Diethylaniline

Diethylaniline
Names
	IUPAC name N,N-Diethylaniline
	Other names N-Phenyldiethylamine; Diethylaminobenzene
Identifiers
CAS Number	91-66-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	6794;
ECHA InfoCard	100.001.899
PubChem CID	7061;
CompTox Dashboard (EPA)	DTXSID8021800 ;
	InChI InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3 Key: GGSUCNLOZRCGPQ-UHFFFAOYSA-N; InChI=1/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3 Key: GGSUCNLOZRCGPQ-UHFFFAOYAA;
	SMILES N(c1ccccc1)(CC)CC;
Properties
Chemical formula	C10H15N
Molar mass	149.237 g·mol−1
Appearance	Colorless to yellowish liquid
Odor	Aniline-like
Density	0.93 g/mL
Melting point	−38 °C (−36 °F; 235 K)
Boiling point	216 °C (421 °F; 489 K)
Solubility in water	0.13 g/L
Hazards
Flash point	83 °C (181 °F; 356 K)
Autoignition; temperature	330 °C (626 °F; 603 K)
	Except where otherwise noted, data are 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]

References

^ N,N-Diethylaniline at chemicalland21.com
^ ^a ^b ^c ^d ^e ^f ^g ^h Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
^ 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.

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

[1] N,N-Diethylaniline at chemicalland21.com

[GESTIS-2] ^ ^a ^b ^c ^d ^e ^f ^g ^h Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health

[3] 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.

[4] 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.

[1]

[2]

[3]

[4]

See also

References