Basic information Safety Supplier Related

1-Methylpiperazin-2-one

Basic information Safety Supplier Related

1-Methylpiperazin-2-one Basic information

Product Name:
1-Methylpiperazin-2-one
Synonyms:
  • 1-METHYL-PIPERAZIN-2-ONE
  • 2-Piperazinone, 1-methyl-
  • 1-Methylpiperazin-2-one ,98%
  • 1-Methylpiperazin-2-one ,97%
  • -Methyl-piperazin-2-one
  • 1-methylpiperazin-2-one(SALTDATA: HCl)
  • 1-Methyl-2-piperazinone
  • 1-METHYL-PIPERAZINE-2-ONE
CAS:
59702-07-7
MF:
C5H10N2O
MW:
114.15
Mol File:
59702-07-7.mol
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1-Methylpiperazin-2-one Chemical Properties

Boiling point:
242.1±33.0 °C(Predicted)
Density 
1.037±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Liquid
pka
7.42±0.20(Predicted)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C5H10N2O/c1-7-3-2-6-4-5(7)8/h6H,2-4H2,1H3
InChIKey
KJCIMSSFGUGTGA-UHFFFAOYSA-N
SMILES
N1(C)CCNCC1=O
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Safety Information

Hazard Codes 
Xi
Risk Statements 
43
Safety Statements 
36/37
HS Code 
2933599590
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1-Methylpiperazin-2-one Usage And Synthesis

Synthesis

110-85-0

59702-07-7

The general procedure for the synthesis of 1-methylpiperazin-2-one using piperazine as starting material was as follows: piperazine was dissolved in 70 mL of a 50% aqueous acetone solution containing 2.2 g of sodium hydroxide, and the resulting solution was stirred and reacted for 3 hours at room temperature. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was added to acetone to precipitate insoluble impurities. The insoluble material was separated by filtration and the filtrate was removed from the acetone by distillation under reduced pressure. Finally, the residue was distilled under reduced pressure to give 5.2 g of 1-methylpiperazin-2-one with a boiling point of 104°C/4 mmHg in 91% yield.

References

[1] Patent: US4087424, 1978, A
[2] Patent: US4112090, 1978, A

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