CAS 62-55-5
:Tioacetamida
- Acetamide, thio-
- Acetimidic acid, thio-
- Acetothioamide
- Nsc 2120
- TAA
- Thiacetamide
- Thioacetamid
- Thioacetamide
- Tioacetamida
- Ethanethioamide
Thioacetamide
CAS:Fórmula:C2H5NSPureza:>98.0%(GC)(T)Cor e Forma:White to Light yellow to Light orange powder to crystalPeso molecular:75.13Thioacetamide, ACS, 99% min
CAS:Thioacetamide is used in qualitative inorganic analysis as an in-situ source for sulfide ions. It is used in analytical chemistry as a source of hydrogen sulfide. It is an additive in enantioselective reduction of beta-keto esters with immobilized bakers yeast. It is also used as a vulcanizing agent
Fórmula:C2H5NSPureza:99%Peso molecular:75.13Thioacetamide, 98%
CAS:Thioacetamide is used in qualitative inorganic analysis as an in-situ source for sulfide ions. It is used in analytical chemistry as a source of hydrogen sulfide. It is an additive in enantioselective reduction of beta-keto esters with immobilized bakers yeast. It is also used as a vulcanizing agent
Fórmula:C2H5NSPureza:98%Cor e Forma:White to cream to pale yellow, Crystals or powder or crystalline powderPeso molecular:75.13Thioacetamide
CAS:Fórmula:C2H5NSPureza:≥ 99.0%Cor e Forma:White, off-white or faint yellow or beige crystalline powder or crystalsPeso molecular:75.13Thioacetamide
CAS:ThioacetamideFórmula:C2H5NSPureza:99%Cor e Forma: colorless/white to off-white/yellow solidPeso molecular:75.1328g/molThioacetamide
CAS:Produto ControladoApplications Thioacetamide is a carcinogen, a hepatotoxicant. Thioacetamide induces acute chronic liver injury through the activation of protein synthesis of RNA, DNA, and gamma-glutamyl transpeptitase. Thioacetamide has been used in the synthesis of [email protected] nano-array core-shell structure.
References Akhtar, T., Sheikh, N.: Toxin Reviews, 32, 43 (2013); Yuan, A., et. al.: Adv. Mater. Res., 652, 683 (2013)Fórmula:C2H5NSCor e Forma:NeatPeso molecular:75.13Thioacetamide
CAS:Produto ControladoThioacetamide is a chemical compound that has been used as a model system to study apoptosis. It is also known to cause injury and biochemical changes in cells. Thioacetamide is metabolized by cytochrome P450 enzymes and conjugated with glucuronic acid, which prevents it from binding to DNA or protein. The oxidation of thioacetamide by cytochrome P450 enzymes leads to the formation of reactive oxygen species that may cause DNA damage. Apoptosis induced by thioacetamide has been shown to be mediated through the mitochondrial pathway, which involves the release of cytochrome C, activation of caspase-9, and cleavage of poly (ADP-ribose) polymerase (PARP). Thioacetamide also inhibits sorbitol dehydrogenase activity, which leads to an accumulation of sorbitol in cells. This accumulation can activate transcriptional factors such as nuclear factor kappa B (NF-κB), leading toFórmula:C2H5NSPureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:75.13 g/molThioacetamide extrapure AR, ACS, ExiPlus, Multi-Compendial, 99%
CAS:Fórmula:C2H5NSPureza:min. 99.0%Cor e Forma:White, Crystalline powder, Clear, ColourlessPeso molecular:75.13Thioacetamide extrapure AR, 99%
CAS:Fórmula:C2H5NSPureza:min. 99.0%Cor e Forma:White, Crystalline powder, Clear, ColourlessPeso molecular:75.13Thioacetamide
CAS:Thioacetamide, a hepatotoxicant, induces liver lesions and cell necrosis without neutrophil infiltration in rats.Fórmula:C2H5NSPureza:99.48% - 99.6%Cor e Forma:White Solid CrystallinePeso molecular:75.13











