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When is DMT ready to smoke, after scraping it off?
- Thread starter tele
- Start date
- Merits
- 117
Ideally one should redissolve in a (pure) less toxic solvent such as ethanol, IPA or acetone, and let it evap again.. This will take care that any solvent traces trapped inside crystal formations are freed and evaporated completely
actualfactual
Rising Star
- Merits
- 42
Myco said:
No need to heat because it should go into solution easily. Only heat if you want the IPA to evaporate faster..
- Merits
- 1,056
tele said:
Step 1: Take a small glass
Step 2: Fill the glass with Ethenol,IPA or Acetone (whichever you have handy)
Step 3: Put your scraped up spice crystals in the same glass
Step 4: Stir a little bit and you will see that the DMT will easely dissolve
Step 5: Pour the content of the glass into a pyrex dish (or any other evap dish with a large surface)
Step 6: Let it completely dry
Step 7: Scrape up and chop it up with a razor blade into very fine crystals
Step 8: Let it sit for a day while chopping it up again once in a while
Fininsh!
Kind regards,
The Traveler
- Merits
- 42
it will seem gooey at first if you use acetone/IPA. Don't worry about it, this is normal. It will turn waxy and semi-crystalline once you move it and chop it some and let it dry some more. It's def. not as pretty as freeze precipitated crystals but that shouldn't matter 
The Traveler said:
Sounds easy, but just to make sure, couple questions:
-For about 200mg of crystals, how many milliliters would be enough(is it enough just to cover them)
-How long should the crystals sit in the substance after stirring?
-Most important: I suppose the crystals will be in different form after evaporating off the Acetone/substance, what should I expect it to look like? Some sort of crust on the bottom of the pyrex dish??
And is this step really necessary? Wouldn't it be enough just to chop the normal crystals into fine powder, to evaporate every last bit of naphtha that might be trapped in them?
The Traveler said:
Hello, i was wondering why this would work? Surely unevaporable solvent traces would not evaporate by being redissolved into another solvent?
Or is it that the dirty solvent traces won't dissolve into the cleaner solvent, ethenol acetone etc.. ?
I am wondering if during a freeze precipiation extraction, as much dirty solvent elements are left remaining in the end result as opposed to the results of an evaporation extraction?
I am also curious as to whether redissolving a cleaner solvent, would be enough purification?
I have read that freeze precip/recrystalisation would remove lye + not leave dirty solvent elements, if using a cleaner solvent for reevaporization, then the only difference would be the possibiltiy of some lye remaining in the spice as the dirty to clean solvent evaporisation method would also not leave dirty solvent elements.
So it would not seem worth it to go through the extra effort of a recrystalisation method (all other things being equal) for a such a small amount of improvement of purity?
- Merits
- 117
There are different kinds of impurities, some might be ok to have, others might be unwanted.
Regarding solvent traces, redissolving in a cleaner solvent will help get rid of it because the solvent (For example naphtha) might be trapped inside crystal formations and therefore not be able to evaporate. But when you redissolve the whole thing in a cleaner solvent, the crystal formations will be broken and the trapped solvent will be released. When it is released, it will mix with the cleaner solvent, diluting itself over that bigger volume, and will evaporate together as the other solvent evaporates. Does it make sense now?
Even freeze precipitated crystals will suffer from the same issue of quite possibly having trapped solvent because regardless of being in the freezer or not, fact is that crystals formed inside a solvent can trap small amounts of that solvent, so personally I would also recommend doing that redissolution and re-evap for freeze precipitated crystals.
Regarding lye and impurities and so on, check these threads/links out, maybe they can be of help:
Spice purity and color falacy: Is my spice ok to smoke?
FAQ: Should I wash my spice?
Regarding solvent traces, redissolving in a cleaner solvent will help get rid of it because the solvent (For example naphtha) might be trapped inside crystal formations and therefore not be able to evaporate. But when you redissolve the whole thing in a cleaner solvent, the crystal formations will be broken and the trapped solvent will be released. When it is released, it will mix with the cleaner solvent, diluting itself over that bigger volume, and will evaporate together as the other solvent evaporates. Does it make sense now?
Even freeze precipitated crystals will suffer from the same issue of quite possibly having trapped solvent because regardless of being in the freezer or not, fact is that crystals formed inside a solvent can trap small amounts of that solvent, so personally I would also recommend doing that redissolution and re-evap for freeze precipitated crystals.
Regarding lye and impurities and so on, check these threads/links out, maybe they can be of help:
Spice purity and color falacy: Is my spice ok to smoke?
FAQ: Should I wash my spice?
About redissolving, can someone please reply to these questions, as I wouldn't want to ruin first ever crystals!
-For about 200mg of crystals, how many milliliters would be enough(is it enough just to cover them)
-How long should the crystals sit in the substance after stirring?
-Most important: I suppose the crystals will be in different form after evaporating off the Acetone/substance, what should I expect it to look like? Some sort of crust on the bottom of the pyrex dish??
-For about 200mg of crystals, how many milliliters would be enough(is it enough just to cover them)
-How long should the crystals sit in the substance after stirring?
-Most important: I suppose the crystals will be in different form after evaporating off the Acetone/substance, what should I expect it to look like? Some sort of crust on the bottom of the pyrex dish??
tele said:
1- You're going to want enough to completely dissolve the spice but not so much that it takes forever to evaporate. Covering them won't be an issue since they will soon be disappearing in solution.
2- Once again the point is to dissolve them and then evaporate them so they will sit there as long as it takes for the solvent to evaporate leaving nice white dry crystals behind.
3-I don't know what they look like now but in the end you should end up with a white/off-white powder.
As someone said the last stages of evaporation can be misleading. Sometimes an oily goo will be left on the dish but this will eventually start to solidify naturally, especially by mixing it around chopping it up a bit.
DudeMeetTyler
Rising Star
- Merits
- 42
So would dissolving your spice in acetone to make enhanced leaf also allow for naphtha impurities trapped in crystals to dissipate (i dont know why it wouldnt, but Im not sure hence the question lol)
- Merits
- 117
yes dudemeetyler, acetone wold also help with that.
tele, just read above posts and the links I posted. There isnt a right amount of time because it depends on many factors.
tele, just read above posts and the links I posted. There isnt a right amount of time because it depends on many factors.
- Merits
- 42
tele said:
Scrape out your crystals and smell a can of naptha. Lay your crystals out and take a quick whiff you should smell the same naptha smell. When you can no longer detect that smell comming from your crystals you should be fine. I usually give it stir to make sure none is trapped. You shouldn't be able to smell it at all.
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