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Merck
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523801

Sigma-Aldrich

N,N-Dimethylphenethylamine

98%

Sinonimo/i:

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

Formula condensata:
C6H5CH2CH2N(CH3)2
Numero CAS:
1126-71-2
Peso molecolare:
149.23
Numero MDL:
MFCD00177940
Codice UNSPSC:
12352100
ID PubChem:
24874370
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

Indice di rifrazione

n20/D 1.502 (lit.)

P. ebollizione

207-212 °C (lit.)

Densità

0.89 g/mL at 25 °C (lit.)

Gruppo funzionale

amine
phenyl

Stringa SMILE

CN(C)CCc1ccccc1

InChI

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

Categorie correlate

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

159.8 °F - closed cup

Punto d’infiammabilità (°C)

71 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
MKCG9582
MKBX8766V
MKBT8978V
MKBL7175V
MKBJ2252V

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2-Phenylethylamine for synthesis

Sigma-Aldrich

8.07334

2-Phenylethylamine

Phenethylamine 99%

Sigma-Aldrich

128945

Phenethylamine

Phenethylamine ≥99%

Sigma-Aldrich

241008

Phenethylamine

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
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
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
Leon van Haandel et al.
Bioanalysis, 3(24), 2783-2796 (2011-12-22)
Low-dose methotrexate is used for the treatment of rheumatoid arthritis and juvenile idiopathic arthritis, but its effectiveness greatly varies between individuals. Therapeutic drug monitoring of intracellular methotrexate metabolites, the γ-polyglutamates (MTXGlu(n)), in human erythrocytes has shown promise in providing a
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