Skip to Content
Merck
All Photos(1)

Key Documents

Y0000165

Tribenoside

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

Ethyl 3,5,6-tri-O-benzyl-D-glucofuranoside

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C29H34O6
CAS Number:
Molecular Weight:
478.58
EC Number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

tribenoside

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

shipped in

wet ice

storage temp.

−20°C

SMILES string

O1[C@@H]([C@@H]([C@H](C1OCC)O)OCc4ccccc4)C(OCc3ccccc3)COCc2ccccc2

InChI

1S/C29H34O6/c1-2-32-29-26(30)28(34-20-24-16-10-5-11-17-24)27(35-29)25(33-19-23-14-8-4-9-15-23)21-31-18-22-12-6-3-7-13-22/h3-17,25-30H,2,18-21H2,1H3/t25?,26-,27-,28-,29?/m1/s1

InChI key

ULLNJSBQMBKOJH-NUZMXOBKSA-N

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

Tribenoside 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.

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

Yamato Kikkawa et al.
Biological & pharmaceutical bulletin, 33(2), 307-310 (2010-02-02)
Tribenoside has been used clinically for hemorrhoidal disease associated with coagulation, inflammation, and wounds. However, the pharmacological mechanism of tribenoside activity has never been clear. In this study we examined whether tribenoside affected expression and deposition of laminins that are
[Glyvenol electrophoresis in the correction of microcirculation disorders in parodontitis].
Iu V Zil'berman
Voprosy kurortologii, fizioterapii, i lechebnoi fizicheskoi kultury, (5)(5), 54-55 (1983-09-01)
[Centella asiatica extract in venous pathology of the lower limbs and its evaluation as compared with tribenoside].
F Marastoni et al.
Minerva cardioangiologica, 30(4), 201-207 (1982-04-01)
A Sioufi et al.
Journal of pharmaceutical sciences, 69(2), 167-169 (1980-02-01)
The determination of alpha-tribenoside at concentrations down to 10 ng/ml and beta-tribenoside at concentrations down to 5 ng/ml in human plasma is described. After addition of an internal standard, alpha- and beta-tribenosides are extracted at basic pH into benzene. Both
D A Kalbhen et al.
Zeitschrift fur Rheumatologie, 40(2), 72-86 (1981-03-01)
Animal experiments with chemically induced osteoarthrosis in the knee joint of adult hens have shown that the daily treatment with tribenoside (Glyvenol(R)) using single oral doses of 50 mg/kg or 150 mg/kg, will result in a marked reduction of the

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