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The crystal structure of cyproterone (systematic name: 6-chloro-1,2-dihydro-17-hydr­oxy-3'H-cyclo­propa[a]pregna-1,4,6-triene-3,20-dione), C22H27ClO3, is compared with cyproterone acetate, a potent anti-androgen steroid. The two compounds adopt a similar conformation, except for the cyclo­propyl ring attached to the cyclohexenone ring (ring A). Cyproterone further adopts a crystal packing distinct from that of the acetate form. These differences result from hydrogen bonding between the free hydr­oxy group and the carbonyl group of ring A.
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