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Merck

P6513

Sigma-Aldrich

2-Phenylethylamine hydrochloride

≥98%

Sinónimos:

β-Phenylethylamine hydrochloride, Phenethylamine hydrochloride

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About This Item

Fórmula lineal:
C6H5CH2CH2NH2 · HCl
Número de CAS:
Peso molecular:
157.64
Beilstein/REAXYS Number:
3624163
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98%

form

powder

mp

220-222 °C (lit.)

SMILES string

Cl.NCCc1ccccc1

InChI

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

InChI key

SKHIBNDAFWIOPB-UHFFFAOYSA-N

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General description

2-Phenylethylamine hydrochloride is a biogenic aromatic amine.

Application

  • 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).

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

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


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Los clientes también vieron

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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

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