1-Aminoethanol: Difference between revisions

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Revision as of 14:13, 19 August 2014 editSmokefoot (talk \| contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,236 edits redirect toalkanolamine as test← Previous edit		Revision as of 14:39, 19 August 2014 edit undoSmokefoot (talk \| contribs)Autopatrolled, Extended confirmed users, Pending changes reviewers, Rollbackers74,236 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 enantiomerNext edit →
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			{{notability\|\|date=August 2014}}
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			{{Chembox
			\| ImageFile = L-aminoethanol.jpg
			\| ImageSize = 200px
			\| ImageName = L-aminoethanol
			\| SystematicName = 1-Aminoethanol
			\| OtherNames = Alanaminol, Acetaldehyde ammonia, 1-Aminoethanol
			\| Section1 = {{Chembox Identifiers
			\| ChemSpiderID = 455852
			\| PubChemID = 522583
			\| InChI = 1S/C2H7NO/c1-2(3)4/h2,4H,3H2,1H3
			\| InChIKey = UJPKMTDFFUTLGM-UHFFFAOYSA-N
			\| SMILES = CC(N)O
			\| CASNo = 75-39-8
			}}
			\| Section2 = {{Chembox Properties
			\| C = 2
			\| N = 1
			\| O = 1
			\| H = 7
			\| ExactMass = 61.052764
			\| MolecularWeight = 61.08308
			}}
			}}

			'''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> ] to form the amino acid ], releasing water.

			==References==
			<references />

			]
			]

			{{alcohol-stub}}

Revision as of 14:39, 19 August 2014

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1-Aminoethanol
Names
L-aminoethanol
Systematic IUPAC name 1-Aminoethanol
Other names Alanaminol, Acetaldehyde ammonia, 1-Aminoethanol
Identifiers
CAS Number	75-39-8
3D model (JSmol)	Interactive image
ChemSpider	455852
ECHA InfoCard	100.000.790
CompTox Dashboard (EPA)	DTXSID60996495
InChI InChI=1S/C2H7NO/c1-2(3)4/h2,4H,3H2,1H3Key: UJPKMTDFFUTLGM-UHFFFAOYSA-N
SMILES CC(N)O
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

Chemical compound

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 ammonia. [[Alanaminol can react with formic acid to form the amino acid Alanine, releasing water.

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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