Any chemistryfag there ?
Does any1 know how to extract nicotine from ciggaretes or tobacco ?
>>723373354
just vape... that's as close as you're gunna get to it
Just squeeze them real hard
>>723373354
Butane, like your making BHO.
>>723373354
Try google. Or ask someone like nile red or nerdrage to do a video
>>723373354
i heard if you wrap it in cling film and smoke it the cling flim filters out the bad stuff really well
The problem is google says me GTFO, dont do that mate. Id like to try to do this in home conditions.
Light it and inhale.
Step1: dissolve in bleach
Step2: add any kind of acid
Put in water
Tar and nicotine will sink to the bottom in a glob
chew it for about 15 mins and keep spitting, all the spit you collect is basically 100% pure nicotine, if you want to make it pure gently heat it in a pan
>>723373354
Put it in alcohol, then damp the alcohol away. You will have a brown oily liquid. Don't touch it.
>>723373354
Put it in water and let the water evaporate. What should be left is nicotine and the rest of the chrmicals in a cigarette. Make sure not to touch the water as nicotine absorbed by the skin that way is much more potent.
cat urine breaks the chemical compound down, something to do with the ammonia in cat urine, it has to be fresh though
>>723375208
Listen to this guy. Dont forget to swallow the remaining tobacco as your mouth will change it's ph value to dangerous levels if you don't let it dissolve by the acid in your stomach
>>723375208
OP, I can confirm this kinda works. Probably your best bet.
>>723373354
See for yourself how you should do it:
Nicotine, C10H14N2. The pure alkaloid is a colourless oil, b.p. 246.1 °/
730-5 mm. It can be purified
through the crystalline zincichloride, B,ZnCl2,2HCl,H20, the regenerated
base being distilled under reduced pressure (20-40 mm.) in presence of
nitrogen or hydrogen. It distils unchanged in a current of steam and is
readily soluble in alcohol, ether or light petroleum. The behaviour of
nicotine with water has been studied by several workers.19 It is miscible
in all proportions with water below 60° and above 210°; at intervening
temperatures soluble hydrates are not formed and miscibility is limited.
According to Kelly et al.19 an azeotrope is formed, which contains 2.45 per
cent, of nicotine and boils at 99-6°/760 mm. The salts are readily soluble
in water, do not crystallise easily and are dextrorotatory.