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291145

Sigma-Aldrich

N-Ethylmethylamine

97%

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Synonym(s):
N-Methylethylamine, NMEA
Linear Formula:
C2H5NHCH3
CAS Number:
624-78-2
Molecular Weight:
59.11
Beilstein:
1730786
EC Number:
210-862-1
MDL number:
MFCD00009030
PubChem Substance ID:
24857515
NACRES:
NA.22

vapor pressure

8.53 psi ( 20 °C)

Quality Level

200

Assay

97%

refractive index

n20/D 1.374 (lit.)

bp

36-37 °C (lit.)

density

0.688 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCNC

InChI

1S/C3H9N/c1-3-4-2/h4H,3H2,1-2H3

InChI key

LIWAQLJGPBVORC-UHFFFAOYSA-N

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1 of 4

This Item
549134147400B25606
N-Ethylmethylamine 97%

Sigma-Aldrich

291145

N-Ethylmethylamine

1-(4-Methylphenyl)ethylamine 96%

Sigma-Aldrich

549134

1-(4-Methylphenyl)ethylamine

N-Ethylacetamide 99%

Sigma-Aldrich

147400

N-Ethylacetamide

N-Benzylmethylamine 97%

Sigma-Aldrich

B25606

N-Benzylmethylamine

refractive index

n20/D 1.374 (lit.)

refractive index

n20/D 1.5210 (lit.)

refractive index

n20/D 1.433 (lit.)

refractive index

n20/D 1.522 (lit.)

bp

36-37 °C (lit.)

bp

211-212 °C (lit.)

bp

90-92 °C/8 mmHg (lit.)

bp

184-189 °C (lit.)

density

0.688 g/mL at 25 °C (lit.)

density

0.926 g/mL at 25 °C (lit.)

density

0.924 g/mL at 25 °C (lit.)

density

0.939 g/mL at 25 °C (lit.)

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

-

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

General description

The kinetics of reaction of guanosine 5′-phospho-2-methylimidazolide with N-ethylmethylamine has been studied in water at 37°C.

Application

N-Ethylmethylamine has been used in the synthesis of N-ethylmethylacrylamide via reaction with acryloyl chloride.

related product

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

-29.2 °F - closed cup

Flash Point(C)

< -34 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Zhigang Li et al.
Chemosphere, 212, 872-880 (2018-09-09)
In this study, the molecularly imprinted polymers (MIPs) with high specific surface area and extraction efficiency of N-Nitrosodiphenylamine (NDPhA) were successfully prepared and a highly sensitive and selective method was developed for determination of NDPhA in water samples using MIPs
Xianze Wang et al.
Journal of environmental sciences (China), 50, 65-71 (2016-12-31)
The presence of mutagenic and carcinogenic nitrosamines in water is of great concern. In this study, seven nitrosamines including N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA), N-nitrosomethylethylamine (NMEA), N-nitrosopyrrolidine (NPyr), N-nitrosopiperidine (NPip), N-nitrosodi-n-propylamine (NDPA), and N-nitrosodi-n-butyl-amine (NDBA) were investigated in river water and
Synthesis of low-polydispersity poly (N-ethylmethylacrylamide) by controlled radical polymerizations and their thermal phase transition behavior.
Xu J, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(1), 60-69 (2008)
A Kanavarioti et al.
The Journal of organic chemistry, 60(3), 632-637 (1995-02-10)
Aliphatic amines react with phosphoimidazolide-activated derivatives of guanosine and cytidine (ImpN) by replacing the imidazole group. The kinetics of reaction of guanosine 5'-phospho-2-methylimidazolide (2-MeImpG) with glycine ethyl ester, glycinamide, 2-methoxyethylamine, n-butylamine, morpholine, dimethylamine (Me2NH), ethylmethylamine (EtNHMe), diethylamine (Et2NH), pyrrolidine, and
Sidsel D Schrøder et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 173, 201-206 (2016-11-05)
Absolute intensities of NH-stretching fundamental and overtone transitions of gas phase aniline, methylamine, ethylamine, cyclopropylamine, methylethylamine, diethylamine and pyrrolidine have been measured with long path length conventional absorption spectroscopy. To support the assignments of NH-stretching transitions, transition frequencies and intensities
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