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404810

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

Name: <I>N,N′</I>-Bis(3-aminopropyl)-1,3-propanediamine
Brand: ALDRICH

technical grade, 90%

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About This Item

Linear Formula:

H₂N(CH₂)₃NH(CH₂)₃NH(CH₂)₃NH₂

CAS Number:

4605-14-5

Molecular Weight:

188.31

NACRES:

NA.22

PubChem Substance ID:

24865272

UNSPSC Code:

12352100

EC Number:

225-007-8

MDL number:

MFCD00008213

Assay:

90%

Form:

liquid

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Properties

grade

technical grade

assay

90%

form

liquid

refractive index

n20/D 1.491 (lit.)

bp

98-103 °C/1 mmHg (lit.)

density

0.92 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCCCNCCCNCCCN

InChI

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

InChI key

ZAXCZCOUDLENMH-UHFFFAOYSA-N

Description

General description

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

Application

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

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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

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Specific type of interactions in the quaternary system of Cu(II), adenosine 5'-triphosphate, 1,11-diamino-4,8-diazaundecane and uridine.

Anna Gasowska et al.

Journal of inorganic biochemistry, 101(10), 1362-1369 (2007-07-04)

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

Polyamine derivatives as selective RNaseA mimics.

Sandra Fouace et al.

Nucleic acids research, 32(1), 151-157 (2004-01-06)

Site-selective scission of ribonucleic acids (RNAs) has attracted considerable interest, since RNA is an intermediate in gene expression and the genetic material of many pathogenic viruses. Polyamine-imidazole conjugates for site-selective RNA scission, without free imidazole, were synthesized and tested on

Chemical features of the protein kinase CK2 polyamine binding site.

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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Global Trade Item Number

SKU	GTIN
404810-5G	04061831987010