60-35-5
Chemical Structure
Acetamide
- CAS No.: 60-35-5
- Formula:C2H5NO
- Molecular Weight:59.07
IUPAC Name: acetamide
InChIKey: DLFVBJFMPXGRIB-UHFFFAOYSA-N
SMILES: CC(N)=O
Biological Activity: Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. Acetamide derivatives may has antioxidant activity and potential anti-inflammatory activity. Acetamide holds promise for research in the fields of anti-inflammatory and cancer studies[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Acetamide | 99.95% | Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. Acetamide derivatives may has antioxidant activity and potential anti-inflammatory activity. Acetamide holds promise for research in the fields of anti-inflammatory and cancer studies. | ||||||||||||||||||||
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Acetamide (Standard) | ≥98% | Acetamide (Standard) is the analytical standard of Acetamide. This product is intended for research and analytical applications. Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. Acetamide derivatives may has antioxidant activity and potential anti-inflammatory activity. Acetamide holds promise for research in the fields of anti-inflammatory and cancer studies. | ||||||||||||||||||||
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Acetamide-15N | 99.0% | Acetamide-15N is the 15N-labeled Acetamide. Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. | ||||||||||||||||||||
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Acetamide-d5 | 98.9% | Acetamide-d5 is the deuterium labeled Acetamide. Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. | ||||||||||||||||||||
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Acetamide-13C2 | ||||||||||||||||||||||
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Acetamide-d3 | 98.0% | Acetamide-d3 (Trideuteroacetamide-d3) is the deuterated-labeled Acetamide (HY-Y0946). Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. Acetamide derivatives may has antioxidant activity and potential anti-inflammatory activity. Acetamide holds promise for research in the fields of anti-inflammatory and cancer studies. | ||||||||||||||||||||
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Acetamide-13C2,15N | Acetamide-13C2,15N is the 13C- and 15N-labeled Acetamide (HY-Y0946). Acetamide is used as an intermediate in the synthesis of methylamine, thioacetamide, and insecticides, and as a plasticizer in leather, cloth and coatings. Acetamide has carcinogenicity. Acetamide derivatives may has antioxidant activity and potential anti-inflammatory activity. Acetamide holds promise for research in the fields of anti-inflammatory and cancer studies. | |||||||||||||||||||||
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Methacrylamide (Standard) | ≥98% | Methacrylamide (2-Methylacrylamide) (Standard) is the analytical standard of Methacrylamide (2-Methylacrylamide) (HY-W020027). This product is intended for research and analytical applications. Methacrylamide is a vinyl monomer and gelatin derivatization reagent that enables chemical crosslinking of Gelatins (HY-Y1365) via free radical polymerization, facilitating the formation of chemically stable hydrogels and the synthesis of pyridine-containing polymers. Methacrylamide is used in research related to biomaterials and polymer synthesis. | ||||||||||||||||||||
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Thioacetamide | 98.0% | Thioacetamide (TAA) is an indirect hepatotoxin and causes parenchymal cell necrosis. Thioacetamide requires metabolic activation by microsomal CYP2E1 to thioacetamide-S-oxide initially and then to thioacetamide-S-dioxide, which is a highly reactive metabolite, and its reactive metabolites covalently bind to proteins and lipids thereby causing oxidative stress and centrilobular necrosis. Thioacetamide can induce chronic liver fibrosis, encephalopathy and other events model. | ||||||||||||||||||||
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References
- [1]. Acetamide. IARC Monogr Eval Carcinog Risks Hum. 1999;71 Pt 3:1211-21. [Content Brief]
- [2]. Moore MM, et, al. The food contaminant acetamide is not an in vivo clastogen, aneugen, or mutagen in rodent hematopoietic tissue. Regul Toxicol Pharmacol. 2019 Nov;108:104451. [Content Brief]
- [3]. Autore G, et al. Acetamide derivatives with antioxidant activity and potential anti-inflammatory activity. Molecules. 2010 Mar 23;15(3):2028-38. [Content Brief]