Skeletal formula of d-Glucosone
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Names | |
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IUPAC name
d-arabino-Hexos-2-ulose
[1]
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Systematic IUPAC name
(3S,4R,5R)-3,4,5,6-tetrahydroxy-2-oxohexanal | |
Other names
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Identifiers | |
3D model (
JSmol)
|
|
MeSH | glucosone |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
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|
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Properties | |
C6H10O6 | |
Molar mass | 178.140 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Glucosone is a reactive carbonyl compound that can be produced by an Amadori rearrangement of a derivative of glucose. It is a dicarbonyl intermediate of the Maillard reaction whose production is higher under oxidative versus non-oxidative conditions. [2]
Skeletal formula of d-Glucosone
| |
Names | |
---|---|
IUPAC name
d-arabino-Hexos-2-ulose
[1]
| |
Systematic IUPAC name
(3S,4R,5R)-3,4,5,6-tetrahydroxy-2-oxohexanal | |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
MeSH | glucosone |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H10O6 | |
Molar mass | 178.140 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Glucosone is a reactive carbonyl compound that can be produced by an Amadori rearrangement of a derivative of glucose. It is a dicarbonyl intermediate of the Maillard reaction whose production is higher under oxidative versus non-oxidative conditions. [2]