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128945

Sigma-Aldrich

Phenethylamine

99%

Sinonimo/i:

2-Phenethylamine, β-Phenylethylamine, 2-Phenylethylamine

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About This Item

Formula condensata:
C6H5CH2CH2NH2
Numero CAS:
64-04-0
Peso molecolare:
121.18
Beilstein:
507488
Numero CE:
200-574-4
Numero MDL:
MFCD00008184
Codice UNSPSC:
12352100
ID PubChem:
24847881
NACRES:
NA.22

Densità del vapore

4.18 (vs air)

Livello qualitativo

200

Saggio

99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.533 (lit.)

P. eboll.

197-200 °C (lit.)

Densità

0.962 g/mL at 20 °C (lit.)

Gruppo funzionale

amine

Stringa SMILE

NCCc1ccccc1

InChI

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

Informazioni sul gene

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

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Categorie correlate

Applicazioni

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

Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H290,H301,H314

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

177.8 °F - closed cup

Punto d’infiammabilità (°C)

81 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBK4536
STBK2756
STBK1044
STBJ4084
STBJ1131

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Sigma-Aldrich

P32406

3-Phenyl-1-propylamine

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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