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Ethanolamine (2-aminoethanol, monoethanolamine, ETA, or MEA) is a naturally occurring organic chemical compound with the formula HOCH 2 CH 2 NH 2 or C 2 H 7 NO. [8] The molecule is bifunctional, containing both a primary amine and a primary alcohol.
Inhalation and skin contact are expected to be the primary ways of occupational exposure to this chemical. Based on single exposure animal tests, it is considered to be slightly toxic if swallowed or inhaled, moderately toxic if absorbed through skin as well as being corrosive to eyes and skin. [1]
Diethylethanolamine is used as a corrosion inhibitor in steam and condensate lines by neutralizing carbonic acid and scavenging oxygen. Diethylethanolamine reacts with 4-aminobenzoic acid to make procaine. DEAE is a precursor for DEAE-cellulose resin, which is commonly used in ion exchange chromatography.
Aminoethanol may refer to: 1-Aminoethanol; Ethanolamine (2-aminoethanol, ETA, or MEA) This page was last edited on 1 February 2021, at 07:11 (UTC). Text is available ...
Dimethylethanolamine (DMAE or DMEA) is an organic compound with the formula (CH 3) 2 NCH 2 CH 2 OH. It is bifunctional, containing both a tertiary amine and primary alcohol functional groups. It is a colorless viscous liquid. It is used in skin care products for improving skin tone and also taken orally as a nootropic.
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N-Methylethanolamine is an alkanolamine with the formula CH 3 NHCH 2 CH 2 OH. It is flammable, corrosive, colorless, viscous liquid. [2] It is an intermediate in the biosynthesis of choline. With both an amine and a hydroxyl functional groups, it is a useful intermediate in the chemical synthesis of various products including polymers and ...
2-Aminoalcohols are an important class of organic compounds that are often generated by the reaction of amines with epoxides: C 2 H 4 O + R−NH 2 → RNHC 2 H 4 OH. Simple alkanolamines are used as solvents, synthetic intermediates, and high-boiling bases. [2] Hydrogenation or hydride reduction of amino acids gives the