I left the H. hostilis powdered root bark sit in sulfuric acid for a couple days, shaking off and on.
Filled mason jar with enough acid so that it was 1/3 bark 2/3 acid.
This gave a DARK red (black) sludge and red fluid (separated).
coffee filtered fluid to get red fluid only. took sludge and placed in fresh acid.
Confirmed red fluid is acidic.
Next added the sodium carbonate
(made by heating sodium bicarb at 500*F for >30min)
Na2CO3 was added until solution stopped fizzing. formed a thick gray fluid, but very viscous, not thick, did not resist stirring
Confirmed fluid is alkaline.
after setting there were then two layers...no siphoning or filtering done here.
Next added (all to same container) acetone and vigorously shook.
This left three distinct layer; bottom appeared to be Na2CO3 gray material, middle layer was black sludge, top layer was tan/brown acetone...resisted stirring a little.
Acetone siphoned off, filtered...only clear layers were kept.
the syringe is for NS but was emptied, filled straight from mason jar, but it shows how it appears...in my's opinion...quit diluted.
I placed a plate with a pool of brown acetone and a mason jar half filled with brown acetone in the oven set to 280*F and as dry layers appeared around edges of fluid on the plate warm fluid from mason jar in oven was lightly applied to edges...this caused the center to grow darker and darker, the edges remained nearly clear (until dried, then brownish)
Here is another pic...This was done 5-7x's so far
btw...the plate is flat, the outside is freshly added dilute solution, the center is not more fluid but more concentrated.
curious
1. what exactly do I have here? DMT dissolved in acetone? Forming fast flakes of dmt crystal from fast evap?
2. By darkening the center through evap really concentrating dmt levels in the center?
If yes How much darker should I let it get?
If no should it go through a fresh acetone/coffee filter bath top layer only pull off?
If no...does it really affect the end viability?
3. can I place these concentrated "flakes" and place with some tobacco or other herbs and smoke or will it need to have its form altered again.
4. I'm assuming this will form a yellow sludge, yes
5. can it be smoked as is once the acetone dries out?
Appreciate any help
Filled mason jar with enough acid so that it was 1/3 bark 2/3 acid.
This gave a DARK red (black) sludge and red fluid (separated).
coffee filtered fluid to get red fluid only. took sludge and placed in fresh acid.
Confirmed red fluid is acidic.
Next added the sodium carbonate
(made by heating sodium bicarb at 500*F for >30min)
Na2CO3 was added until solution stopped fizzing. formed a thick gray fluid, but very viscous, not thick, did not resist stirring
Confirmed fluid is alkaline.
after setting there were then two layers...no siphoning or filtering done here.
Next added (all to same container) acetone and vigorously shook.
This left three distinct layer; bottom appeared to be Na2CO3 gray material, middle layer was black sludge, top layer was tan/brown acetone...resisted stirring a little.
Acetone siphoned off, filtered...only clear layers were kept.
the syringe is for NS but was emptied, filled straight from mason jar, but it shows how it appears...in my's opinion...quit diluted.
I placed a plate with a pool of brown acetone and a mason jar half filled with brown acetone in the oven set to 280*F and as dry layers appeared around edges of fluid on the plate warm fluid from mason jar in oven was lightly applied to edges...this caused the center to grow darker and darker, the edges remained nearly clear (until dried, then brownish)
Here is another pic...This was done 5-7x's so far
btw...the plate is flat, the outside is freshly added dilute solution, the center is not more fluid but more concentrated.
curious
1. what exactly do I have here? DMT dissolved in acetone? Forming fast flakes of dmt crystal from fast evap?
2. By darkening the center through evap really concentrating dmt levels in the center?
If yes How much darker should I let it get?
If no should it go through a fresh acetone/coffee filter bath top layer only pull off?
If no...does it really affect the end viability?
3. can I place these concentrated "flakes" and place with some tobacco or other herbs and smoke or will it need to have its form altered again.
4. I'm assuming this will form a yellow sludge, yes
5. can it be smoked as is once the acetone dries out?
Appreciate any help

thanks