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Merck
CN

P2641

2-Phenethylamine

liquid

Synonym(s):

β-Phenylethylamine, 2-Phenylethylamine

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About This Item

Linear Formula:
C6H5CH2CH2NH2
CAS Number:
64-04-0
Molecular Weight:
121.18
EC Number:
200-574-4
UNSPSC Code:
12352100
PubChem Substance ID:
329820144
Beilstein/REAXYS Number:
507488
MDL number:
MFCD00008184

Key Documents

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InChI key

BHHGXPLMPWCGHP-UHFFFAOYSA-N

InChI

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

SMILES string

NCCc1ccccc1

vapor density

4.18 (vs air)

form

liquid

color

clear colorless

refractive index

n20/D 1.533 (lit.)

bp

197-200 °C (lit.)

density

0.962 g/mL at 20 °C (lit.)

storage temp.

2-8°C

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Preparation Note

Redistilled

Other Notes

This product has been replaced by 407267-ALDRICH | Phenethylamine purified by redistillation, ≥99.5%

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

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

Storage Class

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

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
068K3734
057K3722
047K3661
096K3678
056K3685

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Scott P Runyon et al.
Journal of medicinal chemistry, 51(21), 6808-6828 (2008-10-14)
The effects of 3-position substitution of 9-aminomethyl-9,10-dihydroanthracene (AMDA) on 5-HT 2A receptor affinity were determined and compared to a parallel series of DOB-like 1-(2,5-dimethoxyphenyl)-2-aminopropanes substituted at the 4-position. The results were interpreted within the context of 5-HT 2A receptor models
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
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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