ThatChemGuy
Rising Star
Hi everybody, swim is having problems sourcing clean aliphatic hydrocarbons and is planning on using different solvents for an extraction from mimosa.
Swim can source only Ether and DCM, cleaniest source of naphta is Zippo LF.
Swim is planning on distilling it to get a crystallization solvent but can do it only in small bathces (so not enought for an extraction).
What we know is that with xylene or toluene Jungle Spice will come along with the N,N,and that Jungle is mainly actual DMT with some "impurities".
A quick look to the polarity table and we read:
Heptane....0.1
Toluene....2.4
Xylene.....2.5
Ether......2.8
DCM........3.1
Seems safe to say that if Ether is used for a main extraction instead of naphta, pure yeld should increase a bit but the product will be overall pretty dirty (probably not just alkaloids, some plant junk will come along too); this trend should increase with DCM, lowering purity a lot.
Big problem with these solvents is that Ether is really flammable and DCM is carcinogenic and very eco UN-friendly.
Source plant material is not much and it's nearly 10yo, so swim was going to run some tests before the bulk extraction.
Has swiy any experience extracting with non-hydrocarbon solvents? Swim should really go with ether but he can't work outside or in a fume hood so DCM can actually be safer, but purity (even after crystallization) will be much lower.
Another question is about test batch size: swim has 90g mhrb left, with a bulk extraction size of 30/40g (and at least two of them), swim is left with 10g to 30g for testing. Has swiy any experience with very small batches? Is a 5 or 10g extraction possible? If we consider a 0.5% mean source we are talking about 50mg to 25mg of product if full efficency, with a very dirty pre-crystallization reagent this can lead to many problems like actually getting some crystals. Sadly no TLC are available for now, just a scale and a pair of lungs.
All in all I think 10g batches should be fine; we'll begin as soon as the lab glassware arrives.
I'll keep you up to date with the results.
ThatChemGuy out, peace.
Swim can source only Ether and DCM, cleaniest source of naphta is Zippo LF.
Swim is planning on distilling it to get a crystallization solvent but can do it only in small bathces (so not enought for an extraction).
What we know is that with xylene or toluene Jungle Spice will come along with the N,N,and that Jungle is mainly actual DMT with some "impurities".
A quick look to the polarity table and we read:
Heptane....0.1
Toluene....2.4
Xylene.....2.5
Ether......2.8
DCM........3.1
Seems safe to say that if Ether is used for a main extraction instead of naphta, pure yeld should increase a bit but the product will be overall pretty dirty (probably not just alkaloids, some plant junk will come along too); this trend should increase with DCM, lowering purity a lot.
Big problem with these solvents is that Ether is really flammable and DCM is carcinogenic and very eco UN-friendly.
Source plant material is not much and it's nearly 10yo, so swim was going to run some tests before the bulk extraction.
Has swiy any experience extracting with non-hydrocarbon solvents? Swim should really go with ether but he can't work outside or in a fume hood so DCM can actually be safer, but purity (even after crystallization) will be much lower.
Another question is about test batch size: swim has 90g mhrb left, with a bulk extraction size of 30/40g (and at least two of them), swim is left with 10g to 30g for testing. Has swiy any experience with very small batches? Is a 5 or 10g extraction possible? If we consider a 0.5% mean source we are talking about 50mg to 25mg of product if full efficency, with a very dirty pre-crystallization reagent this can lead to many problems like actually getting some crystals. Sadly no TLC are available for now, just a scale and a pair of lungs.
All in all I think 10g batches should be fine; we'll begin as soon as the lab glassware arrives.
I'll keep you up to date with the results.
ThatChemGuy out, peace.