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Key Documents

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M68423

Sigma-Aldrich

N-Methyl-phenethylamine

99%

Sinónimos:

N-Methyl-2-phenylethylamine

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About This Item

Fórmula lineal:
C6H5CH2CH2NHCH3
Número de CAS:
589-08-2
Peso molecular:
135.21
Beilstein/REAXYS Number:
636347
EC Number:
209-632-3
MDL number:
MFCD00008291
UNSPSC Code:
12352100
PubChem Substance ID:
24897119
NACRES:
NA.22

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.516 (lit.)

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

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Application

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.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Phenethylamine 99%

Sigma-Aldrich

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Phenethylamine

2-(p-Tolyl)ethylamine 97%

Sigma-Aldrich

132020

2-(p-Tolyl)ethylamine

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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