Impurity reference standards
Deflazacort impurities & reference standards
Characterised Deflazacort impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
10reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
![2-((6AR,6bS,7S,8aS,8bS,11aR,12aS,12bS)-7-Hydroxy-6a,8a,10-trimethyl-4-oxo-1,2,4,6a,6b,7,8,8a,11a,12,12a,12b-dodecahydro-8bH-naphtho[2',1':4,5]indeno[1,2-d]oxazol-8b-yl)-2-oxoacetaldehyde chemical structure](/media/structures/AVMGJZDNRTWZEK-RVUAFKSESA-N.svg)
2-((6AR,6bS,7S,8aS,8bS,11aR,12aS,12bS)-7-Hydroxy-6a,8a,10-trimethyl-4-oxo-1,2,4,6a,6b,7,8,8a,11a,12,12a,12b-dodecahydro-8bH-naphtho[2',1':4,5]indeno[1,2-d]oxazol-8b-yl)-2-oxoacetaldehyde
- CAS
- 3035569-86-6
- Formula
- C23H27NO5
- MW
- 397.5 g/mol
VQ-036606
FAQs — Deflazacort impurities
Which Deflazacort impurities do you supply?
We list 10 Deflazacort-related reference materials, including process impurities, degradation products, stable-isotope-labelled standards and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Deflazacort 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 Deflazacort 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 Deflazacort impurity standards
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