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4-Chloro-3-Pyridinesulfonamide

    • Product Name 4-Chloro-3-Pyridinesulfonamide
    • Alias 3-Pyridinesulfonamide, 4-chloro-
    • Einecs 629-803-5
    • 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

    348177

    Chemical Name 4-Chloro-3-Pyridinesulfonamide
    Cas Number 139174-62-2
    Molecular Formula C5H5ClN2O2S
    Molecular Weight 192.63
    Appearance Off-white to light brown crystalline powder
    Melting Point 203-206°C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep container tightly closed and dry
    Smiles NS(=O)(=O)c1cnccc1Cl
    Inchi InChI=1S/C5H5ClN2O2S/c6-4-1-2-7-3-5(4)11(8,9)10/h1-3H,(H2,8,9,10)

    As an accredited 4-Chloro-3-Pyridinesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Chloro-3-Pyridinesulfonamide; tightly sealed, labeled with hazard and handling information.
    Shipping 4-Chloro-3-pyridinesulfonamide is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. It should be transported as a non-hazardous laboratory chemical under standard conditions. Ensure packaging is labeled according to applicable regulations and handled by trained personnel. Store in a cool, dry place away from incompatible substances.
    Storage 4-Chloro-3-pyridinesulfonamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature, ensuring the storage area is appropriately labeled and secure, limiting access to authorized personnel trained in handling chemicals.
    Application of 4-Chloro-3-Pyridinesulfonamide

    Applications of 4-Chloro-3-Pyridinesulfonamide in Industrial Manufacturing

    We supply 4-Chloro-3-Pyridinesulfonamide for direct formulation in specialized chemical industries, supporting downstream manufacturers with strict quality controls, process traceability, and regulatory compliance for reliable end-product performance in consistently defined sectors.

    1. Agrochemical Intermediate in Sulfonylurea Herbicide Synthesis

    This compound serves as a critical building block in the synthesis of sulfonylurea herbicides, especially where strict impurity profiles are enforced by regional regulations. Formulators apply it in the condensation stage to create core sulfonylurea structures, supporting high selectivity against grassy and broadleaf weeds in staple crop protection. Downstream procedures rely on controlled reactivity and substitution, minimizing by-product generation and ensuring the production of herbicides with field-validated performance.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical manufacturing
    • EU Regulation (EC) No 1107/2009 on the placing of plant protection products on the market
    • Chinese GB/T 38390-2019 standards for pesticide active ingredient purity
    • FAO/WHO specification for technical active ingredients used in agrochemicals

    Typical usage ratio

    • 0.18–0.26 molar equivalents in the core condensation reaction, adjusted for the specific sulfonylurea analog required

    Downstream process integration

    • Dosed in the high-temperature aromatic substitution step during synthesis of sulfonylurea rings
    • Isolated and refined through crystallization to remove overchlorinated and desulfonated by-products

    Final product types

    • Sulfometuron-methyl technical concentrate
    • Chlorimuron-ethyl technical material
    • Granular and liquid herbicide formulations for rice, soybean, wheat, and maize fields

    2. Pharmaceutical Intermediate for Antibacterial Drug Development

    The compound is utilized as a key sulfonamide moiety supplier in custom synthesis routes for third-generation antibacterial agents targeting resistant gram-negative bacterial strains. Process chemists incorporate it specifically during heterocyclic core assembly, with reactivity and impurity control determining final batch validity under medicinal-grade standards. Scale-up protocols address aqueous solubility and minimized residual solvents to meet pharmaceutical registration requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF monographs referencing sulfonamide synthetic process controls
    • European Pharmacopoeia 11.0 for sulfonamide intermediates
    • Chinese Pharmacopoeia (ChP) guidelines for raw material purity

    Typical usage ratio

    • 0.95–1.05 mol equivalents as the principal sulfonamide donor in stepwise N-heterocycle formation, ratio based on exact API design

    Downstream process integration

    • Fed into the N-arylation or amidation step post-halide activation
    • Refined via liquid-liquid extraction and activated carbon treatment for pharmaceutical purity

    Final product types

    • Active pharmaceutical intermediates for sulfonamide-based antibiotics
    • Precursors to veterinary antibacterial drugs
    • Development lots for new chemical entities in anti-infective research

    3. Dyestuff Intermediate for Reactive Dye Manufacture

    4-Chloro-3-Pyridinesulfonamide provides a functionalized pyridine ring for azo and reactive dye production, supporting color-fast textile dyes with enhanced migration and bonding properties. Producers utilize its sulfonamide group for improved hydrophilicity and covalent fiber attachment, essential in modern textile coloration lines meeting eco-labeling requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances
    • REACH Regulation (EC) No 1907/2006 registration and SVHC clearance
    • ISO 14001:2015 in dyestuff plant environment management
    • ZDHC MRSL (Manufacturing Restricted Substances List) compliance for textile auxiliaries

    Typical usage ratio

    • 0.25–0.31 mol in coupling reactions per 1 mol diazonium salt precursor, adjusted to dye shade and hue target

    Downstream process integration

    • Introduced during diazo coupling or nucleophilic aromatic substitution steps in dye synthesis
    • Subjected to controlled pH and temperature protocols for consistent chromophore attachment

    Final product types

    • Reactive dyes for cellulosic fibers (cotton and viscose rayon)
    • Azo-based disperse dyes for polyester blends
    • Textile auxiliaries with sulfonamide functionalization for improved wash fastness

    4. Functionalized Ligand Component in Metal Complex Catalyst Production

    Industrial catalyst manufacturers apply this material as a tailored sulfonamide ligand precursor in the synthesis of pyridine-based metal complex catalysts, targeting processes requiring enhanced electronic effects and structure-activity correlation. Integration centers on controlling coordination chemistry, which impacts downstream catalyst selectivity and recyclability in olefin polymerization and fine chemical synthesis.

    Industry compliance standards

    • ISO 22449:2021 for catalyst traceability and quality assurance
    • EU REACH for non-pharmaceutical, non-food industrial chemical registration
    • ASTM D3245-17 for transition metal catalyst analysis (where applicable)
    • Company-specific protocols for trace impurity limits in ligand precursors

    Typical usage ratio

    • 0.08–0.15 mol per mol of metal salt in ligand complexation step, tuned to desired coordination environment and catalyst end-use

    Downstream process integration

    • Reacted with metal salts in ligand exchange under inert atmosphere
    • Purified via column chromatography to ensure ligand purity before catalyst use

    Final product types

    • Catalytic complexes for oligomerization of olefins
    • Process catalysts for asymmetric synthesis in specialty chemicals
    • Pyridine-based homogeneous and supported catalysts for academic and pilot industrial runs
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