Greetings all. I just joined but am not new to psychedelics. I am hoping to get advice from more experienced folks here than I believe is available elsewhere. Ive used marijuana for 5 years, once a week. I have tried mushrooms once (weak), salvia probably 20 times (20x), mescaline (strong) (from IPA extractions of San Pedro, and boiled tea) maybe ten times, 2ce twice, and an attempt or two at LSA (hbwr seeds) and blue lily. I have worked with Ayahuasca 3 times, and was successful in getting it to work all the way once. I have tried A/B extractions with San Pedro (failures) a couple of times, and have attempted a failed STB extraction of MHRB powdered once before. I have a college degree, am a skydiver, used to be a BASE jumper (7 years), scuba diver, sailer, backpacker, and extensive world traveler. I have done enough reading in my life to basically be a permanent liberal arts sort of person, so Im a bit hamstrung, chemically speaking. Its nice to meet everyone, thanks in advance for your support and help.
On a whim, and with no expectations of success, I set off another attempt at a STB extraction of MHRB (powdered) fully expecting a dismal failure. But as fate would have it, well, it succeeded. Im so bad at extractions that even though I should continue with the process, I REALLY dont want to lose what I have. I used "Spicey Cats" stickied tek from Hipforums DMT forum which is apparently a combinative, simplified version of Lazymans tek, and/or Noman's tek. With 100 grams of powdered MHRB, around 13 tablespoons NaOH (I do not have a scale), warmed Naptha vm+p, distilled water, and after a double eye dropper decant, I intended to do a freeze precipitate with the five 80 ml warm naptha pulls, all of which came off as a clear as water, with no visible hitchhikers. I was under the impression that when I evaporated 1/2 the naptha, the remaining amount would be cloudy, indicating that it was ready for freeze precipitation. After a little more than half was gone, was still clear as water. I kept evaporating. When it finally started looking maybe like some texture or cloudiness was occurring, the amount of Naptha remaining was pretty small. Thought was a dud. Allowed to completely evaporate. Two days have passed. Like 50 little islands of furry, spikey crystals appeared on the pyrex glass pan. Many of these are white, some are white/light pale yellow, and they are of varying sizes. I have no idea how much. Maybe 1 dose. maybe 5? In addition there are some colorless crystalline patterns here and there. It looks pretty clean. Except for the thin clear sticky film which coats 75% or so of the bottom of the pan. Its not thick, you cant leave a fingerprint in it, and the islands of crystals seem unaffected by it, although the crystalline patterns are flat in this coating. The light thin coating doesnt cover the spiky, furry crystals. Honestly, I dont know what to do with it, now. I wasnt expecting this to work. Normally, anything I do chemically is a disaster and a comedy all rolled into one.
My actual question. I dont want to mess up by continuing further, is it useable now? I was anticipating scraping crystals off the bottom of the pan, chopping them fine, giving them good dry time and then figuring out dose. (I have no scale of any sort, and have been told that a scale that is actually accurate in low milligram doses is REALLY expensive). But as clean and useable and clear as the crystals are, to get them I would be scraping up this thin tacky clear layer, which in my limited experience is probably extracted plant fats and waxes. Im guessing this may make vaporizations harder? or make the smoke harsher/less palatable? or bulk up the amount of vapor to be inhaled? Possibly the film is something more toxic? I could use the point of a knife to axe out the crystal islands (with some loss, particularly the diffuse crystalline patterns) and physically eliminate 90% of this film, I suppose. But I believe Im supposed to use warm solvent to redissolve all this, then freeze precipitate to lose the plant fats/waxes, and, or do a recrystallization with heptane, but, again, Id hate to lose the progress Ive made by continuing my crippled chemistry. Plus, Id be back to square one in terms of not having cloudy saturated naptha except in a minute 30 ml amount, which Id guess is too small an amount to do this well, or easily.
Can I reasonably use this product? Or must I continue? Thank You doesnt cover it...
Ps. Im going to try and attach an equally crippled picture. Glass pan is square 8.5 inches by 8.5 inches. The crystal islands are like 30 rice kernels scattered over 1/2 the pan...more seem to have faint yellow tint now...
doc savant attached the following image(s):

IMG_0540.JPG
(1,339kb) downloaded 124 time(s).A Civilization is born spartan, and dies Epicurean...