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Merck

404810

Sigma-Aldrich

N,N′-Bis(3-aminopropyl)-1,3-propandiamin

technical grade, 90%

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About This Item

Lineare Formel:
H2N(CH2)3NH(CH2)3NH(CH2)3NH2
CAS-Nummer:
Molekulargewicht:
188.31
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualität

technical grade

Assay

90%

Form

liquid

Brechungsindex

n20/D 1.491 (lit.)

bp

98-103 °C/1 mmHg (lit.)

Dichte

0.92 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amine

SMILES String

NCCCNCCCNCCCN

InChI

1S/C9H24N4/c10-4-1-6-12-8-3-9-13-7-2-5-11/h12-13H,1-11H2

InChIKey

ZAXCZCOUDLENMH-UHFFFAOYSA-N

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Allgemeine Beschreibung

N,N′-Bis(3-aminopropyl)-1,3-propanediamine, a linear polyamine, has been identified in white shrimp Penaeus setiferus by gas chromatography-mass spectrometry.[1]

Anwendung

N,N′-Bis(3-aminopropyl)-1,3-propanediamine (bappn) may be used in the preparation of [Ni(bappn)(ttcH)]·5H2O complex (ttch= trithiocyanurate dianion).[2]

Piktogramme

Corrosion

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Eye Dam. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

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


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Complexation reactions in the quaternary system Cu/ATP/3,3,3-tet/Urd have been studied. The stability constants of the complexes of the Cu(ATP)(3,3,3-tet)H(x)(Urd) type have been determined by computer analysis of the potentiometric titration. On the basis of the results of spectroscopic as well
D Leroy et al.
Biochemistry, 36(6), 1242-1250 (1997-02-11)
Protein kinase CK2 is a ubiquitous eukaryotic Ser/Thr kinase whose catalytic activity is enhanced several times by polyamines. We have shown previously that the regulatory beta-subunit of CK2 bears a polyamine binding site located in the region Asp51-Tyr110. In the
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The Biochemical journal, 328 ( Pt 1), 307-316 (1998-01-10)
Treatment of Chinese hamster ovary cells with alpha-difluoromethylornithine for 3 days, followed by exposure to cycloheximide, led to an unregulated, rapid and massive accumulation of polyamine analogues. This accumulation led to cell death by apoptosis within a few hours. Clear
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Bioorganic & medicinal chemistry letters, 19(9), 2478-2481 (2009-04-01)
We have previously shown that simple N-acyl or N-alkyl polyamines bind to and sequester Gram-negative bacterial lipopolysaccharide, affording protection against lethality in animal models of endotoxicosis. Several iterative design-and-test cycles of SAR studies, including high-throughput screens, had converged on compounds

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