Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

17799

Supelco

Rhamnetin

analytical standard

Synonym(s):

β-Rhamnocitrin, 3,3′,4′,5-Tetrahydroxy 7-methoxyflavone, 7-Methoxyquercetin, 7-Methylquercetin, Quercetin 7-methyl ether

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C16H12O7
CAS Number:
90-19-7
Molecular Weight:
316.26
Beilstein:
47741
EC Number:
201-974-1
MDL number:
MFCD00016931
UNSPSC Code:
85151701
PubChem Substance ID:
329751568
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥99.0% (HPLC)

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

COc1cc(O)c2C(=O)C(O)=C(Oc2c1)c3ccc(O)c(O)c3

InChI

1S/C16H12O7/c1-22-8-5-11(19)13-12(6-8)23-16(15(21)14(13)20)7-2-3-9(17)10(18)4-7/h2-6,17-19,21H,1H3

InChI key

JGUZGNYPMHHYRK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCG6507
BCCC9882
BCBZ3141
BCBW6198
BCBV3729

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

Harmane 98%

Sigma-Aldrich

103276

Harmane

Myricetin ≥96.0%, crystalline

Sigma-Aldrich

M6760

Myricetin

Chrysin ≥96.5%

Sigma-Aldrich

C80105

Chrysin

Kaempferol analytical standard

Supelco

96353

Kaempferol

Apigenin analytical standard

Supelco

42251

Apigenin

Quercetin ≥95% (HPLC), solid

Sigma-Aldrich

Q4951

Quercetin

Leena Pohjala et al.
Molecules (Basel, Switzerland), 17(9), 10774-10790 (2012-09-11)
Previous descriptions of quercetin, a widely studied flavonoid, as a frequently reported nonspecific screening hit due to aggregating behavior has raised questions about the reliability of in vitro bioactivity reports of phenolic compounds. Here a systematic study on 117 phenolic
Andreas Schieber et al.
Journal of agricultural and food chemistry, 51(17), 5006-5011 (2003-08-09)
Flavonol O- and xanthone C-glycosides were extracted from mango (Mangifera indica L. cv. "Tommy Atkins") peels and characterized by high-performance liquid chromatography-electrospray ionization mass spectrometry. Among the fourteen compounds analyzed, seven quercetin O-glycosides, one kaempferol O-glycoside, and four xanthone C-glycosides
W F Hodnick et al.
Biochemical pharmacology, 47(3), 573-580 (1994-02-09)
A continuation of our structure-activity study on flavonoids possessing varied hydroxyl ring configurations was conducted. We tested six additional flavonoids for their ability to inhibit beef heart mitochondrial succinoxidase and NADH-oxidase activities. In every case, the IC50 observed for the
Bushra Naseem et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(4), 1341-1346 (2010-02-19)
Quantitative parameters for interaction of flavonoids-the naturally occurring antioxidants, with solvents and surfactants are determined using UV-visible absorption spectroscopy. The availability of flavonoids; kaempferol, apigenin, kaempferide and rhamnetin in micelles of sodium dodecyl sulfate (SDS) is reflected in terms of
María A Ponce et al.
Phytochemistry, 65(13), 1925-1930 (2004-07-29)
White clover (Trifolium repens) plants were grown in the presence or absence of the arbuscular mycorrhizal fungus Glomus intraradices. Flavones, 4',5,6,7,8-pentahydroxy-3-methoxyflavone and 5,6,7,8-tetrahydroxy-3-methoxyflavone, as well as two flavones 3,7-dihydroxy-4'-methoxyflavone and 5,6,7,8-tetrahydroxy-4'-methoxyflavone never previously reported in plants, were isolated. The known
View All Related Papers

Articles

Dietary Antioxidants

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service