Budesonide EP Impurity K (Mixture of Epimer) CAS 51333-05-2

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.51333-05-2
Molecular FormulaC27H36O7
Molecular Weight472.57 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Budesonide EP Impurity K (Mixture of Epimer) CAS 51333-05-2 chemical structure

Description

CATO supplies Budesonide EP Impurity K (Mixture of Epimer) (CAS 51333-05-2), a pharmacopoeial impurity reference standard (molecular formula C27H36O7, MW 472.57 g/mol) used for the identification and quantification of trace impurities in APIs.

Budesonide EP Impurity K (Mixture of Epimer) (C27H36O7) contains a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system. 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).

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

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.

Physical & Chemical Properties

Molecular FormulaC27H36O7
Molecular Weight472.57 g/mol
AppearancePale yellow to yellow crystalline powder
Purity>95%
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971

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