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Merck
CN

C65408

2-(4-Chlorophenyl)ethylamine

98%

Synonym(s):

4-Chlorophenethylamine

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About This Item

Linear Formula:
ClC6H4CH2CH2NH2
CAS Number:
156-41-2
Molecular Weight:
155.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24892877
EC Number:
205-853-4
Beilstein/REAXYS Number:
508247
MDL number:
MFCD00008191
Assay:
98%
Form:
liquid

Key Documents

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InChI

1S/C8H10ClN/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2

InChI key

SRXFXCKTIGELTI-UHFFFAOYSA-N

SMILES string

NCCc1ccc(Cl)cc1

assay

98%

form

liquid

Quality Level

100

bp

60-65 °C/0.1 mmHg (lit.)

density

1.112 g/mL at 25 °C (lit.)

drug control

Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

222.8 °F - closed cup

flash_point_c

106 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBM3949
SHBD0161V
65997PJV
65997PJ
04404EH

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E Chung Hwang et al.
The Journal of pharmacology and experimental therapeutics, 213(2), 254-260 (1980-05-01)
A series of substituted phenylethylamines were examined for their relative potencies to 1) release and inhibit accumulation of labeled serotonin in brain synaptosomes, 2) compete with serotonin receptor binding and 3) induce the "serotonin syndrome" in mice. In general, the
T N Mellin et al.
The American journal of tropical medicine and hygiene, 32(1), 83-93 (1983-01-01)
Neuropharmacological studies of Schistosoma mansoni were conducted in vitro using visual observations of motor activity and measurements of worm length and extracellular electrical activity. The instrumentation and methodology described quantitatively measure extracellular electrical potentials associated with motor activity, and provide
Khalid Touiki et al.
Psychopharmacology, 182(4), 562-569 (2005-09-01)
Harmane and norharmane (two beta-carbolines) are tobacco components or products. The effects of harmane and norharmane on serotonergic raphe neurons remain unknown. Harmane and norharmane are inhibitors of the monoamine oxidases A (MAO-A) and B (MAO-B), respectively. To study the
Giulia Guiducci et al.
Nucleic acids research, 47(8), 4240-4254 (2019-02-28)
Enzymes of intermediary metabolism are often reported to have moonlighting functions as RNA-binding proteins and have regulatory roles beyond their primary activities. Human serine hydroxymethyltransferase (SHMT) is essential for the one-carbon metabolism, which sustains growth and proliferation in normal and
G B Baker et al.
Progress in neuro-psychopharmacology & biological psychiatry, 6(4-6), 343-346 (1982-01-01)
1. The accumulation of p-chlorophenylethylamine (pCPE) in rat brain after administration of pargyline plus p-chlorophenylalanine (pCPA) is demonstrated. 2. Measurements of pCPE in brain were performed at 0.25 h, 1 h and 4 h after administration of pCPA to pargyline-pretreated
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