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4-Iodobenzenesulfonyl Chloride

    • Product Name 4-Iodobenzenesulfonyl Chloride
    • Alias IBS-Cl
    • Einecs 223-975-4
    • 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

    633625

    Chemical Name 4-Iodobenzenesulfonyl Chloride
    Cas Number 6232-72-4
    Molecular Formula C6H4ClIO2S
    Molecular Weight 302.52
    Appearance White to off-white crystalline powder
    Melting Point 110-114°C
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed
    Solubility Reacts with water; soluble in organic solvents
    Synonyms 4-Iodobenzene-1-sulfonyl chloride, p-Iodobenzenesulfonyl chloride
    Density 2.06 g/cm³
    Smiles C1=CC(=CC=C1S(=O)(=O)Cl)I
    Hazard Statements Causes severe skin burns and eye damage
    Ec Number 228-312-1

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

    Packing & Storage
    Packing 250g of 4-Iodobenzenesulfonyl Chloride is packaged in a sealed amber glass bottle with hazard labeling and tamper-evident cap.
    Shipping 4-Iodobenzenesulfonyl Chloride is shipped in tightly sealed containers to prevent moisture exposure and protect against degradation. It is transported under dry, cool conditions as a regulated hazardous material. Packaging follows relevant safety guidelines to ensure secure handling and compliance with international and local chemical transportation regulations.
    Storage 4-Iodobenzenesulfonyl chloride should be stored in a cool, dry, well-ventilated area away from direct sunlight, moisture, and incompatible materials such as strong bases and oxidizers. Keep the container tightly closed and properly labeled. Use corrosion-resistant containers (preferably amber glass) to minimize light exposure and decomposition. Handle under an inert atmosphere if possible to prevent hydrolysis and degradation.
    Application of 4-Iodobenzenesulfonyl Chloride

    Applications of 4-Iodobenzenesulfonyl Chloride in Industrial Manufacturing

    4-Iodobenzenesulfonyl chloride is an essential intermediate in specialty chemical, pharmaceutical, and advanced material industries. With our direct production and rigorous quality management, we serve clients seeking reliable input for critical synthesis and high-value downstream manufacturing.

    1. Pharmaceutical Intermediate for Sulfonamide Synthesis

    Pharmaceutical manufacturers utilize this material as a sulfonylating agent within multi-step synthesis workflows, particularly in the production of active pharmaceutical ingredients (APIs) such as sulfonamide-based drugs. It enables the selective introduction of sulfonyl chloride groups onto aromatic or heterocyclic scaffolds under controlled temperature and solvent conditions, facilitating further substitution or cyclization steps per patent and pharmacopoeial standards. Operator training, cleanroom measures, drainage controls, and validated cleaning are enforced throughout GMP-compliant API manufacturing.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • United States Pharmacopeia (USP) monographs for sulfonamide APIs
    • EDQM CEP, European Pharmacopoeia (Ph. Eur.)
    • Environmental Protection Law (China), REACH (EU)

    Typical usage ratio

    • 1.05–1.30 equivalents relative to the amine substrate; excess adjusted by final purity required in each batch

    Downstream process integration

    • Charged during sulfonylation of aromatic amines, often after base-catalyzed amination
    • Temperature maintained at 0–25°C to avoid hydrolysis; solvents such as dichloromethane or DMF used to control reactivity
    • Subsequent reactions may use purified output for condensation or ring closure, still within the closed production environment

    Final product types

    • Sulfonamide antibacterials (e.g., sulfathiazole derivatives)
    • Antiviral intermediates
    • API building blocks shipped for further synthesis or clinical use
    • Reference standards for regulated pharmaceutical supply

    2. Agrochemical Intermediate in Herbicide Production

    In crop protection, this raw material plays a pivotal role during the synthesis of sulfonylurea and benzothiadiazole herbicides. Production chemists employ it in the selective sulfonylation of heterocyclic amines or phenylthio compounds under anhydrous conditions. Stringent environmental, safety, and residue control requirements govern both open and closed-system manufacturing in this sector due to the hazardous nature of chlorinated and iodinated intermediates. On-line monitoring supports verification of complete conversion and byproduct minimization to meet regulatory residue guidelines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in agrochemical production
    • Globally Harmonized System (GHS) for labelling and transport
    • FAO/WHO Guidelines on Manufacture of Pesticides
    • China National Standards (GB) for residual iodine/chlorine in agrochemical actives

    Typical usage ratio

    • 0.95–1.10 molar equivalents, optimized for minimal excess following pilot trials

    Downstream process integration

    • Added after base-mediated formation of primary or secondary amines
    • Mixed and reacted in continuous stirred tank reactors equipped for dust and vapor control
    • Automated phase separation and washing downstream ensures trace byproducts remain below regulatory maximums

    Final product types

    • Sulfonylurea herbicide actives (e.g., metsulfuron-methyl, chlorsulfuron)
    • Benzothiadiazole derivatives for disease control
    • Weed control formulations for cereals and paddy rice
    • Technical concentrate shipped to crop chemical formulators

    3. Advanced Dye and Pigment Synthesis

    The dye manufacturing sector relies on this unique sulfonylating agent for the stepwise preparation of water-soluble, halogen-functionalized dyes. It enables introduction of the iodosulfonyl moiety onto aromatic dye precursors, providing key handles for further coupling or polymer grafting reactions. Recipe, temperature, and order of addition are tightly controlled due to sensitivity to moisture and light, and product isolation must reduce residual organoiodine below colorant industry thresholds. Occupational exposure and waste minimization measures align with zero discharge and staff health mandates.

    Industry compliance standards

    • ZDHC MRSL Compliance (Zero Discharge of Hazardous Chemicals)
    • Oeko-Tex Standard 100 (dyestuffs for textiles)
    • ISO 14001 Environmental Management
    • REACH Registered for finished dyes containing aryl sulfonyl chloride

    Typical usage ratio

    • 0.90–1.15 equivalents depending on dye structure and desired color strength

    Downstream process integration

    • Charged during late-stage functionalization of diazo or triphenylmethane scaffolds
    • Introduced after initial coupling reactions, before final work-up and purification
    • Solvent and temperature control reduces byproduct halogenation, with inline filtration to achieve color conformity

    Final product types

    • Anionic and cationic textile dyes
    • Acid and direct dyes for paper and leather coloration
    • Specialty pigment intermediates for plastics
    • Grafted polymer-dye adducts for inkjet dyes

    4. Electronic Material Precursor for Liquid Crystal and Specialty Polymer Manufacturing

    Electronics sector suppliers leverage this compound as a highly effective halogen-sulfonyl donor for functionalization of aryl groups on high-purity intermediates. It enters manufacturing streams at critical stages in the production of advanced liquid crystal molecules or as a crosslinking agent during the fabrication of arylsulfonated engineering polymers. Facilities must comply with rigorous ISO and electronic grade material standards, managing contamination risks and byproduct traces to meet final device reliability and performance certification requirements.

    Industry compliance standards

    • ISO 9001 and ISO 14644 for cleanroom polymer synthesis
    • RoHS Directive (Restriction of Hazardous Substances) for polymer additives
    • IPC-4101 (Base Materials for Printed Boards)
    • REACH/CLP for high-purity specialty chemicals

    Typical usage ratio

    • 1.0–1.05 equivalents based on precise stoichiometric balance in liquid crystal synthesis or 0.5–2% w/w for polymer modification systems

    Downstream process integration

    • Reacted during late-stage functionalization of biphenyl or tolane units for liquid crystal molecules
    • Employed as a crosslinking or chain-terminating agent in sulfonated aromatic polymer production
    • Careful material handling and storage under inert gas maintain purity, with downstream vacuum distillation or chromatography to remove residual halides

    Final product types

    • Liquid crystal display (LCD) intermediates
    • High-performance arylsulfonated engineering resins
    • Polymer electrolytes and proton exchange membranes
    • Substrates for high-frequency circuit fabrication

    5. Specialty Fluorochemical Preparation

    Manufacturers serving high-value fluorochemical sectors use 4-iodobenzenesulfonyl chloride as a selective leaving group during the development of functionalized aryl-fluoride compounds. Its strategic placement allows for nucleophilic aromatic substitution and introduction of perfluoroalkyl or aryl-fluoride groups under phase-transfer or transition-metal catalysis methods. Controlled operations and strict monitoring manage thermal, pressure, and ventilation parameters due to reactivity and toxicity of byproducts. Purity protocols ensure intermediates meet or exceed global fluorochemical supply standards.

    Industry compliance standards

    • ISO 9001 for fluorochemical production
    • REACH Registration for perfluorinated substances
    • Hazardous Waste Operations (OSHA, US)
    • National Environmental Standards for Fluorine Chemistry, China

    Typical usage ratio

    • 0.90–1.10 molar equivalents, adjusted for each perfluoroalkylation pathway following pilot reaction scale-up

    Downstream process integration

    • Introduced after initial aryl coupling and before perfluoroalkylation via phase transfer or transition metal catalysis
    • Temperature and pH adjusted online to maximize conversion and minimize decomposition
    • All intermediates are monitored by HPLC to control halide and sulfonate impurities before isolation

    Final product types

    • Specialty aryl-fluoride building blocks
    • Technical-grade perfluoroalkylated reagents for electronics or surface treatment
    • Materials for water- and oil-repellent coatings
    • Traceable performance intermediates for integrated circuit fabrication
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