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Merck
CN

523801

N,N-Dimethylphenethylamine

98%

Synonym(s):

2-Phenylethyl-N,N-dimethylamine, Dimethyl(2-phenylethyl)amine, N,N-Dimethyl-β-phenethylamine, N,N-Dimethyl-2-phenylethylamine, N,N-Dimethylbenzeneethanamine, N,N-Dimethylphenylethylamine, N-(2-Phenylethyl)dimethylamine, N-Phenethyldimethylamine, [(Dimethylamino)ethyl]benzene

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About This Item

Linear Formula:
C6H5CH2CH2N(CH3)2
CAS Number:
1126-71-2
Molecular Weight:
149.23
NACRES:
NA.22
PubChem Substance ID:
24874370
UNSPSC Code:
12352100
MDL number:
MFCD00177940

Key Documents

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Product Name

N,N-Dimethylphenethylamine, 98%

InChI

1S/C10H15N/c1-11(2)9-8-10-6-4-3-5-7-10/h3-7H,8-9H2,1-2H3

SMILES string

CN(C)CCc1ccccc1

InChI key

TXOFSCODFRHERQ-UHFFFAOYSA-N

assay

98%

refractive index

n20/D 1.502 (lit.)

bp

207-212 °C (lit.)

density

0.89 g/mL at 25 °C (lit.)

functional group

amine
phenyl

Quality Level

100

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

159.8 °F - closed cup

flash_point_c

71 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

监管及禁止进口产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000234474
0000234474
0000210518
0000206206
0000210518

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S Shirolkar et al.
Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics, 11(1), 41-47 (1995-01-01)
In an effort to develop a long-term topically active tear stimulant, it was important to determine if tolerance developed following the repeated instillation of N,N-Dimethyl-2-phenylethylamine hydrochloride (AF2975) to the albino rabbit eye. New Zealand white rabbits were administered AF2975 (0.15%)
O Inoue et al.
Journal of neurochemistry, 44(1), 210-216 (1985-01-01)
N-[methyl-14C]N,N-dimethylphenylethylamine (DMPEA) was synthesized and its availability as a selective radiotracer for in vivo measurement of mouse brain monoamine oxidase (MAO) activity was examined. Relatively high incorporation of labelled DMPEA into brain (about 10% of the injected dose/per gram of
R D Schoenwald et al.
Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics, 14(3), 253-262 (1998-07-22)
Acini cells were obtained from the lacrimal gland of the white New Zealand rabbit. Following isolation and purification, the cells were used to study the uptake of N,N'-dimethyl-2-phenylethylamine HCl (AF2975), which was found to be sodium- and proton-independent, but energy-dependent.
H Shinotoh et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 28(6), 1006-1011 (1987-06-01)
Carbon-11-labeled N,N-dimethylphenylethylamine ([11C]DMPEA) was synthesized by the reaction of N-methylphenylethylamine with [11C]methyl iodide. This newly synthesized radiotracer was developed for the purpose of in vivo measurement of monoamine oxidase-B activity in the brain using a metabolic trapping method. Initially, biodistribution
C Halldin et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 40(7), 557-560 (1989-01-01)
Dimethylphenethylamine (DMPA), a substrate for the B-form of the monoamine oxidase enzyme (MAO, EC 1.4.3.4), was labelled with 11C in two different positions; in the methyl group (M-DMPA) and in the phenethyl group (P-DMPA). M-DMPA was prepared by N-alkylation of
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