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线性分子式:
H2N(CH2)3NH(CH2)3NH(CH2)3NH2
化学文摘社编号:
分子量:
188.31
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
225-007-8
MDL number:
Assay:
90%
Form:
liquid
InChI key
ZAXCZCOUDLENMH-UHFFFAOYSA-N
InChI
1S/C9H24N4/c10-4-1-6-12-8-3-9-13-7-2-5-11/h12-13H,1-11H2
SMILES string
NCCCNCCCNCCCN
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
General description
采用气相色谱-质谱法对白对虾中的线性多胺成分 N,N′-双(3-氨丙基)-1,3-丙二胺进行了鉴定。
Application
N,N′-双(3-氨丙基)-1,3-丙二胺 (bappn) 可用于制备 [Ni (bappn) (ttcH)] ·5H2O 络合物(ttcH= 三硫氰酸盐二价阴离子)。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
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
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
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
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
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
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