I dont see why it would not work with disty. Ive seen it done before.
A quick way to tell is, is the disty more stable then it was? D8 is stable
What is the definition of stable with d8? Viscosity? Lack of crystallization? It definitely behaved more like thc than CBD coming out of the head and down in to the collection flask. It lightened the color a bit also. Much clearer than that first pic looks. I can’t hold the phone still for closeups to save my life.
Ime cbd disty is runny and sticky.
D8 is usually hard enough to knock on. If theres crystallization thatd be weird. Indicating not d8
Yeah, it appears to have converted. Lab is slow here so we’ll find out for sure in about a week.
Please excuse my ignorance, but if you’re reacting your base material with an acid in order to produce your desired isomers, is there a need for a pH correction in the polishing phase? If not: Does the reaction self correct the pH (using T41 or Citric), or is the pH likely to be at an acceptable value for consumption without further correction?
Haha, thank you for posting my next question. I was wondering the same thing. Does the reaction take care of that or do I need to rebalance the ph? There’s a slight pinkish tint and a very faint rubbery smell. I’d like both to go away.
correct the ph before consumption is what i’ve understood
Thanks. Can anyone chime in on how to correct the pH safely for consumption? I’d hate for someone to follow 90% of this thread and hurt themselves, although citric acid is a weak acid so I know it won’t be like xenomorph blood (couldn’t resist).
From what i have read you would simply dissolve it in a solvent and use ph down (bicarb). Please someone tell me if this is wrong
Classic liquid liquid alkaline wash, followed by water wash… Thats all…
Is it going to mess up the lab results if I don’t balance the ph and wash it before I test it?
Will a “freeze and pour off” be adequate following the water wash, or is a rotovap/double boiler needed?
Rotovap and distillation, or Just straight distillation
What percentage T41 did you use?
20200301_164254|375x500 ? I did 5% and it came out with the same color as yours but less viscous than what it should’ve been for high amounts of D8.
If you have color change you used too much acid.
You can adjust the PH with titration to fix color imbalance
Bicarb will work to remove the acid but it’s not strong enough to correct the color imbalance
Is there any concern from the color imbalance other than aesthetics?
As long as you do neutral water washes to remove any acid there shouldnt be any concern
I used 10%. Dried in the oven and then mixed in before it went in the boiling flask. It went to the lab this morning. Should have some results by Friday at latest.
Today’s experiments, ac, t5, and citric acid. Who knows which of these work best?