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Product No: AF0533

Myricetin, 98%

Name: Myricetin
Brand: Chempure

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CAS Number

529-44-2

Molecular Weight

318.24

Formula

C15H10O8

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About this item

IUPAC name	3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
canonical smiles	C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
inchi	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
inchi key	IKMDFBPHZNJCSN-UHFFFAOYSA-N
molecular formula	C15H10O8
synonyms	myricetin 529-44-2 Cannabiscetin Myricetol Myricitin
Compound Description	Myricetin is a hexahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 3', 4', 5, 5' and 7. It has been isolated from the leaves of Myrica rubra and other plants. It has a role as a cyclooxygenase 1 inhibitor, an antineoplastic agent, an antioxidant, a plant metabolite, a food component, a hypoglycemic agent and a geroprotector. It is a hexahydroxyflavone and a 7-hydroxyflavonol. It is a conjugate acid of a myricetin. Myricetin is a natural product found in Caragana frutex, Camellia sinensis, and other organisms with data available. Myricetin is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Quercetin .

Computed Properties

Molecular Weight:	318.23 g/mol
XLogP3:	1.2
Hydrogen Bond Donor Count:	6
Hydrogen Bond Acceptor Count:	8
Rotatable Bond Count:	1
Exact Mass:	318.03756727 g/mol
Monoisotopic Mass:	318.03756727 g/mol
Topological Polar Surface Area:	148 Å²
Heavy Atom Count:	23
Formal Charge:	0
Complexity:	506
Isotope Atom Count:	0
Defined Atom Stereocenter Count:	0
Undefined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
Covalently-Bonded Unit Count:	1
Compound Is Canonicalized:	Yes

Related Compounds

Quercetin

Apigenin

Diosmetin

Taxifolin

Cianidanol

Delphinidin

Kaempferol

Luteolin

Chrysin

Fisetin

Myricetin

Isorhamnetin

Galangin

Morin

Baicalein

hazard signal	Warning
hazard classes and categories	Skin Irrit. 2 (100%) Eye Irrit. 2 (100%) STOT SE 3 (100%)
precautionary statement codes	P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
hazard statements	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

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About this item

Documentation

Certificate of Analysis

Lot Number

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CAS #

*This document is like a lab demo—an example Certificate of Analysis (COA) that showcases what a COA looks like but may not match the latest batch in all its glory. Think of it as a chemistry experiment: close, but not quite the final reaction!

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About this item

IUPAC name	3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
canonical smiles	C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
inchi	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
inchi key	IKMDFBPHZNJCSN-UHFFFAOYSA-N
molecular formula	C15H10O8
synonyms	myricetin 529-44-2 Cannabiscetin Myricetol Myricitin
Compound Description	Myricetin is a hexahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 3', 4', 5, 5' and 7. It has been isolated from the leaves of Myrica rubra and other plants. It has a role as a cyclooxygenase 1 inhibitor, an antineoplastic agent, an antioxidant, a plant metabolite, a food component, a hypoglycemic agent and a geroprotector. It is a hexahydroxyflavone and a 7-hydroxyflavonol. It is a conjugate acid of a myricetin. Myricetin is a natural product found in Caragana frutex, Camellia sinensis, and other organisms with data available. Myricetin is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Quercetin .

Computed Properties

Molecular Weight:	318.23 g/mol
XLogP3:	1.2
Hydrogen Bond Donor Count:	6
Hydrogen Bond Acceptor Count:	8
Rotatable Bond Count:	1
Exact Mass:	318.03756727 g/mol
Monoisotopic Mass:	318.03756727 g/mol
Topological Polar Surface Area:	148 Å²
Heavy Atom Count:	23
Formal Charge:	0
Complexity:	506
Isotope Atom Count:	0
Defined Atom Stereocenter Count:	0
Undefined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
Covalently-Bonded Unit Count:	1
Compound Is Canonicalized:	Yes

Related Compounds

Quercetin

Apigenin

Diosmetin

Taxifolin

Cianidanol

Delphinidin

Kaempferol

Luteolin

Chrysin

Fisetin

Myricetin

Isorhamnetin

Galangin

Morin

Baicalein

hazard signal	Warning
hazard classes and categories	Skin Irrit. 2 (100%) Eye Irrit. 2 (100%) STOT SE 3 (100%)
precautionary statement codes	P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
hazard statements	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Product No: AF0533

Myricetin, 98%

Product No: AF0533

About this item

NAME AND IDENTIFIERS

CHEMICAL AND PHYSICAL PROPERTIES

Related Compounds

SAFETY AND HAZARDS

About this item

Documentation

Certificate of Analysis

Require a Sample Certificate of Analysis (COA) ?

Reviews

Product No: AF0533

About this item

NAME AND IDENTIFIERS

CHEMICAL AND PHYSICAL PROPERTIES

Related Compounds

SAFETY AND HAZARDS

Require a Sample Certificate of Analysis (COA) ?