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84082

Sigma-Aldrich

Rutin trihydrate

≥90% (HPLC)

Synonym(s):

Quercetin-3-rutinoside trihydrate, Vitamin P trihydrate

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About This Item

Empirical Formula (Hill Notation):
C27H30O16 · 3H2O
CAS Number:
250249-75-3
Molecular Weight:
664.56
Beilstein/REAXYS Number:
75455
EC Number:
205-814-1
MDL number:
MFCD00149490
UNSPSC Code:
12352200
PubChem Substance ID:
57652986

assay

≥90% (HPLC)

optical activity

[α]20/D +9±2°, c = 0.5% in absolute ethanol

SMILES string

O.O.O.C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C27H30O16.3H2O/c1-8-17(32)20(35)22(37)26(40-8)39-7-15-18(33)21(36)23(38)27(42-15)43-25-19(34)16-13(31)5-10(28)6-14(16)41-24(25)9-2-3-11(29)12(30)4-9;;;/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3;3*1H2/t8-,15+,17-,18+,20+,21-,22+,23+,26+,27-;;;/m0.../s1

InChI key

NLLBWFFSGHKUSY-JPRRWYCFSA-N

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Biochem/physiol Actions

Rutin is the major mutagenic component of red wine; it is not itself mutagenic, but is activated to a mutagen by treatment both liver microsomal enzymes and fecal enzymes.[1]

Other Notes

Review[2]

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCBJ3371V
BCBD7904V
BCBB3481V
BCBB3481
1445885

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T.I. Khalifa et al.
Anal. Profiles Drug Subst., 12, 623-623 (1983)
C L Yu et al.
Mutation research, 170(3), 103-113 (1986-06-01)
The polyphenolics of a red wine were concentrated by salt-induced phase separation into acetone-alcohol and fractionated by Sephadex LH-20 and multi-layer counter-current chromatography. The mutagenicity of each fraction was evaluated by the Salmonella mutagenesis assay. The mutagen of red wine
Nattapon Supkamonseni et al.
Indian journal of experimental biology, 52(10), 965-971 (2014-10-28)
In vitro study revealed that pancreatic lipase inhibitory activity of C. asiatica extract was significantly higher than rutin but lower than orlistat, an anti-obesity drug. alpha-Amylase inhibitory activities of C. asiatica extract and rutin were significantly lower than acarbose, an
L M Berger et al.
Journal of dairy science, 98(8), 5688-5698 (2015-06-22)
The aim of the present study was to investigate the ruminal degradation of the flavonol quercetin and to determine its potential antimicrobial effects on ruminal fermentation in cows. Ruminal degradation of quercetin (0 or 100μmol/L, respectively) as well as its
Snezana Agatonovic-Kustrin et al.
Journal of chromatography. A, 1385, 103-110 (2015-02-11)
The present study describes a simple high performance thin layer chromatographic (HPTLC) method for the simultaneous quantification of apigenin, chamazulene, bisabolol and the use of DPPH free radical as a post-chromatographic derivatization agent to compare the free radical scavenging activities

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