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Merck

128945

Sigma-Aldrich

Phenethylamin

99%

Synonym(e):

2-Phenylethylamin, β-Phenylethylamin, 2-Phenethylamin

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About This Item

Lineare Formel:
C6H5CH2CH2NH2
CAS-Nummer:
Molekulargewicht:
121.18
Beilstein:
507488
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

4.18 (vs air)

Qualitätsniveau

Assay

99%

Form

liquid

Brechungsindex

n20/D 1.533 (lit.)

bp

197-200 °C (lit.)

Dichte

0.962 g/mL at 20 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

NCCc1ccccc1

InChI

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

InChIKey

BHHGXPLMPWCGHP-UHFFFAOYSA-N

Angaben zum Gen

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

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Anwendung

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

Piktogramme

Skull and crossbonesCorrosion

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 1

Flammpunkt (°F)

177.8 °F - closed cup

Flammpunkt (°C)

81 °C - closed cup

Persönliche Schutzausrüstung

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


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Kunden haben sich ebenfalls angesehen

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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