158917
Triethanolamine hydrochloride
≥99%
Synonym(s):
2,2′,2′′-Nitrilotriethanol hydrochloride, Tris(2-hydroxyethyl)amine hydrochloride
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About This Item
Linear Formula:
(HOCH2CH2)3N · HCl
CAS Number:
Molecular Weight:
185.65
EC Number:
211-284-2
UNSPSC Code:
12161700
MDL number:
Beilstein/REAXYS Number:
3909940
assay
≥99%
useful pH range
7.3-8.3
pKa (25 °C)
7.8
mp
177-179 °C (lit.)
solubility
H2O: soluble 33%, clear, colorless
SMILES string
Cl.OCCN(CCO)CCO
InChI
1S/C6H15NO3.ClH/c8-4-1-7(2-5-9)3-6-10;/h8-10H,1-6H2;1H
InChI key
HHLJUSLZGFYWKW-UHFFFAOYSA-N
Application
Triethanolamine hydrochloride was used to study the chemical cross linking of chloroplast coupling factor l. It was used in assay medium for assaying ADP.
Biochem/physiol Actions
Triethanolamine is a short chain alkanolamine that acts as surfactant and emulsifier in topical skin formulations.Constant use sensitizes skin to allergic response.
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Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
监管及禁止进口产品
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Regulation of glucose uptake by muscle. 7. Effects of fatty acids, ketone bodies and pyruvate, and of alloxan-diabetes, starvation, hypophysectomy and adrenalectomy, on the concentrations of hexose phosphates, nucleotides and inorganic phosphate in perfused rat heart.
E A Newsholme et al.
The Biochemical journal, 93(3), 641-651 (1964-12-01)
Allergic contact dermatitis from triethanolamine in a sunscreen.
C Y Chu et al.
Contact dermatitis, 44(1), 41-42 (2001-01-13)
B A Baird et al.
The Journal of biological chemistry, 251(22), 6953-6962 (1976-11-25)
Cross-linking reagents have been used to link covalently adjacent subunits of solubilized spinach chloroplast coupling factor 1, which is a latent ATPase. 1,5-Difluoro-2,4-dinitrobenzene, dimethyl-3,3'-dithiobispropionimidate, and dimethylsuberimidate are able to form bridges of 3 to 11 A between amino groups, and