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188441

3,3′-Diamino-N-methyldipropylamine

96%

Synonym(s):

(7-Amino-4-methyl-4-azaheptyl)amine, 1,7-Diamino-4-aza(methyl)heptane, 1,7-Diamino-4-methyl-4-azaheptane

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About This Item

Linear Formula:
CH3N(CH2CH2CH2NH2)2
CAS Number:
105-83-9
Molecular Weight:
145.25
NACRES:
NA.22
PubChem Substance ID:
24851162
UNSPSC Code:
12352100
EC Number:
203-336-8
MDL number:
MFCD00008217
Assay:
96%
Form:
liquid
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vapor pressure

6 mmHg ( 110 °C)

Quality Level

200

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.)

functional group

amine

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

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

Skull and crossbonesCorrosion
GHS06,GHS05

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

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCV2198
MKCL5393
MKCG5912
MKCF4644
MKBZ5748V

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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
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Global Trade Item Number

SKUGTIN
188441-500G04061836825560
188441-100G04061838758842