Substance
ID:361496
Names and Identifiers
IUPAC name
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
IUPAC Traditional name
kaempferol
Synonyms
Robigenin3,4′,5,7-Tetrahydroxyflavone3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-oneKaempferol
Registration numbers
Beilstein Number
MDL Number
CAS Number
EC Number
Properties
Product Information
Empirical Formula (Hill Notation)
C15H10O6
Purity
≥99.0% (HPLC)
Grade
analytical standard
Shelf Life
(limited shelf life, expiry date on the label)
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
Risk Statements
25-68
MSDS Link
GHS Signal Word
Danger
GHS Precautionary statements
P281-P301+P310
Storage Temperature
2-8°C
European Hazard Symbols
Toxic (T)Safety Statements
36/37-45
German water hazard class
3
GHS Hazard statements
H301-H341
Molecule Details
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
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
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data