| Weight | 121.183 g/mol |
|---|---|
| Formula | C8H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Phenethylamine (64-04-0)
2-phenethylamine · phenethylamine hydrobromide · phenethylamine sulfate (2:1)
Score:
#559 in Biochemistry
,
#1679 in Biology
,
#1980 in Chemistry
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- Sigma-Aldrich - Phenethylamine20.50 - 416.50 USD
- Fisher Scientific - Search for Phenethylamine
- TCI - Phenethylamine14.00 - 70.00 USD
- Novel Dual Inhibitors of AChE and MAO Derived from Hydroxy Aminoindan and Phenethylamine as Potential Treatment for Alzheimer's Disease (Journal of Medicinal Chemistry, 2002)
- Thermodynamic and Nuclear Magnetic Resonance Study of the Interactions of .alpha.- and .beta.-Cyclodextrin with Model Substances: Phenethylamine, Ephedrines, and Related Substances (Journal of the American Chemical Society, 1995)
- Phenethylamine and related compounds in plants (Phytochemistry, 1977)
- Molecular Interaction of Serotonin 5-HT2A Receptor Residues Phe339(6.51) and Phe340(6.52) with Superpotent N-Benzyl Phenethylamine Agonists (Molecular Pharmacology, 2006)
- Liquid scintillation counting of C14O2 with phenethylamine (Analytical Biochemistry, 1961)
- LSD and the phenethylamine hallucinogen DOI are potent partial agonists at 5-HT2A receptors on interneurons in rat piriform cortex. (Journal of Pharmacology and Experimental Therapeutics, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H227: Combustible liquid
Warning Flammable liquids - Category 4 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - 2-phenethylamine
- phenethylamine hydrobromide
- phenethylamine sulfate (2:1)
- diphenethylamine sulfate
- beta-phenethylamine
- phenethylamine perchlorate
- phenethylamine tosylate
- phenethylamine, 15N-labeled cpd
- 2-phenylethylamine
- phenethylamine sulfate
- phenethylamine, monolithium salt
- 2-phenylethylammonium chloride
- phenethylamine conjugate acid
- beta-phenylethylamine
- phenethylamine mesylate
- phenethylamine, beta-(14)C-labeled cpd
- phenethylamine hydrochloride
-
SMILESC1=CC=C(C=C1)CCN
-
InChIKeyBHHGXPLMPWCGHP-UHFFFAOYSA-N
- Pubchem - Phenethylamine
- Wikipedia - phenethylamine
Phenethylamine (PEA), also known as -phenylethylamine (-PEA) and 2-phenylethan-1-amine, is an organic compound, natural monoamine alkaloid, and trace amine which acts as a central nervous system stimulant in humans. Phenylethylamine functions as a monoaminergic neuromodulator and, to a lesser extent, a neurotransmitter in the human central nervous system. It is biosynthesized from the amino acid L-phenylalanine by enzymatic decarboxylation via the enzyme aromatic L-amino acid decarboxylase.
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(60-19-5)
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(13203-39-9)
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(877-95-2)
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(2158-04-5)
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(103-63-9, 31620-80-1)
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(103-65-1)
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3 safety hazards
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(68333-89-1, 98-82-8, 68411-37-0, 101316-43-2)
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(93-88-9)
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(5969-39-1)
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2-(4-fluorophenyl)-N-methylethanamine
(459-28-9, 405-68-5)
18 alternate names
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(1629-33-0)
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(7763-96-4)
18 alternate names
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76935-60-9
(76935-60-9)
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(370-98-9)
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(10147-11-2)
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(21404-88-6)
18 alternate names
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(25550-14-5, 611-14-3 (2-ethyl toluene), 611-14-3)
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(140-29-4)
18 alternate names
3 safety hazards
3 suppliers
5468-37-1
(5468-37-1)
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hexyl(2-phenylethyl)amine
(24997-83-9)
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(404-70-6)
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3458-98-8
(3458-98-8)
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(6830-82-6)
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(102-25-0, 102806-99-5)
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(103-29-7, 38888-98-1)
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(3333-13-9)
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(3333-13-9)
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(1609401-16-2)
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(25198-48-5)
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1,2-DIETHYLBENZENE
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P-CYMENE
(99-87-6, 4939-75-7, 25155-15-1)
18 alternate names
2 safety hazards
3 suppliers
1,4-DIISOPROPYLBENZENE
(100-18-5)
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(13078-79-0)
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(23068-44-2)
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(98-84-0, 618-36-0)
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3-(4-methylphenyl)propan-1-amine
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2,3,4,5-Tetrahydro-1H-benzo[d]azepine
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104-09-6
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(1081-75-0)
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tert-Butylbenzene
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1633-22-3
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4,4'-Dimethylbibenzyl
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1-ethyl-4-ethynylbenzene
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4-PHENYL-1-BUTENE
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2-bromo-N-(2-phenylethyl)acetamide
(64297-92-3)
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N-methyl-3-phenylpropan-1-amine
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Bicyclo[4.2.0]octa-1,3,5-triene
(694-87-1)
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(3-CHLOROPROPYL)BENZENE
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(13156-95-1)
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4489-84-3
(4489-84-3)
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Phenethylamine
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