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Merck
CN

234486

Sigma-Aldrich

3-(二甲基氨基)丙腈

98%

别名:

DMAPN

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关于此项目

线性分子式:
(CH3)2NCH2CH2CN
化学文摘社编号:
分子量:
98.15
Beilstein:
773779
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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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。

象形图

Exclamation mark

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
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历史批次信息供参考:

分析证书(COA)

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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
J P Keogh
American journal of industrial medicine, 4(3), 479-489 (1983-01-01)
Dimethylaminopropionitrile, used as a catalyst in the manufacture of polyurethane, was responsible for two epidemics of urinary retention, sexual dysfunction, and peripheral neuropathy in 1978. Most affected workers recovered promptly, but some have had persisting neuropathy, sexual and bladder dysfunction
J R Froines et al.
Journal of toxicology and environmental health, 16(3-4), 449-460 (1985-01-01)
Cyanide release from neurotoxic aminonitriles was measured following in vitro incubation with both microsomes and liver slices. Investigation of cyanide released as urinary thiocyanate following ip aminonitrile administration to rats was also measured. The yield of cyanide in the in

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