Hi everyone!
I registered a bit over a year ago - some FOAF had just done their first extractions and wanted me to tell you all about it. Somehow, I never posted that essay and now I can't find it anymore. There was an STB and an A/B from MHRB powder, both with KOH, d-Limonene, Acetic Acid, then Sodium Carbonate, both yielding ca. 1%. The STB resulted first in a nasty emulsion, then in a very dark jimjam freebase that was absolutely delightful both on its own and in changa, with a very strong forest presence. The A/B went smooth and resulted in slightly tan jimjam freebase crumble with slightly less of that forest vibe. They also extracted some rue alk freebase and experimented a bit with changa proportions. I liked Harmalas:Carrier:Spice at 1:2:3 best, and they seem to agree.
So far, our preferred carrier herb is Salvia Officinalis, it's pretty easy on the lungs. I plan to test-smoke many different herbs and spices though to come up with a mixture to improve taste. Cinnamon is surprisingly nice to smoke - I'll have to see if it fits in a mixture.
Now, a few days ago, those FOAF decided to try a Limtek.
- They mixed 300g MHRB powder with 390g Calcium Hydroxide in a glass bowl. Once well mixed, they added water until the consistency was doughy.
- They then stirred this mixture using a hand mixer with dough hooks, for a minute every few minutes during about an hour.
- They then poured ~500ml d-Limonene into the bowl and stirred a bit every now and then for maybe 25 minutes. Then they decanted the limonene through a coffee filter into a sep funnel, trying to get as much of it as possible.
- They pulled 3 times with ~50ml FASW (shaking limo/FASW in the sep funnel for 3x3mins each time), put the combined FASW pulls on a stove at maybe 60°C and called it a day. It took almost 36h to evaporate and yielded 2.1g jimjam fumarates (~1.6g freebase?) with little fumaric acid contamination. Once the evaporation dish was free again, they did another 2 FASW pulls which yielded almost only fumaric acid. They washed the limonene twice with demineralized water, then poured it back into the MHRB dough in the bowl.
- They did the second limonene pull (at ca. 48h after mixing the dough), this time leaving the limo and bark together for almost an hour. They then pulled with FASW 3 times, combined the pulls and put them in the evap dish on the stove. They're still waiting for evaporation to complete, but from the looks/color of it, they expect a similar yield to the first limonene pull. They have a 4th FASW pull in the sep funnel waiting for the dish to be free, and won't make a 5th. They suspect that the 4th won't yield anything either, in which case they will stick to 3 from now on.
- They plan another limonene pull at the 7 day mark, and if that yields well, another one at the 14 day mark, and so on until the bark is depleted. They keep stirring the dough a few times every day, whenever they think of it.
Lucky me, they gave me some of the fumarates from the first pull. I wanted to smoke some in changa, but I was out of Sodium Carbonate for freebase conversion.
I still had some sage infused with rue harmalas (2:1 sage:harmalas) that I had prepared some time ago (for mixing 1:1 with spice freebase -> 1:2:3 changa). And I wanted to smoke some of the new spice really badly. So I dissolved 0.13g fumarates in a bit of water in a shot glass, added 0.1g of the harmalas sage, and put it on the stove overnight. I thought if it doesn't work, it'll have been worth a try. And boy, it did work! I first smoked a third in the bong, which was buzzing but not very much. I then smoked the rest for a nice visit to an inner crystal palace.
Now I wanted to know more. I also had some rue harmalas HCl. I dissolved 0.12g rue HCl and 0.35g spice fumarates in some water, added 0.18g of sage, and put it on the stove overnight. A few hours ago, I tested it, and this also works great! In effect, it means that with Limtek, FASW, Manske, and water, one can make changa without ever needing any base other than lime, and no alcohol or acetone.
Because I had never thought of smoking fumarates (my FOAF only worked with vinegar before), I wanted to know whether anyone on the nexus had already tried it. As it turns out, some people have talked about it in 2010.
In that thread, some health concerns were raised, which I take very seriously. One was the possibility of toxic burn products of fumaric acid when smoking fumarates, a second one was about smoking HCl salts, my guess is because that might produce Cl gas (noone seems to have tried that?).
I can't say anything about the first one, I don't think one can assume that fumarate ions behave the same as fumaric acid molecules, but then again, if the DMT works, it was probably transformed from ion to molecule as well, so if anyone actually knows what's going on there, I'd like to understand.
About the second one, I can definitely say that no noticable chlorine gas was produced, no suspicious or unpleasant smell/taste, no pain or difficulty breathing. The opposite is the case, somehow the smoke was a bit sweet and felt nice.
As per my bioassay, I'm really tempted to only work with salts in the future. But I'd like to know if that's safe. I think it would be interesting to burn a bit of all-salt changa in a gas chromatography. Is there a way for mere mortals to do that?
So, I'm Homo Trypens, I stop by the nexus every now and then, and now I have spoken for the first time
I registered a bit over a year ago - some FOAF had just done their first extractions and wanted me to tell you all about it. Somehow, I never posted that essay and now I can't find it anymore. There was an STB and an A/B from MHRB powder, both with KOH, d-Limonene, Acetic Acid, then Sodium Carbonate, both yielding ca. 1%. The STB resulted first in a nasty emulsion, then in a very dark jimjam freebase that was absolutely delightful both on its own and in changa, with a very strong forest presence. The A/B went smooth and resulted in slightly tan jimjam freebase crumble with slightly less of that forest vibe. They also extracted some rue alk freebase and experimented a bit with changa proportions. I liked Harmalas:Carrier:Spice at 1:2:3 best, and they seem to agree.
So far, our preferred carrier herb is Salvia Officinalis, it's pretty easy on the lungs. I plan to test-smoke many different herbs and spices though to come up with a mixture to improve taste. Cinnamon is surprisingly nice to smoke - I'll have to see if it fits in a mixture.
Now, a few days ago, those FOAF decided to try a Limtek.
- They mixed 300g MHRB powder with 390g Calcium Hydroxide in a glass bowl. Once well mixed, they added water until the consistency was doughy.
- They then stirred this mixture using a hand mixer with dough hooks, for a minute every few minutes during about an hour.
- They then poured ~500ml d-Limonene into the bowl and stirred a bit every now and then for maybe 25 minutes. Then they decanted the limonene through a coffee filter into a sep funnel, trying to get as much of it as possible.
- They pulled 3 times with ~50ml FASW (shaking limo/FASW in the sep funnel for 3x3mins each time), put the combined FASW pulls on a stove at maybe 60°C and called it a day. It took almost 36h to evaporate and yielded 2.1g jimjam fumarates (~1.6g freebase?) with little fumaric acid contamination. Once the evaporation dish was free again, they did another 2 FASW pulls which yielded almost only fumaric acid. They washed the limonene twice with demineralized water, then poured it back into the MHRB dough in the bowl.
- They did the second limonene pull (at ca. 48h after mixing the dough), this time leaving the limo and bark together for almost an hour. They then pulled with FASW 3 times, combined the pulls and put them in the evap dish on the stove. They're still waiting for evaporation to complete, but from the looks/color of it, they expect a similar yield to the first limonene pull. They have a 4th FASW pull in the sep funnel waiting for the dish to be free, and won't make a 5th. They suspect that the 4th won't yield anything either, in which case they will stick to 3 from now on.
- They plan another limonene pull at the 7 day mark, and if that yields well, another one at the 14 day mark, and so on until the bark is depleted. They keep stirring the dough a few times every day, whenever they think of it.
Lucky me, they gave me some of the fumarates from the first pull. I wanted to smoke some in changa, but I was out of Sodium Carbonate for freebase conversion.
I still had some sage infused with rue harmalas (2:1 sage:harmalas) that I had prepared some time ago (for mixing 1:1 with spice freebase -> 1:2:3 changa). And I wanted to smoke some of the new spice really badly. So I dissolved 0.13g fumarates in a bit of water in a shot glass, added 0.1g of the harmalas sage, and put it on the stove overnight. I thought if it doesn't work, it'll have been worth a try. And boy, it did work! I first smoked a third in the bong, which was buzzing but not very much. I then smoked the rest for a nice visit to an inner crystal palace.
Now I wanted to know more. I also had some rue harmalas HCl. I dissolved 0.12g rue HCl and 0.35g spice fumarates in some water, added 0.18g of sage, and put it on the stove overnight. A few hours ago, I tested it, and this also works great! In effect, it means that with Limtek, FASW, Manske, and water, one can make changa without ever needing any base other than lime, and no alcohol or acetone.
Because I had never thought of smoking fumarates (my FOAF only worked with vinegar before), I wanted to know whether anyone on the nexus had already tried it. As it turns out, some people have talked about it in 2010.
In that thread, some health concerns were raised, which I take very seriously. One was the possibility of toxic burn products of fumaric acid when smoking fumarates, a second one was about smoking HCl salts, my guess is because that might produce Cl gas (noone seems to have tried that?).
I can't say anything about the first one, I don't think one can assume that fumarate ions behave the same as fumaric acid molecules, but then again, if the DMT works, it was probably transformed from ion to molecule as well, so if anyone actually knows what's going on there, I'd like to understand.
About the second one, I can definitely say that no noticable chlorine gas was produced, no suspicious or unpleasant smell/taste, no pain or difficulty breathing. The opposite is the case, somehow the smoke was a bit sweet and felt nice.
As per my bioassay, I'm really tempted to only work with salts in the future. But I'd like to know if that's safe. I think it would be interesting to burn a bit of all-salt changa in a gas chromatography. Is there a way for mere mortals to do that?
So, I'm Homo Trypens, I stop by the nexus every now and then, and now I have spoken for the first time