![]() | |
![]() | |
Names | |
---|---|
Preferred IUPAC name
1,3-Dimethyl-1,3-diazinan-2-one[1] | |
Other names
N,N′-Dimethyl-N,N′-trimethyleneurea | |
Identifiers | |
3D model (JSmol) |
|
Abbreviations | DMPU |
ChEMBL | |
ChemSpider |
|
ECHA InfoCard | 100.027.841 ![]() |
EC Number |
|
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C6H12N2O | |
Molar mass | 128.175 g·mol−1 |
Density | 1.064 g/cm3 |
Melting point | −20 °C; −4 °F; 253 K |
Boiling point | 246.5 °C (475.7 °F; 519.6 K) (Source) |
miscible | |
Refractive index (nD) |
1.4875-1.4895 |
Hazards | |
GHS labelling: | |
![]() ![]() ![]() | |
Danger | |
H302, H318, H361f | |
P201, P202, P264, P270, P280, P281, P301+P312, P305+P351+P338, P308+P313, P310, P330, P405, P501 | |
Flash point | 121 °C (250 °F; 394 K) |
Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
N,N′-Dimethylpropyleneurea (DMPU) is a cyclic urea sometimes used as a polar, aprotic organic solvent. In 1985, Dieter Seebach showed that it is possible to replace the suspected carcinogen hexamethylphosphoramide (HMPA) with DMPU.[2]
![]() | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |