N-Ethyl-N-(2-chloroethyl)aniline

N-Ethyl-N-(2-chloroethyl)aniline
Names
	Preferred IUPAC name N-(2-Chloroethyl)-N-ethylaniline
	Other names Ethyl(chloroethyl)aniline
Identifiers
CAS Number	92-49-9;
3D model (JSmol)	Interactive image;
ChemSpider	6826;
ECHA InfoCard	100.001.964
EC Number	202-159-3;
PubChem CID	7093;
UNII	YRZ30ATK2G;
CompTox Dashboard (EPA)	DTXSID6052615 ;
	InChI InChI=1S/C10H14ClN/c1-2-12(9-8-11)10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3 Key: DBDNQNARCHWMSP-UHFFFAOYSA-N;
	SMILES CCN(CCCl)C1=CC=CC=C1;
Properties
Chemical formula	C10H14ClN
Molar mass	183.68 g·mol−1
Appearance	Colorless or white solid
Melting point	45.5–46.5 °C (113.9–115.7 °F; 318.6–319.6 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H311
Precautionary statements	P264, P270, P280, P301+P310, P302+P352, P312, P321, P322, P330, P361, P363, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

N-Ethyl-N-(2-chloroethyl)aniline is the organic compound with the formula C₆H₅N(Et)(CH₂CH₂Cl) (Et = ethyl). It is a low-melting colorless solid that is an alkylating agent. The compound is a precursor to several cationic azo dyes via reaction of the chloroethyl group with tertiary amines or pyridine followed by azo coupling. Examples of derived dyes include C. I. Basic Red 18, Maxilon Red 2GL, and Yoracryl Red 2G.^[1]

References

↑ Klaus Hunger; Peter Mischke; Wolfgang Rieper; et al. (2005). "Azo Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_245. ISBN 3-527-30673-0..

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[Azodye-1] Klaus Hunger; Peter Mischke; Wolfgang Rieper; et al. (2005). "Azo Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_245. ISBN 3-527-30673-0..

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