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Merck

241008

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

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vapor density

4.18 (vs air)

Quality Level

100

description

Drug Control: Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet

Assay

≥99%

form

liquid

drug control

Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet

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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1 of 4

This Item
4072671289458.07334
Phenethylamine ≥99%

Sigma-Aldrich

241008

Phenethylamine

Phenethylamine purified by redistillation, ≥99.5%

Sigma-Aldrich

407267

Phenethylamine

Phenethylamine 99%

Sigma-Aldrich

128945

Phenethylamine

2-Phenylethylamine for synthesis

Sigma-Aldrich

8.07334

2-Phenylethylamine

assay

≥99%

assay

≥99.5%

assay

99%

assay

≥99.0% (GC)

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

solubility

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

solubility

-

solubility

-

solubility

63.25 g/L

bp

197-200 °C (lit.)

bp

197-200 °C (lit.)

bp

197-200 °C (lit.)

bp

200-202 °C/1013 hPa

refractive index

n20/D 1.533 (lit.)

refractive index

n20/D 1.533 (lit.)

refractive index

n20/D 1.533 (lit.)

refractive index

-

density

0.962 g/mL at 20 °C (lit.)

density

0.962 g/mL at 20 °C (lit.)

density

0.962 g/mL at 20 °C (lit.)

density

0.96 g/cm3 at 20 °C

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[1].

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
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
Marion Seitter et al.
International journal of food microbiology, 145(2-3), 483-487 (2011-02-22)
In connection with a study on the DNA microarray based detection of genes involved in safety and technologically relevant properties (Seitter (née Resch) et al., 2011), food-associated coagulase-negative staphylococci (CNS) were investigated phenotypically with regard to their ability to bind
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
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