D8 thca

Hempire Building Hemp Outlet
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Has anyone made some stones yet?

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Out of curiosity, where do you propose deriving enough d8 thca from to make d8 diamonds? I think this would involve recarboxilating a conversion

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I was thinking CBDA isolate, for the best yield, or non decarbed high potency extract.

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You’re high

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I don’t think you understand how this works my friend…

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Care to elaborate?

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I think you’ll have a hard time holding on to your “a”

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During the isomerization?

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Cleanup is where I think you will have a problem without distillation.

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I was thinking of running the isomerization in a lower bp solvent like pentane to help the purging. I was also considering using a polymer supported catalyst to avoid a LLE step and just filter it out.

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Got excited cause I thought this was going to be another recarb thread… Damn…

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Im slowly getting the things together to do some carboxylations using the methyl magnesium carbonate in DMF method. It looks like the yields are horrible for THC, but ill still make a few grams of D8THCA for fun (and for science). I’ll keep yall updated

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Why? I’m not saying this cbda to d8thca will work as I’m not qualified enough to make that statement.

But I can say I have made 95% TAC d8/d9 blend and never took anything above 80c during the reaction or cleanup. Which in theory wouldn’t decarb the solution. Finished product had final solvent removal done in a rotovap and was clear, which also shows water clear isnt only made by distillation.

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This is one of the reasons behind me wanting to winterize with membranes in hydrocarbons

Cbd a > d8 thc a is very possible and wouldn’t be hard with the correct sop

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Recrystallization of the THCA alone should be sufficient cleanup and doesn’t require any.heat

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I guess i need to put some of my higher cbda stuff aside and do a few reactions. I think i have a little bit of 75% cbda 20% cbd from an old run i could use.

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:eyes:keep us posted. I’d like to see d8 diamonds. I’m ASSuming the d9thca will crystallize right along with it, yes?

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I dono, i did a little digging, it sounds like @RockSteady has tried this a few different ways and its broken the carboxyl group.

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Looks like we’re back to recarboxylation

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