synovex h

Ive been doing some serious studying on the whole fina/finaplix
experiment, and along the way i've discovered a couple different experiments on synovex h. I know its basically test prop, but with a high amount of esters. There is a experiment kit available on bigtrenkits.com that offers a decent kit at a pretty good price.
What I would like to know is there anybody out there that could give me some links, or some personal advice, besides the instructions that come with the kit, on how to convert this shit?
I have a stack of papers about how to convert fina, well, now I want a stack of papers on how to convert synovex!

ive got some more info on the converting process. Here is what i've got....
This idea is to wash out the estrogen from the pellets with water, acetone,methanol, or some other solvent. I've heard this wont work though because nothing will dissolve out the estradiol benzoate(eb) while leaving the TP behind. Organic solvents such as acetone or methanol will dissolve the TP even more easily than the EB. Water will do nothing since both TP and EB are practically insoluble in water.
Another concept is to dissolve the TP in acetone, methanol, ether, or some other organic solvent, leaving the EB behind. The problem with this is that no organic solvent will dissolve TP while leaving the EB untouched. You will always have a significant percentage of dissolved EB.
Now, realizing that "if" the esters were removed from the steroids-yielding test and estradiol-these probably could be seperated from each other. Again, both are soluble in organic solvents and both are practically insoluble in water, but there's a trick.Estradiol will react with a strong base, such as sodium hydroxide, to yield the sodium salt of estradiol, which is soluble in water. Therefor one might be able to extract the test into an organic solvent, such as ether, and the estradiol benzoate into alkaline water....MAYBE.
One guy lost more than half the test in this process, and the test was kind of a nasty yellow.
The sodium salt of estradiol acts just like a bile acid-a steroid molecule thats actually quite similar. What you have here is a molecule thats largely hydrophobic or oil like, but one end of the molecule is very hydrophilic. These can cluster together into spheres and present the hydrophilic end on the outside, into the water, with the oil like parts on the inside. Any kind of oily or waxy material can then be carried on the inside of the sphere.
This is how bile acids dissolve fats and steroids in the GI tract. The same thing might be going on here, allowing the sodium estradiol to carry away a lot of test into the discarded water.

Hope this info might help some of you guys out there. Maybe someone could send me a kite. I'm always looking for something new, and then again, even something old....

I see you've been reading T-mag as your post contains excerpts from an article written by Bill Roberts. He may be on to something although I don't think he knows what.