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Supelco

Rhamnetin

analytical standard

Synonym(s):

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

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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

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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG6507
BCCC9882
BCBZ3141
BCBW6198
BCBV3729

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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
F Bucar et al.
Die Pharmazie, 53(12), 875-878 (1999-01-08)
From the methylene chloride extract of the leaves of Guiera senegalensis a novel naphthopyran, 5-methylflavasperone (5,8,10-trimethoxy-2-methyl-4 H-naphtho[1,2-b]pyran-4-one), as well as rhamnetin were isolated. Rhamnetin showed a strong inhibitory activity on 5-lipoxygenase from porcine leucocytes with an IC50 value of 0.7
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
H Jiang et al.
Natural product research, 23(10), 953-959 (2009-06-13)
Preliminary studies with the four extracts of Oxytropis falcate Bunge exhibited that the chloroform and ethyl acetate extracts showed stronger antibacterial activities against the nine tested Gram-positive and Gram-negative bacteria. The HPLC-scanned and bioassay-guided fractionation led to the isolation and
Andrea Mattarei et al.
Molecules (Basel, Switzerland), 15(7), 4722-4736 (2010-07-27)
The regioselective synthesis of several quercetin (3,3',4',5,7-pentahydroxy flavone) tetraesters bearing a single free OH on 5-C was achieved in good yield by proper choice of reaction conditions using common esterification procedures. Tetracetylated quercetin with the free OH on 7-C was
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