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
Beilstein:
1730786
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
SMILES string
CCNC
InChI
1S/C3H9N/c1-3-4-2/h4H,3H2,1-2H3
InChI key
LIWAQLJGPBVORC-UHFFFAOYSA-N
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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.
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Signal Word
Danger
Hazard Statements
Precautionary Statements
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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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)
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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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
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