfonamide as a key intermediate for etchant component synthesis, supporting controlled surface modification and cleaning within semiconductor fabs. Its chemical stability allows for precise integration in fluorochemical blends, while trace-level addition ensures compliance with stringent insoluble-matter and metallic contamination limits common in cleanroom environments.

    Industry compliance standards

    • SEMI C23-0216: Guide for purity specifications of chemical reagents in semiconductor manufacturing
    • IEC 61340-5-1: Electrostatic discharge protection requirements
    • ISO 14644: Cleanroom and associated controlled environments
    • RoHS (for finished product compliance)

    Typical usage ratio

    • 0.01–0.10% by total mass of formulated etchant, adjusted to precise contamination and reactivity profiles required by wafer size and substrate metallurgy

    Downstream process integration

    • Dosed into high-purity fluorochemical or sulfonamide solution during final composition blending; strict filtration and impurity analysis conducted prior to packaging into single-use cleanroom containers

    Final product types

    • High-purity etchants and cleaning solvents used in IC wafer processing
    • Photolithography auxiliary chemicals for advanced node semiconductor fabrication
    Free Quote

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