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C4265

Sigma-Aldrich

p-Chloro-β-methylphenethylamine hydrochloride

≥98%

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About This Item

Empirical Formula (Hill Notation):
C9H12ClN · HCl
CAS Number:
4806-79-5
Molecular Weight:
206.11
EC Number:
225-365-5
MDL number:
MFCD00056126
UNSPSC Code:
12352100
PubChem Substance ID:
57654014
NACRES:
NA.22

Assay

≥98%

form

powder

storage temp.

2-8°C

SMILES string

Cl[H].CC(CN)c1ccc(Cl)cc1

InChI

1S/C9H12ClN.ClH/c1-7(6-11)8-2-4-9(10)5-3-8;/h2-5,7H,6,11H2,1H3;1H

InChI key

RTPMRVSAKBTCBG-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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H Kinemuchi et al.
Research communications in chemical pathology and pharmacology, 54(1), 125-128 (1986-10-01)
In order to develop new and potent reversible MAO-B-selective inhibitors, we examined the inhibitory effects of two substrate-analogues, 5-fluoro-alpha-methyltryptamine (5-FMT) and p-chloro-beta-methylphenethylamine (p-CMP) on rat brain MAO-A and -B activity in vitro. Studies of the inhibitory effects of both analogues
H Kinemuchi et al.
Japanese journal of pharmacology, 46(2), 197-199 (1988-02-01)
To further clarify highly MAO-A- or -B-selective inhibitory properties of 5-fluoro-alpha-methyltryptamine (5-FMT) and p-chloro-beta-methylphenethylamine (p-CMPEA), we determined the types and K1 values of inhibition of rat brain MAO-A and -B activity in vitro. The kinetic data obtained showed that 5-FMT
S K Kim et al.
Neuropharmacology, 30(4), 329-335 (1991-04-01)
Various intraperitoneal doses of 5-fluoro-alpha-methyltryptamine (5-FMT), given to mice, dose-dependently inhibited only MAOA activity, with similar degrees of inhibition in the striatum, hypothalamus and the rest of the forebrain. The activity inhibited in these regions, completely recovered to control levels

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