distillate test results: 12.3% cannabinoids???

F&^k !!!

lol!!! NOOO!

@anon56994712 yahh man it gets you high AF

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Good vacuum when distilling. ?
Cbc can be formed when O2 is present
And breaks down to cbl

first pass is usually around 1000micron, second pass down to 150-250.

just felt like normal run. i know i get some conversion because my gear is crappy chinese, but this is absurd lol

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The most astonishing i find the thc-a
Not even the CBL

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right. compare that to the other test above. nothing seems right. there’s no way 5% TCHa in 3 times distilled oil

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First lab saw no thca. Which brings everything into question…

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I sugest you send samples to other members with analitics
@qga @tweedledew @Rowan
Let s find out

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I have had several batches along the way with these kind of mistery s
I always keep them to see if they crystelize or for what ever other Discovery that they are involved
Of non i can Defenatly appoint the culprit

problem is i have 1500 more lb of this material to process… i’m in the rec market so i need THC! gotta figure out what’s going on.

thank you for all your insights everyone

If you have smaller gear do a perfect run (low vac) see what that brings
One could water wash the biomass before extracting then dry and proceed
For ethanol
Or humid for hexane to rid the sulfor

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What’s the best way to up the ph of ethanol/oil solution? (After filtration, before solvent recovery)

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Best and safest is a water wash
MgO is used as is baking soda

Awww man, I really don’t want to add a whole new process… i need to buy a big reactor and do the whole seperatory funnel thing?

You can Mickey mouse a separatory funnel for real cheap, it only needs to work a few times. Get creative with jugs and buckets. You may need a glass turkey baster to get the last drops of the aqueous layer…

@Ruwan might be able to isolate this compound for further testing

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CBL formation via CBC degradation is one route, I believe
(Has anyone here seen or worked with CBC isolate?)

Any labs that are currently testing for CBT? I would be willing to bet it’s one of the impurities in some of my recent ∆8-THC samples.

so does this mean i can get rich by overcooking sulfur contaminated hemp to remediate thc?

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