Kojic acid

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
  • 207-922-4
3620
KEGG
RTECS number
  • UQ0875000
UNII
  • InChI=1S/C6H6O4/c7-2-4-1-5(8)6(9)3-10-4/h1,3,7,9H,2H2 Y
    Key: BEJNERDRQOWKJM-UHFFFAOYSA-N Y
  • InChI=1/C6H6O4/c7-2-4-1-5(8)6(9)3-10-4/h1,3,7,9H,2H2
  • O=C1/C=C(\O/C=C1/O)CO
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).
N verify (what is YN ?)
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.