Dictionary:
eth·a·nol·a·mine (ĕth'ə-nŏl'ə-mēn', -nō'lə-) ![]() |
| 5min Related Video: ethanolamine |
| Chemistry Dictionary: ethanolamine |
Any of three low-melting hygroscopic colourless solids. They are strong bases, smell of ammonia, and absorb water readily to form viscous liquids. Monoethanolamine, HOCH2CH2NH2, is a primary amine, m.p. 10.5°C; diethanolamine, (HOCH2CH2)2NH, is a secondary amine, m.p. 28°C; and triethanolamine, (HOCH2CH2)3N, is a tertiary amine, m.p. 21°C. All are made by heating ethylene oxide with concentrated aqueous ammonia under pressure and separating the products by fractional distillation. With fatty acids they form neutral soaps, used as emulsifying agents and detergents, and in bactericides and cosmetics.
| Food and Nutrition: ethanolamine |
One of the water-soluble bases of phospholipids, chemically it is 2-aminoethanol. Used as softening agent for hides, as dispersing agent for agricultural chemicals, and to peel fruits and vegetables.
| Veterinary Dictionary: ethanolamine |
A colorless, moderately viscous liquid with an ammoniacal odor contained in cephalins and phospholipids, and derived metabolically by decarboxylation of serine.
| Wikipedia: Ethanolamine |
| Ethanolamine | |
|---|---|
| IUPAC name |
2-Aminoethanol
|
| Other names | 2-Amino-l-Ethanol, Ethanolamine, Monoethanolamine, β-Aminoethanol, β-hydroxyethylamine, β-Aminoethyl alcohol, Glycinol, Olamine, MEA, UN 2491 |
| Identifiers | |
| CAS number | 141-43-5 |
| PubChem | 700 |
| EC number | 205-483-3 |
| KEGG | C00189 |
| ChEBI | 16000 |
| RTECS number | KJ5775000 |
| SMILES |
NCCO
|
| InChI |
1/C2H7NO/c3-1-2-4/h4H,1-3H2
|
| Properties | |
| Molecular formula | C2H7NO |
| Molar mass | 61.08 g/mol |
| Appearance | Viscous colourless liquid with ammonia odour |
| Density | 1.012 g/cm3 |
| Melting point |
10.3°C |
| Boiling point |
170°C |
| Solubility in water | Miscible |
| Vapor pressure | 25 Pa (20°C) |
| Hazards | |
| MSDS | ScienceLab.com |
| R-phrases | R20, R34, R36/37/38 |
| S-phrases | S26, S27, S36/37, S39, S45 |
| NFPA 704 | |
| Flash point | 85°C c.c. |
| Autoignition temperature |
410°C |
| Explosive limits | 5.5 - 17% |
| U.S. Permissible exposure limit (PEL) |
3 ppm |
| Related compounds | |
| Related compounds | N-Methylethanolamine diethanolamine triethanolamine |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
|
| Infobox references | |
Ethanolamine, also called 2-aminoethanol or monoethanolamine (often abbreviated as ETA or MEA), is an organic chemical compound that is both a primary amine (due to an amino group in its molecule) and a primary alcohol (due to a hydroxyl group). Like other amines, monoethanolamine acts as a weak base. Ethanolamine is a toxic, flammable, corrosive, colorless, viscous liquid with an odor similar to that of ammonia. Refractive index of ethanolamine is 1.4539.
Ethanolamine is commonly called monoethanolamine or MEA in order to be distinguished from diethanolamine (DEA) and triethanolamine (TEA). Ethanolamine is the second-most-abundant head group for phospholipids, substances found in biological membranes.
Contents |
Monoethanolamine is produced by reacting ethylene oxide with aqueous ammonia; the reaction also produces diethanolamine and triethanolamine. The ratio of the products can be controlled by changing the stoichiometry of the reactants.[1]
Note that this reaction is exothermic and that controls are needed to prevent a runaway reaction.
MEA is used in aqueous solutions for scrubbing certain acidic gases. It is used as feedstock in the production of detergents, emulsifiers, polishes, pharmaceuticals, corrosion inhibitors, chemical intermediates.[1][2] For example, reacting ethanolamine with ammonia gives the commonly used chelating agent, ethylenediamine:[1]
In pharmaceutical formulations, MEA is primarily used for buffering or preparation of emulsions.[citation needed]
Aqueous solutions of MEA (solutions of MEA in water) are used as a gas stream scrubbing liquid in amine treaters. For example, aqueous MEA is used to remove carbon dioxide (CO2) from flue gas. Aqueous solutions can weakly dissolve certain kinds of gases from a mixed gas stream. The MEA in such solutions, acting as a weak base, then neutralizes acidic compounds dissolved in the solution to turn the molecules into an ionic form, making them polar and considerably more soluble in a cold MEA solution, and thus keeping such acidic gases dissolved in this gas-scrubbing solution. Therefore, large surface area contact with such a cold scrubbing solution in a scrubber unit can selectively remove such acidic components as hydrogen sulfide (H2S) and CO2 from some mixed gas streams. For example, basic solutions such as aqueous MEA or aqueous potassium carbonate can neutralize H2S into hydrosulfide ion (HS-) or CO2 into bicarbonate ion (HCO3-).
H2S and CO2 are only weakly-acidic gases. An aqueous solution of a strong base such as sodium hydroxide (NaOH) will not readily release these gases once they have dissolved. However, MEA is rather weak base and will re-release H2S or CO2 when the scrubbing solution is heated. Therefore, the MEA scrubbing solution is recycled through a regeneration unit, which heats the MEA solution from the scrubber unit to release these only slightly-acidic gases into a purer form and returns the regenerated MEA solution to the scrubber unit again for reuse.
Ethanolamine is often used for alkalinization of water in steam cycles of power plants, including nuclear power plants with pressurized water reactors. This alkalinization is performed to control corrosion of metal components. ETA (or sometimes a similar organic amine, e.g., morpholine) is selected because it does not accumulate in steam generators (boilers) and crevices due to its volatility, but rather distributes relatively uniformly throughout the entire steam cycle. In such application, ETA is a key ingredient of so-called "all-volatile treatment" of water (AVT).
| This article needs additional citations for verification. Please help improve this article by adding reliable references. Unsourced material may be challenged and removed. (May 2008) |
|
|||||
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
| phosphatidylethanolamine | |
| olamine | |
| trimethobenzamide |
| What is the difference between ammonia and Ethanolamine? Read answer... |
| What is the reaction of phosphoric acid and ethanolamine? | |
| Ethanolamine role in reaction of hydantoin with benzaldehyde? | |
| Is ethanolamine another name for ethylenediamine dihydrochloride? |
Copyrights:
![]() | Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved. Read more | |
![]() | Chemistry Dictionary. A Dictionary of Chemistry. Sixth Edition. Copyright © Market House Books Ltd, 2008. All rights reserved. Read more | |
![]() | Food and Nutrition. A Dictionary of Food and Nutrition. Copyright © 1995, 2003, 2005 by A. E. Bender and D. A. Bender. All rights reserved. Read more | |
![]() | Veterinary Dictionary. Saunders Comprehensive Veterinary Dictionary 3rd Edition. Copyright © 2007 by D.C. Blood, V.P. Studdert and C.C. Gay, Elsevier. All rights reserved. Read more | |
![]() | Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Ethanolamine". Read more |