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P6513

Sigma-Aldrich

2-Phenylethylamine hydrochloride

≥98%

Synonym(s):

β-Phenylethylamine hydrochloride, Phenethylamine hydrochloride

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About This Item

Linear Formula:
C6H5CH2CH2NH2 · HCl
CAS Number:
156-28-5
Molecular Weight:
157.64
Beilstein:
3624163
EC Number:
205-849-2
MDL number:
MFCD00012893
UNSPSC Code:
12352100
PubChem Substance ID:
57654546
NACRES:
NA.22

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
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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