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2-Chloro-5-Nitrobenzenesulfonic Acid

    • Product Name 2-Chloro-5-Nitrobenzenesulfonic Acid
    • Alias 5-Nitro-2-chlorobenzenesulfonic acid
    • Einecs 221-586-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    315146

    Chemical Name 2-Chloro-5-Nitrobenzenesulfonic Acid
    Cas Number 96-99-1
    Molecular Formula C6H4ClNO5S
    Molecular Weight 253.62 g/mol
    Appearance Yellow to orange solid
    Melting Point 180-185°C
    Solubility In Water Soluble
    Boiling Point Decomposes before boiling
    Density 1.85 g/cm³ (approx)
    Smiles C1=CC(=C(C=C1S(=O)(=O)O)[N+](=O)[O-])Cl
    Inchi InChI=1S/C6H4ClNO5S/c7-4-1-2-6(14(10,11)12)5(3-4)8(9)13/h1-3H,(H,10,11,12)
    Synonyms 2-Chloro-5-nitrobenzenesulphonic acid

    As an accredited 2-Chloro-5-Nitrobenzenesulfonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with secure screw cap, labeled "2-Chloro-5-Nitrobenzenesulfonic Acid, 100g," displays hazard and handling information.
    Shipping 2-Chloro-5-Nitrobenzenesulfonic Acid is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is classified as a hazardous chemical, requiring appropriate labeling and documentation. Transport must comply with local and international regulations for hazardous materials, ensuring safety during handling, storage, and delivery to prevent leaks or contamination.
    Storage 2-Chloro-5-Nitrobenzenesulfonic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and reducing agents. Protect from moisture and direct sunlight. Use appropriate secondary containment and label storage vessels clearly. Store at room temperature, following all institutional and regulatory guidelines for hazardous chemical storage.
    Application of 2-Chloro-5-Nitrobenzenesulfonic Acid

    Applications of 2-Chloro-5-Nitrobenzenesulfonic Acid in Industrial Manufacturing

    As a primary manufacturer of 2-Chloro-5-Nitrobenzenesulfonic Acid, we supply this specialty intermediate to established chemical sectors where reliability, compliance, and batch consistency are essential. Below we outline key downstream uses, including formulation standards, practical ratio guidance, process positions, and the types of finished goods produced in each specialization.

    1. Synthesis of Reactive Dyes for Cellulosic Fibers

    Reactive dye manufacturers employ this compound as a diazo component to introduce both solubility and chromophore capacity in final dye molecules. The sulfonic acid group promotes high fiber affinity, while the chloro and nitro substituents enable precise chromatic modifications during coupling and finishing operations. Batch-to-batch quality directly affects dye reproducibility and textile fastness.

    Industry compliance standards

    • Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers (ETAD) requirements
    • OEKO-TEX Standard 100 Annex 4 (Textile ecology limits)
    • ZDHC MRSL 3.0 (Manufacturing Restricted Substances List)
    • ISO 9001:2015 quality management during dye synthesis

    Typical usage ratio

    • 10–25% by mole in the diazonium coupling stage, adjusted per hue depth and fiber compatibility

    Downstream process integration

    • Charged after diazotization and before coupling in liquid-phase synthesis reactors
    • Monitored under controlled pH (1.5–2.5) and temperature (0–5°C) for safe and complete transformation

    Final product types

    • Reactive dyes for cotton, viscose, and lyocell yarns
    • Granular dye powders and high-concentration aqueous dispersions for industrial textile printing

    2. Sulfonamide Pharmaceutical Intermediate Production

    Pharmaceutical manufacturers use this chemical as a key intermediate for producing certain sulfonamide antibiotics and related APIs. The electron-withdrawing nitro and chloro functions support targeted sulfonation and subsequent amination steps, with strict impurity control required. GMP validation addresses both cross-contamination and residual solvent limits.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, ICH Q7)
    • USP-NF monographs for sulfonamide APIs
    • European Pharmacopoeia (Ph. Eur.) and JP standards for intermediates
    • REACH substance registration and hazard labelling compliance

    Typical usage ratio

    • Stoichiometric ratios ranging from 1.0 to 1.1 equivalent, depending on target API impurity profile and reactivity

    Downstream process integration

    • Incorporated directly after core aromatic sulfonation
    • Feeds into reduction or nucleophilic aromatic substitution, monitored by HPLC for trace byproducts

    Final product types

    • Synthesized sulfonamide antibiotics (e.g., sulfamethoxazole derivatives)
    • Specialty drug intermediates for anti-infective class compounds

    3. Agrochemical Formulation for Herbicide Manufacturing

    Agrochemical producers utilize this compound as a building block during the synthesis of selective herbicides. The strong electron-withdrawing groups allow subsequent reactive modifications for targeted weed control agents, enhancing the solubility and stability of pre-emergence and post-emergence formulations. End quality impacts the ultimate field performance and crop safety indices.

    Industry compliance standards

    • FAO and WHO pesticide specification guidelines
    • ISO 9001:2015 traceability standards for input chemicals
    • European Union Regulation (EC) No 1107/2009 for plant protection product active substances
    • US EPA Registration requirements for formulated herbicides

    Typical usage ratio

    • 15–30% by mole as an aromatic precursor, tailored according to the selectivity profile of the active ingredient

    Downstream process integration

    • Dosed after chlorosulfonation and before condensation or ring-closure steps in multi-step syntheses
    • Processed in continuous reactors with automated QC sampling of intermediates

    Final product types

    • Systemic herbicide actives (triazines, sulfonylureas)
    • Concentrated technical-grade agrochemical intermediates

    4. Electroplating Auxiliary Agent Synthesis

    The electronics and surface finishing industry integrates this compound into additives for electroplating baths, where the sulfonic acid group optimizes metal ion dispersion and brightener action during deposition. The nitro and chloro substituents shape the additive’s reactivity, influencing deposit morphology for end-use in printed circuit board (PCB) manufacturing and precision components.

    Industry compliance standards

    • IPC-A-600 acceptability requirements for PCBs
    • RoHS Directive (2011/65/EU) for hazardous substance limits in electronics
    • ISO 9001:2015 for process traceability in chemical additives
    • SEMI S2 for semiconductor industry chemical safety

    Typical usage ratio

    • 0.5–2.5% by weight in the auxiliary additive premix, with dosing refined based on the target metal plating layer uniformity

    Downstream process integration

    • Added to electroplating bath solution during make-up or maintenance
    • Dissolved directly into aqueous solution under agitation, followed by filtration prior to plating

    Final product types

    • Electroplated copper, nickel, or tin layers for PCBs and connectors
    • High purity metal finishers for microelectronics sector

    5. Advanced Photographic Chemical Manufacturing

    In the imaging sector, this material functions as a specialty intermediate in the synthesis of complex photographic couplers and color developers. The precise orientation and reactivity of the nitro and sulfonic groups enable high efficiency color formation and minimization of competing side reactions during photographic processing.

    Industry compliance standards

    • ISO 18902:2013 for imaging materials chemical composition
    • ANSI IT9.1 for photographic archival quality standards
    • REACH and GHS labeling for hazardous imaging chemicals
    • ISO 14001 for environmentally responsible manufacturing

    Typical usage ratio

    • 5–15% by mole in developer coupler synthesis, tailored to image density and fading resistance requirements

    Downstream process integration

    • Introduced after sulfonation in multi-stage organic syntheses
    • Purified by crystallization and solvent extraction prior to formulation into developer solutions

    Final product types

    • Photographic color developers for film and paper processing
    • Special-purpose emulsions for digital and analog imaging
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