Kojic acid
| Names | |
|---|---|
| Preferred IUPAC name
5-Hydroxy-2-(hydroxymethyl)-4H-pyran-4-one | |
| Other names
Kojic acid, 5-Hydroxy-2-(hydroxymethyl)-4-pyrone, 2-hydroxymethyl-5-hydroxy-γ-pyrone | |
| Identifiers | |
3D model (JSmol) |
|
| 120895 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.007.203 |
| EC Number |
|
| 3620 | |
| KEGG | |
PubChem CID |
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| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C6H6O4 | |
| Molar mass | 142.110 g·mol−1 |
| Appearance | white |
| Melting point | 152 to 155 °C (306 to 311 °F; 425 to 428 K) |
| Slight | |
| Acidity (pKa) | 9.40 |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H351 | |
| P201, P280, P308+P313 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Kojic acid is an organic compound with the formula HOCH2C5H2O2OH. It is a derivative of 4-pyrone that functions in nature as a chelation agent produced by several species of fungus, especially Aspergillus oryzae, which has the Japanese common name koji. Kojic acid is a by-product in the fermentation process of malting rice, for use in the manufacturing of sake, the Japanese rice wine. It is a mild inhibitor of the formation of pigment in plant and animal tissues, and is used in food and cosmetics to preserve or change colors of substances. It forms a bright red complex with ferric ions.