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TEK Ethyl acetate approach [CIELO]

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I did a small potency test on 50g of Noid bridgesii. 0.55g yield fumerate. dissapointing. This was a lower-in-the-stem cutting, aged for 6 months, no dark stress. Shows that bridges aren't always the most mescaline.
Thanks for sharing. 1.1% fumarate is not too bad. Lower stem is not as potent as the midsection as I understand it.

And yes, there is a large variability.

Extracting and propagating the spicer as cacti with precise mescaline measurements is a very worthwhile enterprise. I think it will make cacti in captivity more consistent/potent over the next decades.
 
Probably a mixture of sodium carbonate (maybe in various states of hydration), sodium bicarbonate (trace?), and the sodium salt(s) of whatever acid was in the EA.

[Edit: possibly also a bit of sodium acetate from hydrolysis of the EA as well]
Oh, and one shouldn't assume it's anything, nor not anything. Ideally, test for alkaloids as there may have been an unknown reason for slow precipitation, although this seems exceedingly unlikely if we're looking at a post-SC-treatment situation.
I did a small potency test on 50g of Noid bridgesii. 0.55g yield fumerate. dissapointing.
1.1% isn't all that bad, just not stellar. It did make me consider that the precipitation may have been incomplete due to some component of bridgesii interfering with the crystallisation process - hence the preceeding paragraph.
Extracting and propagating the spicer as cacti with precise mescaline measurements
species, perhaps?
 
Oh, and one shouldn't assume it's anything, nor not anything. Ideally, test for alkaloids as there may have been an unknown reason for slow precipitation, although this seems exceedingly unlikely if we're looking at a post-SC-treatment situation.

1.1% isn't all that bad, just not stellar. It did make me consider that the precipitation may have been incomplete due to some component of bridgesii interfering with the crystallisation process - hence the preceeding paragraph.

species, perhaps?
Unfortunately the precipitate was from another batch. That batch was coreless PC which came out to .5% and I feebly pulled until strips were clean. The amount of white crust was over 10g.

Does anyone experience their coffee filters dropping in flow pretty quickly? Mine do with pretty much everything I pour through them that has the slightest hint of particulates. I think half of my tek time is waiting for draining. Any filter recommendations would be appreciated.
 
Thanks for sharing. 1.1% fumarate is not too bad. Lower stem is not as potent as the midsection as I understand it.

And yes, there is a large variability.

Extracting and propagating the spicer as cacti with precise mescaline measurements is a very worthwhile enterprise. I think it will make cacti in captivity more consistent/potent over the next decades.

I will be doing a bunch of testing in the next few years.

Is there a mini FIELO we can do to save time? Like one big pull with a liter of EA on 10g dry?
 
I will be doing a bunch of testing in the next few years.

Is there a mini FIELO we can do to save time? Like one big pull with a liter of EA on 10g dry?
That would give you bad data.
Which i guess could be normalized if you did the same poor performing process against all samples.
But you'd wind up with results that indicate your source material is less potent than it actually is.

Given the same total volume of solvent, multiple smaller extractions will always outperform a single larger extraction.
 
That would give you bad data.
Which i guess could be normalized if you did the same poor performing process against all samples.
But you'd wind up with results that indicate your source material is less potent than it actually is.

Given the same total volume of solvent, multiple smaller extractions will always outperform a single larger extraction.
Why would it give bad data?
 
I think i made a mistake. I didnt notice you said 1L ea pulling 10g powder.
Thats a much higher ration of solvent to cactus and may actually overcome the partition coefficient issue i mentioned in my last post.

I'll step back and let someone who knows more about chemistry take it from here
 
Is this the place to report results?

I did a PC extract this weekend. This was from some cuttings that had been sitting in the sun for 5 months and then in the dark for a month. They were sun grown and new growth.

I haven't weighed it out but it looks like it's well over 1%! My guess is 1.75% from eyeballing previous pulls. The EA is cloudy so I have to wait.

I have a question though. The final pull still was reading green on the ph strip. I want to do another pull but it will have to be into a different vessel than the one I've already salted. If I do this last pull with 1L of EA, how much fumaric acid should I add? 3g?
 
Is this the place to report results?

I did a PC extract this weekend. This was from some cuttings that had been sitting in the sun for 5 months and then in the dark for a month. They were sun grown and new growth.

I haven't weighed it out but it looks like it's well over 1%! My guess is 1.75% from eyeballing previous pulls. The EA is cloudy so I have to wait.

I have a question though. The final pull still was reading green on the ph strip. I want to do another pull but it will have to be into a different vessel than the one I've already salted. If I do this last pull with 1L of EA, how much fumaric acid should I add? 3g?


Ok I was actually spot on. Total was 1.6g yield from 200g dry. That means this PC results are 0.8% fumaric. 3 foot long tip cutting, sat in sun 5 months, dark one month, no core!

Vigorous sun grown super sawtooth looking quintessential garden center PC. Even had TMV.

I am pretty happy about that. It's as good as that bridgesii lower mid. If I do another run with it I will try to cut out most of the white.
 
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