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128945

Sigma-Aldrich

Phenethylamine

99%

Synonym(s):

2-Phenethylamine, β-Phenylethylamine, 2-Phenylethylamine

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About This Item

Linear Formula:
C6H5CH2CH2NH2
CAS Number:
64-04-0
Molecular Weight:
121.18
Beilstein:
507488
EC Number:
200-574-4
MDL number:
MFCD00008184
UNSPSC Code:
12352100
PubChem Substance ID:
24847881
NACRES:
NA.22

vapor density

4.18 (vs air)

Assay

99%

form

liquid

refractive index

n20/D 1.533 (lit.)

bp

197-200 °C (lit.)

density

0.962 g/mL at 20 °C (lit.)

SMILES string

NCCc1ccccc1

InChI

1S/C8H11N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6-7,9H2

InChI key

BHHGXPLMPWCGHP-UHFFFAOYSA-N

Gene Information

human ... AOC3(8639)
mouse ... Aoc3(11754)
rat ... Htr2a(29595)

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Application

Phenethylamine was used to study the mass spectra of [2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2,3-methylenedioxyphenyl)methyl]ethanamine], a psychoactive substance.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H290,H301,H314

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

Flash Point(F)

177.8 °F - closed cup

Flash Point(C)

81 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Douwe de Boer et al.
Pharmacy world & science : PWS, 26(2), 110-113 (2004-04-17)
To collect data related to phenethylamine drugs-of-abuse of the 2C-series, to review possible health risks of their use and to discuss legal counter actions of authorities in the European Union (EU). Dutch smartshops. In the period of 1994-2002, all products
Deepak Narang et al.
The Journal of pharmacology and experimental therapeutics, 351(1), 164-171 (2014-08-15)
The trace amine β-phenylethylamine (PEA) is normally present in the body at low nanomolar concentrations but can reach micromolar levels after ingestion of drugs that inhibit monoamine oxidase and primary amine oxidase. In vivo, PEA elicits a robust pressor response
Christian Brand et al.
The journal of physical chemistry. A, 115(34), 9612-9619 (2011-04-20)
A remarkable influence of the orientation of a polar side chain on the direction of the S(1) ← S(0) transition dipole moment of monosubstituted benzenes was previously reported from high-resolution electronic spectroscopy. In search for a more general understanding of
José L García Ruano et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(22), 6142-6147 (2011-04-15)
The preparation of a stabilized monofluorobenzyl carbanion by means of a remote homochiral sulfinyl group and its completely stereoselective reactions with N-p-tolylsulfinylimines are described. The use of these reactions followed by the simultaneous removal of both chiral auxiliaries with tBuLi
Xin-Long Ni et al.
Organic & biomolecular chemistry, 10(23), 4618-4626 (2012-05-17)
The lower rim functionalized hexahomotrioxacalix[3]arene derivatives cone-3 and cone-5 bearing three benzyl and three N,N-diethyl-2-aminoethoxy groups, respectively, were synthesized from triol 1. Their complexation with 2-(3,4-dihydroxyphenyl)ethylamine (dopamine), 5-hydroxytryptamine (serotonin), and 2-phenylethylamine (phenethylamine), which have biologically important activities, has been studied
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