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.[1]
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).[2]
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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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)
K Hamana et al.
Journal of biochemistry, 91(4), 1321-1328 (1982-04-01)
Seven phyla of eukaryotic algae were analyzed to determine their contents of diamines and polyamines. The algae examined included Rhodophyta, Pyrrophyta, Chrysophyta, Phaeophyta, Euglenophyta, Chlorophyta, and Charophyta. Both putrescine and spermidine were detected in all the algae studied, while appreciable
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
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)
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