Aminoethylethanolamine

Aminoethylethanolamine
Names
	Preferred IUPAC name 2-[(2-Aminoethyl)amino]ethan-1-ol
	Other names N-(2-Hydroxyethyl)ethylenediamine
Identifiers
CAS Number	111-41-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	7821 ;
ECHA InfoCard	100.003.516
PubChem CID	8112;
UNII	RC78W6NPXT ;
CompTox Dashboard (EPA)	DTXSID7025423 ;
	InChI InChI=1S/C4H12N2O/c5-1-2-6-3-4-7/h6-7H,1-5H2 Key: LHIJANUOQQMGNT-UHFFFAOYSA-N ; InChI=1/C4H12N2O/c5-1-2-6-3-4-7/h6-7H,1-5H2 Key: LHIJANUOQQMGNT-UHFFFAOYAR;
	SMILES OCCNCCN;
Properties
Chemical formula	C4H12N2O
Molar mass	104.153 g·mol−1
Density	1.03 g/cm3
Melting point	−28 °C (−18 °F; 245 K)
Boiling point	243 °C (469 °F; 516 K)
Vapor pressure	0.01 mmHg @ 20 °C; 8.17×10−4mmHg @ 25 °C
Hazards
NFPA 704 (fire diamond)	2 1 0
Flash point	132 °C (270 °F; 405 K)
Autoignition; temperature	368 °C (694 °F; 641 K)
	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

Aminoethylethanolamine or AEEA is an organic base used in the industrial manufacture of fuel and oil additives, chelating agents, and surfactants.

Synthesis

AEEA may be produced by the ethoxylation of ethylenediamine in the presence of water. Multiple ethoxylations result in undesirable byproducts, so the reaction is conducted with an excess of diamine.^[2]

References

↑ "N-(2-Hydroxyethyl)ethylenediamine". Sigma-Aldrich.
↑ US patent 6013801, Juhan Koll and Magnus Frank, "Method for producing aminoethylethanolamine and/or hydroxyethyl piperazine", issued 2000-01-11

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[1] "N-(2-Hydroxyethyl)ethylenediamine". Sigma-Aldrich.

[2] US patent 6013801, Juhan Koll and Magnus Frank, "Method for producing aminoethylethanolamine and/or hydroxyethyl piperazine", issued 2000-01-11

[1]

[2]