Diethylaniline
 | |
| Names | |
|---|---|
| IUPAC name
N,N-Diethylaniline | |
| Other names
N-Phenyldiethylamine; Diethylaminobenzene[1] | |
| Identifiers | |
91-66-7  | |
| ChemSpider | 6794 |
| |
| Jmol-3D images | Image |
| PubChem | 7061 |
| |
| Properties | |
| Molecular formula |
C10H15N |
| Molar mass | 149.23 g·mol−1 |
| Appearance | Colorless to yellowish liquid[2] |
| Odor | Aniline-like[2] |
| Density | 0.93 g/mL[2] |
| Melting point | −38 °C (−36 °F; 235 K)[2] |
| Boiling point | 216 °C (421 °F; 489 K)[2] |
| 0.13 g/L[2] | |
| Hazards | |
| Flash point | 83 °C (181 °F; 356 K)[2] |
| 330 °C (626 °F; 603 K)[2] | |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
Diethylaniline is a chemical compound with the molecular formula C10H15N. It is used as an intermediate in the manufacture of dyes, pharmaceuticals and other chemicals, and also as a reaction catalyst. In organic synthesis, the complex diethylaniline·borane (DEANB) is used as a reducing agent.[3]
Diethylaniline may be genotoxic because it has been found to increase the rate of sister chromatid exchange.[4]
See also
References
- ↑ N,N-Diethylaniline at chemicalland21.com
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Record in the GESTIS Substance Database of the IFA
- ↑ Salunkhe, Ashok M.; Burkhardt, Elizabeth R. (1997). "N,N-Diethylaniline·borane, an efficient reducing agent for reduction of representative functional groups". Tetrahedron Letters 38 (9): 1519. doi:10.1016/S0040-4039(97)00127-5.
- ↑ Li, Q; Minami, M (1997). "Sister chromatid exchanges of human peripheral blood lymphocytes induced by N,N-diethylaniline in vitro". Mutation research 395 (2–3): 151–7. doi:10.1016/s1383-5718(97)00162-9. PMID 9465926.