This impurity is related to Triamcinolone Impurity C PG Hemi Acetal 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 Impurity C PG Hemi Acetal is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6aS,6bR,7S,8aS,8bS,11aR,12aS,12bS)-6b-fluoro-7-hydroxy-8b-(2-hydroxy-2-(2-hydroxypropoxy)acetyl)-6a,8a,10,10-tetramethyl-1,2,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Triamcinolone Molecular Formula: C27H37FO8
Molecular Weight: 508.6
Storage: Store in a cool, dry place.