1,3-Dimethyl-2-imidazolidinone

From Wikipedia, the free encyclopedia
Jump to: navigation, search
1,3-Dimethyl-2-imidazolidinone
Structural formula of 1,3-dimethyl-2-imidazolidinone
Ball-and-stick model of the 1,3-dimethyl-2-imidazolidinone molecule
Names
IUPAC name
1,3-Dimethyl-2-imidazolidinone
Other names
Dimethylethyleneurea
N,N'-Dimethylimidazolidinone
Identifiers
3D model (JSmol)
Abbreviations DMI
ChemSpider
ECHA InfoCard 100.001.187
Properties
C5H10N2O
Molar mass 114.1457
Appearance colorless liquid
Melting point 8.2[1] °C (46.8 °F; 281.3 K)
Boiling point 225 °C (437 °F; 498 K)
Hazards
Flash point 120 °C (248 °F; 393 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

1,3-Dimethyl-2-imidazolidinone (DMI) is a cyclic urea used as a high-boiling polar aprotic solvent.[2] It is colourless, highly polar solvent has high thermal and chemical stability. It is a homolog of the related solvent DMPU. It can be prepared from 1,2-dimethylethylenediamine by reaction with phosgene.

Solvent[edit]

DMI has excellent solvating ability for both inorganic and organic compounds. In many applications, DMI (as well as DMPU) can be used as a substitute or replacement for the carcinogenic solvent HMPA.[3]

DMI is used in a variety of applications including detergents, dyestuffs, electronic materials and in the manufacture of polymers.[citation needed]

DMI is toxic in contact with skin.[4]

References[edit]

  1. ^ DMI at Mitsui Chemicals
  2. ^ Leahy, Ellen M. "1,3-Dimethyl-2-imidazolidinone" e-EROS Encyclopedia of Reagents for Organic Synthesis (2001),doi:10.1002/047084289X.rd342
  3. ^ Lo, C.-C.; Chao, P.-M. (1990). "Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis". Journal of Chemical Ecology. 16 (12): 3245–3253. doi:10.1007/BF00982095. 
  4. ^ DMI at TCI