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Merck

291145

Sigma-Aldrich

N-乙基甲基胺

97%

别名:

N-甲基乙胺, NMEA

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About This Item

线性分子式:
C2H5NHCH3
CAS号:
分子量:
59.11
Beilstein:
1730786
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽壓力

8.53 psi ( 20 °C)

化驗

97%

折射率

n20/D 1.374 (lit.)

bp

36-37 °C (lit.)

密度

0.688 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CCNC

InChI

1S/C3H9N/c1-3-4-2/h4H,3H2,1-2H3

InChI 密鑰

LIWAQLJGPBVORC-UHFFFAOYSA-N

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一般說明

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

應用

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

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

<-29.2 °F - closed cup

閃點(°C)

< -34 °C - closed cup

個人防護裝備

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
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
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

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