Ibuprofen EP Impurity B CAS 3585-49-7

Purity >90%In StockPharmacopoeial Impurity Standards
CAS No.3585-49-7
Molecular FormulaC13H18O2
Molecular Weight206.28 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Ibuprofen EP Impurity B CAS 3585-49-7 chemical structure

Description

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.

CATO supplies Ibuprofen EP Impurity B (CAS 3585-49-7), a pharmacopoeial impurity reference standard (molecular formula C13H18O2, MW 206.28 g/mol) used for the identification and quantification of trace impurities in APIs.

Ibuprofen EP Impurity B (C13H18O2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

Physical & Chemical Properties

Molecular FormulaC13H18O2
Molecular Weight206.28 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity>90%
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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