First off, I like to preface this by saying I do realize that the Methyl group on these compounds allows for the most efficient and complete delivery in most cases. However, delivery and efficiency are not my concern, hepatoxicity is.
The compound of particular concern to me is Superdrol. I have run it twice, both times with relatively stellar blood panels; however, this was at a soft cap of three weeks and 30mgs, I would be very interested in possibly extending these cycles by converting some SDrol to injectable form.
Now, I also realize that Superdrol is basically unmethylated Masteron; however, anecdotally at least, these compounds are very different. My question, basically, is a two parter:
1) Given that small structure changes can vastly alter the effects/efficacy of steroids, would removing the methyl group for injection drastically alter an oral's performance
2) Does anybody know how to safely perform this 'experiment'?
The compound of particular concern to me is Superdrol. I have run it twice, both times with relatively stellar blood panels; however, this was at a soft cap of three weeks and 30mgs, I would be very interested in possibly extending these cycles by converting some SDrol to injectable form.
Now, I also realize that Superdrol is basically unmethylated Masteron; however, anecdotally at least, these compounds are very different. My question, basically, is a two parter:
1) Given that small structure changes can vastly alter the effects/efficacy of steroids, would removing the methyl group for injection drastically alter an oral's performance
2) Does anybody know how to safely perform this 'experiment'?