Basic information Safety Supplier Related

5-Amino-1-methylpyrazole-4-carboxamide

Basic information Safety Supplier Related

5-Amino-1-methylpyrazole-4-carboxamide Basic information

Product Name:
5-Amino-1-methylpyrazole-4-carboxamide
Synonyms:
  • 5-AMINO-1-METHYLPYRAZOLE-4-CARBOXAMIDE
  • 5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOXAMIDE
  • 5-AMINO-1-METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID AMIDE
  • BUTTPARK 94\04-11
  • 5-Amino-1,3-dimethyl-1H-pyrazole-4-carboxamide
  • 5-Amino-1-methylpyrazole-4-carboxamide, tech
  • 5-Amino-1-methyl-1h-pyrazole-4-carboxamide, tech
  • 1H-Pyrazole-4-carboxamide,5-amino-1-methyl-(9CI)
CAS:
18213-75-7
MF:
C5H8N4O
MW:
140.14
EINECS:
200-258-5
Product Categories:
  • Miscellaneous
  • AMIDE
Mol File:
18213-75-7.mol
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5-Amino-1-methylpyrazole-4-carboxamide Chemical Properties

Melting point:
224-226°C
Boiling point:
355.1±22.0 °C(Predicted)
Density 
1.56±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
15.26±0.50(Predicted)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
36/37/38-25
Safety Statements 
26-36/37/39-24/25-22-45
RIDADR 
UN 2811 6.1 / PGIII
HazardClass 
IRRITANT
HS Code 
2933199090
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5-Amino-1-methylpyrazole-4-carboxamide Usage And Synthesis

Synthesis

5334-41-8

18213-75-7

The general procedure for the synthesis of 5-amino-1-methyl-1H-pyrazole-4-carboxamide from 1-methyl-4-cyano-5-amino-1,2-pyrazole was carried out as follows: a mixture of 1-methyl-4-cyano-5-amino-1,2-pyrazole (0.11 mol) and concentrated sulfuric acid (30 mL, 0.6 mol) was stirred for 1 h at room temperature. Upon completion of the reaction, the mixture was slowly poured into ice water and the pH was adjusted to 8 with 50% aqueous ammonium hydroxide under ice bath conditions.Subsequently, the precipitated solid product was filtered and washed with cold water to give the final 5-amino-1-methyl-1H-pyrazole-4-carboxamide (13.5 g, 91% yield).

References

[1] Patent: WO2009/97446, 2009, A1. Location in patent: Page/Page column 64
[2] Patent: WO2009/97446, 2009, A1. Location in patent: Page/Page column 64
[3] Journal of Organic Chemistry, 1956, vol. 21, p. 1240,1242
[4] Patent: EP2025678, 2009, A1. Location in patent: Page/Page column 18-19

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