Ibuprofen EP Impurity N is a structural analog of ibuprofen characterized by a substituted aromatic ring and a propionic acid moiety. It features a 4-ethyl-2-phenylpropanoic acid framework, differing from the parent drug by the replacement of the isobutyl group with an ethyl substituent. This impurity arises via alkylation pathway deviations during ibuprofen synthesis, retaining the core 2-phenylpropanoic acid scaffold. Its ethyl substitution reduces steric bulk compared to the isobutyl group, altering hydrophobic interactions. This compound serves as a critical HPLC reference standard for quantifying process-related impurities in ibuprofen formulations.
On RequestCCC1=CC=C(C=C1)C(C)C(=O)O
InChI=1S/C11H14O2/c1-3-9-4-6-10(7-5-9)8(2)11(12)13/h4-8H,3H2,1-2H3,(H,12,13)
VGMCZELQCNPMQV-UHFFFAOYSA-N