3-Carboxy Mefenamic Acid Acyl-β-D-glucuronide CAS 152832-30-9

Purity 97%+In StockPharmaceutical Standards
CAS No.152832-30-9
Molecular FormulaC21H21NO10
Molecular Weight447.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Carboxy Mefenamic Acid Acyl-β-D-glucuronide CAS 152832-30-9 chemical structure

Description

CATO manufactures 3-Carboxy Mefenamic Acid Acyl-β-D-glucuronide 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.

3-Carboxy Mefenamic Acid Acyl-β-D-glucuronide (CAS 152832-30-9), molecular formula C21H21NO10 and molecular weight 447.39 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, 3-Carboxy Mefenamic Acid Acyl-β-D-glucuronide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 447.39 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC21H21NO10
Molecular Weight447.39 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2000
Nitrogen Atoms1

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