I imagine it’s going to come down to ease of access.
I appreciate the insight, it hadn’t occurred to me to try and ‘mix’ reactions. Plenty of papers out there describing olivetol+something else to make CBD or otherwise.
If there’s a reasonably accessible terpene that can convert resulting olivetol during the reaction, that’d be pretty intriguing.
I think we’re all curious to how your runs this weekend go, and what kind of byproducts are there!
Just going to throw verbenol into the discussion since it seems you guys are looking at relevant SOP’s. That’ll lead you to some of the other old school reactions that I feel like iontrap is hinting at.
I’ve seen olivetol in CRC’d extracts at like 0.02% but that’s pretty much it. Accompanied by trace amounts of D8. Phenol/butyl phenol etc has been documented in cannabisheadspace studies so some definitely exists outside of conversions but the question is which ones, how much, and if it’s a contaminant to begin with. It’s possible that a lot of these things could occur under natural circumstances (natural degradation or non) but the concentration is going to be a drop in the bucket compared to what you could see as a reaction byproduct.
Pthalates are a pretty common contaminant in general but I only am familiar with them in the context of plastics leaching. Cannabis definitely produces a wide range of things that could theoretically go astray under the right conditions. 2-ethylhexanol pops into my head which I’ve seen several times. Usually the pthalates I’m familiar with are just from bad lab practices like handling plastic materials that are not apt for solvents. I’d be curious to see some more insight in the context of cannabinoid conversions since I think plasticizers are already a widely unrecognized, common contaminant in cannabis extracts.
we have found that treatment of equimolar quantities of these materials in the presence of 1% BF3.Et20 and anhydrous magnesium sulfate in methylene chloride at 0" for 1.5 hr yielded A’-THC as the major product and practically no A’@) isomer was formed. When the reaction was carried out either in the absence of magnesium sulfate or at room tem- perature, considerable amounts of AI@)-THC(5) were formed.
If you get something iontrap and/or KCA labs signs off on, count me in. As a consumer I’ll gladly pay double the current retail prices for a clean, safe product.
On the business side, if you get there, I’d love to discuss getting your product in stores nationwide in the USA. We work with some big names in the CBD and headshop space on the marketing and strategic business relationship side of things.
I only wish that they put more focus on labs because it’s really helpful to get a little background before you start working with folks that really know what the heck they’re doing.
A college education does not an accomplished chemist make. It takes years of chemical synthesis to get there.