| Weight | 137.182 g/mol |
|---|---|
| Formula | C8H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
2-Amino-1-phenylethanol (4561-43-7, 7568-93-6)
beta Phenylethanolamine · 2-Hydroxyphenethylamine · beta-Hydroxyphenethylamine
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- Sigma-Aldrich - 2-Amino-1-phenylethanol95.30 - 279.50 USD
- Fisher Scientific - Search for 2-Amino-1-phenylethanol
- TCI - 2-Amino-1-phenylethanol63.00 - 196.00 USD
- Infrared Ion Dip Spectroscopy of a Noradrenaline Analogue: Hydrogen Bonding in 2-Amino-1-phenylethanol and Its Singly Hydrated Complex (Journal of Physical Chemistry A, 1999)
- Genetic regulation of the catecholamine biosynthetic enzymes. II. Inheritance of tyrosine hydroxylase, dopamine-beta-hydroxylase, and phenylethanolamine N-methyltransferase. (Journal of Biological Chemistry, 1974)
- Self-administration of the endogenous trace amines beta-phenylethylamine, N-methyl phenylethylamine and phenylethanolamine in dogs. (Journal of Pharmacology and Experimental Therapeutics, 1982)
- Activity of the enzymes dopamine-beta-hydroxylase and phenylethanolamine-N-methyltransferase in discrete brain regions of the copper-zinc deficient rat following aluminum ingestion. (Neurotoxicology, 1982)
- Immunohistochemical localization of 3 beta-hydroxysteroid/delta 5-delta 4-isomerase, tyrosine hydroxylase and phenylethanolamine N-methyl transferase in adrenal glands of sheep fetuses throughout gestation and in neonates. (Reproduction, 1992)
- Lipase catalysis in the optical resolution of 2-amino-1-phenylethanol derivatives (Journal of The Chemical Society-perkin Transactions 1, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - beta Phenylethanolamine
- 2-Hydroxyphenethylamine
- beta-Hydroxyphenethylamine
- 2-Phenylethanolamine
- beta Hydroxyphenethylamine
- beta-Phenylethanolamine
- Bisnorephedrine
- 2 Hydroxyphenethylamine
- 2 Phenylethanolamine
-
SMILESC1=CC=C(C=C1)C(CN)O
-
InChIKeyULSIYEODSMZIPX-UHFFFAOYSA-N
- Pubchem - 2-Amino-1-phenylethanol
- Wikipedia - phenylethanolamine
Phenylethanolamine (sometimes abbreviated PEOH), or -hydroxyphenethylamine, is a trace amine with a structure similar to those of other trace phenethylamines as well as the catecholamine neurotransmitters dopamine, norepinephrine, and epinephrine. As an organic compound, phenylethanolamine is a -hydroxylated phenethylamine that is also structurally related to a number of synthetic drugs in the substituted phenethylamine class. In common with these compounds, phenylethanolamine has strong cardiovascular activity and, under the name Apophedrin, has been used as a drug to produce topical vasoconstriction.
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