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Merck
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文件

188441

Sigma-Aldrich

N,N-双(3-氨丙基)甲胺

96%

别名:

(7-氨基-4-甲基-4-氮杂庚基)胺, 1,7-二氨基-4-甲基-4-氮杂庚烷

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About This Item

线性分子式:
CH3N(CH2CH2CH2NH2)2
CAS号:
105-83-9
分子量:
145.25
EC號碼:
203-336-8
MDL號碼:
MFCD00008217
分類程式碼代碼:
12352100
PubChem物質ID:
24851162
NACRES:
NA.22

蒸汽壓力

6 mmHg ( 110 °C)

化驗

96%

形狀

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 字串

CN(CCCN)CCCN

InChI

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

InChI 密鑰

KMBPCQSCMCEPMU-UHFFFAOYSA-N

相关类别

應用

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

象形圖

Skull and crossbonesCorrosion
GHS06,GHS05

訊號詞

Danger

危險分類

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

儲存類別代碼

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

水污染物質分類（WGK）

WGK 1

閃點（°F）

217.4 °F - closed cup

閃點（°C）

103 °C - closed cup

個人防護裝備

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

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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
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
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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