407275
N,N-二甲基苯胺
purified by redistillation, ≥99.5%
别名:
N,N-Dimethylaniline, N,N-Dimethylphenylamine, DMA, Dimethylaniline, Dimethylphenylamine
质量水平
方案
≥99.5%
表单
liquid
纯化方式
glass distillation
redistillation
折射率
n20/D 1.557 (lit.)
pH值(酸碱度)
7.4 (20 °C, 1.2 g/L)
沸点
193-194 °C (lit.)
mp
1.5-2.5 °C (lit.)
密度
0.956 g/mL at 25 °C (lit.)
官能团
amine
SMILES字符串
CN(C)c1ccccc1
InChI
1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3
InChI key
JLTDJTHDQAWBAV-UHFFFAOYSA-N
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一般描述
通过常规和循环伏安法对在酸性缓冲液中铂电极上N,N-二甲基苯胺的阳极氧化进行了研究。采用皮秒-飞秒激光光解和时间分辨瞬态吸收光谱研究了DMA在乙腈溶液中对兴奋二苯甲酮(BP)的光还原反应。
应用
N,N-二甲基苯胺(DMA)可用于通过DMA的阳极氧化制备聚(N,N-二甲基苯胺)膜。
警示用语:
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 2
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
167.0 °F - closed cup
闪点(°C)
75 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Electrochemically polymerized N, N-dimethylaniline film with ion-exchange properties as an electrode modifier.
Oyama N, et al.
Analytical Chemistry, 57(8), 1526-1532 (1985)
Femtosecond-picosecond laser photolysis studies on photoreduction process of excited benzophenone with N,N-dimethylaniline in acetonitrile solution.
Miyasaka H, et al.
Bulletin of the Chemical Society of Japan, 63(12), 3385-3397 (1990)
Anodic oxidation studies of N,N-dimethylaniline. I. Voltammetric and spectroscopic investigations at platinum electrodes.
Mizoguchi T and Adams RN.
Journal of the American Chemical Society, 84(11), 2058-2061 (1962)
Marius Koch et al.
Journal of the American Chemical Society, 134(8), 3729-3736 (2012-01-31)
The fluorescence quenching of 3-cyanoperylene upon electron transfer from N,N-dimethylaniline in three room-temperature ionic liquids (RTILs) and in binary solvent mixtures of identical viscosity has been investigated using steady-state and time-resolved fluorescence spectroscopy. This study was stimulated by previous reports
Yong Wang et al.
The journal of physical chemistry. B, 114(8), 2964-2970 (2010-02-12)
This paper addresses the experimentally observed mechanistic differences between the cytochrome P450-catalyzed N-demethylation of substituted N,N-dimethylanilines (DMA) and of N,N-dimethylbenzamides (DMBA). The two reactions of these substrates are initiated by C-H activation of the methyl groups on the nitrogen. Thus
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