Online Database of Chemicals from Around the World

Kojic acid
[CAS# 501-30-4]

List of Suppliers
Spec-Chem Industry Inc. China Inquire  
+86 (25) 8452-3390 ex 111
sc@specchemind.com
Chemical manufacturer since 1995
chemBlink standard supplier since 2006
3C Chemical Co., Ltd. China Inquire  
+86 (25) 8320-4626
kelly@3cchem.com
Chemical manufacturer since 2003
chemBlink standard supplier since 2007
Sichuan Huamai Technology Co., Ltd. China Inquire  
+86 (28) 8012-5218
wqkoa.newland@gmail.com
Chemical manufacturer since 2003
chemBlink standard supplier since 2007
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Jarchem Industries Inc. USA Inquire  
+1 (973) 344-0600
marketing@jarchem.com
Chemical manufacturer
chemBlink standard supplier since 2009
Extrasynthese Chemical S.A.S. France Inquire  
+33 (47) 898-2034
info@extrasynthese.com
Chemical manufacturer
chemBlink standard supplier since 2009
Hubei Artec Biotechnology Co., Ltd. China Inquire  
+86 (710) 312-5319
312-5180
artec@artec.cc
Chemical manufacturer since 2006
chemBlink standard supplier since 2009
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
Complete supplier list of Kojic acid
Identification
Classification Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Pyran compound
Name Kojic acid
Synonyms 5-Hydroxy-2-hydroxymethyl-4-pyrone; 5-Hydroxy-2-(hydroxymethyl)-4H-pyran-4-one
Molecular Structure CAS # 501-30-4, Kojic acid, 5-Hydroxy-2-hydroxymethyl-4-pyrone, 5-Hydroxy-2-(hydroxymethyl)-4H-pyran-4-one
Molecular Formula C6H6O4
Molecular Weight 142.11
CAS Registry Number 501-30-4
EC Number 207-922-4
SMILES C1=C(OC=C(C1=O)O)CO
Properties
Solubility soluble (water)
Density 1.5±0.1 g/cm3, Calc.*
Melting point 152-155 ºC (Expl.)
Index of Refraction 1.607, Calc.*
Boiling Point 401.7±45.0 ºC (760 mmHg), Calc.*
Flash Point 179.9±22.2 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS08 Warning    Details
Hazard Statements H351    Details
Precautionary Statements P203-P260-P263-P264-P270-P280-P318-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
CarcinogenicityCarc.2H351
SDS Available
up Discovory and Applicatios
Kojic acid is a naturally occurring compound that is widely used in the cosmetic and pharmaceutical industries for its skin-lightening properties. It was first discovered in 1907 by Japanese researchers, who isolated it from the fermentation process of a type of fungus, *Aspergillus oryzae*, used in the production of sake (a Japanese rice wine). The compound is produced as a byproduct of the fermentation of certain fungi, as well as from other natural sources, such as the rice bran.

Kojic acid is a chelation agent that works by inhibiting the activity of tyrosinase, an enzyme responsible for the production of melanin in the skin. By blocking melanin production, kojic acid helps lighten hyperpigmentation such as age spots, freckles, and melasma. This property has made kojic acid a popular ingredient in many skin-lightening products and treatments.

Apart from its cosmetic uses, kojic acid has also been studied for its potential antimicrobial properties. It has been found to have antifungal and antibacterial effects, which make it useful in treating skin conditions such as acne and fungal infections. In addition to its application in dermatology, kojic acid has been investigated for its potential in food preservation due to its ability to inhibit microbial growth.

In cosmetic products, kojic acid is commonly found in serums, creams, lotions, and soaps. It is often included in formulations aimed at reducing the appearance of dark spots, improving skin tone, and providing an even complexion. Due to its strong tyrosinase-inhibiting effect, kojic acid is also utilized in depigmenting agents for conditions like post-inflammatory hyperpigmentation and sunspots.

Despite its widespread use, there are some concerns regarding the safety of long-term or high-dose use of kojic acid, especially in higher concentrations found in some products. Prolonged exposure can lead to skin irritation, and, in rare cases, it may cause allergic reactions. As a result, the concentration of kojic acid in cosmetic formulations is regulated in many countries to ensure its safe use.

In summary, kojic acid, discovered in 1907 from the fermentation of fungi, has become a well-known and widely used compound in the cosmetic industry due to its ability to lighten hyperpigmentation and improve skin tone. Its antimicrobial properties have also led to its application in treating skin conditions and in food preservation. However, it is essential to use kojic acid products in appropriate concentrations to avoid potential skin irritation.

References

2024. The Skin-Lightening Power of Tirbanibulin 1% Ointment. Dermatology and Therapy, 14(12).
DOI: 10.1007/s13555-024-01310-0

2024. Activated carbon as a catalyst to promote the reactivity of hydroquinone in skin whitening cosmetics. Journal of Porous Materials, 31(6).
DOI: 10.1007/s10934-024-01720-7

2024. Profiling of bioactive secondary metabolites from Aspergillus niger against a guava wilt pathogen, Fusarium oxysporum f. sp. psidii. Archives of Microbiology, 206(12).
DOI: 10.1007/s00203-024-04199-7
Market Analysis Reports
List of Reports Available for Kojic acid
Related Products
Knapsack MIS  KN-92 hydrochloride  Knidilin  KN-92 phosphate  Ko 143  Koaburaside  Koaburaside monomethyl ether  Kobophenol A  Kobusone  Kojibiose  Kojic acid dipalmitate  Kolavenol  Kongensin A  Konjac glucomannan  Koumine  Koumine N-oxide  Kovanol  KP 1461  KPT 330  KR 134BS