Procedure: 1. Begin by Adding 100g Cacti Powder or Diced 12in Cacti Cutting(s) To A Pot. Add 30g Citric Acid

Procedure
Procedure for Mescaline HCl Extract

1. Begin by adding 100g cacti powder or diced 12in cacti cutting(s) to a pot. Add 30g citric acid
or 200ml vinegar or 10ml glacial. If using cacti powder, add enough water to make it wet but
not watery.
2. To this add 2L H2O and simmer for 2hrs. Mix occasionally. Any cacti snot will boil off
eventually and the tea should become nonviscous and watery.
3. Filter out liquid from plant matter with a cloth filter and funnel, and add the liquid to another
pot. Reduce this to a low volume by boiling. Add plant material back to original pot, cover
with 2L H2O, and simmer for 1hr. Mix occasionally.
4. Repeat step 3 atleast four to six times total until the liquid filtered out has very little color.
Discard plant material after final time and reduce all the aqueous cacti extract to around 300
ml. This can be put in a glass pickle jar. Allow to sit overnight to precipitate unwanted fine
particles, but this is optional.
5. Now it is time to basify. Mix 50g NaOH in 100ml H2O. It will get VERY hot, it is
recommended to cool the mixing container while stirring with a cold water bath or under the
faucet. Add the NaOH solution to the aqueous cacti extract.
6. Add 200ml toluene (or xylene) and mix for 10-15 minutes. Let the mixture settle and use a
hot water bath to seperate the layers from the emulsion if necessary. Seperate the layers with
a pipet, separatory funnel, or syringe. Save the toluene in another glass container and put
basic aqueous cacti solution back in original container.
7. Repeat previous step atleast 4 times total. Discard basic aqueous layer after, saving the
toluene extract which contains the alkaloids.
8. To the toluene extract add 100ml H2O. Add 0.5ml concentrated HCl to this and mix well for
5 minutes. Check the pH. If it is still basic (pH 9+) then add incriments of 0.5ml HCl with
mixing and checking pH until it tests acidic (below pH 7). Continue mixing for 10 minutes
after. Only one acid salting pull is usually necessary, but more can be performed and may be
necessary for larger scale extraction.
9. Seperate layers, hot water bath may be necessary to seperate emulsion quickly. Filter and
save acidic H2O layer and discard/recycle toluene. Evaporate the aqueous layer on a dish
with aid of a fan and/or hot water bath. Never use direct heat it will scorch your product.
Scrape up the crystals.
10. Wash crystals with 50ml cold MEK (or anhydrous acetone, ethyl acetate). You will notice
the solvent become discolored and the crystals become cleaner. Decant off the solvent
carefully, leaving behind the cleaned crystals.
-You will usually be left with light tan Mescaline HCl if pachanoi was used. Yield will be
largely dependent on how efficiently you performed the extraction, but most importantly the
quality of cacti used in the beginning. 0.5-1.5% yield of dry starting weight is average, but
can range anywhere from 0-3%. Enjoy!
Procedure Notes
-Reducing the initial liquid: After each filtration the liquid is put into a pot, the "reducing
pot". This can be boiled on high heat, just make sure it doesnt boil over. Once the liquid has
boiled down to a low volume, stop reducing it when it becomes different in appearance and
syrupy. Make sure not to reduce beyond this point and obviously dont boil it completely dry.
Doing so will destroy alkaloids.
-Filtering plant material: This can be quite a frustrating step if working with cacti powder,
though you get the hang of it over time. It is easiest to seperate out the liquid from cacti
material by using cloth cut from a shirt and then pouring the sludge into a funnel through the
cloth filter. Get a pair of rubber gloves and squeeze out the liquid from the filter. Dont
squeeze too hard or cacti sludge will press through. Filtering is easiest to do while the liquid
is hot and should be done atleast twice after each water boil. It also gets easier after each
boil.
-Checking pH: The pH can be checked with pH paper by dipping it in the toluene/H2O
solution while mixing. The paper must come in contact with the water layer as pH cannot be
read from the nonpolar layer.
-Washing the crystals: It is important to wash your end crystals with a solvent like MEK or
anhydrous acetone to remove impurities. The solvent dissolves resins and impurities, leaving
behind cleaner non-sticky crystals.
Additional Purification
Procedure for White Mescaline
NOTE
Doesnt change effects much, but increases purity and looks awful pretty! This procedure can be used to obtain pure
white mescaline, and solvent ratios must be followed exactly. Solvent ratio affects the rate crystals precipitate out and
more importantly their size. If they are too small/precipitate too quickly, they will be too fine to filter or decant liquid
from. More nonpolar-> decreases solubility, more methanol-> increases solubility.
1. To a glass container with 1g cleaned Mescaline Hcl add 50ml H2O + 1ml HCl. Mix well until
crystals completely dissolve.
2. Add 50ml toluene.
3. Mix 10g NaOH with 50ml water and add this to the solution, turning it basic. Mix well for 10
minutes.
4. Seperate layers, saving toluene and discarding aqueous.
5. To another glass container pour 40ml methanol (HEET antifreeze remover) and add 0.5g
fumaric acid. Mix well until fumaric acid dissolves.
6. Add the fumaric methanol to the toluene and mix it alittle. After a short time, the solution
turns cloudy and crystals begin to form. Once crystals settle, mix it alittle more and pour into a
dish.
7. Very carefully decant by pouring off liquid and leaving behind white crystals. With no
remaining liquid on the plate, let crystals dry and scrape up, yielding pure white Mescaline
Fumarate. Enjoy!
Additional Purification Notes

It is important to remove all the liquid to avoid fumaric acid contamination. Alternatively to
decanting, you can filter if the crystals are big enough. This purification SWIM imagines 
could be used for larger amounts of mescaline keeping to the solvent ratios. It is also 
possible to use other solvent combinations and acids for precipitation, though this is left up to
you. One could also get a pretty pure product if they simply did another hcl salting from the
toluene instead of precipitation.
Dosage Information
The good thing about making a purified mescaline extract is that you can easily measure exactly how
much you are consuming and the experience is more clear. Mescaline is a very "friendly" feeling
substance that is probably the least edgy of the traditional psychedelics imho. The experience is
usually associated with euphoria, brightened colors, increased sociability, altered thinking, and
morphing rainbows/patterns/environment. While dosages vary for everyone, I believe this to be a
fairly accurate scale of dosage for the extraction procedure:
 Threshold <100 mg
 Light 100 - 200 mg
 Common 200 - 400 mg
 Strong 400 - 600 mg
 Heavy >600 mg
Pictures
Materials Required
Source Material:
 100g cacti powder or 1-2 12in cutting(s).

Solvents:
 1L Toluene or Xylene
 50ml MEK, anhydrous acetone, or ethyl acetate
 H2O
 40ml Methanol (Optional)

Reagents/Desiccants:
 30g Citric Acid or 200ml white vinegar (10ml glacial)
-->Citric Acid Appears More Likely To Cause Emulsions
 50g NaOH (Lye)
 Hcl (Muriatic Acid)
 0.5g Fumaric Acid (Optional)

Equipment:
 Pots
 Glassware
 1L glass pickle jar
 Evaporating dish/bowl
 Stir utensils
 Pipet/syringe/separatory funnel
 Coffee filters and funnel
 Cloth filters (shirt)
 Rubber gloves

Procedure: 1. Begin by Adding 100g Cacti Powder or Diced 12in Cacti Cutting(s) To A Pot. Add 30g Citric Acid

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Procedure: 1. Begin by Adding 100g Cacti Powder or Diced 12in Cacti Cutting(s) To A Pot. Add 30g Citric Acid

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What is the procedure for extracting mescaline HCl?

What is the procedure for extracting mescaline HCl?

What are some tips for filtering plant material and checking pH?

What are some tips for filtering plant material and checking pH?

Procedure

Procedure for Mescaline HCl Extract

from. More nonpolar-> decreases solubility, more methanol-> increases solubility.

 Light 100 - 200 mg

 Common 200 - 400 mg

 Strong 400 - 600 mg

 100g cacti powder or 1-2 12in cutting(s).

 50ml MEK, anhydrous acetone, or ethyl acetate

 40ml Methanol (Optional)

 30g Citric Acid or 200ml white vinegar (10ml glacial)

-->Citric Acid Appears More Likely To Cause Emulsions

 50g NaOH (Lye)

 Hcl (Muriatic Acid)

 0.5g Fumaric Acid (Optional)

 1L glass pickle jar

 Coffee filters and funnel

 Cloth filters (shirt)

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