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方案
98%
折射率
n20/D 1.426 (lit.)
沸点
171 °C/750 mmHg (lit.)
mp
−43 °C (lit.)
密度
0.87 g/mL at 25 °C (lit.)
SMILES字符串
CN(C)CCC#N
InChI
1S/C5H10N2/c1-7(2)5-3-4-6/h3,5H2,1-2H3
InChI key
MTPJEFOSTIKRSS-UHFFFAOYSA-N
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一般描述
3-（二甲氨基）丙腈通过钯催化剂的的加氢反应已被研究。
应用
3-（二甲氨基）丙腈已被用于：
- 在I类杂化聚（N-异丙基丙烯酰胺）/二氧化硅水凝胶的合成过程中引发有机聚合
- 制备基于溶剂化变色荧光团4-N,N-二甲基氨基-1,8-萘二甲酰亚胺（4-DMN）的半胱氨酸修饰剂
类似于TEMED的催化剂用于从过硫酸铵形成氧自由基。自由基可引起丙烯酰胺和双丙烯酰胺的聚合。
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
145.4 °F - closed cup
闪点(°C)
63 °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
Hydrogenation of 3-(dimethylamino) propionitrile over palladium catalysts.
Krupka J, et al.
Collection of Czechoslovak Chemical Communications, 65(11), 1805-1819 (2000)
Galen Loving et al.
Bioconjugate chemistry, 20(11), 2133-2141 (2009-10-14)
The solvatochromic fluorophore 4-N,N-dimethylamino-1,8-naphthalimide (4-DMN) possesses extremely sensitive emission properties due largely to the low intrinsic fluorescence it exhibits in polar protic solvents such as water. This makes it well suited as a probe for the detection of a wide
P Banet et al.
The journal of physical chemistry. B, 113(45), 14914-14919 (2009-11-06)
Class I hybrid poly(N-isopropylacrylamide)/silica hydrogels, PNIPAM/SiO2, were prepared by a new one shot synthesis. In this approach, the free-radical polymerization of vinyl groups of N-isopropylacrylamide (NIPAM) and the hydrolysis-condensation of alkoxy groups of tetramethoxysilane (TMOS) are performed concomitantly using sodium
K R Wilmarth et al.
Journal of toxicology and environmental health, 32(4), 415-427 (1991-04-01)
Oxidation of aminopropionitriles was measured in vitro with both rat liver mitochondria and bovine plasma monoamine oxidase (MAO). The nonneurotoxic aminonitrile beta-aminopropionitrile (BAPN) was oxidized at a significantly higher rate (p less than .05) than either of the neurotoxic aminonitriles
Inhibition of acetylcholinesterase by neurotoxic aminonitriles.
J R Froines
Biochemical pharmacology, 34(17), 3185-3187 (1985-09-01)
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