This impurity is related to Triamcinolone EP Impurity A is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Triamcinolone EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:9-Fluoro-11?,17-dihydroxy-3,20-dioxopregna-1,4-diene-16a,21-diyl diacetate ; 9-Fluoro-11?,16a,17,21-tetrahydroxypregna-1,4-diene-3,20-dione 16,21-diacetate (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Triamcinolone Molecular Formula: C25H31FO8
Molecular Weight: 478.5
Storage: Store in a cool, dry place.