I've been hearing mixed reviews about the conversion. Some say this technique will work and others are saying I need a non polar solvent to extract the DPT freebase from the solution. Which is right, or are they both right? Is this just one step shorter? Do I NEED to solvent to get the freebase correctly? It's almost all evaporated, a few more hours. It's still all pure white.
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All is dried and I now have some nice light orange chunks on DPT freebase (I hope) I'll test it out and report back with the weight as well
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Someone please explain how I got 1.05g out of this when I only put in 350mg DPT hcl and 50mg NaOH....??????
I thought weight was lost when converting HCL to freebase....?
I'm stumped
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I don't know what I made, but it's something other than DPT freebase....the chunks I had put into my base pipe they rocked up even more. It didn't melt to an oil or anything, just stayed solid. It smoked and it deffinatly hit me harder than straight HCL. My heart rate went way up, felt somewhat nauseated, and things are deffinatly swaying and my vision is odd. I'm very confused as to what I have now.......
After the pinkish burns off I'm left with a white/tan rock... I took it out and crumbles once I apply pressure. Still feels slightly waxy when I crush it. Please tell me I wasn't smoking lye, as I did not want to do that. Even if I did, just once, would there be any ill or noticeable effects of toxicity?
EDIT : Next time I'm going to break it up before hand and see if that works better.
Shit, another thing I just realized. Why wouldn't there be NaOH in there?! I was just a mixture of NaOH and DPT, evaporated. Isn't that what I get in the end product??? NaOH is a solid and doesn't evaporate :-/
I think next time I'll be using the non polar solvent to extract the DPT from the solution.....
I'm assuming the extra weight is H2O trapped inside.....