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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.
N,N-Dimethylethanolamine bitartrate contains tertiary ammonium cations (dimethyl(2-hydroxyethyl)ammonium [HN(CH 3) 2 CH 2 CH 2 OH] +) and bitartrate anions (HOOC−CH(OH)−CH(OH)−COO −). Tertiary ammonium cation is a cation in which three hydrogen atoms of ammonium are replaced with organyl groups.
Methylhexanamine (also known as methylhexamine, 1,3-dimethylamylamine, 1,3-DMAA, dimethylamylamine, and DMAA; trade names Forthane and Geranamine) is an indirect sympathomimetic drug invented and developed by Eli Lilly and Company and marketed as an inhaled nasal decongestant from 1948 until it was voluntarily withdrawn from the market in the 1980s.
Bitartrate is an anion which is the conjugate base of tartaric acid. It may also refer to any salt or monoester of tartaric acid. Some examples of bitartrate salts include: Choline bitartrate; Cysteamine bitartrate; Dihydrocodeine bitartrate; Dimethylaminoethanol bitartrate; Hydrocodone bitartrate; Metaraminol bitartrate; Norepinephrine ...
N,N-DMPEA has been found to be safe for use as a flavoring agent by the Flavor and Extract Manufacturers Association (FEMA) Expert Panel [7] and also by the Joint Expert Committee on Food Additives (JECFA) [8] —a collaboration between the Food and Agricultural Organization of the United Nations (FAO) and the World Health Organization.
2-Dimethylaminoethyl acrylate is prepared via transesterification of acrylic acid esters such as methyl acrylate (R = -CH 3) [3] or ethyl acrylate (R = -CH 2-CH 3) [4] with 2-dimethylaminoethanol under acid catalysis with tin compounds (for example stannoxanes [5]) or titanium compounds (for example tetraisopropyl orthotitanate [6]).
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The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: . CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −
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