Budesonide EP Impurity L
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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

216453-74-6Budesonide EP Impurity L

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Catalogue No.:VL34007
CAS No.:216453-74-6
Mol. Formula:C25H32O6
Mol. Weight:428.52 g/mol

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50 mg $417.50
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Additional information on CAS 216453-74-6

Parent drug

Budesonide

IUPAC Name

16α,17-[(1RS)-Butylidenebis(oxy)]-21-hydroxypregna-1,4-diene-3,11,20-trione

Synonyms

Budesonide Related Compound L / 11-Ketobudesonide

Description

Budesonide EP Impurity L, also designated Budesonide Related Compound L and 11-Ketobudesonide, is an oxidative degradation product of the inhaled glucocorticoid budesonide rather than a distinct synthetic excipient impurity. The structure retains the corticosteroid scaffold but contains an 11-keto function, consistent with metabolic or stress-induced oxidation at C-11. CAS 216453-74-6; molecular formula C25H32O6; molecular weight 428.52 g/mol. Its presence is evaluated in pharmacopeial impurity profiling by orthogonal chromatographic methods, typically HPLC with UV detection and LC-MS/MS for structural confirmation and trace-level quantification.

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