Catégorie
Triamcinolone hexacetonide
Numéro CAS
NA
Formule moléculaire
C30H41ClO7
Masse moléculaire
549.1
Synonyme

2-((6aS,6bR,7S,8aS,8bS,11aR,12aS,12bS)-6b-Chloro-7-hydroxy-6a,8a,10,10-tetramethyl-4-oxo-2,4,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-8b-yl)-2-oxoethyl 3,3-dimethylbutanoate; 9-chloro-11ß-hydroxy-2',2'-dimethyl-3,20-dioxo-(16ßH)-[1,3]dioxolo[4',5':16,17]pregna-1,4-dien-21-yl 3,3-dimethylbutanoate

Mots-clés
Metabolites.
Impurities
Pharmaceutical Standards
Intermediates
Fine Chemicals
Slide 1.GIF
Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Triamcinolone hexacetonide Impurity-C is a certified reference standard used in the quality control and impurity profiling of Triamcinolone hexacetonide. It supports analytical method validation, stability studies, and regulatory compliance in pharmaceutical development.