5,7,4'-trihydroxy-6,8-diprenylisoflavone 5,7-dihydroxy-3-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one 51225-28-6 6,8-diisoprenyl-5,7,4'-trihydroxyisoflavone 6,8-diprenylgenistein 8-(gamma,gamma-dimethylallyl)-wighteone 8-prenylwighteone CHEBI:66263 CAS 51225-28-6

Purity 97%+In StockPharmaceutical Standards
CAS No.51225-28-6
Molecular FormulaC25H26O5
Molecular Weight406.47 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5,7,4'-trihydroxy-6,8-diprenylisoflavone 5,7-dihydroxy-3-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one 51225-28-6 6,8-diisoprenyl-5,7,4'-trihydroxyisoflavone 6,8-diprenylgenistein 8-(gamma,gamma-dimethylallyl)-wighteone 8-prenylwighteone CHEBI:66263 CAS 51225-28-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 5,7,4'-trihydroxy-6,8-diprenylisoflavone 5,7-dihydroxy-3-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one 51225-28-6 6,8-diisoprenyl-5,7,4'-trihydroxyisoflavone 6,8-diprenylgenistein 8-(gamma,gamma-dimethylallyl)-wighteone 8-prenylwighteone CHEBI:66263.

CATO supplies 5,7,4'-trihydroxy-6,8-diprenylisoflavone 5,7-dihydroxy-3-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one 51225-28-6 6,8-diisoprenyl-5,7,4'-trihydroxyisoflavone 6,8-diprenylgenistein 8-(gamma,gamma-dimethylallyl)-wighteone 8-prenylwighteone CHEBI:66263 (CAS 51225-28-6), a certified reference material (molecular formula C25H26O5, MW 406.47 g/mol) for analytical method development and quality control.

The molecular framework of 5,7,4'-trihydroxy-6,8-diprenylisoflavone 5,7-dihydroxy-3-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one 51225-28-6 6,8-diisoprenyl-5,7,4'-trihydroxyisoflavone 6,8-diprenylgenistein 8-(gamma,gamma-dimethylallyl)-wighteone 8-prenylwighteone CHEBI:66263 (C25H26O5) is characterized by a flavonoid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC25H26O5
Molecular Weight406.47 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971

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