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D22606

Sigma-Aldrich

Cadaverine

95%

Sinônimo(s):

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

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About This Item

Fórmula linear:
NH2(CH2)5NH2
Número CAS:
462-94-2
Peso molecular:
102.18
Beilstein:
1697256
Número CE:
207-329-0
Número MDL:
MFCD00008239
Código UNSPSC:
12352100
ID de substância PubChem:
24893671
NACRES:
NA.22

Ensaio

95%

forma

liquid

índice de refração

n20/D 1.458 (lit.)

pb

178-180 °C (lit.)

pf

14-16 °C (lit.)

densidade

0.873 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

NCCCCCN

InChI

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

chave InChI

VHRGRCVQAFMJIZ-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

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.

Pictogramas

Corrosion
GHS05

Palavra indicadora

Danger

Frases de perigo

H314

Classificações de perigo

Eye Dam. 1 - Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

143.6 °F - closed cup

Ponto de fulgor (°C)

62 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

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1,9-Diaminononane 98%

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187127

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Putrescine dihydrochloride ≥98% (TLC)

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1,6-Diaminohexane for synthesis

Sigma-Aldrich

8.04323

1,6-Diaminohexane

F Konikoff et al.
Liver, 10(3), 173-176 (1990-06-01)
Lithogenicity of human bile is dependent not only on cholesterol saturation, but also on the presence of nucleating and antinucleating factors. Most of the research in this field is directed toward biliary proteins, particularly glycoproteins. In the present study we
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)
CuI-catalyzed hetarylation of natural di-and polyamines with halopyridines.
Panchenko SP, et al.
Russian Chemical Bulletin, 66(9), 1611-1617 (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
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