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Merck
CN

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%
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产品名称

N-乙基甲基胺, 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

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

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

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

历史批次信息供参考:

分析证书(COA)

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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
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
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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