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241008

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:
24854450
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.)

solubility

alcohol: freely soluble(lit.)
diethyl ether: freely soluble(lit.)
water: soluble(lit.)

density

0.962 g/mL at 20 °C (lit.)

functional group

amine
phenyl

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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General description

Phenethylamine, a new stimulant designer drug, was analyzed by the liquid chromatography high-resolution mass spectrometry quadrupole-time-of-flight (LC-HRMS-QTOF) method.

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBL1546
STBK4536
STBK2756
STBK1044
STBJ4084

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Michael Paul et al.
Analytical and bioanalytical chemistry, 406(18), 4425-4441 (2014-05-16)
The development of a liquid chromatography high-resolution mass spectrometry quadrupole-time-of-flight (LC-HRMS-QTOF) method for the analysis of new stimulant designer drugs (e.g. phenethylamine, amphetamine, cathinone and piperazine derivatives) and common drugs of abuse (e.g. ketamine and ritalinic acid) in urine is
Nickolaj J Petersen et al.
Electrophoresis, 33(6), 1021-1031 (2012-04-25)
The traditional way of calculating mobility and peak areas in capillary electrophoresis does not take into account the changes in the buffer viscosity at different thermostatic control and that the analytes may accelerate during the individual runs due to Joule
Ke-Jing Huang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(9-10), 579-584 (2011-02-15)
A simple and efficient method, ionic liquid-based ultrasound-assisted liquid-liquid microextraction, has been developed for the determination of three biogenic amines including octopamine (OCT), tyramine (TYR) and phenethylamine (PHE). Fluorescence probe 2,6-dimethyl-4-quinolinecarboxylic acid N-hydroxysuccinimide ester was applied for derivatization of biogenic
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
David M Ferrero et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(27), 11235-11240 (2011-06-22)
Predator-prey relationships provide a classic paradigm for the study of innate animal behavior. Odors from carnivores elicit stereotyped fear and avoidance responses in rodents, although sensory mechanisms involved are largely unknown. Here, we identified a chemical produced by predators that
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