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HS Code |
350771 |
| Product Name | 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide |
| Molecular Formula | C5H6N2O2S |
| Molecular Weight | 158.18 g/mol |
| Appearance | Off-white to light yellow powder |
| Melting Point | Approx. 210-215°C (literature value, may vary) |
| Purity | Typically ≥ 95% |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Smiles | C1=NC(=CS1)CC(=O)N |
| Inchi | InChI=1S/C5H6N2O2S/c6-4(8)2-3-7-5(9)1-10-3/h1,9H,2H2,(H2,6,8) |
As an accredited 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide is sealed in an amber glass bottle with a screw cap and labeled for laboratory use. |
| Shipping | The chemical **2-(4-Hydroxy-Thiazol-2-Yl)Acetamide** is securely packaged in sealed, clearly labeled containers to prevent contamination and moisture exposure. Shipping complies with all safety regulations, including cushioning material and leak-proof packaging. Material Safety Data Sheets (MSDS) accompany the shipment, and it is transported via certified chemical couriers to ensure safe and compliant delivery. |
| Storage | Store **2-(4-Hydroxy-Thiazol-2-Yl)acetamide** in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from moisture, direct sunlight, and incompatible substances such as strong oxidizers. Keep away from sources of ignition and store at room temperature (20–25°C) unless otherwise specified. Ensure appropriate chemical labeling and access is restricted to trained personnel. |
Applications of 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide in Industrial ManufacturingAs a specialized manufacturer of 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide, we support key sectors by supplying this high-purity intermediate for demanding downstream applications. Our production and quality management systems reflect the needs of customers who depend on consistent batch quality, full traceability, and documented compliance from source to final integration. Below are core application scenarios, each aligned with sector-specific regulations and end-use needs. 1. Pharmaceutical Intermediate in Cephalosporin SynthesisMany global API plants utilize 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide as a thiazole-derivative intermediate for cefotaxime, ceftriaxone, and related β-lactam antibiotics. Its high thiazole ring purity supports key condensation reactions, enabling a controlled building block for side-chain modification steps during cephalosporin manufacturing. Downstream pharmaceutical integrators make regular use of our traceability documentation and impurity profile data to pass EU and US batch release protocols. Industry compliance standards
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2. Specialty Dye Intermediate for Reactive Textile ColorantsDye manufacturers employ 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide as a key raw material to synthesize sulfur-containing heterocyclic azo dyes, particularly for deep yellows and proprietary brown or gold textile shades. The material’s unique electronic structure supports high dye fixation rates on cellulosic fibers. Our QC protocol for metal content and trace residuals suits the stringent textile dye supply chain, where product consistency directly impacts environmental discharge compliance. Industry compliance standards
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3. Agricultural Chemical Synthesis for Fungicide FormulationSeveral major agchem companies integrate 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide during the manufacturing of specific thiazole-based fungicide actives. This compound forms a backbone in multi-step syntheses yielding soil treatment products that address fungal blights on cereals and vegetables. Its ring integrity and controlled impurity profile assist downstream partners in meeting residue tolerances for international crop export markets. Industry compliance standards
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4. Photographic Chemical Intermediate for Silver Halide EmulsionsPhotographic material producers rely on 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide to develop anti-fogging agents and spectral sensitizers. The unique thiazole acetamide moiety can alter the precipitation kinetics of silver halide materials, thereby improving sensitivity and granularity in professional imaging films. We support customers through analytical batch verification aligned with strict photochemical purity requirements. Industry compliance standards
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5. Electronic Chemical Precursor for Conductive Polymer SynthesisElectronics-sector manufacturers utilize 2-(4-Hydroxy-Thiazol-2-Yl)Acetamide to introduce thiazole functionality during the production of specialty heterocyclic monomers for antistatic polymer coatings. The precise position of the hydroxy and acetamide groups determines polymer surface energy and conductivity, making analytical-grade material mandatory for downstream integrators operating within electronics-grade cleanroom environments. Industry compliance standards
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