68625
N-Methyl-phenethylamine
purum, ≥96.0% (GC)
Synonym(s):
N-Methyl-2-phenylethylamine
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About This Item
Linear Formula:
C6H5CH2CH2NHCH3
CAS Number:
Molecular Weight:
135.21
EC Number:
209-632-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
636347
MDL number:
grade
purum
assay
≥96.0% (GC)
refractive index
n20/D 1.516
bp
203 °C (lit.)
density
0.93 g/mL at 25 °C (lit.)
SMILES string
CNCCc1ccccc1
InChI
1S/C9H13N/c1-10-8-7-9-5-3-2-4-6-9/h2-6,10H,7-8H2,1H3
InChI key
SASNBVQSOZSTPD-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
163.4 °F - closed cup
flash_point_c
73 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Xulin Tan et al.
Journal of separation science, 30(12), 1888-1892 (2007-07-20)
A novel chiral stationary phase (CSP) for HPLC was prepared by bonding (R)-1-phenyl-2-(4-methylphenyl)ethylamine amide derivative of (S)-valine to aminopropyl silica gel through a 2-amino-3,5-dinitro-1-carboxamido-benzene unit. The CSP was used for the separation of some amino acid derivatives and pyrethroid insecticides
D Reid et al.
Pharmacology, biochemistry, and behavior, 24(6), 1547-1553 (1986-06-01)
The discriminative stimulus (cue) properties of phenylethylamine (PEA) were analysed in rodents in a conventional two lever FR10 operant drug discrimination task. Rats trained to discriminate phenylethylamine at 30 mg/kg showed complete dose-related generalization to PEA and to two potential
K A Moore et al.
Drug and alcohol dependence, 39(2), 83-89 (1995-08-01)
Methamphetamine is a popular drug of abuse, readily synthesized in clandestine laboratories. Illicitly obtained methamphetamine is frequently impure, containing various purposefully added diluents and adulterants, as well as impurities of manufacture and origin. Few impurities have been studied in vivo
Aron D Mosnaim et al.
Neurochemical research, 38(4), 842-846 (2013-02-08)
Phenylethylamine and its monomethylated derivatives p-methylphenylethylamine, α-methylphenylethylamine, phenylethylamine itself, N-methylphenylethylamine, o-methylphenylethylamine, and β-methylphenylethylamine, readily cross the blood-brain barrier showing a brain-uptake index (%) ± SD (water considered 100 %), of 108 ± 11, 98 ± 14, 83 ± 6, 78
H E Shannon et al.
The Journal of pharmacology and experimental therapeutics, 222(1), 52-60 (1982-07-01)
beta-Phenylethylamine and phenylethanolamine are biogenic amines structurally related to amphetamine which are known to occur endogenously in trace amounts in mammalian brain. The purpose of the present experiments was to determine whether these endogenous biogenic amines, like amphetamine, have reinforcing
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