CAS 62-55-5

Tioacetamida

Descripción:

Tioacetamida es un compuesto orgánico con la fórmula química C2H5NS, caracterizado por la presencia de un grupo funcional tioamida. Aparece como un sólido cristalino blanco con un leve olor a azufre y es soluble en agua, alcohol y éter. Tioacetamida es conocido por su papel en la síntesis orgánica, particularmente como un reactivo en la preparación de tioamidas y otros compuestos que contienen azufre. También se utiliza en diversas aplicaciones, incluida la producción de productos farmacéuticos y agroquímicos. El compuesto tiene un perfil de toxicidad relativamente bajo, pero puede ser peligroso al ser ingerido o inhalado, lo que requiere precauciones de seguridad adecuadas durante su manipulación. Tioacetamida puede sufrir hidrólisis para formar ácido acético y sulfuro de hidrógeno, y también se sabe que participa en varias reacciones químicas, como sustituciones nucleofílicas. Debido a su reactividad, es importante almacenar Tioacetamida en un lugar fresco y seco, alejado de agentes oxidantes fuertes.

Fórmula: C₂H₅NS

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

Clave 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)

Forma y color: 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%

Forma y color: 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%

Forma y color: 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%

Forma y color: 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%

Forma y color: Solid, Crystalline

Peso molecular: 75.12999725341797

Ref: 10-F012744

Thioacetamide

Producto controlado

CAS: 62-55-5

Fórmula: C₂H₅NS

Forma y color: Neat

Peso molecular: 75.13

Ref: 04-C17469000

Thioacetamide

CAS: 62-55-5

Thioacetamide

Fórmula: C₂H₅NS

Pureza: 99%

Forma y color: colorless/white to off-white/yellow solid

Peso molecular: 75.1328g/mol

Ref: 54-OR28604

Thioacetamide

Producto 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

Forma y color: Neat

Peso molecular: 75.13

Ref: TR-T344295

Thioacetamide

Producto 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-%

Forma y color: 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%

Forma y color: 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%

Forma y color: 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%

Forma y color: White Solid Crystalline

Peso molecular: 75.13

Ref: TM-T35367