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1-Methyl-1H-Imidazole-4-Sulfonyl Chloride

    • Product Name 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride
    • Alias N-Methylimidazole-4-sulfonyl chloride
    • Einecs 629-761-6
    • 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

    332045

    Product Name 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride
    Cas Number 127126-21-8
    Molecular Formula C4H5ClN2O2S
    Molecular Weight 196.62
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 80-85°C
    Solubility Soluble in organic solvents such as dichloromethane
    Smiles CN1C=NC=C1S(=O)(=O)Cl
    Inchi InChI=1S/C4H5ClN2O2S/c1-7-2-3-6-4(7)10(5,8)9/h2-3H,1H3
    Storage Conditions Store at 2-8°C, protected from moisture
    Reactivity Reacts with water, alcohols, and amines
    Hazard Statement Corrosive; causes burns

    As an accredited 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride 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, sealed with a screw cap and equipped with tamper-evident seal, labeled with hazard warnings.
    Shipping **Shipping Description:** 1-Methyl-1H-Imidazole-4-sulfonyl chloride should be shipped in tightly sealed containers under dry, cool conditions. As a moisture-sensitive and potentially corrosive chemical, it must comply with regulations for hazardous materials. Appropriate hazard labeling and documentation are required. Handle with caution and avoid exposure to heat or incompatible substances during transit.
    Storage Store 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride in a cool, dry, and well-ventilated area, tightly sealed in a corrosion-resistant container. Keep away from moisture, heat, light, and incompatible substances such as water, strong bases, and oxidizing agents. Use in a chemical fume hood and ensure proper labeling. Avoid exposure to humidity to prevent hydrolysis and decomposition.
    Application of 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride

    Applications of 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride in Industrial Manufacturing

    As a core upstream supplier, we specialize in 1-Methyl-1H-Imidazole-4-Sulfonyl Chloride for advanced chemical synthesis. This intermediate sees established use in regulated fields where strict control of process, purity, and compliance underpin high-value manufacturing. Below, we outline verified downstream industrial sectors, providing details on specification, compliance, application ratio, integration method, and the type of final goods produced by leading manufacturers.

    1. Pharmaceutical API Synthesis—Sulfonamide-Based Drug Intermediates

    Pharmaceutical companies use this intermediate for the preparation of sulfonamide motifs during active pharmaceutical ingredient (API) synthesis, particularly in anti-infective and oncology pipelines. The compound acts as a sulfonyl donor in the formation of N-sulfonyl imidazole fragments, often at the late-stage functionalization step to minimize side reactions and optimize batch yields. Manufacturers ensure traceability from incoming raw materials to finished API lots, with high purity (>99%) essential for reproducible reactivity during multi-step synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • US FDA 21 CFR Part 211
    • EU EudraLex Volume 4 GMP
    • USP–NF monographs for relevant pharmaceuticals

    Typical usage ratio

    • 0.9–1.1 molar equivalents relative to amine substrates in sulfonylation steps
    • Adjusted based on yield optimization and reaction scale (lab/pilot/plant)

    Downstream process integration

    • Used in batch and continuous flow reactors, typically post-protected amine deprotection
    • Dosed into controlled, inert atmosphere vessels; isolated as intermediate or directly into telescoped transformations

    Final product types

    • N-sulfonylated drug candidates in early- and late-phase development
    • Key intermediates for antimicrobial, antiviral, and anticancer APIs approved for global markets

    2. Specialty Agrochemical Synthesis—Herbicide and Fungicide Actives

    Agrochemical formulators employ the sulfonyl chloride as a functionalizing agent to produce sulfonamide-linked intermediates central to select post-emergence herbicides and fungicides. Used during phase-transfer catalysis steps, the raw material allows precise introduction of the sulfonyl moiety, which enhances bioactivity and crop selectivity of the finished products. Compliance with pesticide GMP is essential to support regulatory submissions in main agricultural economies.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • ISO 9001:2015 for chemical production systems
    • REACH Regulation (EC) No 1907/2006 for European market entry

    Typical usage ratio

    • 0.8–1.2 equivalents to core heterocyclic precursors
    • Adjusted for batch purity and downstream conversion efficiency

    Downstream process integration

    • Applied at late-stage functionalization of active ingredient backbones
    • Reacted via phase transfer with strong bases; product isolated by crystallization or continuous extraction

    Final product types

    • Sulfonylurea herbicides such as nicosulfuron and rimsulfuron intermediates
    • Sulfonamide-based fungicide actives for cereals and specialty crops

    3. Advanced Material Synthesis—Polymer Crosslinking and Surface Modification

    The sulfonyl chloride serves as a reactive crosslinker in advanced polymer synthesis, enabling surface functionalization of membranes and resins for filtration and ion exchange. Process engineers incorporate it during post-polymerization modification to install functional groups that tune hydrophilicity, selectivity, and ion transport properties. Purity grade and reaction control directly affect membrane uniformity and final performance in separation technologies.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer manufacturing
    • ASTM D4696 for crosslinked polymer membranes characterization
    • UL 94 verification for final plastic part safety

    Typical usage ratio

    • 1–5 wt% relative to overall polymer matrix in modification steps
    • Adjusted based on required surface density and crosslinking architecture

    Downstream process integration

    • Introduced in post-polymerization batch reactors or inline modification chambers
    • Processed with precise metering and temperature control to prevent undesired side reactions

    Final product types

    • Functional membrane sheets for ultrafiltration, nanofiltration, reverse osmosis
    • Specialty ion-exchange and adsorbent resins for industrial water treatment

    4. Specialty Chemical Synthesis—Heterocyclic Compound Functionalization

    Experienced contract synthesis and fine chemical companies use this specialty intermediate for introducing sulfonyl groups onto heterocyclic frameworks, especially in the construction of molecular scaffolds for advanced research or as building blocks for dye, pigment, or catalyst development. Process design requires rigorous control of reaction stoichiometry, solvent system, and workup to achieve high specificity in functionally rich, multi-nitrogen ring systems.

    Industry compliance standards

    • ISO 14001 for environmental management during specialty chemical synthesis
    • GLP (Good Laboratory Practice) for analytical verification
    • REACH Registration for production volumes entering Europe

    Typical usage ratio

    • 0.8–1.3 equivalents based on heterocycle electron density and targeted substitution pattern
    • Ratios refined in pilot and scale-up based on yield and byproduct analysis

    Downstream process integration

    • Charged into stirred tank reactors post-heterocycle synthesis and isolation
    • Employed in controlled addition with in-process monitoring for exothermicity

    Final product types

    • Functionalized heterocyclic intermediates for fine chemical portfolios
    • Specialty ligands, dyes, and catalyst precursors for R&D and industrial application
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