Save your unusable raws Guaranteed.

As said by others surface solvents are easy to remove via vacuum and mild heat. But solvent/impurities can and will get trapped in the lattice and amorphous regions if crystals rapid form. This is why we are recrystallizing in the first place. Its the shit that gets trapped behind from yield being more important than quality. Just did recryst on some of the shit TC from AASraw I just got. Off to Jano Monday with before and after samples. MP is good at 101.2 initial and 102 clear. Nice sharp MP. Happy with the result on it. Just ethanol as solvent and carbon wash/filter through celite and slow cool from 60c. Seeded at 40c. MP video starts at 101c 1c/min rate. Out of the bag MP was 90c initial and 100c clear. So both depressed and extended. Powder looked fairly white(light beige)but was yellow as piss once in BB, would not go into dissolution. I ran it up to 250mg/ml in straight BB and up to 150c.


Were you able to figure out where the yellowing came from?
 
Were you able to figure out where the yellowing came from?
Some non soluble garbage. Maybe oxidation? Crystals all dropped and came out clean. Once filter dried out it looked like dust bunnies on the filter. All the color stayed in mother liquor. Crystals washed. Pretty clean.IMG_6507.webpIMG_6507.webp
 
what is the current tele? just read through the entire thread excited to try this for myself since I just got 92-93 percent purity test prop raws
i do been nuked a few times but each time some hater decides to nuke i grow 10x the size so i consider it a celebration for growth lol last time i was nuked i had 300 then i got 900 i expect 1500 soon
 
how difficult is this to do on a large scale for kilos
by the process itself its already done in LARGE vats at the synthesis labs at least officially. when i made this thread i was reading how industrial purification is done and i simply scaled it down to home use. if you have the time and the lots of energy then yeah it should be pretty easy to process kilos and kilos at a time assuming you got enough solvents....however its better to do it small batches at time instead if you really want to make sure you get the best you can. getting to 97 to 98% pure is the easy part.

getting to 99% and 99,9999% ...yeah thats a vast vast vast effort level there. if you got kilos better to split your batch into 500 to 300 Grams at one time and process it untill you get something clean. then repeat. going all at once will give large error and harder to control

i processed like 500 grams of eq however that was a whole other ball game had to do vacuum distill and liquid to liquid extraction

if you got some AAS raws test just process your stuff in small batches.
 
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