291145
N-Ethylmethylamine
97%
Sinónimos:
N-Methylethylamine, NMEA
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Fórmula lineal:
C2H5NHCH3
Número CAS:
Peso molecular:
59.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-862-1
Beilstein/REAXYS Number:
1730786
MDL number:
Assay:
97%
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Permítanos ayudarleInChI key
LIWAQLJGPBVORC-UHFFFAOYSA-N
InChI
1S/C3H9N/c1-3-4-2/h4H,3H2,1-2H3
SMILES string
CCNC
vapor pressure
8.53 psi ( 20 °C)
assay
97%
refractive index
n20/D 1.374 (lit.)
bp
36-37 °C (lit.)
density
0.688 g/mL at 25 °C (lit.)
functional group
amine
storage temp.
2-8°C
Quality Level
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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.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 2
flash_point_f
<-29.2 °F - closed cup
flash_point_c
< -34 °C - closed cup
ppe
Faceshields, Gloves, Goggles
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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
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
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
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