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Scope Pharmachem Plus LLP is a reliable contract research organization (CRO) specialized in the custom synthesis of pharmacopeial & non-pharmacopeial reference standards, working standards, drug metabolites, glucuronides, and nitrosamine impurities for global pharmaceutical quality assurance.

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11-a.-hydroxyprednisolone sodium phosphate | Scope Pharmachem Reference Standards
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Home/Pharmaceutical Reference Standards/Pharmaceutical Reference Standards/11-a.-hydroxyprednisolone sodium phosphate

11-a.-hydroxyprednisolone sodium phosphate

11-a.-hydroxyprednisolone sodium phosphate
CAT No:SPP-P027054
CAS No:NA
Mol. F:C21H27Na2O8P
Mol. Wt.:484.4
Chemical Name:Sodium 2-((10R,11R,13S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl phosphate
Purity:>99.0%
SMILES:C[C@@](C(CC1)=CC2=O)(C=C2)C3C1C(CC[C@]4(O)C(COP(O[Na])(O[Na])=O)=O)[C@]4(C)C[C@H]3O
Inventory Status:In Stock
Storage Conditions:Store at 2°C - 8°C
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Origin: India • Standard Dossier Available

This impurity is related to 11-a.-hydroxyprednisolone sodium phosphate and is provided with comprehensive characterization data in accordance with international regulatory guidelines.

Suitable for analytical method development (AMD), analytical method validation (AMV), Quality Control (QC) release testing, Abbreviated New Drug Applications (ANDA), DMF filing, and commercial production batch release.

Standard Analytical Dossier Included:
  • Certified Certificate of Analysis (COA) with quantitative purity determination
  • High-Performance Liquid Chromatography (HPLC) chromatogram
  • Proton Nuclear Magnetic Resonance (1H-NMR) spectral confirmation
  • Mass Spectrometry (MS) molecular confirmation

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