N,N-Dimethylethylamine
 | |
| Names | |
|---|---|
| IUPAC name
N,N-Dimethylethanamine | |
| Other names
Dimethylethylamine | |
| Identifiers | |
598-56-1  | |
| ChemSpider | 11230 |
| 5523 | |
| Jmol interactive 3D | Image |
| PubChem | 11723 |
| |
| Properties | |
| C4H11N | |
| Molar mass | 73.14 g·mol−1 |
| Appearance | Volatile liquid at room temp. |
| Density | 0.7±0.1 g/cm3 |
| Melting point | −140 °C (−220 °F; 133 K) |
| Boiling point | 36.5 °C (97.7 °F; 309.6 K) |
| Vapor pressure | 495.4±0.1 mmHg |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is  ?) | |
| Infobox references | |
N,N-Dimethylethylamine (DMEA), sometimes referred to as dimethylethylamine, is an organic compound with formula C4H11N. It is an industrial chemical that is mainly used in foundries as a catalyst for sand core production.[1] Dimethylethylamine is a malodorous, volatile liquid at room temperature that is excreted at greater concentrations with larger dietary intake of trimethylamine.[2] It has recently been identified as an agonist of human trace amine-associated receptor 5.[3]
See also
References
- ↑ "Dimethylethylamine". BASF The Chemical Company. Retrieved 4 May 2014.
- ↑ "N,N-Dimethylethylamine". Toxnet. Hazardous Substance Data Bank. Retrieved 4 May 2014.
The aim was to study the effect of trimethylamine (TMA) on the metabolism of the industrial catalyst N,N-dimethylethylamine to ascertain whether biological monitoring of industrial exposure to N,N-dimethylethylamine is compromised and excretion of the malodorous N,N-dimethylethylamine in sweat and urine is increased by dietary intake of TMA....Although the increased urinary and hidrotic excretion of N,N-dimethylethylamine may contribute to body odor problems, they were primarily due to TMA excretion, which is much the greater.
- ↑ Wallrabenstein I, Kuklan J, Weber L, Zborala S, Werner M, Altmüller J, Becker C, Schmidt A, Hatt H, Hummel T, Gisselmann G (2013). "Human trace amine-associated receptor TAAR5 can be activated by trimethylamine". PLoS ONE 8 (2): e54950. doi:10.1371/journal.pone.0054950. PMC 3564852. PMID 23393561.
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