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== Collect πŸ’–==  
 
== Collect πŸ’–==  
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Catch crystals in a coffee filter. Rinse jar/filter with room temperature ethyl acetate a couple times and dry (Fig. 6).  
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Catch crystals in a coffee filter. Rinse jar/filter with a couple ounces of room temperature ethyl acetate a couple times and dry (Fig. 6).  
  
  

Revision as of 03:25, 9 June 2021

CIELO

Introduction πŸ™

CIELO stands for Crystals In Ethyl-acetate Leisurely Over-the-counter.


In this technique (TEK), cold alkaline cactus paste (Fig. 2) is extracted with chilled ethyl acetate (Fig. 3). Mescaline citrate is precipitated with citric acid (Fig. 4-5) and collected (Fig. 6).


Thanks to everyone who contributed: someblackguy, Benzyme, shroombee, Metta-Morpheus, Downwardsfromzero, Kash, grollum, Mindlusion, Doubledog, Dreamer042, Loveall, and others.


Safety ⛑️

Review ethyl acetate's safety information[1]. Verify MSDS, plastic compatibility, and clean evaporation.


Following this advice does not guarantee safety. It is up to each adult individual to make their own decision.


Materials πŸ›’

  • French press (or similar ensemble)
  • 300g ice cold water
  • 25g lime
  • 100g dry cactus powder
  • 1qt freezer chilled (~0F) ethyl acetate
  • Coffee filter, support basket, and funnel
  • Quart jar
  • 5g of citric acid
  • 4oz of room temperature ethyl acetate
  • Washing soda (for solvent reclaim)


IMG 20210603 180858748 copy 800x600.jpg
Fig. 1: Materials.

Process πŸ“œ

Paste 🌡

Mix ice cold water, lime, and cactus in french press for a few minutes to a smooth paste (Fig. 2).


IMG 20210603 183405358 copy 800x600.jpg
Fig. 2: Alkaline cactus paste.

Extract πŸ‘¨πŸΎβ€πŸ”¬

Cover cold paste with chilled ethyl acetate (~0F), mix for for 60 seconds and filter to quart jar. Repeat until jar is full (~5x).


Inspect extract for droplets or particles. If present, remove them. Extract needs to be clean (see Fig. 3).


IMG 20210601 122315740 copy 600x800.jpg
Fig. 3: Ethyl acetate extract.

Crystalize ✨

Drop (do not stir) citric acid into extract, forming clouds (Fig. 4). After a few hours mescaline citrate crystals form (Fig. 5). Allow crystalization to complete undisturbed (~12 hours).


IMG 20210604 165954132 copy 800x600.jpg
Fig 5.: Crystals in ethyl acetate.

Collect πŸ’–

Catch crystals in a coffee filter. Rinse jar/filter with a couple ounces of room temperature ethyl acetate a couple times and dry (Fig. 6).


If some crystals stubbornly remain on the jar walls, dissolve them in hot water, dry in a shallow dish, and scrape.


Yield depends on the cactus and is usually between 0.2% to 2% with ~1% being most common[2].


IMG 20210603 130102387 copy 600x800 copy 800x600.jpg
Fig. 6: Collected mescaline citrate crystals.


Mass spectrometry (MS) results from solaris analytical[3] indicate the product is very clean mescaline (Fig. 7).


Cactus-extract copy 800x600 1.jpg
Fig. 7: Mass spectrometry result. Peak near 210.5 is mescaline. Lower mass peaks are mescaline with cleaved functional groups. The peak at 239.5 is not attributed to mescaline.

Reclaim Solvent πŸ’š

Reusing solvents is encouraged[4] at the DMT nexus.


Wash spent extract with sodium carbonate saturated water shaking vigorously (emulsions do not form). Citric acid removal is complete when CO2 bubbling stops. Remove water layer. Freeze and filter out ice crystals. Store for reuse.

Appendix: Development Notes πŸ”¬

Paste 🌡

No improvements were seen with longer basing time, microwaving, drying, or increasing the ionic strength.

Extract πŸ‘¨πŸΎβ€πŸ”¬

Longer pull times or higher temperatures result in more (1) off colors, (2) difficult crystalization, (3) absorbed solvent, and (4) tendency for paste to congeal. These negatives come with no yield improvement.


Chemically drying the extract before salting had no crystallization or yield benefit.

Crystalize ✨

During crystallization, every 233mg of citric acid (H3Cit) react with free base mescaline (Mes) to form to 1g of mescaline citrate (or slightly more if a hydrate is precipitating):


3Mes(↑) + H3Cit(↑) β‡’ 3(MesH)Cit(↓)


The TEK calls for more citric acid than would be needed for titration because excess citric acid shifts the precipitation reaction to the right (Le Chatelier's principle), helping overcome water and plant material. There is a lot room for excess citric acid in solution since its solubility is 50mg/g in ethyl acetate. The TEK recommends ~5mg/g but since cacti and pull techniques can vary, users may find other values work better for their specific situation (in one example with whole cactus powder 20mg/g was used [5]).


Several factors can make crystals smaller: Reusing ethyl acetate, warmer pulls, longer pulls, higher citric acid concentration, and mechanical agitation. Small crystals can look like a fine powder. Potency does not seem affected by the crystallization appearance, and a powdery precipitate is not a problem unless it becomes difficult to decant/filter.


After the initial crystallization, adding more citric acid and/or moving the extract to the refrigerator did not result in any more precipitation. Moving the extract to the freezer produced ice crystals.


Other dry organic acids could work. Fumaric, Malic, Tartaric, Ascorbic, Succinic, etc can be tested in future investigations.

Collect πŸ’–

Washing crystals over a filter gave better results than decanting washes from a jar. The filter paper wicked away the off colors forming a ring. Unlike the pulls, warmer ethyl acetate is an advantage because the goal is to dissolve away plant matter.


The jar wash should be done immediately. If any straggler crystals dry they can become stuck to the jar walls.

References πŸ—οΈ

  1. ↑ Ethyl acetate safety[1]
  2. ↑ Cactus analysis thread[2]
  3. ↑ Solaris analytical service[3]
  4. ↑ On reusing non polar solvent[4]
  5. ↑ Ethyl acetate approach[5]