CBD isolates usually contain some 0.1-0.8% CBDv, plus another one in similar or lower poportions (CBD dimer ? CBD quinone ? I’m still not sure), even after several crystallization. So each 99+ isolate has in fact it own identity. You can discern them with a finely tuned GC.
@PaulyFerg
I would consider over 2% difference from a commercial standard on your quality checks a no-no.
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Did you generate the calibration curve yourself? What is R2? Should be 0.999-ish.
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If yes, where did you buy standards? There are issues with standards:
a. if you dont keep them in a freezer and don
t try to use them rather soon after opening; building a calibration curve at 10% off can happen easily - then all your analyses will be 10% off.
b. If you built your calibration curve with a standard from one company, did you validate against the same standard from a different company?
Some companiesstandards are downright awful - Restek - an established standards company sends out d9-THC prepared gravimetrically, no CoA; says purity is 98% - guess what the standard really is. We purchase standards from Absolute Standards - can
t say enough good words about their work. -
This way you eliminate the standards issue.
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I assume you use auto-pipettes when you say you do their calibration - they are not very good with organic solvents. Switch to a glass pipette.
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Do you know how to properly use HPLC injection microsyringe? While trivial, many people don`t.
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What injection volume you use? Why not over the injector volume (usually 20 uL)? This way you assure consistency.
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What analytical balance are you using? If cheap balance and not with at least 1mg precision, then this can be an issue too.
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During your HPLC runs, do you control temperature? It has a significant impact on peak RT, as well as height.
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Is this lab you are referring to doing anything above and you are actually right and they are wrong? Just because it is a certified lab, doesn`t mean the person setting up the method was doing things correctly.
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How do you prep sample?