291145
N-Ethylmethylamine
97%
Synonym(s):
N-Methylethylamine, NMEA
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About This Item
Linear Formula:
C2H5NHCH3
CAS Number:
Molecular Weight:
59.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-862-1
Beilstein/REAXYS Number:
1730786
MDL number:
Product Name
N-Ethylmethylamine, 97%
InChI 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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Application
N-Ethylmethylamine has been used in the synthesis of N-ethylmethylacrylamide via reaction with acryloyl chloride.
General description
The kinetics of reaction of guanosine 5′-phospho-2-methylimidazolide with N-ethylmethylamine has been studied in water at 37°C.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A
Storage Class
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
Regulatory Information
危险化学品
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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
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
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)
Ya Ji et al.
Journal of hazardous materials, 368, 452-458 (2019-02-02)
Nowadays, drinking water treatment involves large usage of chloramines making control of N-nitrosamines formation very challenging. Detecting and removing N-nitrosamine precursors in water is the most effective method to reduce N-nitrosamine formation. Therefore, it is essential to develop methods to
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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