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4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride

    • Product Name 4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride
    • Alias BS-TS-Cl
    • Einecs 405-020-4
    • 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
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    Specifications

    HS Code

    426972

    Product Name 4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride
    Cas Number 1154087-88-7
    Molecular Formula C10H7ClO4S2
    Molecular Weight 306.75 g/mol
    Synonyms 4-(Phenylsulfonyl)thiophene-2-sulfonyl chloride
    Appearance Off-white to pale yellow solid
    Solubility Soluble in organic solvents (e.g., dichloromethane, chloroform)
    Purity Typically ≥ 97%
    Storage Temperature Store at 2-8°C, under dry conditions
    Smiles C1=CC=C(C=C1)S(=O)(=O)C2=CSC(=C2)S(=O)(=O)Cl
    Inchi InChI=1S/C10H7ClO4S2/c11-17(14,15)9-6-12-7-10(9)18(16,17)8-4-2-1-3-5-8/h1-7H

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

    Packing & Storage
    Packing The chemical is packaged in a sealed amber glass bottle, labeled "4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride, 10 grams," with safety information.
    Shipping 4-(Benzenesulfonyl)thiophene-2-sulfonyl chloride is shipped in secure, sealed containers compliant with hazardous material regulations. It should be handled with proper labeling and documentation, and transported under cool, dry conditions, avoiding moisture and incompatible substances. Ensure compliance with all relevant local, national, and international shipping regulations for corrosive chemicals.
    Storage Store **4-(Benzenesulfonyl)thiophene-2-sulfonyl chloride** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as bases and strong oxidizers. Protect from direct sunlight and sources of ignition. Handle under an inert atmosphere if possible, and ensure proper labeling. Use appropriate PPE when handling to avoid contact and inhalation.
    Application of 4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride

    Applications of 4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride in Industrial Manufacturing

    As a chemical manufacturer with advanced synthesis and purification capabilities, we supply 4-(Benzenesulfonyl)Thiophene-2-Sulfonyl Chloride for high-value downstream applications where specialty sulfonyl chloride intermediates play a critical functional role. We support our partners in regulated sectors with consistent quality and transparent compliance, contributing expertise directly to their formulation, processing, and QC protocols.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers regularly deploy this compound in constructing heterocyclic sulfonylated building blocks and introducing aromatic sulfonyl groups crucial to several API synthesis routes. Its high reactivity allows selective functionalization steps in respiratory, oncology, and anti-infective molecule assembly, with precise molar equivalents added to protect strategic amine or hydroxyl groups in multistep batch reactions. We support integration compliant with current Good Manufacturing Practice (cGMP) standards, validating traceability from incoming material through to finished dosage formulation.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia monographs and GMP requirements
    • EU REACH registration for pharmaceutical intermediates

    Typical usage ratio

    • Applied in the 0.05–0.3 molar equivalent range relative to key intermediates; exact ratio determined by amine/hydroxyl substrate loading and process-specific protection/deprotection cycles.

    Downstream process integration

    • Charged in situ during the early to mid-stage synthesis steps for functional group transformation and protection.
    • Utilized in closed-system reactors under nitrogen with automated addition control.
    • Purge, clean-in-place, and waste stream handling per cGMP with validated residue removal protocols.

    Final product types

    • Sulfonamide APIs for anti-infectives
    • Small-molecule kinase inhibitors
    • Thiophene-based API cores for medicinal products
    • Solid oral and parenteral finished dosage forms

    2. Specialty Agrochemical Intermediate Production

    Producers within the agrochemical sector use this material as a building block for custom synthesis of herbicide and fungicide active ingredients containing sulfonyl-aryl moieties, critical to biological selectivity. The compound reacts smoothly under phase-transfer catalysis and anhydrous conditions to introduce the sulfonyl chloride motif into target molecules, which can later be converted to functional sulfonamides or sulfonylureas. Usage ratios depend on the active's molecular scaffold requirements and batch scale, with all handling controlled under strict environmental and operator safety protocols.

    Industry compliance standards

    • FAO/WHO technical specifications for pesticide active ingredients
    • ISO 9001:2015 Quality Management Systems
    • EU REACH Annex requirements for agrochemical intermediates
    • National environmental protection standards for chemical synthesis

    Typical usage ratio

    • Typical addition range of 2–6% by mol relative to core heterocycles; adjusted based on desired sulfonyl substitution level and downstream reaction efficiency.

    Downstream process integration

    • Introduced at the sulfonylation step post-initial heteroaromatic ring closure.
    • Operated in jacketed glass-lined reactors with real-time temperature and pH controls.
    • Byproduct neutralization and phase separation managed per industry safety guidelines.

    Final product types

    • Pre-emergence and selective herbicides
    • Foliar fungicides with thiophene functionalization
    • Intermediates for pesticide sulfonamide derivatives
    • Technical grade crop protection compounds

    3. Electronic Material Synthesis for Polymer Additives

    Manufacturers in the specialty polymers and electronics sector rely on this sulfonyl chloride to introduce sulfonyl-thiophene units into conjugated polymers, optimizing film stability and charge transport in thin-film transistor (TFT), organic photovoltaic (OPV), and sensor applications. The material is critical during macromolecular chain extension by sulfonamide coupling or direct sulfonation, ensuring final conductivity and processability align with strict sector requirements for performance and purity. All process steps are performed in controlled atmospheres to prevent contamination and preserve product integrity.

    Industry compliance standards

    • IEC 60749 Semiconductor device processing standards
    • IPC-4101/126 for electronic substrate materials
    • ISO 14001 Environmental Management for chemical production
    • RoHS and REACH compliance for restricted substances

    Typical usage ratio

    • Dosed between 0.5–3% w/w relative to polymer precursors, adjustable for molecular weight scaling and target conductivity range.

    Downstream process integration

    • Fed into polymerization reactors at the monomer activation or sulfonylation stage.
    • Undergoes thermal or microwave-assisted coupling depending on application.
    • Works with vacuum transfer systems to prevent ambient moisture ingress.

    Final product types

    • Electron transport layers in OPV cells
    • OLED display sensor films
    • Photoresist and dielectric polymer materials
    • Flexible printed circuit board coatings

    4. Dye and Pigment Intermediate Manufacture

    Producers of sulfur-containing dyes and pigments use this compound to form stable aromatic sulfonyl linkages essential for waterfastness and colorbright formulations. In colorant production, it acts as a reactive intermediate for forming sulfonamide-bonded chromophores or as a connector group in azo dye synthesis. Industrial processes require strict batch monitoring for sulfonylation extent and by-product removal, especially where products must comply with textile, food contact, or consumer safety standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textiles and dye safety
    • EN 71-3 (EU Toy Safety) for pigment migration limits
    • REACH Annex XVII (restricted substances in colorants)
    • Quality Control protocols per ISO 9001 and in-house methods

    Typical usage ratio

    • Recommended addition of 1–7% mol, determined by the target chromophore length and desired intensity; ratio optimized in pilot batches for reproducible shade strength.

    Downstream process integration

    • Engages at early-stage diazo coupling or post-azo coupling as a conversion step.
    • Feedstream monitored for reaction completion and byproduct suppression using inline spectroscopy.
    • Post-reaction purification by crystallization and solvent extraction methods.

    Final product types

    • Sulfonamide-based water-soluble dyes for textiles and leathers
    • Azo pigments for plastics and paints
    • Colorant intermediates for inkjet formulation
    • Sulfur-containing lake pigments for food contact materials

    5. Fine Chemical Intermediate Synthesis for Material Science

    Advanced material science firms employ this sulfonyl chloride in the documented preparation of complex molecular scaffolds for liquid crystal displays, specialty coatings, and surface modification agents. The reactivity profile supports targeted sulfonation of heterocyclic substrates, allowing precise control over substitution patterns essential to electronic, optical, and surface-active property tuning. Close monitoring and dedicated hazard management enable production scaling while adhering to environmental and occupational health standards.

    Industry compliance standards

    • ISO 9001 and ISO 14001 (Quality and Environmental Management)
    • EN 62431 for liquid crystal raw materials
    • OSHA 29 CFR 1910.1200 Hazard Communication
    • REACH registration for substances used in advanced materials

    Typical usage ratio

    • Standard application at 0.5–4.0% mol depending on complexity of target molecule, substitution degree needed, and post-reaction yield coefficients.

    Downstream process integration

    • Added as sulfonylation agent to functionalize advanced heterocyclic cores in multipurpose flasks with controlled environment.
    • Integrated with downstream quenching and extraction setups to streamline impurity removal.
    • Process validated with real-time chromatographic and spectroscopic monitoring.

    Final product types

    • Alignment layers for LCD panels
    • Functionalized surface coatings with hydrophilic/hydrophobic balance
    • Reactives for display and optoelectronic films
    • Intermediate scaffolds for specialty additive packages
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