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Y0000105

Rutoside trihydrate

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

Rutin trihydrate, 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:
75455
MDL number:
MFCD00149490
UNSPSC Code:
41116107
PubChem Substance ID:
329830846
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

rutoside

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

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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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.
For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Rutoside trihydrate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Other Notes

Sales restrictions may apply.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

监管及禁止进口产品

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Determination of Specific proteolytic activity of Trypsin and Bromelain and simultaneous estimation of Rutoside Trihydrate, Diclofenac sodium, Trypsin and Bromelain in tablet formulation.
Wani S S, et al.
International Journal of PharmTech Research, 6(4), 1236-1244 (2014)
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
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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