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Sigma-Aldrich

3,3′-Diamino-N-methyldipropylamine

96%

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Synonym(s):
(7-Amino-4-methyl-4-azaheptyl)amine, 1,7-Diamino-4-aza(methyl)heptane, 1,7-Diamino-4-methyl-4-azaheptane
Linear Formula:
CH3N(CH2CH2CH2NH2)2
CAS Number:
Molecular Weight:
145.25
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

6 mmHg ( 110 °C)

Quality Level

assay

96%

form

liquid

refractive index

n20/D 1.4725 (lit.)

bp

110-112 °C/6 mmHg (lit.)

density

0.901 g/mL at 25 °C (lit.)

SMILES string

CN(CCCN)CCCN

InChI

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

InChI key

KMBPCQSCMCEPMU-UHFFFAOYSA-N

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This Item
676438631698536393
2,2′-Dibromo-1,1′-binaphthyl 96%

676438

2,2′-Dibromo-1,1′-binaphthyl

1,1′-Binaphthyl-2,2′-diamine 96%

631698

1,1′-Binaphthyl-2,2′-diamine

4,4′-Dinitrodiphenyl ether 96%

536393

4,4′-Dinitrodiphenyl ether

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

form

liquid

form

solid

form

solid

form

-

refractive index

n20/D 1.4725 (lit.)

refractive index

-

refractive index

-

refractive index

-

bp

110-112 °C/6 mmHg (lit.)

bp

-

bp

-

bp

-

density

0.901 g/mL at 25 °C (lit.)

density

-

density

-

density

-

Application

3,3′-Diamino-N-methyldipropylamine was used in the synthesis of:
  • new bischromone derivatives, potential anticancer drugs
  • polyamine derivatives containing dimeric quinolone, cinnoline and phthalimide moieties
  • 3-(2,4-dinitroanilino)-3′-amino-N-methyldipropylamine

pictograms

CorrosionSkull and crossbones

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 1

flash_point_f

217.4 °F - closed cup

flash_point_c

103 °C - closed cup

ppe

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


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Customers Also Viewed

Slide 1 of 2

1 of 2

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
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
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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