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4-Chloro-5-Sulphamoylbenzoic Acid

    • Product Name 4-Chloro-5-Sulphamoylbenzoic Acid
    • Alias 4-Chloro-5-sulfamoylbenzoic acid
    • Einecs 242-770-8
    • 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
    VTB
    Specifications

    HS Code

    989568

    Productname 4-Chloro-5-Sulphamoylbenzoic Acid
    Casnumber 121-49-3
    Molecularformula C7H6ClNO4S
    Molecularweight 235.64 g/mol
    Appearance White to off-white solid
    Meltingpoint 273-275 °C
    Solubility Slightly soluble in water
    Boilingpoint Decomposes before boiling
    Density Approx. 1.7 g/cm3
    Storagetemperature Store at room temperature
    Purity Typically ≥98%
    Synonyms 4-Chloro-5-sulfamoylbenzoic acid
    Iupacname 4-chloro-5-sulfamoylbenzoic acid
    Smiles O=S(=O)(N)c1cc(Cl)cc(C(=O)O)c1

    As an accredited 4-Chloro-5-Sulphamoylbenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 4-Chloro-5-Sulphamoylbenzoic Acid is supplied in a sealed, amber glass bottle with tamper-evident cap and label.
    Shipping 4-Chloro-5-Sulphamoylbenzoic Acid should be shipped in tightly sealed containers, clearly labeled according to hazardous materials regulations. Protect from moisture and direct sunlight. Package with appropriate cushioning to prevent breakage. Handle with gloves and eye protection. Ship via a certified carrier specializing in chemical transport, complying with all local, national, and international shipping laws.
    Storage **4-Chloro-5-sulphamoylbenzoic acid** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from direct sunlight, moisture, and incompatible materials such as strong oxidizing agents. Store at room temperature and keep away from sources of ignition. Clearly label the container and restrict access to trained personnel only.
    Application of 4-Chloro-5-Sulphamoylbenzoic Acid

    Applications of 4-Chloro-5-Sulphamoylbenzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 4-Chloro-5-Sulphamoylbenzoic Acid, our material supports multiple specialized industrial processes across pharmaceuticals, diagnostics, agrochemicals, dye intermediates, and advanced polymer synthesis. Each downstream application calls for specific compliance, control over formulation ratios, precise process steps, and tight end use standards, furthering the full traceability and regulatory requirements of our production partners.

    1. Synthesis of Thiazide Diuretic Pharmaceuticals

    This compound acts as an essential intermediate in the synthesis of several thiazide-based diuretic agents. Its sulphonamide and chloro substituents allow for efficient ring closure and controlled functionalization in the transformation into active pharmaceutical ingredients. Bulk pharmaceutical manufacturers rely on its high assay and low impurity specification to guarantee process yield and finished product purity.

    Industry compliance standards

    • USP, Ph. Eur., JP compendial standards for APIs
    • ICH Q7A Good Manufacturing Practice Guidelines
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • EDQM CEP quality requirements

    Typical usage ratio

    • Input levels range 0.7–1.2 molar equivalents relative to target product
    • Ratio optimized based on reaction conversion efficiency, impurity control, and solvent system

    Downstream process integration

    • Material charged during cyclization or condensation step in API synthesis
    • Introduced after initial arylation, before chlorosulphonation or amide coupling
    • In-process controls monitor completion prior to downstream purification

    Final product types

    • Hydrochlorothiazide
    • Bendroflumethiazide
    • Chlorothiazide
    • Metolazone and similar diuretic pharmaceutical actives

    2. In Vitro Diagnostic Reagent Production

    Diagnostic kit and reagent formulators utilize this raw material as a fine chemical intermediate to prepare sulphonamide-based analyte detectors and specialized enzyme substrates. Its precise molecular structure contributes to high signal specificity in colorimetric and enzymatic assays manufactured under strictly regulated environments.

    Industry compliance standards

    • ISO 13485:2016 (Medical devices – QMS for IVD)
    • IVDR (EU) 2017/746 regulation
    • FDA 21 CFR Part 820 (Quality System Regulation for medical devices)
    • REACH Annex XVII (SVHC candidate qualification)

    Typical usage ratio

    • Usually 1–5% by mass in coupling reactions for reagent semi-finished preparation
    • Level adjusted for response sensitivity and shelf-life stability

    Downstream process integration

    • Added during synthesis or functionalization of assay substrates
    • Purified intermediate isolated prior to formulation with buffers or preservatives
    • Component tracked by batch-to-batch traceability protocols

    Final product types

    • Colorimetric test strips for clinical analytes
    • Enzyme-linked IVD reagents
    • P-point of care diagnostic cartridges
    • Immunoassay kits for laboratory use

    3. Herbicide and Plant Growth Regulator Intermediate

    Agrichemical synthesis routes employ this material as a key structural fragment for the assembly of sulphonylurea-type herbicides and regulatory actives. Its reactivity supports high-conversion coupling with amine and urea building blocks under anhydrous or aqueous phase, allowing predictable process scaleups and consistent residue control in final crop-protection agents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical raw materials
    • EU Regulation (EC) No 1107/2009 (placing of plant protection products on the market)
    • National pesticide residue limits (e.g., EPA, EFSA MRLs)

    Typical usage ratio

    • Utilized at 0.5–1.5 molar ratio based on target synthesis
    • Ratio tuned to maximize target compound yield and minimize total organic residue

    Downstream process integration

    • Charged at initial condensation with urea or carbamate reagents
    • Handled in solvent or slurried addition, integrated with in-process chromatographic monitoring
    • Purification proceeds after completion of coupling and hydrolysis

    Final product types

    • Sulphonylurea herbicide actives (e.g., chlorsulfuron)
    • Growth regulating compounds with sulphonamide motifs
    • Precursor blends for field formulation of herbicidal agents
    • Concentrated technical grade substances for agricultural use

    4. Synthesis of Azo Dye Intermediates

    The sulphonamide and chloro functionalities in this compound make it a preferred choice for dye manufacturers as a diazo coupling component. Its controlled introduction produces specific shades and enhances fastness in textile, leather, and paper application colors. Strict batch consistency is critical to large-scale pigment synthesis customers.

    Industry compliance standards

    • Oeko-Tex Standard 100 (chemical conformance in textiles)
    • REACH Regulation (EC) No 1907/2006 (dangerous substances in dyes)
    • ISO 9001:2015 (colorant production management)
    • ZDHC MRSL (zero discharge of hazardous chemicals list)

    Typical usage ratio

    • 1.0–1.4 equivalents relative to primary aromatic amine
    • Ratio refined for tint strength, hue target, and migration restrictions

    Downstream process integration

    • Added post-diazotization as coupling partner in batch or continuous reactors
    • Pre-treated via purification to reduce off-tones and maximize color yield
    • Intermediate filtered and dried before blending with auxiliary components

    Final product types

    • Disperse dyes for polyester textiles
    • Azo pigments for printing inks
    • Reactive dyes for cellulosic fibers
    • Leather coloring agents

    5. Advanced Polymer Modifier Synthesis

    Specialty polymer producers use this compound to introduce sulphonamide and aromatic functionalities into engineering plastics and high-performance copolymers. The controlled addition imparts charge, thermal stability, and structural features to block copolymers for membrane, filter, and electronics applications. Strict control of monomer feed ratios and impurity levels supports downstream regulatory audits for high-technology end uses.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for engineered polymers)
    • ISO 10993-5 (for medical device polymer toxicity testing, where relevant)
    • RoHS (EU Restriction of Hazardous Substances Directive, for electronics-grade polymers)
    • UL94 flammability standards for plastic materials

    Typical usage ratio

    • 0.2–1.0% by weight in copolymer feed blend
    • Ratio adjusted for target polymer chain length, charge density, and mechanical properties

    Downstream process integration

    • Blended in monomer mixture prior to polymerization
    • Dissolved in solvent or melt depending on process environment
    • Monitored by in-line spectrometry for consistent incorporation

    Final product types

    • Charged block copolymers for lithium battery separators
    • Functional membranes for water and gas filtration
    • Antistatic additives in electronics-grade films
    • High-performance engineering plastic blends
    Free Quote

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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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