CAS 62-55-5

Tioacetamida

Descrição:

Tioacetamida é um composto orgânico com a fórmula química C2H5NS, caracterizado pela presença de um grupo funcional tioamida. Aparece como um sólido cristalino branco com um leve odor de enxofre e é solúvel em água, álcool e éter. Tioacetamida é conhecido por seu papel na síntese orgânica, particularmente como um reagente na preparação de tioamidas e outros compostos que contêm enxofre. Também é utilizado em várias aplicações, incluindo a produção de produtos farmacêuticos e agroquímicos. O composto tem um perfil de toxicidade relativamente baixo, mas pode ser perigoso quando ingerido ou inalado, necessitando de precauções de segurança adequadas durante o manuseio. Tioacetamida pode sofrer hidrólise para formar ácido acético e sulfeto de hidrogênio, e também é conhecido por participar de várias reações químicas, como substituições nucleofílicas. Devido à sua reatividade, é importante armazenar Tioacetamida em um local fresco e seco, longe de agentes oxidantes fortes.

Fórmula: C₂H₅NS

InChI: InChI=1S/C2H5NS/c1-2(3)4/h1H3,(H2,3,4)

Chave InChI: InChIKey=YUKQRDCYNOVPGJ-UHFFFAOYSA-N

SMILES: C(C)(N)=S

Sinónimos:

• Acetamide, thio-
• Acetimidic acid, thio-
• Acetothioamide
• Nsc 2120
• TAA
• Thiacetamide
• Thioacetamid
• Thioacetamide
• Tioacetamida
• Ethanethioamide

Thioacetamide

CAS: 62-55-5

Fórmula: C₂H₅NS

Pureza: >98.0%(GC)(T)

Cor e Forma: White to Light yellow to Light orange powder to crystal

Peso molecular: 75.13

Ref: 3B-T0187

Thioacetamide, 98%

CAS: 62-55-5

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: C₂H₅NS

Pureza: 98%

Cor e Forma: White to cream to pale yellow, Crystals or powder or crystalline powder

Peso molecular: 75.13

Ref: 02-A12926

Thioacetamide, ACS, 99% min

CAS: 62-55-5

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: C₂H₅NS

Pureza: 99%

Peso molecular: 75.13

Ref: 02-030638

Ethanethioamide

CAS: 62-55-5

Fórmula: C₂H₅NS

Pureza: 97%

Cor e Forma: Solid

Peso molecular: 75.1328

Ref: IN-DA0035OS

Thioacetamide

CAS: 62-55-5

Fórmula: C₂H₅NS

Peso molecular: 75.13

Ref: 4Z-A-133002

Thioacetamide, 10mM (in DMSO)

CAS: 62-55-5

Thioacetamide, 10mM (in DMSO)

Pureza: ≥98%

Peso molecular: 75.13g/mol

Ref: 54-BUP18998

Thioacetamide

CAS: 62-55-5

Fórmula: C₂H₅NS

Pureza: ≥ 99.0%

Cor e Forma: White, off-white or faint yellow or beige crystalline powder or crystals

Peso molecular: 75.13

Ref: 7W-GK1732

Thioacetamide

CAS: 62-55-5

Pureza: 98.0%

Cor e Forma: Solid, Crystalline

Peso molecular: 75.12999725341797

Ref: 10-F012744

Thioacetamide

Produto Controlado

CAS: 62-55-5

Fórmula: C₂H₅NS

Cor e Forma: Neat

Peso molecular: 75.13

Ref: 04-C17469000

Thioacetamide

CAS: 62-55-5

Thioacetamide

Fórmula: C₂H₅NS

Pureza: 99%

Cor e Forma: colorless/white to off-white/yellow solid

Peso molecular: 75.1328g/mol

Ref: 54-OR28604

Thioacetamide

Produto Controlado

CAS: 62-55-5

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.
References Akhtar, T., Sheikh, N.: Toxin Reviews, 32, 43 (2013); Yuan, A., et. al.: Adv. Mater. Res., 652, 683 (2013)

Fórmula: C₂H₅NS

Cor e Forma: Neat

Peso molecular: 75.13

Ref: TR-T344295

Thioacetamide

Produto Controlado

CAS: 62-55-5

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

Fórmula: C₂H₅NS

Pureza: Min. 98 Area-%

Cor e Forma: Powder

Peso molecular: 75.13 g/mol

Ref: 3D-FT45494

Thioacetamide extrapure AR, ACS, ExiPlus, Multi-Compendial, 99%

CAS: 62-55-5

Fórmula: C₂H₅NS

Pureza: min. 99.0%

Cor e Forma: White, Crystalline powder, Clear, Colourless

Peso molecular: 75.13

Ref: SR-48979

Thioacetamide extrapure AR, 99%

CAS: 62-55-5

Fórmula: C₂H₅NS

Pureza: min. 99.0%

Cor e Forma: White, Crystalline powder, Clear, Colourless

Peso molecular: 75.13

Ref: SR-17942

Thioacetamide

CAS: 62-55-5

Thioacetamide, a hepatotoxicant, induces liver lesions and cell necrosis without neutrophil infiltration in rats.

Fórmula: C₂H₅NS

Pureza: 99.48% - 99.6%

Cor e Forma: White Solid Crystalline

Peso molecular: 75.13

Ref: TM-T35367