4,5-dimethyl-2-phenylfuran-3-carboxylic acid CAS 4414-38-4

Purity 97%+In StockPharmaceutical Standards
CAS No.4414-38-4
Molecular FormulaC13H12O3
Molecular Weight216.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,5-dimethyl-2-phenylfuran-3-carboxylic acid CAS 4414-38-4 chemical structure

Description

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.

4,5-dimethyl-2-phenylfuran-3-carboxylic acid (CAS 4414-38-4) is a high-purity analytical reference standard with the molecular formula C13H12O3 and a molecular weight of 216.23 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, 4,5-dimethyl-2-phenylfuran-3-carboxylic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 216.23 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 4,5-dimethyl-2-phenylfuran-3-carboxylic acid 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 FormulaC13H12O3
Molecular Weight216.23 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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