| Dimethylethanolamine | |
|---|---|
| IUPAC name |
2-(dimethylamino)ethanol
|
| Other names | dimethylamino ethanol Deanol |
| Identifiers | |
| Abbreviations | DMAE |
| CAS number | 108-01-0 |
| SMILES |
CN(C)CCO
|
| Properties | |
| Molecular formula | C4H11NO |
| Molar mass | 89.14 g/mol |
| Density | 0.89 g/mL |
| Melting point |
-70 °C |
| Boiling point |
133–134 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
|
| Infobox references | |
Dimethylaminoethanol, also known as DMAE or dimethylethanolamine, is an organic compound. This compound also goes by the names of N,N-dimethyl-2-aminoethanol, beta-dimethylaminoethyl alcohol, beta-hydroxyethyldimethylamine and Deanol. It is a liquid with a color that ranges from clear to pale-yellow.
Contents |
Industrial uses
Dimethylaminoethanol is used as a curing agent for polyurethanes and epoxy resins. It is also used in mass quantities for water treatment, and to some extent in the coatings industry. It is used in the synthesis of dyestuffs, textile auxiliaries, pharmaceuticals, emulsifiers, and corrosion inhibitors. It is also an additive to paint removers, boiler water and amino resins. It forms a number of salts with melting points below room temperature (ionic liquids) such as N,N-dimethylethanolammonium acetate and N,N-dimethylethanolammonium octanoate, which have been used as alternatives to conventional solvents[citation needed].
Biochemical precursor
Dimethylaminoethanol is related to choline and is a biochemical precursor to the neurotransmitter acetylcholine, and found naturally in fish like sardines and anchovies. It is reported to have nootropic effects, although research on this chemical has found both positive and negative potential results.
It is believed that dimethylaminoethanol is methylated to produce choline in the brain[1]. It is known that dimethylaminoethanol is processed by the liver into choline; however, the choline molecule is charged and cannot pass the blood-brain barrier.[citation needed]
Research
Short-term studies have shown an increase in vigilance and alertness, with a positive influence on mood.[2] Research for Attention Deficit Hyperactivity Disorder (ADHD) has been promising, though inconclusive.[3] Long-term studies are equivocal. Some showed dimethylaminoethanol to increase the lifespan of animals in which it was tested, while others indicate a possible reduction in the average life span of quail.[4]
See also
References
- ^ Zahniser NR, Chou D, Hanin I (March 1977). "Is 2-dimethylaminoethanol (deanol) indeed a precursor of brain acetylcholine? A gas chromatographic evaluation". J. Pharmacol. Exp. Ther. 200 (3): 545–59. PMID 850128. http://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=850128.
- ^ Dimpfel W, Wedekind W, Keplinger I (May 2003). "Efficacy of dimethylaminoethanol (DMAE) containing vitamin-mineral drug combination on EEG patterns in the presence of different emotional states". Eur. J. Med. Res. 8 (5): 183–91. PMID 12844472.
- ^ Knobel M (1974). "Approach to a combined pharmacologic therapy of childhood hyperkinesis". Behav Neuropsychiatry 6 (1-12): 87–90. PMID 4619768.
- ^ Cherkin A, Exkardt MJ (January 1977). "Effects of dimethylaminoethanol upon life-span and behavior of aged Japanese quail". J Gerontol 32 (1): 38–45. PMID 830732. http://geronj.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=830732.
Studies
- Earliest research
- Pfeiffer CC, Jenney EH, Gallagher W, et al. (September 1957). "Stimulant effect of 2-dimethylaminoethanol; possible precursor of brain acetylcholine". Science 126 (3274): 610–1. PMID 13467254. http://www.sciencemag.org/cgi/pmidlookup?view=long&pmid=13467254.
- As a treatment for tardive dyskinesia
- As an unsuccessful treatment for Alzheimer's disease
- Fisman M, Mersky H, Helmes E (July 1981). "Double-blind trial of 2-dimethylaminoethanol in Alzheimer's disease". Am J Psychiatry 138 (7): 970–2. PMID 7020434. http://ajp.psychiatryonline.org/cgi/pmidlookup?view=long&pmid=7020434.
|
|||||||||||||||||||||||||||||||||||||
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)




