N-Methylsuccinimide

Suppliers

Names

[ CAS No. ]:
1121-07-9

[ Name ]:
N-Methylsuccinimide

[Synonym ]:
1-Methyl-2,5-pyrrolidinedione
2,5-Pyrrolidinedione, 1-methyl-
MFCD00005517
1-Methylpyrrolidine-2,5-dione
N-Methylsuccinimide

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
234.0±0.0 °C at 760 mmHg

[ Melting Point ]:
61-70 °C(lit.)

[ Molecular Formula ]:
C5H7NO2

[ Molecular Weight ]:
113.115

[ Flash Point ]:
105.9±11.1 °C

[ Exact Mass ]:
113.047676

[ PSA ]:
37.38000

[ LogP ]:
-0.95

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.493

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S26-S36/37

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
2

[ RTECS ]:
UY1028650

[ HS Code ]:
2925190090

Synthetic Route

Customs

[ HS Code ]: 2925190090

[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

nfrared Study of the Hydrogen Bond Complexes Between N-Methylsuccinimide and Phenols. Bruyneel K, et al.

Spectrosc. Lett. 29(4) , 739-47, (1996)

N-Methylsuccinimide in plasma and urine as a biomarker of exposure to N-methyl-2-pyrrolidone. Jönsson BAG and Åkesson B.

Int. Arch. Occup. Environ. Health 74(4) , 289-94, (2004)

Modeling the enolization of succinimide derivatives, a key step of racemization of aspartic acid residues: importance of a two-H2O mechanism.

Chem. Biodivers. 7(6) , 1349-56, (2010)

Racemization of aspartic acid residues in peptides and proteins is assumed to proceed via succinimide intermediates. An enolization of the succinimide intermediate is required for the racemization to ...


More Articles


Related Compounds

  • 2-Ethyl-N-methylsuccinimide
  • 2-Benzyl-N-methylsuccinimide
  • 2-hydroxy-N-methylsuccinimide
  • 3-hydroxy-N-methylsuccinimide
  • 3-hydroxy-N-methylsuccinimide
  • 2-(p-Iodophenyl)-N-methylsuccinimide
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 2-Methyl-4-(thiolan-3-yloxy)-6-(trifluoromethyl)pyrimidine
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • tert-Butyl 2-amino-2-(tetrahydro-2H-pyran-4-yl)acetate
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine