407275
N,N-二甲基苯胺
purified by redistillation, ≥99.5%
别名:
N,N-Dimethylaniline, N,N-Dimethylphenylamine, DMA, Dimethylaniline, Dimethylphenylamine
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关于此项目
线性分子式:
C6H5N(CH3)2
化学文摘社编号:
分子量:
121.18
Beilstein:
507140
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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
此项目有
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)
Molecular fibers and wires in solid-state and solution self-assemblies of cyclodextrin [2]rotaxanes.
Subashani Maniam et al.
Organic letters, 10(10), 1885-1888 (2008-04-16)
Cyclodextrin [2]rotaxanes have been prepared by coupling dimethylanilines with dicarboxylic acids using DMT-MM, in aqueous solutions of alpha-cyclodextrin, and the example illustrated shows unusual fluorescence emission and other spectroscopic behavior characteristic of the formation of molecular wires in solution, similar
Kenji Hirai et al.
Chemical communications (Cambridge, England), 48(52), 6472-6474 (2012-04-21)
Spatiospecific functionalisation of a shell crystal was performed in a core-shell crystal of a porous coordination polymer (PCP) via post-synthetic modification (PSM). The shell crystal allowed the core crystal to selectively accumulate N,N-dimethylaniline (DMA) and afford the intense exciplex fluorescence.
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