1,2,3,4-Tetramethoxydibenzo[b,d]furan CAS 88256-07-9

Purity 97%+In StockPharmaceutical Standards
CAS No.88256-07-9
Molecular FormulaC16H16O5
Molecular Weight288.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2,3,4-Tetramethoxydibenzo[b,d]furan CAS 88256-07-9 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 288.30 g/mol gives 1,2,3,4-Tetramethoxydibenzo[b,d]furan distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1,2,3,4-Tetramethoxydibenzo[b,d]furan (CAS 88256-07-9), molecular formula C16H16O5 and molecular weight 288.30 g/mol, is a CATO reference standard with documented purity and traceability.

1,2,3,4-Tetramethoxydibenzo[b,d]furan (C16H16O5) contains a flavonoid core, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC16H16O5
Molecular Weight288.30 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.)1982

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Why CATO?