Molecular structure of Thioacetamide, CAS Number: 62-55-5
Thioacetamide (CAS 62-55-5)
Alternate Names:
Acetothioamide
Application:
Thioacetamide is a hepatotoxin
CAS Number:
62-55-5
Purity:
≥98%
Molecular Weight:
75.13
Molecular Formula:
CH3CSNH2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Thioacetamide, a versatile organic compound, finds extensive application in organic synthesis and scientific research. With its sulfur-containing nature, thioacetamide proves valuable in synthesizing various organic molecules. Moreover, it plays a significant role in the production of dyes, pigments, and specialty chemicals. In scientific research, thioacetamide serves as a reagent for synthesizing organic compounds. Additionally, thioacetamide facilitates the synthesis of diverse compounds, including esters, amides, and thiols. Given its broad range of applications, thioacetamide can serve as a useful reagent in many organic synthesis and research applications.
Thioacetamide (CAS 62-55-5) References
- Thioacetamide, an anti-thyroid compound. | MALOOF, F. and SOODAK, M. 1961. Endocrinology. 68: 125-9. PMID: 13765931
- Kynurenic Acid Protects against Thioacetamide-Induced Liver Injury in Rats. | Marciniak, S., et al. 2018. Anal Cell Pathol (Amst). 2018: 1270483. PMID: 30327755
- Nicotinamide mononucleotide inhibits hepatic stellate cell activation to prevent liver fibrosis via promoting PGE2 degradation. | Zong, Z., et al. 2021. Free Radic Biol Med. 162: 571-581. PMID: 33220424
- Toxicity of thioacetamide and protective effects of quercetin in zebrafish (Danio rerio) larvae. | Wang, K., et al. 2021. Environ Toxicol. 36: 2062-2072. PMID: 34227734
- Electrochemiluminescence of Ru(bpy)32+/thioacetamide and its application for the sensitive determination of hepatotoxic thioacetamide. | Kitte, SA., et al. 2021. Analyst. 146: 5198-5203. PMID: 34308456
- Ingestion of mannose ameliorates thioacetamide-induced intrahepatic oxidative stress, inflammation and fibrosis in rats. | Shaker, ME., et al. 2021. Life Sci. 286: 120040. PMID: 34637794
- Hepatoprotective effect of Baicalin against thioacetamide-induced cirrhosis in rats: Targeting NOX4/NF-κB/NLRP3 inflammasome signaling pathways. | Zaghloul, RA., et al. 2022. Life Sci. 295: 120410. PMID: 35182557
- Fisetin alleviates thioacetamide-induced hepatic fibrosis in rats by inhibiting Wnt/β-catenin signaling pathway. | El-Fadaly, AA., et al. 2022. Immunopharmacol Immunotoxicol. 44: 355-366. PMID: 35255766
- Toxic effects of thioacetamide-induced femoral damage in New Zealand white rabbits by activating the p38/ERK signaling pathway. | Cheng, L., et al. 2022. Physiol Res. 71: 285-295. PMID: 35275703
- Nephrotoxicity evaluation and proteomic analysis in kidneys of rats exposed to thioacetamide. | Lim, JY., et al. 2022. Sci Rep. 12: 6837. PMID: 35477741
- Acute bone damage through liver-bone axis induced by thioacetamide in rats. | Jin, X., et al. 2022. BMC Pharmacol Toxicol. 23: 29. PMID: 35526079
- Liver cirrhosis: An overview of experimental models in rodents. | Faccioli, LAP., et al. 2022. Life Sci. 301: 120615. PMID: 35526595
- New Aspects of the Reaction of Thioacetamide and N-Substituted Maleimides. | Aseeva, YV., et al. 2022. Molecules. 27: PMID: 36557934
- Thioacetamide hepatocarcinogenesis. | Becker, FF. 1983. J Natl Cancer Inst. 71: 553-8. PMID: 6577229
Inhibitor of:
CDO, SF4, and Thyroperoxidase.Activator of:
Glutamate-Pyruvate Transaminase.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Thioacetamide, 25 g | sc-213031 | 25 g | $53.00 |