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trolamine

Structure via PubChem · Public domain (PubChem)

EntityQ424314· pop 23· linked from 75 articles

Also known as triethanolamine, H3tea, tris(beta-hydroxyethyl)amine, nitrilo-2,2',2''-triethanol, tris(2-hydroxyethyl)amine, 2,2',2''-nitrilotris(ethanol), N(CH2CH2OH)3, nitrilotriethanol

Triethanolamine (TEOA) is an organic compound with the chemical formula . It is a colourless, viscous liquid. It is both a tertiary amine and a triol. A triol is a molecule with three alcohol groups. Approximately 150,000 tonnes were produced in 1999. It is a colourless compound although samples may appear yellow because of impurities.

Chemical data

Formula
C6H15NO3
Molecular weight
149.19 g/mol
IUPAC name
2-[bis(2-hydroxyethyl)amino]ethanol
SMILES
C(CO)N(CCO)CCO
InChIKey
GSEJCLTVZPLZKY-UHFFFAOYSA-N
XLogP
-1
Polar surface area
63.9 Ų
H-bond donors
3
H-bond acceptors
4
Formal charge
0

via PubChem

Wikidata facts

Mass
149.105
Show 7 more facts
chemical formula
C₆H₁₅NO₃
Commons category
Triethanolamine
pKa
7.77
canonical SMILES
C(CO)N(CCO)CCO
melting point
20.5
boiling point
335.4
ionization energy
7.90
Sources (2)

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Article

17 sections
Contents
  • Production
  • Applications
  • Cement production
  • Cosmetics and medicine
  • Derivatives
  • In the laboratory and in amateur photography
  • In holography
  • In electroless plating
  • In ultrasonic testing
  • In aluminium soldering
  • Safety and regulation
  • Allergic reactions
  • Tumors
  • Environmental toxicity
  • Regulation
  • See also
  • References

Triethanolamine (TEOA) is an organic compound with the chemical formula . It is a colourless, viscous liquid. It is both a tertiary amine and a triol. A triol is a molecule with three alcohol groups. Approximately 150,000 tonnes were produced in 1999. It is a colourless compound although samples may appear yellow because of impurities.

==Production== Triethanolamine is produced from the reaction of ethylene oxide with aqueous ammonia, also produced are ethanolamine and diethanolamine. The ratio of the products can be controlled by changing the stoichiometry of the reactants.

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