triethanolamine

Synonyms: "2,2',2''-nitrilotriethanol", "sterolamide", "tris(2-hydroxyethyl)amine", "Daltogen", "Triethylolamine", "Nitrilotriethanol", "Trihydroxytriethylamine", "Thiofaco T-35", "Triethanolamin", "Sting-Kill", "Tri(hydroxyethyl)amine", "Sodium ISA", "Ethanol, 2,2',2''-nitrilotris-", "Nitrilo-2,2',2''-triethanol", "Tris(beta-hydroxyethyl)amine", "Alkanolamine 244", "Teoa", "Nitrilotris(ethanol)", "2,2',2''-Nitrilotris(ethanol)", "Tris(hydroxyethyl)amine", "Triethanolamin-NG", "H3tea", "Triaethanolamin-NG", "2,2',2-Nitrilotriethano".

Source: Acrylonitrile is a heavily produced unsaturated nitrile, which is used in the production of synthetic fibers, plastics, resins, and rubber.

Identifiers:

IUPAC Name: 2-[bis(2-hydroxyethyl)amino]ethanol
CAS Number: 102-71-6
PubChem ID: 7618
InChiKey: GSEJCLTVZPLZKY-UHFFFAOYSA-N
Canonical SMILES: C(CO)N(CCO)CCO

Structural Properties:

Molecular Formula: C₆H₁₅NO₃
Molecular Weight: 149.190

Pharmacophore Features:

Number of bond donors: 3
Number of bond acceptors: 4
Number of atoms different from hydrogen: 10

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3D structure (.sdf)
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3D structure (.pdb)
3D structure (.pdbqt)

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

NTP. 1999. NTP Toxicology and Carcinogenesis Studies of Triethanolamine (CAS No. 102-71-6) in F344 Rats and B6C3F1 Mice (Dermal Studies). Natl Toxicol Program Tech Rep Ser 449:1-298. URL: https://ntp.niehs.nih.gov/results/pubs/longterm/ reports/longterm/tr400499/abstracts/tr449/index.html.