New Mushroom Lab in Oregon

Thank you for clarifying questions that were asked about my post!

Cheers,
Sensi

This is why it’s important to make a large batch and store properly…or send samples to Flourish Labs and we’ll test as many batches/lots as you want! :stuck_out_tongue_winking_eye:

Cheers,
Sensi

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One of the main differences between an analytical labs extraction and extraction for producing products is in the analytical setting we dont need to worry much about long term stability as the tests are run within a couple of hours at most after extraction. And once innthe light protected HPLC vial and stored at 4C they are definitely stable for at least a couple of days

So apologies about offering up information with regard to large scale extraction and stability.

If anyone wants to do a longitudinal study on their extracts Flourish can help with that as well.

Cheers,
Sensi

I dropped off 5 samples to Flourish

2 chocolate bars. One a friend made and one someone sold me about a year ago that I bet is RC

3, 2 gram samples of Thrasher PE (ITWs Iso). One of the cap, one of the fat neck thing they get and one of a mini shroom containing cap and stem.

Will share results when I get them

My next step is to powderize a few lbs and mix it as Cyclopath suggested (nice and simple) Then I will test 3 different 2g samples from different areas of the batch and share those as well. See if there is any variance throughout a powdered batch

Any suggestions on something to grind them down to powder? I use a ninja blender right now that works great but I was looking at grain mills too on Amazon

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I’ve had good luck getting a fine powder with a Jawz Blender . It’s obnoxiously powerful.

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I’ve always used an oster and the right size canning jar.

I’ve also lyophilized (freeze dried) first for best results (at that point you can pretty much powderize in the baggy) rather than simply air drying or using a forced air dehydrator.

at scale, a mill will be a better solution than a blender.

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Stability of Psilocybin and Analogs.pdf (930.5 KB)

This paper is pretty informative but I can confirm that freeze drying isn’t the way. Even at moderate temps like -10 C it will certainly completely dephosphorylate psilocybin to psilocin. Using an off the shelf dehydrator preserves the psilocybin almost completely.

As far as homogeneity, if you powderize it’s helpful to sieve it to a uniform size and then mix otherwise there will still be higher concentration pockets and settling.

I prefer extraction to have large lots with an ensured homogenous potency, but I agree drying and grinding to a powder is very simple and effective for home use that is in a timely fashion. For storage though, extraction is far better because the enzymes will degrade even dry biomass. I have independently verified that this paper is pretty accurate from samples I’ve tested: about 50% loss after a month.

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:arrow_up: is another reason Im skeptical about the results from the psilocybin cup. They’ve advertising sample collections for months and the tests don’t occur until the competition…

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Wow!

image

Not how that USUALLY works.

I’d like to see that repeated, and can’t think of any good reason it should be true unless these molecules are part of a “dormancy through times without water” strategy.

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That’s exactly what I thought. It is completely counterintuitive to me but after testing it and test other peoples freeze dried vs air dried on the same batch I can confirm it’s true. I have no idea why this happens but it does.

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The cup was all sorts of sketchy…the magic myco fam didn’t even make the tw2 isolate/culture that won. It was an enigma culture that was gifted to him.

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How’d it go?

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Possible the chitin and other polymers in the mushroom cell walls makes a better barrier to atmosphere when air dried at room temp than when freeze dried?

Seeing as the cell wall polymers are hydrated to begin with, maybe a small amount of water at room temp is helping to keep the polymer gelled/swollen and thus provides a better barrier. Possibly freezing after dried interrupts this gelling? Likewise maybe freeze drying removes too much water?

These are all hypotheses though.

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Yep, all decent hypotheses.

Freezing ruptures membranes…allowing O2

is probably the best fit.

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So far so good I tested a few fruits from the same tub

Strain is Thrasher PE


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Can you explain how to read the potency on this? What’s desired? What’s average?

Im ignorant

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I’m learning myself

So apparently the range for fruits is 0.5% to 1.5%

Which is 5mg/g and 15mg/g

A micro dose is 1-2mg
A breakthrough trip is 25mg
250ug of LSD is similar to 25mg

Anyone feel free to add or correct me if I’m wrong

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Those figures agree with what I have seen.

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Old fruits can be much worse though like .2

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I just blended a pound of these TPE into powder and took samples

I’m going to test them 30 days apart and see how they degrade

Each one has 3 samples taken from the same area of the powdered blend. A was center, B was left side and C was right side. Not a perfect test by any means but will still be interesting to see the results

We will get to see the batch homogeneity triple tested and the degradation over the 60 days

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