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Spiranolactone Impurity F

Spiranolactone Impurity F is a regioisomeric byproduct derived from the synthetic pathway of Spiranolactone, featuring a ฮณ-lactone core fused to a cyclohexene ring with a 6ฮฒ-hydroxy substituent. The compound exhibits a distinct stereochemical configuration at the C-17 position, leading to altered hydrogen bonding and chromatographic properties relative to the parent drug. Its structural divergence arises from a competing nucleophilic attack during lactonization, yielding a minor isomeric fraction. This impurity functions as an HPLC reference standard for quantifying synthetic process variability in Spiranolactone production.

On Request
Molecular Formula C22H28O3
Molecular Weight 340.5000
CAS Number 976-71-6 โœ“ Verified
PubChem CID 13789 โ†—
Purity N/A
Product Type API Impurity
Parent Drug Spiranolactone
Lead Time On Request
IUPAC Name (8R,9S,10R,13S,14S,17R)-10,13-dimethylspiro[2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthrene-17,5'-oxolane]-2',3-dione
Official Reference Standards
Std Catalog # Quantity Price
EP C0410000 โ†— 15 MG EUR 90.00
USP 1619017 โ†— 100 mg USD 930.00

๐Ÿ“ Synonyms

CANRENONE 976-71-6 Aldadiene SC-9376 Canrenonum DTXSID3045930 Spironolactone metabolite m1 78O20X9J0U SC9376 NSC-261713

๐Ÿ”ฌ Chemical Identifiers

C[C@]12CCC(=O)C=C1C=C[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@]45CCC(=O)O5)C
InChI=1S/C22H28O3/c1-20-9-5-15(23)13-14(20)3-4-16-17(20)6-10-21(2)18(16)7-11-22(21)12-8-19(24)25-22/h3-4,13,16-18H,5-12H2,1-2H3/t16-,17+,18+,20+,21+,22-/m1/s1
UJVLDDZCTMKXJK-WNHSNXHDSA-N

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