CAS 62-55-5

Thioacetamide

Description:

Thioacetamide is an organic compound with the chemical formula C2H5NS, characterized by the presence of a thioamide functional group. It appears as a white crystalline solid with a faint sulfur odor and is soluble in water, alcohol, and ether. Thioacetamide is known for its role in organic synthesis, particularly as a reagent in the preparation of thioamides and other sulfur-containing compounds. It is also utilized in various applications, including the production of pharmaceuticals and agrochemicals. The compound has a relatively low toxicity profile, but it can be hazardous upon ingestion or inhalation, necessitating appropriate safety precautions during handling. Thioacetamide can undergo hydrolysis to form acetic acid and hydrogen sulfide, and it is also known to participate in various chemical reactions, such as nucleophilic substitutions. Due to its reactivity, it is important to store thioacetamide in a cool, dry place, away from strong oxidizing agents.

Formula: C₂H₅NS

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

InChI key: InChIKey=YUKQRDCYNOVPGJ-UHFFFAOYSA-N

SMILES: C(C)(N)=S

Synonyms:

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

Thioacetamide

CAS: 62-55-5

Formula: C₂H₅NS

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 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

Formula: C₂H₅NS

Purity: 98%

Color and Shape: White to cream to pale yellow, Crystals or powder or crystalline powder

Molecular weight: 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

Formula: C₂H₅NS

Purity: 99%

Molecular weight: 75.13

Ref: 02-030638

Ethanethioamide

CAS: 62-55-5

Formula: C₂H₅NS

Purity: 97%

Color and Shape: Solid

Molecular weight: 75.1328

Ref: IN-DA0035OS

Thioacetamide

CAS: 62-55-5

Formula: C₂H₅NS

Molecular weight: 75.13

Ref: 4Z-A-133002

Thioacetamide, 10mM (in DMSO)

CAS: 62-55-5

Thioacetamide, 10mM (in DMSO)

Purity: ≥98%

Molecular weight: 75.13g/mol

Ref: 54-BUP18998

Thioacetamide

CAS: 62-55-5

Formula: C₂H₅NS

Purity: ≥ 99.0%

Color and Shape: White, off-white or faint yellow or beige crystalline powder or crystals

Molecular weight: 75.13

Ref: 7W-GK1732

Thioacetamide

CAS: 62-55-5

Purity: 98.0%

Color and Shape: Solid, Crystalline

Molecular weight: 75.12999725341797

Ref: 10-F012744

Thioacetamide

Controlled Product

CAS: 62-55-5

Formula: C₂H₅NS

Color and Shape: Neat

Molecular weight: 75.13

Ref: 04-C17469000

Thioacetamide

CAS: 62-55-5

Thioacetamide

Formula: C₂H₅NS

Purity: 99%

Color and Shape: colorless/white to off-white/yellow solid

Molecular weight: 75.1328g/mol

Ref: 54-OR28604

Thioacetamide

Controlled Product

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)

Formula: C₂H₅NS

Color and Shape: Neat

Molecular weight: 75.13

Ref: TR-T344295

Thioacetamide

Controlled Product

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

Formula: C₂H₅NS

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 75.13 g/mol

Ref: 3D-FT45494

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

CAS: 62-55-5

Formula: C₂H₅NS

Purity: min. 99.0%

Color and Shape: White, Crystalline powder, Clear, Colourless

Molecular weight: 75.13

Ref: SR-48979

Thioacetamide extrapure AR, 99%

CAS: 62-55-5

Formula: C₂H₅NS

Purity: min. 99.0%

Color and Shape: White, Crystalline powder, Clear, Colourless

Molecular weight: 75.13

Ref: SR-17942

Thioacetamide

CAS: 62-55-5

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

Formula: C₂H₅NS

Purity: 99.48% - 99.6%

Color and Shape: White Solid Crystalline

Molecular weight: 75.13

Ref: TM-T35367