7-Chloromethyl 17R-Drospirenone is a stereospecific synthetic derivative of drospirenone featuring a 7-chloromethyl substitution on the 17Ξ±-pregnane scaffold. The 17R configuration at the sulfur-containing thione group distinguishes its spatial orientation relative to the parent hormone. This impurity arises from selective chloromethylation at C-7 during API synthesis, retaining the 13-ethyl, 3-oxo, and 17-thione functionalities critical to drospirenoneβs pharmacophore. Its structural similarity to the parent compound enables use as an HPLC reference standard for impurity profiling in quality control workflows.
On Request| Std | Catalog # | Quantity | Price |
|---|---|---|---|
| USP | 1A04920 β | 25 mg | USD 1725.00 |
C[C@]12CCC(=O)C=C1C[C@@H]([C@@H]3[C@@H]2CC[C@]4([C@H]3[C@@H]5C[C@@H]5[C@]46CCC(=O)O6)C)CCl
InChI=1S/C24H31ClO3/c1-22-6-3-15(26)10-14(22)9-13(12-25)20-17(22)4-7-23(2)21(20)16-11-18(16)24(23)8-5-19(27)28-24/h10,13,16-18,20-21H,3-9,11-12H2,1-2H3/t13-,16-,17+,18+,20-,21+,22+,23+,24-/m1/s1
YGBFZJNESAZJNB-WUVPQEDYSA-N