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2,4-Dimethoxybenzenesulfonyl Chloride

    • Product Name 2,4-Dimethoxybenzenesulfonyl Chloride
    • Alias DMB-Cl
    • Einecs EINECS 221-002-6
    • 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
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    Specifications

    HS Code

    688384

    Productname 2,4-Dimethoxybenzenesulfonyl Chloride
    Casnumber 4396-00-9
    Molecularformula C8H9ClO4S
    Molecularweight 236.68 g/mol
    Appearance White to off-white solid
    Meltingpoint 70-74°C
    Boilingpoint No data available (decomposes)
    Solubility Soluble in organic solvents such as dichloromethane and chloroform
    Density 1.40 g/cm³ (approximate)
    Purity Typically ≥98%
    Synonyms 2,4-Dimethoxybenzenesulfonyl chloride; 2,4-Dimethoxybenzenesulfonic acid chloride
    Chemicalstructure COC1=CC(=C(C=C1OC)S(=O)(=O)Cl)

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

    Packing & Storage
    Packing White, opaque plastic bottle containing 100 grams of 2,4-Dimethoxybenzenesulfonyl Chloride; secure screw-cap; clearly labeled with hazard warnings.
    Shipping 2,4-Dimethoxybenzenesulfonyl chloride should be shipped in tightly sealed containers, protected from moisture and light. It must be clearly labeled, packed in accordance with regulations for corrosive substances, and transported under dry, cool conditions. Appropriate hazard communication and documentation are required to ensure safe handling during transit.
    Storage 2,4-Dimethoxybenzenesulfonyl chloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as bases and strong oxidizers. Protect it from light and sources of ignition. Handle under an inert atmosphere (e.g., nitrogen or argon) if possible, and avoid exposure to air and humidity to prevent decomposition.
    Application of 2,4-Dimethoxybenzenesulfonyl Chloride

    Applications of 2,4-Dimethoxybenzenesulfonyl Chloride in Industrial Manufacturing

    2,4-Dimethoxybenzenesulfonyl Chloride plays a precise role as a sulfonating and protecting reagent in various chemical synthesis routes across multiple industrial sectors. Our production implements strict QC and traceable batch documentation to support advanced manufacturing for pharmaceuticals, agrochemicals, specialty polymers, and electronics intermediates.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturing uses 2,4-Dimethoxybenzenesulfonyl Chloride in selective sulfonyl protection of amine and alcohol functionalities during API intermediate synthesis. The material allows controlled introduction and subsequent removal of sulfonyl groups, securing high regioselectivity and purity for critical steps in antihypertensive, anti-inflammatory, and antibacterial compound preparation. Our QA protocols ensure low residuals according to final product pharmacopoeial requirements.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • United States Pharmacopeia (USP) standards
    • European Pharmacopoeia (Ph. Eur.)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • 1.05–1.25 molar equivalents relative to amine or alcohol substrate
    • Adjusted based on substrate reactivity and desired protection yield

    Downstream process integration

    • Used in the protection step during multi-step organic synthesis of API intermediates
    • Introduced after completion of initial acylation or alkylation
    • Deprotection follows in the penultimate process stage

    Final product types

    • Telmisartan intermediates
    • Macrolide antibacterial intermediates
    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Beta-lactam antibiotic key intermediates

    2. Agrochemical Intermediate Synthesis

    Modern agrochemical production applies this sulfonyl chloride for protection and functionalization steps in the synthesis of pre-emergent herbicide and insecticide actives. Its electrophilic reactivity allows selective transformation of heterocyclic scaffolds and controlled deprotection under mild hydrolysis, ensuring minimal impurity profile and effective downstream reaction management.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • ISO 9001:2015 quality management for crop chemical raw materials
    • China GB 20660-2006 (Pesticide technical material standard)

    Typical usage ratio

    • 1.15–1.30 molar equivalents, flexible according to target heterocycle or side chain modification

    Downstream process integration

    • Added to starting heterocycle or substituted aromatic system after initial cyclization
    • Often followed by nucleophilic displacement or Monsanto oxidation

    Final product types

    • Triazole fungicide intermediates
    • Sulfonylurea herbicide building blocks
    • Organophosphorus insecticide precursors
    • Precursor for safener compounds

    3. Specialty Polymer Functionalization

    The specialty polymers sector utilizes 2,4-Dimethoxybenzenesulfonyl Chloride as a sulfonating agent for modifying aromatic monomers and polymer backbones. This process enables fine-tuning of polymer solubility, ionic conductivity, and chemical resistance. Sulfonated polyaryletherketones, polyimides, and polystyrenes synthesized using this material show improved processing performance and end-use function in high-performance films and membranes.

    Industry compliance standards

    • ASTM D883 terminology and classification for high-performance polymers
    • REACH Regulation (EC) No 1907/2006 for chemical safety in Europe
    • ISO 9001:2015 for advanced polymer manufacturing

    Typical usage ratio

    • 0.5–2.5 wt% based on total monomer or pre-polymer charge, adjusted for desired sulfonation level

    Downstream process integration

    • Introduced during pre-polymer functionalization or as a post-polymerization sulfonation step
    • Often followed by neutralization or hydrolysis before blending or extrusion

    Final product types

    • Sulfonated polyetheretherketone (S-PEEK) membranes
    • Functionalized polystyrene-ion exchange resins
    • High-durability polyimide films
    • Proton-conductive fuel cell components

    4. Electronic Materials and Photoresist Precursors

    In the electronics industry, 2,4-Dimethoxybenzenesulfonyl Chloride serves in the synthesis of sulfonated aromatic compounds that become photoacid generators (PAGs) and charge transport materials for lithography and microelectronics. The high purity required for these applications aligns with rigorous sub-ppm metal and organics control, essential for preventing structural defects in photoresist coatings and thin-film transistor fabrication.

    Industry compliance standards

    • SEMI C3 Standards for Performance Chemicals in Semiconductor Production
    • IEC 62474 Declarable Substances Standard in Electronics
    • RoHS Directive (2011/65/EU) for hazardous substance control

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target aromatic substrate in PAG synthesis
    • Dosage refined by final product required sensitivity

    Downstream process integration

    • Reacted with phenolic or aromatic amine base structure during fine chemical intermediate synthesis
    • PAG intermediates isolated and used in photoresist formulation

    Final product types

    • I-line and DUV photoresist photoacid generator components
    • Charge transport layer additives for OLED and LCD devices
    • Negative tone resist precursor compounds
    • Polymer semiconductors for transistor arrays
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