Methyl 3-(benzyloxy)-4,5-dimethoxybenzoate CAS 26409-24-5

Purity 97%+In StockPharmaceutical Standards
CAS No.26409-24-5
Molecular FormulaC17H18O5
Molecular Weight302.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(benzyloxy)-4,5-dimethoxybenzoate CAS 26409-24-5 chemical structure

Description

The molecular framework of Methyl 3-(benzyloxy)-4,5-dimethoxybenzoate (C17H18O5) 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 Methyl 3-(benzyloxy)-4,5-dimethoxybenzoate (CAS 26409-24-5), a certified reference material (molecular formula C17H18O5, MW 302.32 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), Methyl 3-(benzyloxy)-4,5-dimethoxybenzoate 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 FormulaC17H18O5
Molecular Weight302.32 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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