Myricetin CAS#529-44-2

CAS Number: 529-44-2
Chemical Formula: C15H10O8
Synonyms:

Myricetin, froM Myrica rubra (Lour.) Zucc.
MYRICETIN 95%
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)

Appearance: Yellow Crystal

MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)

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Product Details

Myricetin CAS#529-44-2

Myricetin[529-44-2] is a flavonoid compound found in many fruits and vegetables, including red wine, that acts as a powerful antioxidant. Myricetin inhibits TBARS formation with an IC50 value of 6.34 and at 20 μM, blocks oxLDL uptake by U937-derived macrophages, reducing CD36 expression. Myricetin demonstrates potent chemopreventative potential by binding JAK1/STAT3 to inhibit the neoplastic transformation of murine JB6 P+ cells and inhibiting MEK1 kinase activity.

Myricetin Chemical Properties

Melting point	>300 °C(lit.)
Boiling point	377.41°C (rough estimate)
density	1.4222 (rough estimate)
refractive index	1.4395 (estimate)
storage temp.	2-8°C
solubility	ethanol: soluble10mg/mL, clear to very faintly turbid, yellow to very deep greenish-yellow
form	crystalline
pka	6.30±0.40(Predicted)
color	Yellowish Brown
Water Solubility	Soluble in dimethyl sulfoxide,dimethyl formamide and ethanol. Insoluble in water.
Merck	14,6332
BRN	332331
Stability:	Hygroscopic
Cosmetics Ingredients Functions	ANTIOXIDANT SKIN CONDITIONING
InChI	1S/C15H10O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,16-20,22H
InChIKey	IKMDFBPHZNJCSN-UHFFFAOYSA-N
SMILES	Oc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3cc(O)c(O)c(O)c3
LogP	1.206 (est)
CAS DataBase Reference	529-44-2(CAS DataBase Reference)

Safety Information

Safety Statements	24/25
WGK Germany	3
RTECS	LK8646000
F	10
HS Code	29329990
Storage Class	11 - Combustible Solids
Hazardous Substances Data	529-44-2(Hazardous Substances Data)

Product Application of Myricetin CAS#529-44-2

Myricetin is used as an antioxidant. It is a cell-permeable flavonoid used in inflammatory, diabetes, and cancer studies. It is effective in protecting neurons against oxidative stresses. Further, it inhibits yeast alfa-glucosidase,1 glyoxalase I in vitro and bovine milk xanthine oxidase.

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