3-p-Anisoyl Acacetin CAS 874519-13-8

Purity 97%+In StockPharmaceutical Standards
CAS No.874519-13-8
Molecular FormulaC24H18O7
Molecular Weight418.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-p-Anisoyl Acacetin CAS 874519-13-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 418.40 g/mol gives 3-p-Anisoyl Acacetin distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3-p-Anisoyl Acacetin (CAS 874519-13-8), a certified reference material (molecular formula C24H18O7, MW 418.40 g/mol) for analytical method development and quality control.

The molecular framework of 3-p-Anisoyl Acacetin (C24H18O7) 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.

CATO manufactures 3-p-Anisoyl Acacetin under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC24H18O7
Molecular Weight418.40 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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987

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