The Ranger said:
Yup...As I said earlier, I tried it Back in the Day....awsome shit it was too!!! I've hit the fina pretty hard as well...no comparision between the two...
We can only hope it will go back into production one day very soon....Some of you Chemistry fuckers outa do something about it...<wink>!!!
Ranger
Man, is there really that big of a difference between para and fina? I have only used fina.
Now here's when I should keep my mouth shut....
To be honest, it wouldn't be all that difficult to swap an acetate ester for, say, a cypionate (or whatever) ester. Para's ester cyclohexylmethylcarbonate is in a class of esters by itself. It's not like a straight chain ester (deconate, acetate, propionate) and it's not like a phenyl propionate or cypionate ester either..
But that really shouldn't matter. You could throw a deconate ester on trenbolone and expect a marked decrease in diffusion rate from the injection site.
Anyway, an ester is easily hydrolyzed by boiling in NaOH solution. The mixture would then be extracted several times with a non-polar solvent like either, toluene, chloroform, or hexane. This solvent evaporated and the crystaline, parent steroid would be heated with the organic acid that coorisponds to which ester you wanted along with a few drops of sulfuric acid.
Next, the solution would get neutralized with baking soda, and then extracted several times with your favorite non-polar solvent. Now evaporate this solvent and you have your brand-new ester on trenbolone.
Anyone want to donate some TA to the
Andy Search For a Better Ester (ASFBE) cause?
I've got lots of little toys for when I play chemist too.
Andy