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HS Code |
320201 |
| Name | 2-Chlorothiobenzamide |
| Cas Number | 19788-38-4 |
| Molecular Formula | C7H6ClNS |
| Molecular Weight | 171.65 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 120-124 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Smiles | C1=CC=C(C(=C1)Cl)C(=S)N |
| Storage Temperature | 2-8 °C |
| Synonyms | 2-chlorobenzenecarbothioamide |
As an accredited 2-Chlorothiobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Chlorothiobenzamide is packaged in a 100-gram amber glass bottle with a secure screw cap and appropriate hazard labeling. |
| Shipping | 2-Chlorothiobenzamide is shipped in tightly sealed containers to prevent moisture and contamination. It should be packed in accordance with regulatory guidelines, labelled with appropriate hazard symbols. The chemical must be kept away from incompatible substances and shipped under controlled conditions, ensuring compliance with local, national, and international transportation regulations. |
| Storage | 2-Chlorothiobenzamide should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. The storage location should be secure and clearly labeled, with access limited to trained personnel wearing appropriate protective equipment. Avoid sources of heat or ignition. |
Applications of 2-Chlorothiobenzamide in Industrial Manufacturing2-Chlorothiobenzamide serves as a critical intermediate in multiple specialized sectors, supporting the synthesis of value-added products through controlled processes. As a manufacturer, we supply this raw material to downstream partners with precise technical standards, ensuring traceability and compliance for regulated industries. Detailed below are the principal industrial applications and associated production paths. 1. Agrochemical Active Ingredient SynthesisMajor agrochemical companies utilize 2-Chlorothiobenzamide as a thioamide component for the synthesis of sulfenylurea herbicides and several fungicidal actives. The chlorinated benzamide core enables efficient coupling reactions, supporting high-yield transformations during pesticide and herbicide formulation. Our technical-grade material meets strict input specifications for these transformations, facilitating reliable large-scale batch reactions under controlled temperature and solvent regimes, followed by purification steps suited for regulated agricultural use. Industry compliance standards
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2. Pharmaceutical Intermediate for Thioamide Drug SynthesisPharma companies and contract manufacturing organizations source 2-Chlorothiobenzamide to develop niche APIs, especially as a thioamide precursor in the preparation of drugs for rare inflammatory and metabolic diseases. The controlled reactivity of the compound supports site-specific introduction of the thioamide function into drug candidates through amide bond-forming reactions. Reliable input quality underpins successful scale-up for both clinical and commercial API campaigns, supporting safe patient outcomes under regulatory scrutiny. Industry compliance standards
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3. Custom Synthesis for Specialty Dyes and Optical MaterialsDye and pigment manufacturers employ 2-Chlorothiobenzamide as a key intermediate during the preparation of sulfur-containing heterocyclic chromophores, used for advanced textile, inkjet, and security printing applications. The compound’s ortho-chloro group allows for controlled coupling and ring-closure in chromophore backbones, resulting in high-purity dye components with repeatable performance in commercial colorant manufacturing. Precise material traceability supports downstream QC and batch verification for demanding end customers. Industry compliance standards
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4. Fine Chemical Intermediate for Electron Transport MaterialsManufacturers of organic electronic components value 2-Chlorothiobenzamide for integration into synthesis workflows for electron transport and hole blocking materials. Its structure enables productive derivatization into benzothiazole frameworks, essential for performance materials in OLEDs and organic semiconductors. Stringent impurity control ensures reliable electrical function post-processing, making it suitable for next-generation display and photovoltaic device production. Industry compliance standards
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