AC-42453 - thioacetamide-99-acs-reagent | 62-55-5
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Thioacetamide
CAS:Formel:C2H5NSReinheit:>98.0%(GC)(T)Farbe und Form:White to Light yellow to Light orange powder to crystalMolekulargewicht:75.13Thioacetamide
CAS:Formel:C2H5NSReinheit:≥ 99.0%Farbe und Form:White, off-white or faint yellow or beige crystalline powder or crystalsMolekulargewicht:75.13Thioacetamide
CAS:ThioacetamideFormel:C2H5NSReinheit:99%Farbe und Form: colorless/white to off-white/yellow solidMolekulargewicht:75.1328g/molThioacetamide
CAS:Kontrolliertes Produkt<p>Applications 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.<br>References Akhtar, T., Sheikh, N.: Toxin Reviews, 32, 43 (2013); Yuan, A., et. al.: Adv. Mater. Res., 652, 683 (2013)<br></p>Formel:C2H5NSFarbe und Form:NeatMolekulargewicht:75.13Thioacetamide
CAS:Kontrolliertes Produkt<p>Thioacetamide 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 to</p>Formel:C2H5NSReinheit:Min. 98 Area-%Farbe und Form:PowderMolekulargewicht:75.13 g/molThioacetamide
CAS:Thioacetamide, a hepatotoxicant, induces liver lesions and cell necrosis without neutrophil infiltration in rats.Formel:C2H5NSReinheit:99.48% - 99.6%Farbe und Form:White Solid CrystallineMolekulargewicht:75.13Thioacetamide extrapure AR, 99%
CAS:Formel:C2H5NSReinheit:min. 99.0%Farbe und Form:White, Crystalline powder, Clear, ColourlessMolekulargewicht:75.13Thioacetamide extrapure AR, ACS, ExiPlus, Multi-Compendial, 99%
CAS:Formel:C2H5NSReinheit:min. 99.0%Farbe und Form:White, Crystalline powder, Clear, ColourlessMolekulargewicht:75.13Thioacetamide, ACS, 99% min
CAS:<p>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</p>Formel:C2H5NSReinheit:99%Molekulargewicht:75.13Thioacetamide, 98%
CAS:<p>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</p>Formel:C2H5NSReinheit:98%Farbe und Form:White to cream to pale yellow, Crystals or powder or crystalline powderMolekulargewicht:75.13










