You should see my forearm! Few chemical and steam burns at this point.
I got burnt once with concentrated AcOHā¦
Gives you a whole new view of the word ārespectā.
Straight facts. To this day the worst burn I ever got was by steam. I am hairy motherfucker. I have patches on my left arm because I donāt grow hair anymore lol.
Getting acid on your skin is about as much fun as napalm.
I appreciate the information. Iāll stick to ethanol
Are you saying vinegar can be used as a solvent?
You should try uric acid as your solvent
Thatās what I use to disolve ur girlfriends makeup
Should have said āyo mamas makeupā but it was still a great comeback.
However I donāt think it is a good idea
Anything you extract with vinegar and evaporate will be left with a gooey mess, even if itās something that normally crystallized upon evaporation. Itās just gross
Besides I doubt it would be possible
Hereās one utilizing Menthol (not methanol) and acetic acid to extract cannabinoids.
Closest thing I found while searching
thank you.
they used an analytical trick I hadnāt heard used for cannabinoids: Separations | Free Full-Text | Single-Run Separation and Quantification of 14 Cannabinoids Using Capillary Electrophoresis
I would probably not spend too much time or resources investigating this. There is pretty much zero obvious benefit, and any number of disadvantages such as:
- cost
- occupational hazard/general unpleasantness
- increased infrastructure/operations (ventilation, PPE, storage)
- needing to use SS316, PTFE, PE, other expensive high chemical compatibility materials for everything that touches acid
- its high boiling (118C) compared to conventional extraction solvents
- whatever chemistry occurs when you leave cannabinoids in contact with acetic acid/product stability
In general I would ask myself questions like āwhat about ~insert proposed action~ provides me a better extraction?ā Answers to a question like this might be:
- its cheaper
- its safer
- its more selective
- it improves efficiency/reduces operations
Iām not saying donāt compare its extraction selectivity to other solvent in a concise series of experiments if youāre that curious, but I wouldnāt beat my head against this for too long considering the obvious complications using AcOH introduces.
read: AcOH better provide an insanely selective or efficient extraction to offset all the other disadvantages
None of the above.
Nice summary
ā¦ lol Iām not sure you want to make vinegar dabs
Haha why you mad bro? Donāt want to derail this great thread you created, just like the rest you make. Great job!
imho, try a methanol wash, make an oil, dissolve that in etoh for winterization and to possibly further lower the amount of methanol.
personally, I tried so hard to keep etoh as my main solvent and I fucking hated it the more I tried. Itās literally now only used for rso, winterizing bho runs or reclaim/misc clean-ups.
final opinion, I would just keep running butane.
Groove once you aredissolved in methanol
It would be stupid not to winterize as well at the same time for it s the best solvent to winterize of the common solvents
I was just saying in case OP did decide to do MeOH and was afraid of any residual ppm.
MeOH is definitely a solvent i want to try Iām just deadly afraid of working with it.
No fear. Some good ventilation and don t drink your extract and you ll be fine
I work with a ton of methanol. The low vapor pressure makes it relatively unlikely to cause you problems. Iām much more afraid of hexane, and that seems like a way more common solvent round these parts.