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线性分子式:
C6H5N(CH3)2
化学文摘社编号:
分子量:
121.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-493-5
Beilstein/REAXYS Number:
507140
MDL number:
Assay:
≥99.5%
Bp:
193-194 °C (lit.)
Quality Level
InChI key
JLTDJTHDQAWBAV-UHFFFAOYSA-N
InChI
1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3
SMILES string
CN(C)c1ccccc1
assay
≥99.5%
form
liquid
purified by
glass distillation, redistillation
refractive index
n20/D 1.557 (lit.)
pH
7.4 (20 °C, 1.2 g/L)
bp
193-194 °C (lit.)
mp
1.5-2.5 °C (lit.)
density
0.956 g/mL at 25 °C (lit.)
functional group
amine
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General description
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。
Application
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。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
167.0 °F - closed cup
flash_point_c
75 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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)
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)
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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