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1-ACETYL-3-THIOSEMICARBAZIDE

CAS No.
2302-88-7
Chemical Name:
1-ACETYL-3-THIOSEMICARBAZIDE
Synonyms
acetamidothiourea;ACETYLTHIOSEMICARBAZIDE;1-ACETYLTHIOSEMICARBAZIDE;1-ACETYL-3-THIOSEMICARBAZIDE;1-Acetylthiosemicarbazide,95%;2-acetylhydrazinecarbothioaMide;N-{[Thio(carbonoimidyl)]amino}acetamide;Acetic acid, 2-(aminothioxomethyl)hydrazide;Acetic acid N'-(aminothioxomethyl) hydrazide
CBNumber:
CB5400203
Molecular Formula:
C3H7N3OS
Molecular Weight:
133.17
MDL Number:
MFCD00004932
MOL File:
2302-88-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-04 16:00:12
Product description Number Pack Size Price
N-{[Thio(carbonoimidyl)]amino}acetamide TRC-B642518-5G 5g $123
N-{[Thio(carbonoimidyl)]amino}acetamide TRC-B642518-500MG 500mg $76
N-{[Thio(carbonoimidyl)]amino}acetamide TRC-B642518-1G 1g $83
1-Acetyl-3-thiosemicarbazide FA160492 10g $162.2
1-Acetyl-3-thiosemicarbazide FA160492 25g $259.5

1-ACETYL-3-THIOSEMICARBAZIDE Properties

Melting point 165-170 °C
Density 1.280 (estimate)
refractive index 1.7490 (estimate)
storage temp. 2-8°C(protect from light)
solubility DMSO (Sparingly), Methanol (Sparingly)
pka 10.30±0.70(Predicted)
form solid
Appearance Off-white to light yellow Solid
Water Solubility Partly soluble in water.
Stability Hygroscopic
CAS DataBase Reference 2302-88-7(CAS DataBase Reference)
FDA UNII 6EWT2928KE

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Danger
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312a-P330-P501a
Hazard Codes  T
Risk Statements  25-36/37/38
Safety Statements  24/25-45
RIDADR  2811
HazardClass  6.1
PackingGroup  III
HS Code  29309099
REACH Registrations Active
Limited Quantities 5.0 kg (11 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)

1-ACETYL-3-THIOSEMICARBAZIDE price More Price(51)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC TRC-B642518-5G N-{[Thio(carbonoimidyl)]amino}acetamide 2302-88-7 5g $123 2026-06-03 Buy
TRC TRC-B642518-500MG N-{[Thio(carbonoimidyl)]amino}acetamide 2302-88-7 500mg $76 2026-06-03 Buy
TRC TRC-B642518-1G N-{[Thio(carbonoimidyl)]amino}acetamide 2302-88-7 1g $83 2026-06-03 Buy
Biosynth FA160492 1-Acetyl-3-thiosemicarbazide 2302-88-7 10g $162.2 2026-06-04 Buy
Biosynth FA160492 1-Acetyl-3-thiosemicarbazide 2302-88-7 25g $259.5 2026-06-04 Buy
Product number Packaging Price Buy
TRC-B642518-5G 5g $123 Buy
TRC-B642518-500MG 500mg $76 Buy
TRC-B642518-1G 1g $83 Buy
FA160492 10g $162.2 Buy
FA160492 25g $259.5 Buy

1-ACETYL-3-THIOSEMICARBAZIDE Chemical Properties,Uses,Production

Chemical Properties

white to slightly beige crystalline powder

Uses

1-Acetyl-3-thiosemicarbazide is applied in pharmaceutical industry as an intermediate.

Synthesis

thiosemicarbazide

79-19-6

Acetyl chloride

75-36-5

1-ACETYL-3-THIOSEMICARBAZIDE

2302-88-7

General procedure for the synthesis of acetylthiosemicarbazone from aminothiourea and acetyl chloride: preparation of the intermediate 2-acetylcarbazinethioformamide; Acetyl chloride (8.64 g, 0.11 mol) was added slowly and dropwise to an anhydrous tetrahydrofuran (THF, 100 mL) solution of aminothiourea (9.10 g, 0.10 mol) at 0 °C. The reaction mixture was heated to reflux and maintained for 3 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction was quenched by the addition of water (100 mL) followed by extraction with ethyl acetate (3 x 100 mL). The organic phases were combined, washed with saturated saline, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by column chromatography (eluent: methanol/dichloromethane=1/1, v/v) to afford the target compound acetylthiosemicarbazone (8.64 g, 65% yield). The results of mass spectrometry (electrospray ionization, ESI) analysis: m/z calculated value C3H7N3OS [M+H]+ 133.03, measured value 134.0 (MH+).

References

[1] Patent: WO2009/87220, 2009, A1. Location in patent: Page/Page column 57
[2] Yakugaku Zasshi, 1952, vol. 72, p. 376
[3] Chem.Abstr., 1953, p. 3856
[4] Synthetic Communications, 2004, vol. 34, # 22, p. 4189 - 4198
[5] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2010, vol. 76, # 5, p. 531 - 536

1-ACETYL-3-THIOSEMICARBAZIDE Preparation Products And Raw materials

1-ACETYL-3-THIOSEMICARBAZIDE Suppliers

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ACETYLTHIOSEMICARBAZIDE acetamidothiourea 1-ACETYLTHIOSEMICARBAZIDE 1-ACETYL-3-THIOSEMICARBAZIDE Acetic acid N'-(aminothioxomethyl) hydrazide 1-Acetylthiosemicarbazide,95% 2-acetylhydrazinecarbothioaMide Acetic acid, 2-(aminothioxomethyl)hydrazide N-{[Thio(carbonoimidyl)]amino}acetamide 2302-88-7 C3H7N3OS H2NCSNHNHCOCH3 Sulphur Derivatives