Pular para o conteúdo
Merck
Todas as fotos(3)

Documentos Principais

Visualizar Toda a Documentação

P6513

Sigma-Aldrich

2-Phenylethylamine hydrochloride

≥98%

Sinônimo(s):

β-Phenylethylamine hydrochloride, Phenethylamine hydrochloride

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(3)

About This Item

Fórmula linear:
C6H5CH2CH2NH2 · HCl
Número CAS:
156-28-5
Peso molecular:
157.64
Beilstein:
3624163
Número CE:
205-849-2
Número MDL:
MFCD00012893
Código UNSPSC:
12352100
ID de substância PubChem:
57654546
NACRES:
NA.22

Ensaio

≥98%

Formulário

powder

pf

220-222 °C (lit.)

cadeia de caracteres SMILES

Cl.NCCc1ccccc1

InChI

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

chave InChI

SKHIBNDAFWIOPB-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Categorias relacionadas

Descrição geral

2-Phenylethylamine hydrochloride is a biogenic aromatic amine.

Aplicação

  • Multifunctional organic electrolyte additive for batteries: Research outlined a novel application of 2-Phenylethylamine hydrochloride in developing a multifunctional organic electrolyte additive for aqueous zinc ion batteries, enhancing the performance of polyaniline cathodes (Wang et al., 2023).

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H315,H319,H335

Classificações de perigo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
SLCL0768
SLCK6285
SLCH9843
SLCF4354
SLCC5177

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 6

1 of 6

Phenethyl-1,1,2,2-d4-amine 98 atom % D, 98% (CP)

Sigma-Aldrich

615897

Phenethyl-1,1,2,2-d4-amine

Phenethylammonium iodide

Sigma-Aldrich

805904

Phenethylammonium iodide

Cadaverine dihydrochloride ~98%

Sigma-Aldrich

C8561

Cadaverine dihydrochloride

Cadaverine dihydrochloride ≥99.0% (AT)

Sigma-Aldrich

33220

Cadaverine dihydrochloride

Histamine dihydrochloride ≥99% (TLC), powder

Sigma-Aldrich

H7250

Histamine dihydrochloride

Benzylamine hydrochloride

Sigma-Aldrich

B5136

Benzylamine hydrochloride

Simultaneous analysis of biogenic amines in canned fish by HPLC.
Yen GC & Hsieh CL
Journal of Food Science, 56(1), 158-160 (1991)
Calix [5] arene-based heteroditopic receptor for 2-phenylethylamine hydrochloride
Gargiulli C, et al.
The Journal of Organic Chemistry, 74(11), 4350-4353 (2009)
Elena Cichero et al.
Chemical biology & drug design, 81(4), 509-516 (2012-08-14)
Trace amine-associated receptor 1 (TAAR1) is a G protein-coupled receptor that belongs to the family of TAAR receptors and responds to a class of compounds called trace amines, such as β-phenylethylamine (β-PEA) and 3-iodothyronamine (T(1)AM). The receptor is known to
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
Shinsuke Inagaki et al.
Drug testing and analysis, 4(12), 1001-1008 (2012-03-13)
A rapid enantiomeric separation and simultaneous determination method based on ultra high performance liquid chromatography (UHPLC) was developed for phenethylamine-type abused drugs using (R)-(-)-4-(N,N-dimethylaminosulfonyl)-7-(3-isothiocyanatopyrrolidin-1-yl)-2,1,3-benzoxadiazole ((R)-(-)-DBD-Py-NCS) as the chiral fluorescent derivatization reagent. The derivatives were rapidly enantiomerically separated by reversed-phase UHPLC
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica