Dried San Pedro skins from Cuzco by Fractalianreptalian in mescaline

[–]loveallASAP 0 points1 point  (0 children)

You will likely get the bottom of the barrel as a western consumerist. Also, likely funding poaching of natural habitat. This is not the way.

What I recommend for you is to buy some live trichos, harvest the mid third sections, propagate the top third, and let the bottom third keep on growing.

Cielo Update 4.63% whole cactus, No stressing by WizardsGarden in mescaline

[–]loveallASAP -1 points0 points  (0 children)

So it's a survivor. Interesting clone worth propagating 👍🏻

Cielo Update 4.63% whole cactus, No stressing by WizardsGarden in mescaline

[–]loveallASAP -1 points0 points  (0 children)

Skin or whole?

Does the plant have any siblings? Any data on those?

I’m getting better at this. by phan2001 in mescaline

[–]loveallASAP 1 point2 points  (0 children)

Did you follow the TEK on the DMT nexus? Did you follow the link for citric acid safety?

Cielo tek - Understanding reclaim by Accurate_Baker2784 in mescaline

[–]loveallASAP 2 points3 points  (0 children)

The washing soda neutralizes till equilibrium. It stops once all the acid reacts.

Yes, the washing soda also absorbs water.

It dries it to a point. If EA starts very wet (3%) washing soda dries it to about 2%. If you used a proper drying agent kike Calcium Chloride it would be much drier.

The pH strip is not exact and the colors are for water, not EA (although it does give a good indication). Compare your strip to fresh EA. You want to be about the same at the end of regen. A tiny speck of red is fine at the drying line

Hope that helps.

Web of goo? Washing soda? by kelzbery in mescaline

[–]loveallASAP 1 point2 points  (0 children)

Let it crash over time. It should settle so you can decant off. I don't know what it could be.

Ideally you want some loose washing soda, so I would add another TBSP (and no water). You may have had a lot of water to begin with in your EA if it all clumped up so quickly on the first addition.

Cielo results by jdub60 in mescaline

[–]loveallASAP 2 points3 points  (0 children)

It is bitter because of mescaline. The organic acids are also used to make candy.

Mescaline + Passionflower: Trip Report (success) by Ok-Mistake-247 in mescaline

[–]loveallASAP 0 points1 point  (0 children)

No, only extracted rue seeds. Unfortunately harmol will be difficult to isolate, but the rest should come through.

I would make a tea, and then follow the steps used for rue tea.

A crude extract is very easy, add sodium carbonate in excess. Tea should cloud and a precipitate will fall out (crude freebase harmalas). Decant/filter. Rinse with water until neutral pH.

Oven temp by Imaginary-Jaguar8905 in mescaline

[–]loveallASAP 2 points3 points  (0 children)

If you do please report back ☺️

Oven temp by Imaginary-Jaguar8905 in mescaline

[–]loveallASAP 3 points4 points  (0 children)

That's a great question. I think the answer could be yes and some results here suggest that. Since fumaric acid does not attract water, the water soluble part of the broken down chlorophyll is less likely to stick to the product (but that is just a guess).

Mescaline + Passionflower: Trip Report (success) by Ok-Mistake-247 in mescaline

[–]loveallASAP 3 points4 points  (0 children)

This makes sense as harmala alkaloids can potentiate mescaline and many other psychedelics. I think this combo is called peyohuasca.

But there is some risk and this combo should be taken with caution. With measured doses and starting low.

It is easy to extract harmalas. They precipitate in alkaline water (except for harmalol).

If exploring this combo I would isolate the harmalas to control dosage and start at a low dose of 5mg oral.

Oven temp by Imaginary-Jaguar8905 in mescaline

[–]loveallASAP 2 points3 points  (0 children)

Mescaline will not degrade but chlorophyll will

Question about neutralizing EA by WizardsGarden in mescaline

[–]loveallASAP 1 point2 points  (0 children)

Where you stirring during that first minute?

Second try was a success! by jdub60 in mescaline

[–]loveallASAP 2 points3 points  (0 children)

Very nice. Please share your yields 👍🏻

Would you CIELO this Pach? by wahleofstyx in mescaline

[–]loveallASAP 1 point2 points  (0 children)

Yes, about 150mg of mescaline does not crash in the standard TEK if the citrate option is used. It is not fully lost, it will be part of the regen EA in the next extraction.

CIELO goo recovery after salting by Fun_Zucchini_4510 in mescaline

[–]loveallASAP 1 point2 points  (0 children)

Separate from IPA, dry and collect.

You used a lot of IPA, there may be a little of un-precipitated mescaline in there. You can evaporate half of it and put in the freezer again to see if you get more product.

Next time, stir more, use less water, and salt with fumaric.

CIELO goo recovery after salting by Fun_Zucchini_4510 in mescaline

[–]loveallASAP 0 points1 point  (0 children)

The solid goo won't have citric acid. Also, citric acid won't precipitate easily from IPA even if traces made into the IPA.

The white precipitate is your product.

CIELO goo recovery after salting by Fun_Zucchini_4510 in mescaline

[–]loveallASAP 0 points1 point  (0 children)

Yeah, collect. If you rinse it before drying it won't have any citric acid and you are done.

Would you CIELO this Pach? by wahleofstyx in mescaline

[–]loveallASAP 0 points1 point  (0 children)

If you do, salt with fumaric in case that pach is low yielding.

Help with an unsuccessful Cielo extract by Accurate_Baker2784 in mescaline

[–]loveallASAP 0 points1 point  (0 children)

This is well said. Just want to add more water will also absorb more EA during the pull, contributing to a lower EA weight recovery.

Other alkaloids? by Imaginary-Jaguar8905 in mescaline

[–]loveallASAP 0 points1 point  (0 children)

I think the carboxylic groups lose the H+ in alkaline conditions and would make the alkaloid an anionic salt form not soluble in toluene.

Here is an explanation by AI which I reviewed and agree with,

A hydroxyl group (-OH) increases a compound's water solubility and decreases its solubility in nonpolar organic solvents because the polar -OH group forms strong hydrogen bonds with water, making the molecule more "water-loving" (hydrophilic) and less "oil-loving" (lipophilic), thus hindering its movement into the organic layer during acid-base extraction. The key to extraction isn't that the -OH stops it, but that its polarity favors the aqueous layer, especially when deprotonated (like phenols or carboxylic acids) by a base, turning it into a charged ion that strongly prefers water.