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Aminoethylethanolamine

From Wikipedia, the free encyclopedia
Aminoethylethanolamine
Skeletal formula of aminoethylethanolamine
Ball-and-stick model of the aminoethylethanolamine molecule
Names
Preferred IUPAC name
2-[(2-Aminoethyl)amino]ethan-1-ol
Other names
N-(2-Hydroxyethyl)ethylenediamine
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.003.516Edit this at Wikidata
UNII
  • InChI=1S/C4H12N2O/c5-1-2-6-3-4-7/h6-7H,1-5H2 checkY
    Key: LHIJANUOQQMGNT-UHFFFAOYSA-N checkY
  • InChI=1/C4H12N2O/c5-1-2-6-3-4-7/h6-7H,1-5H2
    Key: LHIJANUOQQMGNT-UHFFFAOYAR
  • OCCNCCN
Properties
C4H12N2O
Molar mass104.153 g·mol−1
Density1.03 g/cm3[1]
Melting point−28 °C (−18 °F; 245 K)
Boiling point243 °C (469 °F; 516 K)
Vapor pressure0.01 mmHg @ 20 °C; 8.17x10−4mmHg @ 25 °C
Hazards
NFPA 704 (fire diamond)
Flash point132 °C (270 °F; 405 K)
368 °C (694 °F; 641 K)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Aminoethylethanolamine orAEEA is an organic base used in the industrial manufacture of fuel and oil additives,chelating agents, andsurfactants.

Synthesis

[edit]

AEEA may be produced by theethoxylation ofethylenediamine in the presence ofwater. Multiple ethoxylations result in undesirable byproducts, so the reaction is conducted with an excess of diamine.[2]

References

[edit]
  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 


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