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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 | 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. |
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 SynthesisPharmaceutical 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
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2. Agrochemical Intermediate ManufacturingProducers 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
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3. Dye Additive and Pigment IntermediateSynthetic 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
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4. Material Science—Specialty Polymer ProcessingPolymer 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
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