CasNo: 102-71-6
Molecular Formula: C6H15NO3
Appearance: Clear, amber viscous liquid
General description |
Triethanolamine is a hygroscopic liquid with a weak ammoniacal odor, ranging in color from colorless to pale yellow. It may turn brown upon exposure to air and light, and at lower temperatures, it can form colorless or pale yellow cubic crystals. With a melting point of 21.2°C, a boiling point of 360°C, a flash point of 193°C, a relative density (d420) of 1.1242, and a refractive index (nD20) of 1.4852, triethanolamine is a versatile compound. It is miscible with water, ethanol, and acetone, while being slightly soluble in ether, benzene, and carbon tetrachloride. |
Uses |
Triethanolamine exhibits strong alkalinity, allowing it to function as a base by accepting protons, making it suitable for condensation reactions. In the cement industry, triethanolamine serves as an early strength agent. It accelerates the hydration process of cement in concrete, enhancing early strength, increasing concrete density, and providing anti-permeability and antifreeze properties. In pharmaceutical formulations, triethanolamine is utilized in emulsions and as an alkylating agent. It finds application in various pharmaceutical products, including topical preparations, injectable solutions, topical analgesics, and sunscreens. |
Production Methods |
Triethanolamine is prepared commercially by the ammonolysis of ethylene oxide. The reaction yields a mixture of monoethanolamine, diethanolamine, and triethanolamine, which are separated to obtain the pure products. |
Definition |
ChEBI: A tertiary amino compound that is ammonia in which each of the hydrogens is substituted by a 2-hydroxyethyl group. |
Brand name |
Mobisyl [as salicylate] (Ascher);Sabrilex. |
Shipping |
UN2491 Ethanol amine or Ethanolamine solutions, Hazard class: 8; Labels: 8-Corrosive material. |
Waste Disposal |
Controlled incineration; incinerator equipped with a scrubber or thermal unit to reduce nitrogen oxides emissions |
InChI:InChI=1/C6H15NO3/c8-4-1-7(2-5-9)3-6-10/h8-10H,1-6H2
Triethanolamine (TEA) accelerated the hydration of 3CaO.Al2O3 and 3CaO.Al2O3-CaSO4.2H2O systems and extended the induction period of the hydration of 3CaO.SiO2. In portland cement paste TEA decreased the strength at all ages and setting characteristics were drastically altered, especially at higher TEA contents.
This work reports the measurements of K ...
(IUCr) Structures of monoethanolamine (MEAM), diethanolamine (DEAM) and triethanolamine (TEAM) … 756 MONOETHANOLAMINE, DIETHANOLAMINE AND TRIETHANOLAMINE...
Matteson's asymmetric synthesis via a on...
propylene glycol
triethanolamine
Conditions | Yield |
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1-methylsilatrane
triethanolamine
methylsilanetriol
Conditions | Yield |
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With disodium hydrogenphosphate; potassium dihydrogenphosphate; at 40 - 70 ℃; Kinetics; Thermodynamic data; Mechanism; hydrolysis in neutral medium;
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oxirane
ethanolamine
tris-(2-chloro-ethyl)-amine
tris(2-hydroxyethyl)amine-N-oxide
tris-[2-(4-nitro-benzoyloxy)-ethyl]-amine
Glycolaldehyde
2,2'-iminobis[ethanol]
tris-(2-acetoxy-ethyl)-amine