1,4,6-Trihydroxy-5-methoxy-7-prenylxanthone CAS 160623-47-2

Purity 97%+In StockPharmaceutical Standards
CAS No.160623-47-2
Molecular FormulaC19H18O6
Molecular Weight342.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,4,6-Trihydroxy-5-methoxy-7-prenylxanthone CAS 160623-47-2 chemical structure

Description

The molecular framework of 1,4,6-Trihydroxy-5-methoxy-7-prenylxanthone (C19H18O6) 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).

CATO supplies 1,4,6-Trihydroxy-5-methoxy-7-prenylxanthone (CAS 160623-47-2), a certified reference material (molecular formula C19H18O6, MW 342.34 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 1,4,6-Trihydroxy-5-methoxy-7-prenylxanthone meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC19H18O6
Molecular Weight342.34 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002

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