291145
N-乙基甲基胺
97%
别名:
N-甲基乙胺, NMEA
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关于此项目
线性分子式:
C2H5NHCH3
化学文摘社编号:
分子量:
59.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-862-1
Beilstein/REAXYS Number:
1730786
MDL number:
Assay:
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%
Quality Level
bp
36-37 °C (lit.)
density
0.688 g/mL at 25 °C (lit.)
functional group
amine
storage temp.
2-8°C
General description
鸟苷-5′-磷酸-2-甲基咪唑内酯与N-二乙基甲基胺丙氨酸的反应动力学已在37℃的水中进行了研究。
Application
通过与丙烯酰氯反应，N-乙基甲胺已用于合成 N-乙基甲基丙烯酰胺。
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A
存储类别
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
法规信息
危险化学品
此项目有
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
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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