All Photos(1)
Synonym(s):
1,5-Diaminopentane, 1,5-Pentanediamine, Pentamethylenediamine
Linear Formula:
NH2(CH2)5NH2
CAS Number:
Molecular Weight:
102.18
Beilstein:
1697256
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
95%
form
liquid
refractive index
n20/D 1.458 (lit.)
bp
178-180 °C (lit.)
mp
14-16 °C (lit.)
density
0.873 g/mL at 25 °C (lit.)
SMILES string
NCCCCCN
InChI
1S/C5H14N2/c6-4-2-1-3-5-7/h1-7H2
InChI key
VHRGRCVQAFMJIZ-UHFFFAOYSA-N
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Application
Cadaverine is a diamine that can be used in hetarylation with halopyridines (2-bromo, 2-iodo, and 3-iodo-pyridines) to synthesize N,N′-dipyridinyl diamine derivatives in the presence of CuI-2-isobutyrylcyclohexanone as a catalyst. It can also be used to synthesize a poly-imidazolium polymer with high thermal stability by reacting with acetic acid, pyruvaldehyde and formaldehyde by modified Debus-Radziszewski reaction.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
143.6 °F
Flash Point(C)
62 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
Certificates of Analysis (COA)
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CuI-catalyzed hetarylation of natural di-and polyamines with halopyridines.
Panchenko SP, et al.
Russian Chemical Bulletin, 66(9), 1611-1617 (2017)
Main-Chain Polyimidazolium Polymers by One-Pot Synthesis and Application as Nitrogen-Doped Carbon Precursors.
Grygiel K, et al.
Macromolecular Chemistry and Physics, 218(18), 1600586-1600586 (2017)
S Goldberg et al.
Journal of dental research, 73(6), 1168-1172 (1994-06-01)
Whereas previous studies have shown correlations between volatile sulphur compounds (VSC) and bad breath levels, it is probable that other compounds found in the oral cavity may contribute to oral malodor. In the present investigation, the possibility that diamines (cadaverine
S Kubota et al.
Cancer research, 43(5), 2363-2367 (1983-05-01)
We developed a new simple enzymatic assay method for measuring urinary polyamines (total amount of putrescine, spermidine, and cadaverine), using an acylpolyamine amidohydrolase and a putrescine oxidase. First conjugated polyamines (putrescine, spermidine, and cadaverine) in urine were hydrolyzed by incubation
K Fujita et al.
Clinical chemistry, 26(11), 1577-1582 (1980-10-01)
This method for assay of polyamines (putrescine, spermidine, and spermine) in large numbers of urine samples is based on preliminary analyte isolation by use of a Dowex 50W column, separation by high-voltage paper electrophoresis, reaction with ninhydrin to detect the
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