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Merck
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M68423

Sigma-Aldrich

N-Methyl-phenethylamine

99%

Sinonimo/i:

N-Methyl-2-phenylethylamine

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About This Item

Formula condensata:
C6H5CH2CH2NHCH3
Numero CAS:
589-08-2
Peso molecolare:
135.21
Beilstein:
636347
Numero CE:
209-632-3
Numero MDL:
MFCD00008291
Codice UNSPSC:
12352100
ID PubChem:
24897119
NACRES:
NA.22

Saggio

99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.516 (lit.)

P. eboll.

203 °C (lit.)

Densità

0.93 g/mL at 25 °C (lit.)

Stringa SMILE

CNCCc1ccccc1

InChI

1S/C9H13N/c1-10-8-7-9-5-3-2-4-6-9/h2-6,10H,7-8H2,1H3
SASNBVQSOZSTPD-UHFFFAOYSA-N

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Applicazioni

N-Methyl-phenethylamine can be used as a reactant:
  • To synthesize N-methyl-phenethylamine based tertiary amines by reacting with different alkyl halides in the presence of triphenylphosphine (TPP) and diisopropylazocarboxylate (DIAD) via N-alkylation reaction.
  • To fabricate photochemically stable, super-sensitive, and highly selective fluorescent film for the detection of N-methamphetamine (an illicit drug).
  • To prepare biologically active squaric acid N-hydroxylamide amide derivatives.

Pittogrammi

CorrosionExclamation mark
GHS05,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H302,H318

Classi di pericolo

Acute Tox. 4 Oral - Eye Dam. 1

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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Efficient synthesis of tertiary amines from secondary amines
Michio K, et al.
Tetrahedron Letters, 47, 4871-4875 (2006)
Fabrication of a new fluorescent film and its superior sensing performance to N-methamphetamine in vapor phase
H Meixia, et al.
Sensors and Actuators B, Chemical, 227 (2016)
T D Forbes et al.
Journal of animal science, 72(2), 464-469 (1994-02-01)
Eighteen Suffolk and Suffolk x Hampshire wethers (56.3 +/- 1.3 kg) were used to determine the effects of naturally occurring amines, N-methyl-beta-phenethylamine (NMP) and tyramine (T), on plasma cortisol, norepinephrine (NE), ACTH, and GnRH-stimulated LH concentrations. In each experiment, wethers
J D Duncan et al.
Drug metabolism and disposition: the biological fate of chemicals, 11(1), 15-20 (1983-01-01)
The effects of methyl, ethyl, isopropyl, isobutyl, and benzyl substituents at the alpha-carbon of N-methyl-2-phenethylamine on the kinetics of its N-demethylation in liver microsomes from both control and phenobarbital pretreated rats were studied. In control microsomes, the kinetic studies indicated
I Osamu
European journal of nuclear medicine, 8(9), 385-388 (1983-01-01)
A new type of metabolically trapped agent for measuring regional brain function was designed and evaluated. N-methylphenylethylamine (14C-MPEA) was synthesized with trifluoroacetylphenylethylamine and 14C-methyl iodide. A high concentration of 14C-MPEA accumulated in mouse brain 1 min after injection, and radioactivities
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