Merck
CN

188441

Sigma-Aldrich

N,N-双(3-氨丙基)甲胺

96%

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别名:
(7-Amino-4-methyl-4-azaheptyl)amine, 1,7-Diamino-4-aza(methyl)heptane, 1,7-Diamino-4-methyl-4-azaheptane
线性分子式:
CH3N(CH2CH2CH2NH2)2
CAS号:
分子量:
145.25
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

蒸汽压

6 mmHg ( 110 °C)

质量水平

检测方案

96%

形式

liquid

折射率

n20/D 1.4725 (lit.)

bp

110-112 °C/6 mmHg (lit.)

密度

0.901 g/mL at 25 °C (lit.)

SMILES字符串

CN(CCCN)CCCN

InChI

1S/C7H19N3/c1-10(6-2-4-8)7-3-5-9/h2-9H2,1H3

InChI key

KMBPCQSCMCEPMU-UHFFFAOYSA-N

应用

3,3′-二氨基- N -甲基二丙胺用于合成:
  • 新的双色酮衍生物,潜在的抗癌药物
  • 含有二聚喹啉酮、辛诺林和邻苯二甲酰亚胺基团的多胺衍生物
  • 3-(2,4-二硝基苯胺)-3'-氨基- N -甲基二丙胺

象形图

CorrosionSkull and crossbones

警示用语:

Danger

危险分类

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

闪点(°F)

217.4 °F - closed cup

闪点(°C)

103 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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R G Anderson et al.
Proceedings of the National Academy of Sciences of the United States of America, 81(15), 4838-4842 (1984-08-01)
We report the synthesis of a probe that permits the visualization by electron microscopy of acidic organelles in intact cells. This probe, 3-(2,4-dinitroanilino)-3'-amino-N-methyldipropylamine (DAMP), is a basic congener of dinitrophenol that readily diffuses into intact cells. Its primary and tertiary
Carla Cruz et al.
PloS one, 6(11), e27078-e27078 (2011-12-02)
Useful probes of the intracellular environment that target a specific organelle in order to allow direct observation of the changes in these regions is of high current interest. Macrocyclic ligands have already revealed themselves as important selective hosts in some
Agata Szulawska-Mroczek et al.
Archiv der Pharmazie, 346(1), 34-43 (2012-10-31)
The synthesis of new bischromone derivatives (4a-c and 5a-c) as potential anticancer drugs is described. The difference in the reactivity between 4-oxo-4H-chromene-3-carboxylic acid 2 (or its methyl ester 3) and 4-oxo-4H-chromene-3-carbonyl chloride 1 with three different polyamines: 3,3'-diamino-N-methyldipropylamine (a), 1,4-bis(3-aminopropyl)piperazine
Marta Szumilak et al.
European journal of medicinal chemistry, 45(12), 5744-5751 (2010-10-27)
The synthesis of new polyamine derivatives containing dimeric quinoline (3a-c), cinnoline (4a-c) and phthalimide (7a-c and 8a-c) moieties is described. Three different polyamines: (1,4-bis(3-aminopropyl)piperazine (a), 4,9-dioxa-1,12-dodecanediamine (b), 3,3'-diamino-N-methyldipropylamine (c) were used as linkers. The new compounds were obtained according to
Lucas Vu et al.
Theranostics, 2(12), 1160-1173 (2013-02-06)
A focused library of twenty-one cationic poly(amino ethers) was synthesized following ring-opening polymerization of two diglycidyl ethers by different oligoamines. The polymers were screened in parallel for plasmid DNA (pDNA) delivery, and transgene expression efficacies of individual polymers were compared

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