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Merck
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Documentos Principais

128945

Sigma-Aldrich

Phenethylamine

99%

Sinônimo(s):

2-Phenethylamine, β-Phenylethylamine, 2-Phenylethylamine

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About This Item

Fórmula linear:
C6H5CH2CH2NH2
Número CAS:
Peso molecular:
121.18
Beilstein:
507488
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

densidade de vapor

4.18 (vs air)

Ensaio

99%

Formulário

liquid

índice de refração

n20/D 1.533 (lit.)

p.e.

197-200 °C (lit.)

densidade

0.962 g/mL at 20 °C (lit.)

grupo funcional

amine
phenyl

cadeia de caracteres SMILES

NCCc1ccccc1

InChI

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

chave InChI

BHHGXPLMPWCGHP-UHFFFAOYSA-N

Informações sobre genes

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

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Aplicação

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

Pictogramas

Skull and crossbonesCorrosion

Palavra indicadora

Danger

Frases de perigo

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

177.8 °F - closed cup

Ponto de fulgor (°C)

81 °C - closed cup

Equipamento de proteção individual

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


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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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