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(4-Chlorophenylthio)Acetic Acid

    • Product Name (4-Chlorophenylthio)Acetic Acid
    • Alias 4-CPTAA
    • Einecs 249-655-6
    • 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

    400070

    Chemical Name (4-Chlorophenylthio)acetic acid
    Cas Number 1873-12-7
    Molecular Formula C8H7ClO2S
    Molecular Weight 202.66
    Appearance White to off-white solid
    Melting Point 90-93°C
    Solubility In Water Slightly soluble
    Smiles C1=CC(=CC=C1SCC(=O)O)Cl
    Synonyms 2-(4-Chlorophenylthio)acetic acid
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C

    As an accredited (4-Chlorophenylthio)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of (4-Chlorophenylthio)acetic acid is packed in a sealed amber glass bottle with hazard labeling and tamper-evident cap.
    Shipping (4-Chlorophenylthio)acetic acid is shipped in sealed, chemical-resistant containers to prevent leaks and contamination. The packaging complies with safety regulations for hazardous materials. It is transported with clear labeling, including hazard information. During transit, it is handled by authorized personnel and stored in a cool, dry place away from incompatible substances.
    Storage (4-Chlorophenylthio)acetic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and moisture. Keep it out of direct sunlight and incompatible substances such as strong oxidizers and bases. Properly label the container and ensure it is stored at room temperature or as specified by the manufacturer or material safety data sheet.
    Application of (4-Chlorophenylthio)Acetic Acid

    Applications of (4-Chlorophenylthio)Acetic Acid in Industrial Manufacturing

    (4-Chlorophenylthio)Acetic Acid serves as a specialty intermediate supporting several niche sectors within pharmaceutical and chemical manufacturing. As a direct producer, we collaborate closely with downstream industry engineers to ensure batch consistency, purity, and regulatory conformity from pilot-scale synthesis to routine production.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers deploy this intermediate in the multi-stage synthesis of select active ingredients, particularly as a thiophenyl introduction agent in aromatic compound modifications. Its reactivity enables precise side-chain manipulation under strictly controlled reaction parameters, meeting the scale-up needs for patented APIs. Customers typically source quality-assured lots with low impurity profiles for integration into lead compound development and process optimization cycles.

    Industry compliance standards

    • ICH Q7 GMP compliance for API intermediate stages
    • US FDA 21 CFR Part 211 for process control
    • EU GMP Annex 8 for intermediates
    • Chinese Pharmacopoeia guidance for starting material traceability

    Typical usage ratio

    • 0.2–0.5 molar equivalents relative to precursor substrate
    • Adjustments based on target molecule, reactive site accessibility, and impurity control thresholds

    Downstream process integration

    • Direct addition to aromatic coupling or substitution reactions after solvent charge
    • Usually employed during mid-stage transformations before final API crystallization
    • Requires inert gas blanketing and real-time pH adjustment

    Final product types

    • Antifungal agents with chlorophenyl moieties
    • Non-steroidal anti-inflammatory drugs using thiophenyl intermediates
    • Specialty antihistamines requiring site-specific chlorination
    • Small-molecule oncology candidates with aromatic sulfur linkages

    2. Agrochemical Intermediate Manufacturing

    Producers in the agrochemical sector utilize this compound in the synthesis of sulfur-containing herbicide and fungicide intermediates. Its high reactivity supports sulfonation and further condensation reactions, allowing for the introduction of chlorinated thiol groups in lead molecule frameworks. Agrochemical R&D units choose it for new formulation prototypes and commercial-scale production under robust process containment.

    Industry compliance standards

    • FAO/WHO pesticide specification requirements
    • China National Standard GB 2763 (Maximum Residue Limits)
    • REACH Annex VII-X compliance for chemical intermediates
    • ISO 9001:2015 QA systems for chemical production sites

    Typical usage ratio

    • 5%–15% of total batch weight depending on targeted herbicide or fungicide
    • Ratio adjusted for activity spectrum, residue limits, and conversion yield

    Downstream process integration

    • Batch-fed into thioether synthesis during core intermediate conversion
    • Neutralized post-reaction in aqueous work-up lines
    • Processed before final formulation blending steps

    Final product types

    • Pre-emergent herbicide intermediates with chlorothio functionality
    • Post-emergent fungicide actives using thioether side chains
    • Seed treatment agents for broad-acre crops
    • Plant growth regulators incorporating halogenated sulfur groups

    3. Dye Additive and Pigment Intermediate

    Synthetic dye and pigment manufacturers incorporate this material to introduce sulfur and chlorine substituents in aromatic dye backbones. Its structure permits high-yield sulfidation and halogenation steps, especially in the controlled production of specialty colorants for textiles and functional coatings. Analytical monitoring ensures by-product minimization and stable chromatic properties in the finished dispersions.

    Industry compliance standards

    • ISO 9001:2015 for pigment production lines
    • Oeko-Tex Standard 100 (restricted substance criteria)
    • EU REACH (Substance of Very High Concern screening)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines

    Typical usage ratio

    • 3%–8% as a reactive intermediate in total dye mixture mass
    • Optimized according to chromatic intensity, shade purity, and fastness requirements

    Downstream process integration

    • Charged into diazotization or coupling process steps under controlled pH
    • Blended prior to pigment precipitation in slurry reactors
    • Filtered and washed for downstream paste or powder conversion

    Final product types

    • Sulfur dyes for cellulosic textile applications
    • Anthraquinone derivative colorants with chlorinated thio side groups
    • High-performance organic pigments for industrial coatings
    • Specialty printing ink concentrates requiring chemical stability

    4. Material Science—Specialty Polymer Processing

    Polymer and advanced materials manufacturers employ this compound as a functionalizing monomer or chain transfer agent for select sulfur- and chlorine-modified polymers. Its unique moiety enables tailored molecular weights and controlled branching through step-growth or radical copolymerization. Quality-sensitive production protocols include in-line purification and continuous process analytics to secure particle size and dispersity specifications.

    Industry compliance standards

    • ISO 9001:2015 QMS for specialty polymerization lines
    • ASTM D256-10 for polymer impact strength testing
    • EU REACH registration requirements for new polymer entities
    • RoHS Directive (2011/65/EU) for electronic polymers

    Typical usage ratio

    • 0.5%–2.5% by weight in polymer reaction feed
    • Adjusted according to target polymer structure and desired end-group modification

    Downstream process integration

    • Metered into block or random copolymerization reactors during initial charge
    • Reacted under inert conditions to prevent side-chain oxidation
    • Removed via vacuum or solvent stripping prior to pelletization

    Final product types

    • Functionalized engineering plastics with increased chemical resistance
    • Conductive polymer films for flexible electronics
    • Specialty resin modifiers for impact-resistant composites
    • Photoresist materials for microelectronics manufacturing
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