404810
N,N′-Bis(3-aminopropyl)-1,3-propanediamine
technical grade, 90%
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About This Item
Linear Formula:
H2N(CH2)3NH(CH2)3NH(CH2)3NH2
CAS Number:
Molecular Weight:
188.31
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
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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).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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R H Hu et al.
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
Synthesis and Characterization of Cu (II), Co (II) and Ni (II) Complexes of Trithiocyanuric Acid: The Structure of {N, N'-Bis (3-Aminopropyl)-1, 3-Propanediamine}-(Trithiocyanurato) Nickel (II).
Kopel P, et al.
Journal of Coordination Chemistry, 56(1), 1-11 (2003)
Andrew J Geall et al.
Bioconjugate chemistry, 13(3), 481-490 (2002-05-16)
Polyamine amides have been prepared from lithocholic and cholic acids (5beta-colanes) by acylation of tri-Boc-protected tetraamines spermine and thermine. These designed ligands for DNA are polyammonium ions at physiological pH. In NMR spectra, they display 14N-1H 1J = 51 Hz
Anurupa Shrestha et al.
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
Identification of the unusual polyamines 3,3'-diaminodipropylamine and N,N'-bis(3-aminoproply)-1,3-propanediamine in the white shrimp Penaeus setiferus.
L W Stillway et al.
Biochemical and biophysical research communications, 77(3), 1103-1107 (1977-08-08)
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