![(1R,2R,4R,5R,7S,10R,11S,14S,16S,18S,19S)-5,7-Dihydroxy-10,14-dimethylhexacyclo[9.8.0.02,4.05,10.014,19.016,18]nonadecan-15-one chemical structure](/media/structures/GWUFXQIQXPASJU-VJWUOOCFSA-N.svg)
(1R,2R,4R,5R,7S,10R,11S,14S,16S,18S,19S)-5,7-Dihydroxy-10,14-dimethylhexacyclo[9.8.0.02,4.05,10.014,19.016,18]nonadecan-15-one
- CAS
- 82543-16-6
- Formula
- C21H30O3
- MW
- 330.5 g/mol
VQ-025421
Impurity reference standards
Drospirenone impurities & reference standards
Characterised Drospirenone impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
24reference materials
1isotope-labelled
COAHPLC · NMR · MS on request
3b,5b-Dihydroxy Drospirenone Ring-opened Alcohol Impurity
- CAS
- 82543-18-8
- Formula
- C24H38O4
- MW
- 390.6 g/mol
VQ-025422
5-β-Hydroxy Drospirenone Ring-opened Alcohol Impurity
- CAS
- 1357252-81-3
- Formula
- C24H36O4
- MW
- 388.5 g/mol
VQ-025423
FAQs — Drospirenone impurities
Which Drospirenone impurities do you supply?
We list 24 Drospirenone-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 Drospirenone 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 Drospirenone 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 Drospirenone impurity standards
We reply within one business day with price, pack options, lead time and documentation.