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N-Methylethanolamine is produced industrially by reacting ethylene oxide with excess methylamine in aqueous solution. This reaction yields a mixture of the 1:1 addition product NMEA (1) and - by a further addition of another ethylene oxide - the 1:2 addition product methyl diethanolamine (MDEA) (2):
This list is ordered by the number of carbon atoms in an alcohol. C1. Methanol; C2. Ethanol; C3 1-Propanol ... Isoamyl alcohol; 2-Methyl-1-butanol; Neopentyl alcohol ...
Benzyl alcohol is used effectively for treating lice infestations as the active ingredient in lotion shampoo with 5% benzyl alcohol. [ 13 ] Benzyl alcohol is an ingredient used in the manufacture of soaps, topical creams, skin lotions, shampoos, and facial cleansers and is popular due to its anti-bacterial and anti-fungal properties.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Chemically, phenyethanolamine is an aromatic compound, an amine, and an alcohol. The amino-group makes this compound a weak base , capable of reacting with acids to form salts. Two common salts of phenylethanolamine are the hydrochloride, C 8 H 11 NO.HCl, m.p. 212 °C, [ 6 ] and the sulfate, (C 8 H 11 NO) 2 .H 2 SO 4 , m.p. 239–240 °C.
Benzyl alcohol, m-nitro 3-Nitrobenzyl alcohol Benzenemethanol, 3-nitro- ... The compound 3-nitrobenzyl alcohol is an organic compound with the formula C 7 H 7 NO 3.
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. Ethanolamine is a colorless, viscous liquid with an odor reminiscent of ammonia. [9]
Benzylamine is used as a masked source of ammonia, since after N-alkylation, the benzyl group can be removed by hydrogenolysis: [10] C 6 H 5 CH 2 NH 2 + 2 RBr → C 6 H 5 CH 2 NR 2 + 2 HBr C 6 H 5 CH 2 NR 2 + H 2 → C 6 H 5 CH 3 + R 2 NH. Typically a base is employed in the first step to absorb the HBr (or related acid for other kinds of ...
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