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Kaempferol

Catalog No. 60010 Name Sigma Aldrich
CAS Number 520-18-3 Website http://www.sigmaaldrich.com
M. F. C15H10O6 Telephone 1-800-521-8956
M. W. 286.2363 Fax
Purity ≥97.0% (HPLC) Email
Storage Chembase ID: 1622

SYNONYMS

IUPAC name
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
IUPAC Traditional name
kaempferol
Synonyms
Robigenin
3,4′,5,7-Tetrahydroxyflavone
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

DATABASE IDS

CAS Number 520-18-3
PubChem SID 24881773
MDL Number MFCD00016938
Beilstein Number 304401

PROPERTIES

Empirical Formula (Hill Notation) C15H10O6
Impurities ≤12% water
Purity ≥97.0% (HPLC)
Gene Information human ... CDC2(983), CDK5(1020), CDK6(1021), CYP1A2(1544), CYP2C9(1559), GSK3A(2931)mouse ... Hexa(15211)
GHS Pictograms GHS06
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H301-H341
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements P281-P301 + P310
Risk Statements 25-68
Safety Statements 36/37-45
German water hazard class 3

DETAILS

Description (English)
Application
Chromogenic reagent for antimony in the low ppm range2 and for gallium and indium in the sub-ppm range.3
Biochem/physiol Actions
Potent inhibitor of osteoclastic bone resorption. The effect is believed to be attributable to both the antioxidant and estrogenic activities of kaempferol.1
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 60010.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Description (简体中文)
Application
Chromogenic reagent for antimony in the low ppm range2 and for gallium and indium in the sub-ppm range.3
Biochem/physiol Actions
Potent inhibitor of osteoclastic bone resorption. The effect is believed to be attributable to both the antioxidant and estrogenic activities of kaempferol.1
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 60010.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

REFERENCES