jcam222
Board Supporter
Hello. New to the board and must say WOW this the mac daddy of the boards from what I can see. The plans for lessons etc are amazing. Anyway saw this thread somewhere and wondered if someone might elaborate on the entire process on these. They sound easy and I would love to try them. Any help appreciated. If this is the wrong area to post in for this I apoligize in advance. Just trying to learn here. Here is the thread
Boldenone would be easier to make from 1,4-androstadiene-3,17-diol or the 17-cypionate thereof. One can currently purchase the powder legally in the USA but I think it will soon be illegal.
Anyway, just stirring 1,4-androstadiene-3,17-diol with manganese dioxide (MnO2) will oxidize the allylic 3-OH to a 3-ONE and VOILA, boldenone base in one step from a legal prohormone.
4-androstene-3,17-diol can be oxidized to testosterone the same way. If one were to start with the 17-cypionate of 4-androstenediol, test cyp would be the product.
Nandrolone can be made analogously from 19-nor-4-androstene-3,17-diol. MnO2 oxidations are extremely mild and clean reactions. It is unusual for any side reactions to occur at all.
I also saw this little teaser quote on the 4ad to test conversion " There is no bubbling involved or evolved in this reaction. It is a simple mixing at room temperature of the 4-AD in a solvent with a mild oxidizing reagent "
Again any help greatly appreciated I would love to start my new obsession of research.
Boldenone would be easier to make from 1,4-androstadiene-3,17-diol or the 17-cypionate thereof. One can currently purchase the powder legally in the USA but I think it will soon be illegal.
Anyway, just stirring 1,4-androstadiene-3,17-diol with manganese dioxide (MnO2) will oxidize the allylic 3-OH to a 3-ONE and VOILA, boldenone base in one step from a legal prohormone.
4-androstene-3,17-diol can be oxidized to testosterone the same way. If one were to start with the 17-cypionate of 4-androstenediol, test cyp would be the product.
Nandrolone can be made analogously from 19-nor-4-androstene-3,17-diol. MnO2 oxidations are extremely mild and clean reactions. It is unusual for any side reactions to occur at all.
I also saw this little teaser quote on the 4ad to test conversion " There is no bubbling involved or evolved in this reaction. It is a simple mixing at room temperature of the 4-AD in a solvent with a mild oxidizing reagent "
Again any help greatly appreciated I would love to start my new obsession of research.
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