You can argue all you want, d8 is way less psycho active than d9
Heres from the us patent filed on converting cbd to d9 and d8.
It’s been found to be 3 to 10 times less potent in certain circumstances.
Heres the link
Btw read what it says right under where I underlined.
Side effects of d8 are more prevalent in adults than children
I bet when they say in certain circumstances d8 can be 3 to 10x less potent then d9 they’re talking about children.
I ate a gram edible I made with isomerized d8 from d9. It hit and then.
I was walking around the middle section of Walmart for about 30 minutes looking for jars that were very visible then got even more high and felt like I was going to puke and was sick feeling
what would you price thcv at? do hou have distilled thcv or did you crash w cpc?
Cannot comment on that. Still looking into the legality of THCV and doing research into what pricing should be
Although, I don’t concur with the second sentence of the first paragraph . Due to the fact that isomerizing cbd to delta 8 thc and oxidizing to cbn. I have 78% return rate out of 100 grams . Coa and proof.
Edit:
https://future4200.com/uploads/default/original/3X/7/2/72ec92dd68075f55fcd3e5d7bbd9397e17a9b37b.jpegIntersting tought i wonder if i would distill delta 9 to delta 8 i could have better results in my bubble oxigen treu solution rig with a altered ph
And patience 
The above posted literature talks about how d9 will oxidize into cbn but d8 wont
Treu d8 is more stable
Could you pm me the companies you have seen selling in bulk? I am in need of bulk cbn
The quote that delta 8 wont oxidize i to cbn is wrong, proof is in the puddin.
I dont see how you’ll get that double back to the 9th spot with just oxidation (plus get the rest of the ring up filled up)
Not gonna happen
sure thing. If you “see”.
I am so impressed that someone can get this to 99.9%, I have only gotten it to 93% in production quantities.
@richpel Have you tried crashing it out with a solvent?
Ya and that actually looks real. Will have CBC and D8 and several others at 99.9% as well soon
A dihydrocannabinol intermediate(two double bonds, pictured molecule is formed from d9) is formed before CBN.
Theoretically, for d8s analogous intermediate, the second double bound could form at d10 or d6a,7 without requiring d8 to move backwards to d9 first. I agree, d8 moving backwards is very unlikely under any reasonable conditions.
Not saying that’s the mechanism occurring for what @Thedistillator is observing , but it’s technically possible.
Depending on what method you use to make CBN, you will with form that diene that @Dabatronicus posted or you will force a radical which can do whatever the hell it wants. The location of the double bond is irrelevant since that alkene will behave the same in either position.
