1,3,7,9-Tetramethoxy-2,6-dimethyldibenzo[b,d]furan CAS 24565-66-0

Purity 97%+In StockPharmaceutical Standards
CAS No.24565-66-0
Molecular FormulaC18H20O5
Molecular Weight316.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,3,7,9-Tetramethoxy-2,6-dimethyldibenzo[b,d]furan CAS 24565-66-0 chemical structure

Description

Structurally, 1,3,7,9-Tetramethoxy-2,6-dimethyldibenzo[b,d]furan (C18H20O5) contains a flavonoid core, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 316.35 g/mol, it falls into the moderately-high-molecular-weight range. 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).

1,3,7,9-Tetramethoxy-2,6-dimethyldibenzo[b,d]furan (CAS 24565-66-0), molecular formula C18H20O5 and molecular weight 316.35 g/mol, is a CATO reference standard with documented purity and traceability.

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), 1,3,7,9-Tetramethoxy-2,6-dimethyldibenzo[b,d]furan 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 FormulaC18H20O5
Molecular Weight316.35 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1964

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