CAS 62-55-5

Tioacetamide

Descrizione:

Tioacetamide è un composto organico con la formula chimica C2H5NS, caratterizzato dalla presenza di un gruppo funzionale tioamide. Si presenta come un solido cristallino bianco con un leggero odore di zolfo ed è solubile in acqua, alcol ed etere. Tioacetamide è noto per il suo ruolo nella sintesi organica, in particolare come reagente nella preparazione di tioamidi e altri composti contenenti zolfo. È anche utilizzato in varie applicazioni, inclusa la produzione di farmaci e agrochimici. Il composto ha un profilo di tossicità relativamente basso, ma può essere pericoloso se ingerito o inalato, richiedendo adeguate precauzioni di sicurezza durante la manipolazione. Tioacetamide può subire idrolisi per formare acido acetico e solfuro di idrogeno, ed è anche noto per partecipare a varie reazioni chimiche, come le sostituzioni nucleofile. A causa della sua reattività, è importante conservare Tioacetamide in un luogo fresco e asciutto, lontano da agenti ossidanti forti.

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

Sinonimi:

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

Thioacetamide

CAS: 62-55-5

Formula: C₂H₅NS

Purezza: >98.0%(GC)(T)

Colore e forma: White to Light yellow to Light orange powder to crystal

Peso molecolare: 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

Purezza: 98%

Colore e forma: White to cream to pale yellow, Crystals or powder or crystalline powder

Peso molecolare: 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

Purezza: 99%

Peso molecolare: 75.13

Ref: 02-030638

Ethanethioamide

CAS: 62-55-5

Formula: C₂H₅NS

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 75.1328

Ref: IN-DA0035OS

Thioacetamide

CAS: 62-55-5

Formula: C₂H₅NS

Peso molecolare: 75.13

Ref: 4Z-A-133002

Thioacetamide, 10mM (in DMSO)

CAS: 62-55-5

Thioacetamide, 10mM (in DMSO)

Purezza: ≥98%

Peso molecolare: 75.13g/mol

Ref: 54-BUP18998

Thioacetamide

CAS: 62-55-5

Formula: C₂H₅NS

Purezza: ≥ 99.0%

Colore e forma: White, off-white or faint yellow or beige crystalline powder or crystals

Peso molecolare: 75.13

Ref: 7W-GK1732

Thioacetamide

CAS: 62-55-5

Purezza: 98.0%

Colore e forma: Solid, Crystalline

Peso molecolare: 75.12999725341797

Ref: 10-F012744

Thioacetamide

Prodotto controllato

CAS: 62-55-5

Formula: C₂H₅NS

Colore e forma: Neat

Peso molecolare: 75.13

Ref: 04-C17469000

Thioacetamide

CAS: 62-55-5

Thioacetamide

Formula: C₂H₅NS

Purezza: 99%

Colore e forma: colorless/white to off-white/yellow solid

Peso molecolare: 75.1328g/mol

Ref: 54-OR28604

Thioacetamide

Prodotto controllato

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

Colore e forma: Neat

Peso molecolare: 75.13

Ref: TR-T344295

Thioacetamide

Prodotto controllato

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

Purezza: Min. 98 Area-%

Colore e forma: Powder

Peso molecolare: 75.13 g/mol

Ref: 3D-FT45494

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

CAS: 62-55-5

Formula: C₂H₅NS

Purezza: min. 99.0%

Colore e forma: White, Crystalline powder, Clear, Colourless

Peso molecolare: 75.13

Ref: SR-48979

Thioacetamide extrapure AR, 99%

CAS: 62-55-5

Formula: C₂H₅NS

Purezza: min. 99.0%

Colore e forma: White, Crystalline powder, Clear, Colourless

Peso molecolare: 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

Purezza: 99.48% - 99.6%

Colore e forma: White Solid Crystalline

Peso molecolare: 75.13

Ref: TM-T35367