Hi everyone! I have a problem with my first evaporation and i really hope you can help me! 
Yesterday i've done my first extraction using STB Noman's Tek.
Everything went well, this morning i found my first crystals precipitaded from my first pull (2nd and 3rd are still in the freezer).
So, i poured all the naphtha (i used RONSONOL Lighter Fluid) from my glass bowl and then only nice snow white crystals remained.
So, i put the bowl upside-down with a side up, to let all the naphtha evaporate completely, because a very very very thin wet layer remained on the botton.
But now, after something like 8 hours, i went to check the bowl and it seems that the great part of the crystals are dry because they are more white and sharp than this morning, BUT, there is still the same thin wet layer on the ground, and if i touch it now its a little bit oily.. I know that it could be that thing that you call "goo", but everything in the bowl (naphtha and crystals) is perfectly white, no other alkaloids (i think), absolutely no dirt from the MHRB in the water solution. And i have not heated nothing in all the process, not the water, not the naphtha, not the crystals after the precipitation to help naphtha evaporate, so this shouldn't be dmt oxidate. And it can't be a residue of the RONSONOL, because i left a glass in the kitchen yesterday evening with a little bit of it (like 2-3 ml) and this morning the glass was completely clear and dry, no smell of naphtha at all!
What should i do now in your opinion? Maybe the naphtha requires DAYS to evaporate completely, so i should only wait? Or if not, what can i do?
And, I have the other two pulls in the freezer at the moment, what could i do to let naphtha better evaporate from these two pulls?
I'm probably missing something in this step.. but i can't waste the material from my first extraction!!
Thank you very much!!
Yesterday i've done my first extraction using STB Noman's Tek.
Everything went well, this morning i found my first crystals precipitaded from my first pull (2nd and 3rd are still in the freezer).
So, i poured all the naphtha (i used RONSONOL Lighter Fluid) from my glass bowl and then only nice snow white crystals remained.
So, i put the bowl upside-down with a side up, to let all the naphtha evaporate completely, because a very very very thin wet layer remained on the botton.
But now, after something like 8 hours, i went to check the bowl and it seems that the great part of the crystals are dry because they are more white and sharp than this morning, BUT, there is still the same thin wet layer on the ground, and if i touch it now its a little bit oily.. I know that it could be that thing that you call "goo", but everything in the bowl (naphtha and crystals) is perfectly white, no other alkaloids (i think), absolutely no dirt from the MHRB in the water solution. And i have not heated nothing in all the process, not the water, not the naphtha, not the crystals after the precipitation to help naphtha evaporate, so this shouldn't be dmt oxidate. And it can't be a residue of the RONSONOL, because i left a glass in the kitchen yesterday evening with a little bit of it (like 2-3 ml) and this morning the glass was completely clear and dry, no smell of naphtha at all!
What should i do now in your opinion? Maybe the naphtha requires DAYS to evaporate completely, so i should only wait? Or if not, what can i do?
And, I have the other two pulls in the freezer at the moment, what could i do to let naphtha better evaporate from these two pulls?
I'm probably missing something in this step.. but i can't waste the material from my first extraction!!
Thank you very much!!
The DMT in jungle spice... assuming the impurity of your product will become harder to evaporate...and well just follow my advice and re extract with some nice warm bestine. 
