kaempferol rhamnoside

4H-1-1benzopyran-4-one, e-[(6-deoxy-a-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-

CAS: 482-39-3 C21 H20 O10 MW: 432.38240000

Identification

Namekaempferol rhamnoside
IUPAC5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
CAS Number482-39-3
FDA UNII5M86W1YH7O
Molecular FormulaC21 H20 O10
Molecular Weight432.38240000
MDL NumberMFCD00210589
Nikkaji NumberJ12.243B

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 1212 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesantioxidants

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryantioxidant, emollients, skin conditioning
Recommendation for kaempferol rhamnoside usage levels up tonot for fragrance use.
Recommendation for kaempferol rhamnoside flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

basswood flower ginkgo biloba pollen hazelnut bark hazelnut leaf peach flower peach plant

Synonyms

afzelin 4H-1-1 benzopyran-4-one, e-[(6-deoxy-a-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)- 5,7- dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one kaempferol 3-rhamnoside PubMed: [Absorption of extractive Polygonum orientale in rat everted gut sacs]. PubMed: Antimicrobial and antioxidant activity of kaempferol rhamnoside derivatives from Bryophyllum pinnatum. PubMed: Novel inhibitory activity of the Staphylococcus aureus NorA efflux pump by a kaempferol rhamnoside isolated from Persea lingue Nees. PubMed: Phenolic composition of kiwifruit juice.