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Merck

D22606

Cadaverine

95%

Synonym(s):

1,5-Diaminopentane, 1,5-Pentanediamine, Pentamethylenediamine

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About This Item

Linear Formula:
NH2(CH2)5NH2
CAS Number:
462-94-2
Molecular Weight:
102.18
NACRES:
NA.22
UNSPSC Code:
12352100
PubChem Substance ID:
24893671
EC Number:
207-329-0
Beilstein/REAXYS Number:
1697256
MDL number:
MFCD00008239

Product Name

Cadaverine, 95%

InChI key

VHRGRCVQAFMJIZ-UHFFFAOYSA-N

InChI

1S/C5H14N2/c6-4-2-1-3-5-7/h1-7H2

SMILES string

NCCCCCN

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.)

Quality Level

200

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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.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9426
BCCH2320
MKCX8215
MKCX1699
MKCL6925

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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
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
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
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