ez people. So after deciding to use noman's tek since the qt tek went horribly wrong! swim used 50 of powdered root bark with caustic soda and zippo fuel. by the way the zippo fuel swim used is the one in the red and black tin (swim is from uk) and it seemed better than the naptha containing white spirit swim used recently. Neway after freeze precip and redesolving in warm naptha the precipin again, swim ended up with 0.3g of yellow almost oily powder. smelt plasticy and when smoked smelt like fart gas but got swims mate (the guinea pig) fucked but not to breakthrough. any suggestions why swim didnt get snow globey crystals?is swim on the right track here? much apreciated lads n lasses.
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After thoughts to extraction
- Thread starter reflex
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freedominphilly
Rising Star
maybe you got some of the black/brown gunk in with the solvent mix..i know that when SWIM does his extractions, that is the reason why his doesnt end up completely white.
ChemicalEudaemonia
Rising Star
I wish my farts smelled like DMT. Mmm'mmm. It could be you had too little DMT dissolved in too much naptha.
It just needs cleaning. Barks vary in yellowy content and NP's differ in how much other stuff they pull. If it were more widely available I'd have spec'd heptane as the NP because its much more selective than naptha. At any rate, a recrystalization should take care of it.
No definitley didnt pull any of the lye mhrb mix through to the np solution. swim did recrystal it once with no real effect. goin to use swims last 20g of mhrb n change lighter fuel. then if no difference change root supplier but will def stick to nomans tek. thanks
magic clown
aka Slap Stick Sam
Was the lighter fluid Ronsonol? White tin, red and black print? That stuff is cool. My friend uses that for the first pulls, then switches to Swan for the recrystalizing. My freind wouldn't bother getting out of bed to pull 20g.
Yes 'easily' ... I muse.... aloud... is this another case demonstratring why it is important to do 'proper procdure' when attempting to solubilize and extract tryptamines from MHRB..? Everyone knows now, since I've been saying it over-and-over ... and since any chemist will tell you - "solubilize the tryptamines first" ... ! And that requires pH of 2- 4. That fact plus filtration puts all the dmt in the MHRB at your command. From this you will get the MOST white snow-globe 'shards' of dmt possible per gram of MHRB used. The Lye-stew is bad for you, bad for dmt (pH of 13.5 .>! pwhaah! ..), and yeilds low quality, and 50% of the quantity... when you do it right. Why do you even bother..? Which 'chemist' amongst us, piping up here isn't being convincing enough ..!? The Lye-bucket method is not worth the cost of the MHRB, ... the risk to your body and brain .. lips and face ... not even the hair on your chin..! Clearly newbies especially, ought to stay away from lye-stew 'teks' ... Another side-observation ... Bad teks are good for keeping bulletin board threads going ... about how poor the result is etc etc ... discussing the actual failings in detail.. ! Posting pictures even ... ! But then people keep trying it, and presumably even smoking the suspicious yeild ...!> This is spreading mis-information ... and risk around. I see few threads explaining the failings of an acid-base procedure. I had to learn by mistake too. Practice an acid-base method, learn how to filter the acid extract (Whatman 100 brand works well). Practice 'proper procedure' a few times instead of choosing a 'tek' that seems "easy", and refusing to learn what each stage entails, chemically, logistically etc ... ...
