Apparantly many of you have the wrong idea. Of course I'm not going to run the shit through a coffee filter, call it good and then inject. I know the BA in the gear is what did the dissolving, I mean thats it's soul purpose for being in the gear(as a solvent, not for melting styro). If it can't be recovered then I'll toss it with no regret. But who want to toss 6 bottles of human grade Test? Not me unless I have to. I started this thread to see if there are any chemists out there who could point me towards a method of separating the good form the bad. I know it's possible. Humans can slipt atoms into their component parts for christs sake. That question then becomes one of cost/time/complexity. And about the coffee filters, though I already said this, they are only there to pre filter the solution to remove the larger particulate matter. I was never under any illusion that it would render the material safe for consumption.
Ok, before I lay this out I would like to clarify a couple things...the human body is capable of millions of processes that scientists have yet to replicate in a lab! AND, the human body cannot split atoms into their components any more so than a glass of water can... the body can use ion gradients(electron gradients), etc.... but a glass of water will pull electrons forming ions to....but atoms, on their own, can split into their components... it's called radioactive decay....
Now, onto these two methods...
1. Precipitate the test out of the oil...(filter the foam pieces out first)
you can put the test in the freezer for a day or two and crash it... you will end up with a bunch of test crystals floating, at the bottom, and attached to the walls and bottom of the container it is in(I recommend using a wide glass dish for this, if you have pyrex lab glassware, that would be best...if not, go to walmart and get a half-pint jelly canning jar, with lid(sterilize it by using 91%isopropyl alcohol, fill jar half way, with the lid on, shake the jar... empty, drain, let evaporate til no liquid left in jar...)
you have 18 g of test e there(if it is dosed correctly).. you will not recover all of it, but will recover most if you take your time, and do this right.....
once the test is crystalized out of solution, filter the oil to catch crystals(save the crystals), you can do the freeze process again(using another jar... the one you have you need to sterilize a knife and scrape the edges and bottom, save those crystals....) you may get some more crystals(you can leave it in there for a couple more days) if they didn't fall out to the full extent that they will at that temp...
once you filter the crystals and have them contained, put them into a larger glass beaker. you will then put just enough methanol on them til you can get them to barely dissolve...swirl them as you are slowly adding methanol(if you add too much, it makes this take much longer and you lose way more product)...
once they are dissolved, you will take very cold(as in put the gallon in the fridge for a couple days while you are crystalizing the test... you will need a couple gallons)distilled water, pour 4 cups into the methanol/test solution. the solution will turn white, test will start falling out of solution...let this sit for about 4 -8 hrs(in the fridge, covered). the test will mostly be settled at the bottom(it will be white crystalline). run this through coffee filters(save test crystals, you will need to dry them now)... the water/methanol/test solution, you can add a couple more cups of cold distilled water.. if it turns cloudy again, there is still test in it... repeat last few steps to get it out...
you will dry the test crystals out completely(methanol is highly toxic!!! it does evaporate clean, so if you dry them completely you will not have methanol left)... as an extra precaution, you can rinse the test crystals with distilled water when you finish filtering them(while they are in coffee filter, slowly pour distilled water on top of them so it passes through them and the filter into the glass below)...DRY THEM COMPLETELY!!!
when they are completely dry, you can homebrew them back into test e....
This is not a difficult procedure, but patience, cleanliness, and sterility are key....If you take your time and do this right, you can get 15+g of test back out(i could probably save just over 16g, but I have lots of experience with things like this... if you get 15 you did a good job)
there is another method, but the one I posted is safer, and it yields test e... the other method yields tne, and uses caustic materials....