Category
Beclometasone
CAS Number
205105-83-5
Molecular Formula
C₂₅H₃₂O₆
Molecular Weight
428.52 g/mol
Synonym

9,11ß-Epoxy-17-hydroxy-16ß-methyl-3,20-dioxo-9ß-pregna-1,4-dien-21-yl propanoate ; 
9,11β-Epoxy-17-hydroxy-16β-methyl-3,20-dioxo-9β-pregna-1,4-dien-21-yl propanoate; 16β-Betamethasone 9,11-Epoxide 21-Propionate; (9β,11β,16β)-9,11-Epoxy-17-hydroxy-16-methyl-21-(1-oxopropoxy)pregna-1,4-diene-3,20-dione; Beclomethasone 9,11-Epoxide 21-Propionate;Beclometasone Dipropionate Impurity V;

Keywords
High-Quality Pharmaceutical Reference Standards
Intermediates
Impurities
Metabolites.
Pharmaceutical Standards
Fine Chemicals
Steroids
Impurities Manufacturer in India
Impurities manufacturer and Suppliers in Hyderabad india
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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.

Manasa Life Sciences is a trusted Beclometasone Dipropionate EP Impurity V manufacturer and supplier in India, providing analytical reference material (CAS No. 205105-83-5; Molecular Formula: C₂₅H₃₂O₆; Molecular Weight: 428.52 g/mol) for steroid impurity profiling, related-substances analysis, chromatographic peak identification, and method development and validation. Analytical services include HPLC, LC-MS, NMR, FTIR, and potentiometric analysis, with applicable COA, MSDS/SDS, chromatograms, spectral reports, and batch traceability documentation. Testing and documentation can be tailored to relevant ICH and EMA guidance, EP and USP requirements, and GLP and GDP practices, within the agreed project scope. Request specifications, characterization data, pricing, and availability for your pharmaceutical research and quality-control requirements.