(11-Beta)-11,20-dihydroxy-3-oxo-pregna-1,4,17(20)-trien-21-al
- CAS
- 3372-11-0
- Formula
- C21H26O4
- MW
- 342.4 g/mol
VQ-041615
Impurity reference standards
Prednisone impurities & reference standards
Characterised Prednisone impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
12reference materials
COAHPLC · NMR · MS on request
Parent API: Prednisone WS
53-03-2 · C21H26O5
(17Z)-20-Hydroxy-3,11-dioxopregna-1,4,17(20)-trien-21-al
- CAS
- 118724-35-9
- Formula
- C21H24O4
- MW
- 340.4 g/mol
VQ-027607
FAQs — Prednisone impurities
Which Prednisone impurities do you supply?
We list 12 Prednisone-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Prednisone impurity standards used for?
They are used for analytical method development and validation, impurity identification and quantification, forced-degradation and stability studies, and to support ANDA, DMF and other regulatory submissions under ICH Q3A/Q3B (and ICH M7 for mutagenic impurities).
Can you synthesise a Prednisone impurity that is not listed?
Yes. Our custom synthesis service can prepare and characterise unlisted impurities, metabolites and labelled analogues from milligram to gram scale. Share the structure or name and required quantity for a quotation.
Request Prednisone impurity standards
We reply within one business day with price, pack options, lead time and documentation.