1,3-Dimethyl-2-imidazolidinone

1,3-Dimethyl-2-imidazolidinone
Names
	IUPAC name 1,3-Dimethyl-2-imidazolidinone
	Other names Dimethylethyleneurea; N,N'-Dimethylimidazolidinone
Identifiers
CAS Number	80-73-9 ;
3D model (JSmol)	Interactive image; Interactive image;
Abbreviations	DMI
ChEMBL	ChEMBL12338 ;
ChemSpider	6409 ;
ECHA InfoCard	100.001.187
PubChem CID	6661;
	InChI InChI=1S/C5H10N2O/c1-6-3-4-7(2)5(6)8/h3-4H2,1-2H3 Key: CYSGHNMQYZDMIA-UHFFFAOYSA-N ; InChI=1/C5H10N2O/c1-6-3-4-7(2)5(6)8/h3-4H2,1-2H3 Key: CYSGHNMQYZDMIA-UHFFFAOYAB;
	SMILES O=C1N(C)CCN1C; CN1CCN(C1=O)C;
Properties
Chemical formula	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).
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	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

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.

DMI is toxic in contact with skin.^[4]

References

↑ DMI at Mitsui Chemicals
↑ Leahy, Ellen M. "1,3-Dimethyl-2-imidazolidinone" e-EROS Encyclopedia of Reagents for Organic Synthesis (2001),doi:10.1002/047084289X.rd342
↑ 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.
↑ DMI at TCI

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[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