| Revision as of 14:39, 19 August 2014 editSmokefoot (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,251 edits reinstate this parent compound but trim back on some of the article (list of links), give a generic ref to March for imine formation, rm image of one enantiomer← Previous edit | Revision as of 14:59, 19 August 2014 edit undoSmokefoot (talk | contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,251 editsm rm uncited mention of reaction involving formic acid, probably speculationNext edit → | ||
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| '''1-Aminoethanol''' is the ] with the formula CH<sub>3</sub>CH(NH<sub>2</sub>)OH. It is classified as an ]. Specifically, it is a structural isomer of ] (ethanolamine). These two compounds differ in the position of the amino group. Since the central carbon atom in 1-aminoethanol has four different substitutents, the compound has two ], L-aminoethanol (shown) and R-aminoethanol. It is known as alanaminol because it has the same side chain as ]. Unlike 2-aminoethanol, which is of considerable importance in commerce, 1-aminoethanol is not commonly encountered as a pure material and is mainly of theoretical interest. | '''1-Aminoethanol''' is the ] with the formula CH<sub>3</sub>CH(NH<sub>2</sub>)OH. It is classified as an ]. Specifically, it is a structural isomer of ] (ethanolamine). These two compounds differ in the position of the amino group. Since the central carbon atom in 1-aminoethanol has four different substitutents, the compound has two ], L-aminoethanol (shown) and R-aminoethanol. It is known as alanaminol because it has the same side chain as ]. Unlike 2-aminoethanol, which is of considerable importance in commerce, 1-aminoethanol is not commonly encountered as a pure material and is mainly of theoretical interest. | ||
| 1-Aminoethanol exists in a solution of acetaldehyde and ammonia.<ref>{{March6th}}</ref> |
1-Aminoethanol exists in a solution of acetaldehyde and aqueous ammonia.<ref>{{March6th}}</ref> | ||
| ==References== | ==References== | ||
Revision as of 14:59, 19 August 2014
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| L-aminoethanol | |
| Names | |
|---|---|
| Systematic IUPAC name 1-Aminoethanol | |
| Other names Alanaminol, Acetaldehyde ammonia, 1-Aminoethanol | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.000.790 
|
| CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
| Properties | |
| Chemical formula | C2H7NO |
| Molar mass | 61.084 g·mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references | |
1-Aminoethanol is the organic compound with the formula CH3CH(NH2)OH. It is classified as an alkanolamine. Specifically, it is a structural isomer of 2-aminoethanol (ethanolamine). These two compounds differ in the position of the amino group. Since the central carbon atom in 1-aminoethanol has four different substitutents, the compound has two stereoisomers, L-aminoethanol (shown) and R-aminoethanol. It is known as alanaminol because it has the same side chain as alanine. Unlike 2-aminoethanol, which is of considerable importance in commerce, 1-aminoethanol is not commonly encountered as a pure material and is mainly of theoretical interest.
1-Aminoethanol exists in a solution of acetaldehyde and aqueous ammonia.
References
- Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
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