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Names | |
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IUPAC name
2-O-α-D-Glucopyranosyl-D-glucose
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Systematic IUPAC name
(2R,3S,4R,5R)-3,4,5,6-tetrahydroxy-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanal | |
Other names
2-alpha-D-glucosyl-D-glucose
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Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
MeSH | Kojibiose |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
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Properties | |
C12H22O11 | |
Molar mass | 342.30 g/mol |
Density | 1.688 g/mL |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Kojibiose is a disaccharide. It is a product of the caramelization of glucose. [1] It is also present in honey (approx. 3%). [2]
Kojibiose has a mild sweet taste, but low calorie count. In combination with its prebiotic properties, kojibiose could function as a sugar substitute. However, kojibiose is hard to synthesize on an industrial scale. Recently, two enzyme approaches transforming sucrose and lactose or sucrose and glucose into kojibiose have been developed, potentially solving the synthetization problem. [3] [4]
![]() | |
Names | |
---|---|
IUPAC name
2-O-α-D-Glucopyranosyl-D-glucose
| |
Systematic IUPAC name
(2R,3S,4R,5R)-3,4,5,6-tetrahydroxy-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanal | |
Other names
2-alpha-D-glucosyl-D-glucose
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
MeSH | Kojibiose |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C12H22O11 | |
Molar mass | 342.30 g/mol |
Density | 1.688 g/mL |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Kojibiose is a disaccharide. It is a product of the caramelization of glucose. [1] It is also present in honey (approx. 3%). [2]
Kojibiose has a mild sweet taste, but low calorie count. In combination with its prebiotic properties, kojibiose could function as a sugar substitute. However, kojibiose is hard to synthesize on an industrial scale. Recently, two enzyme approaches transforming sucrose and lactose or sucrose and glucose into kojibiose have been developed, potentially solving the synthetization problem. [3] [4]