How to Make MDMA

How to make MDMA

Overview: 1. 2. 3. 4. 5. 6.

Distillation: of Natural Oil to obtain pure Safrole Rxn: Formaldehyde + Ammonium Chloride -> MethylAmine.HCl (MeAm.HCl) Rxn: Safrole -(Wacker Oxidation(PdCl2+Benzoquinone))-> MDP2P Distillation: of Reaction contents to yield pure MDP2P Rxn: MDP2P -(Al/Hg Amalgam (MeAm.HCl) -> MDMA oil Crystallization: (MDMA oil + HCl in IPA/Xylene) (anhydrous conditions)

What you need: This list is the basics. Do not even start this without ALL the Chemicals and Apparatus. Apparatus and Glass: 

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'The Organic Chem Lab Survival Manual' by James W. Zubrick. (A must, throughout this text, pages from this book will be mentioned. ~32$) (and very handy pictures of glass set-ups) Distillation Apparatus (1x500mL and 1x1000mL Round Bottom Flask, 1x250mL Round Bottom Flask, condenser, distillation adapter, vacuum adapter, thermometer adapter) (Get Ground Glass Joints. These are the best. 19/22 or 24/40 - my first set was 19/22 - and is still used to this day.) Thermometer (0°C to ~300°C) Stand (Home Depot - (2x10in., flange, 2 ft. of ½in pipe)) Clamp (Buy it. Trust me its worth it) (for holding the glassware to the stand - these support several hundred dollars in glass - buy a nice one!) Hotplate/Stirrer combo (got to have it, its worth it) (www.labx.com - spend $200) Magnetic stir bar (look on the Web) (teflon coated) Water Aspirator (or a good vacuum source. But aspirators are cheap MDP2P

This step has been called the Wacker Oxidation. It uses PdCl2 as a catalyst to put and oxygen across a double bond. This step has been worked over many times so do not change the amounts for the fabled 'scale-up'. If you do this correctly, you will have more MDMA.HCl than you know what to do with. (Thanks Strike!) Procedure: Put the following into your CLEAN 1000mL RBFlask: 300mL of dimethylformamide (DMF), 50mL of tap water, 120g of p-Benzoquinone 2g of Palladium Chloride (PdCl2), Magnetic Stirbar. (PS - Don't skimp on the catalyst!)

Start the stir bar on 'slow stir'. Mix 160g of Safrole and 50mL DMF in a cup/jar. Drip the Safrole/DMF Mix into the solution at room temp (30°C) over 30min time. After the addition, the solution was dark reddish orange. Almost black. Make sure the stir bar is spinning - Now - Walk away. Go to bed. Go somewhere else. Set your watch alarm to wake/remind you 7 hours later. Note: This reaction requires NO additional heating! Just stir! Strikes comment: "After 4.5 h the solution will progress on its own to 45°C. Obvious exothermic reaction. After 7 h solution will be back to ~30°C." The reaction mix was flooded with slightly acidic water (~50mL of Muriatic Acid (HCl) in 1.5L of water). The oil fell out of solution to the bottom. It was black/blood red in color. This is when its nice to have a Big Sep Funnel. Now we need to define several things. The upper layer (in this case!) Is the aqueous layer IE it's the layer that contains the WATER - the bottom layer is the organic layer (in this case!). IE it contains oil and other ORGANIC type molecules (IE the stuff you want!). After you flood the reaction contents shake the container to mix the solution, give it about 10 minutes to settle - two layers will form. The upper aqueous layer was a lighter blood red/pink. The upper aqueous layer was decanted from the oil (IE it was poured off). The aqueous Layer washed with 2x100mL DCM (Methylene Chloride / DiChloroMethane). If you can't see the layers, hold the container up to the light, so that the light shines through the container. Keep the DCM washes - They contain the goods. You now should have about 200mL total of DCM washes. You should also have about ~100mL of the 'Organic Layer' that you separated from the reaction contents. Pour the DCM washes and the Organic layer together. Now wash the DCM/Organic layer with 2x150mL 10% NaOH (30g NaOH in 270mL water). This will remove the other reaction by-product hydroquinone. If you don't do this step the hydroquinone will clog your condenser when you try to distill. Keep the DCM/Organic layer. The NaOH layer (Aqueous: is still on top) can be tossed. (Thanks Osmium!) You can stop here and wait for another day - put the DCM/Organic Layer into the freezer. Define Washes - 100mL of DCM was poured into the aqueous layer and then the aqueous layer+DCM was shaken so the two would mix - then it was put down to let it settle out again. When it was settled (notice that the layer now is a different color) the aqueous layer was poured off again into another jar where it was washed again with another 100mL portion of fresh DCM = 2x100mL washes.

Step 4. (4 hours work) 4. Distillation: of Reaction contents to yield pure MDP2P Pour the DCM/Organic layer into your CLEAN 500mL RBFlask. Put several boiling stones in too. Set up for vacuum distillation.

This time we are going to collect a particular fraction in the flask - there is DCM (BP 40°C), water (BP 100°C), DMF (153°C), safrole (232°C), ketone (BP est. ~290°C), and polymerized crap (BP ~300°C+) Now remember when we distilled the safrole? What temp did it come over for you? Well that temp plus approximately 25°C is the temp that the ketone will come over under vacuum. For example, if your safrole comes over at 150°C, then the ketone will come over at 175°C. If your safrole comes over at 130°C then your ketone will come over at 155°C. Get it? WEIGH the receiving flask! Write the weight on a piece of tape and tape it to the flask! Start your vacuum distillation by first turning on your vacuum - if you remembered your boiling stones, then it will begin to boil immediately. This is the DCM coming off first. The boiling may be very vigorous, So watch it, and be prepared to vary the pressure so it won't fly into your receiving flask. Turn on the heat (Hotplate) SLOWLY! and let the temp climb to just over the temp at which safrole came over (SLOWLY: it should take at least 2 hours to reach that temperature - if you do it in under 2 hours you are going WAY to fast). You are going to have to change the flask, when the temp gets to above the safrole temp. This is a bit tricky, because you are going to have to release the vacuum. Release the vacuum at the pump/aspirator and change the flask quickly - you may just dump it out, rinse it once with acetone, or IPA (IsoPropylAlcohol) - and put it back. Start the vacuum immediately, but be careful here, because the Organic layer that you are distilling might jump out of the flask and into the receiving flask - so if you can - vary the vacuum so that the vacuum comes on GRADUALLY! (IE with an aspirator, turn on the water slowly.) The ketone oil is a clear white/yellow hint of green oil. Re-weigh the flask for your yield calculation - you should have over 100g of ketone. With an aspirator you can vary the vacuum when you are turning it on. You simply turn on the water slowly. IE Increase water pressure slowly. By turning it off, you can make water jump into the receiving flask because there is a 'vacuum' in the distillation apparatus and it will suck water out of the aspirator - SO - when you turn off the vacuum, do so by removing the hose from the aspirator - while the aspirator is going. You can also vary the vacuum by removing the hose PARTIALLY - This will take some practice so play and have fun. Strike's excellent post read: "With high vacuum at 100-140°C ~18g safrole came over. At 166°C came over ~125g ketone." When she did this method... Keep the ketone. Smell it. Look at it. Look at how it refracts light. For the brave: taste it. Note all of these 'properties' and remember - After you have judged its properties, put it in the freezer. Note: it won't freeze. It will become a very viscous liquid. If you try to distill the ketone at atmospheric pressure (no vacuum), you will get to about 220°C and then the whole flask will polymerize. Total waste of effort, time, and precursors. So don't mess around and get a vacuum source. The ketone is unstable. It won't explode or anything, but if left to its own devises, it will rearrange. And then it will be useless. At room temp, it will rearrange in about a week depending on where you live - if you keep it in the freezer - it can last months - FREEZER! After its in the freezer you can stop for today.

Step 5. 5. Rxn: MDP2P -(Al/Hg Amalgam (MeAm.HCl) -> MDMA oil

(Thanks Ritter, Osmium, Shulgin!) This is called the Al/Hg Amalgam. This process utilizes the electronegative properties of the Aluminum. Now, something that most people don't realize, is that all aluminum is actually coated with Al2O3. This is the oxidized form of Aluminum. We will remove this part of the foil so that the aluminum can reduce the imine with elemental Al. This reaction actually has two parts. First, there is the ketone → imine condensation. This reaction reacts the ketone with methyl-amine to form an imine - water is produced as a product. Second, the imine is reduced (Hydrogen is added across the double bond) to the amine. The condensation really needs anhydrous (no water) conditions, and the reduction actually needs water - so there is a fine balance here - IE don't mess with the procedure. What you need to have prepared ahead of time:        

CLEAN 500mL RBFlask. 20g of thick aluminum foil cut into ~1cm squares. 0.1g of Hg(salt) (any mercury salt will do, not Hg Metal) (Note: Hg=Mercury) Disposal Jug (milk jug) 1L of Clean water 25mL of 25% NaOH solution (dissolve 25g NaOH in 75g of water, then 25mL of it) 50g of MethylAmine.HCl dissolved in 300mL of 91% Isopropyl Alcohol 40g of 'ketone' dissolved in 50mL of 91% Isopropyl Alcohol

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Cool water bath. (A milk jug with the top cut off) Ice (don't screw around, buy a bag) (or have at least several kilo's handy)

Set up your stand and clamp so that, when the flask is clamped to the stand the bottom of the flask is about 4 inches (10cm) from the table top. This is so that you can put the heating plate and stirbar combo under it. Have your thermometer already in its thermometer adapter so you can throw it in the flask at any second. Prepare the following, put them in a jar and have them ready at a moments notice:  

50g MethylAmine.HCl dissolved in 300mL 91% Isopropyl Alcohol 40g 'ketone' in 50mL of 91% Isopropyl Alcohol

It is very important that these are ready before you start! Before you start! 20g of Al squares are put into the 500mL RBFlask. They are covered with ~350mL of H2O (water). 0.1g of Hg(salt) (or just a very small spatula) is placed in with the Al squares, and given a good stir. Amalgamation was allowed to proceed until there was the evolution of fine bubbles the formation of a light grey precipitate, and the appearance of occasional silvery spots on the surface of the aluminum. (Thanks Dr. Shulgin!) Basically here the Al2O3 is being destroyed, the water is reacting with the Al2O3 to form Al(OH)3 and H2. This should take between 15 and 30 minutes. Just be patient. When amalgamation is complete, pour out the water into the milk jug. Pour in another ~350mL of water and carefully shake the flask to stir up the contents. Pour it out into the jug. Do it again with another ~350mL of water. So basically, you wash the Al pieces with 2x350mL of water. Dump out as much of the water as you can in 10 seconds or so - then immediately go to the next step - leave the Al foil in. This will remove most of the Hg from the solution. Don't worry, the Hg will be completely removed in the successive washes during the work up. If you let the Al squares sit in between washes, they will heat up and re-form the Al2O3 in a matter of seconds. So be quick and have the ingredients ready for the procedure. Now, immediately, add in THIS order:  

50g MethylAmine.HCl dissolved in 300mL 91% Isopropyl Alcohol 40g 'ketone' in 50mL of 91% Isopropyl Alcohol, then drop in a Magnetic Stirbar. Try to get the stirbar going - it might take several minutes.

Now drip this in 25mL of 25% NaOH solution over several minutes. Put the thermometer in the solution. Start being very paranoid about the temperature. The temperature of the reaction flask must not climb above 60°C. Its best if the temp is kept around 50°C. Stirring is necessary so, with the heat off, stirbar on, flask sitting in the cool water bath. When the temp gets to about 50°C, put several chunks of ice in the bath. If the temp falls below 40°C, take some of the ice out. But whatever you do, make sure the temp remains below 60°C. The whole time you are doing this the contents are a grey sludge. Remember to keep the stirbar going! If the stirbar is difficult to start going. Don't worry, trying to get it started seems to work just enough.

At some point you'll notice that the temperature is not rising like it had been (in about 4 hours or so). You have reached the end of the ketone -> imine condensation - Look inside the reaction flask and see if you still see any pieces of Al foil - if you do - continue stirring until the Al foil has been depleted. This reaction should go no less than 6 hours. Now, after you are convinced that the reaction has stopped (6 hours later) - IE the temp of the solution is room temperature, and there is no more foil chips in the mix. Pour in 25mL of the 25% NaOH solution. Stir the contents some more, and then let the stirbar stop and then let the solution rest for at least 30 minutes. The NaOH solution will make that grey sludge into a filterable consistency. If you can't tell there has been a change in the consistency - put in another 25mL of 25% NaOH solution. The grey sludge should abruptly change from a uniform grey to a chunky white/grey blob. Then in a matter of minutes the whole thing will be resting on the bottom of your flask. The reaction contents will settle out. The grey sludge will settle to the bottom, and a clear yellow liquid will rise to the top. Pour off the clear yellow liquid. Save it. Put 200mL of 91% Isopropyl Alcohol into the reaction contents, stir the solution, so that the whole thing is disturbed and swirling in the flask and again wait. Pour off the 2nd clear yellow liquid once it settles. Add the 2nd clear yellow liquid to the first. Do this several times, or until the clear liquid is no longer yellow. This is an extraction out of the reaction contents. The more you do this process, the higher your yield. So don't do it once and get excited and try to complete it with just the first extraction because you will just waste half of your product. You've gone this far - don't fuck it up now. After you have gotten as much of the yellow liquid out as you could. Put the grey sludge in the same milk jug waste container. Dispose of it properly - the milk jug contains elemental Hg - Not a lot - less than 0.1g. But you should dispose of it properly. Not down the sink. Take it to a High School or A University, To the Chemistry department - tell them you broke a thermometer, and then couldn't figure out what to clean it up with. Set up for vacuum distillation (Boiling Stones!) but we're not going to distill. We are going to evaporate the Isopropyl Alcohol (IPA) from the reaction contents. Under an aspirator vacuum, the IPA should come over around 35°C. Make sure you get the alcohol out. When the alcohol is close to being gone - the solution might spontaneously separate in your distillation flask. Not to worry - the top layer is probably your product, and the bottom is water. Don't try to separate it, just dump the whole thing into the next procedure. The next two paragraphs out line a procedure known as an Acid/Base extraction. This works very well for our target molecule, and any molecule that contains an amino group. If the next two paragraphs are not done, then plan on not having any crystals when you're done. After the alcohol has all gone, Take the brown oil that is left and put it into 500mL of ~0.5M HCl solution (470mL water + 30mL of Muriatic Acid). Stir or shake it up. A lot of the brown oil should go into the acid solution. Now pour into this solution 30mL of DCM. Shake again and let it settle. You will notice two layers formed - The top layer is the Aqueous layer which contains your product, and the bottom layer contains the DCM, polymerized crap, and non Nitrogen containing molecules. Pour off the top layer (That contains your product) and discard the DCM layer. Wash the Aqueous layer again with 30mL of DCM, and repeat the

process. Note that the aqueous layer contains the product - Do not discard the aqueous layer! You can discard the DCM washes, because they contain nothing useful what-so-ever. Discard! Now, slowly add 50mL of 25% NaOH solution to the aqueous layer. When you do this the Aqueous layer will turn a milky white and may heat up just a little bit. Not to worry. A light brown oil will fall out of the solution. This is your product (in the freebase form). Before collecting it, wash the 'now basic' Aqueous layer with ~50mL of DCM. Shake and let it settle out. Pour off the top Aqueous layer, and keep the DCM this time! The DCM washes contain the goods! Wash the aqueous layer twice more with 50mL of DCM. Combine those DCM washes that contain your product, and continue. Set up for vacuum distillation, and once again, just boil off the DCM (Boiling Stones!). There might be a little water in it, so this time when you are boiling off the DCM, let the temp of the distillation flask reach ~50°C for several minutes. That should be good enough. You should have a light brown oil in the flask - it kind of looks like thick Newcastle Beer.

Step 6 (2 hours work) 6. Crystallization (MDMA oil + HCl in IPA/Xylene) This must be done in anhydrous conditions. If its not, then you will not get crystals. Anhydrous means 'no-water'. If water is present, then you can expect to get crapola. Procedure: This first step can be done ahead of time. Like, during a distillation or reaction: Get a fresh bottle of 91% Isopropyl Alcohol, and pour out approximately 100mL. Now get some of your DRY Magnesium Sulphate (Epsom Salts) (about 100mL worth) and dump it into the 91% IPA. There might be a little heat evolution, but not to worry .... Shake it up and then let it sit till the MgSO4 settles out. Pour off the IPA, and then put more fresh MgSO4 into it (about 100mL worth). Now shake the bottle and let it sit for 15 minutes. You must do this at least three times - It really is much better to do it four times - Why fuck it up now right? After three times you will have 'Dry' IPA. You can actually do this while you are distilling or waiting for a reaction to proceed. Make a mixture of 100mL 'Dry' IPA and 150mL Xylene. Pour it into the flask that contains the MDMA oil, and drop the stirbar in too. Stir so that the whole thing is mixed up real well Now drip in Muriatic Acid slowly. Test with pH paper every 5 drops or so - keep adding the Muriatic Acid until the pH of the solution is 5-6 - or just barely acidic. Set up for vacuum distillation, and distill the solution, distill this with the stirbar in instead of the boiling stones - IE When the solution has reached a pH of 5-6 - Start distilling. Be careful not to let the solution get above 120°C - When a lot of the solution has boiled away, crystals will spring to life in the flask. Under vacuum, the solution should never get above 70°C.

Filter these with a coffee filter, suspended over a jar - This gets the excess IPA/Xylene out. Scrape the crystals on to a plate and let the crystals dry, by letting the IPA/Xylene (mostly Xylene at this point) evaporate - this might take several hours - a 60 Watt lamp 6 inches (20cm) away from the crystals shining brightly helps. Stir the crystals to promote even heating. The crystals will be a brown-yellow color. Now scrape the crystals into a jar, and pour ~20mL of acetone onto them. Swirl the mixture. The crystals won't dissolve - but a lot of the brown will. The brown-acetone is poured off, and the acetone wash is repeated. After the acetone wash, dry the crystals. You should have around 15g of dry crystals. That's 150 hits. The now 'almost white' crystals have melting point values over the range from 145153 ° C, depending on how much water was in there during crystallization. And these crystals are ready for consumption. 60mg is not enough. 80mg is great for my wife. 100mg is a great dose. 125mg is balls-to-the-wall. 150mg is too much. For me at least. Fun for me is actually 80mg MDMA+70mg MDA in one pill.

How to make dmt

Name:

N,N-Dimethyltryptamine N,N-Dimethyl-1H-indole-3Chemical Name: ethanamine Alternative 3-[2-(dimethylamino)ethyle]indole, Chemical Names: DMT Chemical Formula: C12H 16N2 Molecular Weight: 188.27 Melting Point: 44.6-44.8° (crystals) Boiling Point: 60-80° (crystals) Dosages: 60-100mg (smoking) 350mg (orally) Controlled substance (hallucinogen) U.S. Code of Federal Regulations, Title 21 Part 1308.11 (1985). In modern times there has been a reduction of ritual. The ceremonies, that previously served to cast out an individual from modern associations and throw him into a field of epiphanies, have become merely form, betraying the inner forces that must somehow manifest. Shamen know of these inner forces. They understand the inevitable overwhelming psychological experience that everyone will face if they are to complete their inward path to open the unconscious and fall in. The psychological crisis is the fulcrum of any metaphysical realization the individual may have about himself or his world. Without these intense experiences, without the rituals that convey the message of the journey, and without shamen to show the way, many are lost in the world searching constantly farther for what is contained only within. To chemically force such spiritual breakthrough may be interpreted by some as a way to circumvent the trials that are necessary to test each soul willing to see the truth of their life. But in contemporary society where is the individual to seek these tests of the self or to be struck silent in awe of their own natural beauty or that of the universe? The shamen offered these opportunities to the individuals of their society

for generations, helping people maintain a healthy psychology between the known world and the mystical. I now offer this ability to you in one of many forms, DMT. DMT is perhaps the most powerful hallucinogen known to man. It is related to LSD and psilocybin. There are no drug tests that would show DMT usage. None of the basic NIDA-5 drug tests [Erowid Note: Now called the "SAMHSA-5"] or any extended drug test will show a result for DMT. DMT is naturally formed in the body and has been found in abnormal levels in the body fluids of persons suffering from schizophrenia. DMT is almost never sold through dealers, rarely synthesized, and seldom used. It is, however, easily extracted from common plant materials and has been used in various forms for hundreds of years (timeline). DMT is not a ―social drug‖ however. Respect the drug and its incredible potential. This drug is not for the inexperienced, nor is it recommended to those who are just looking for another ―high.‖ Few seek the visions enabled through DMT, and even fewer return to them. Even avid psychedelic users have had frightening experiences with DMT on their first encounter with the drug. Take care to research and find out if DMT is for you. I stress that educating yourself about this drug (and about all drugs you intend to use) will make you a more competent and prepared chemist, tripper, and guide. This manual is presented as a quick bench guide for the complete novice on how to extract DMT. Although the text and illustrations for the process were all created by myself, there are a few pictures which are not my own. The origins of these pictures are credited in the bibliography. I would like to encourage others to add to this manual their own written observations. When attempting to produce any of these products the reader is encouraged to read through the steps several times to closely familiarize himself with the entire process. Please take note that DMT is an illegal substance in the United States of America and is controlled under federal regulations. The following is for educational purposes only. How to Extract DMT from Natural Sources

(in Ten Easy Steps) First a plant must be selected that contains the chemicals we wish to extract. None of these plants are illegal and they can be found growing wild and free all over the world (much less can be said for some of our other favorite plants.) Most of these plant materials can be ordered through the internet. A little research may reveal a large quantity of some useful plant material growing near you. Alkaloid contents of each plant mary vary according to the growing conditions. Specifics about these plants and how to grow them are beyond the scope of this manual but the information can easily be found. Below is a chart of several plants that contain NNDMT, 5-OH-DMT, and 5-MeO-DMT (DMT‘s close cousin.) Alkaloids reported as percent of total dry plant source mass/weight: Acacia bark

0.71% NN-DMT Acacia maidenii bark

0.36% NN-DMT Acacia simplicifolia bark

0.86% NN-DMT

Mimosa hostilis root (bark)

0.57% NN-DMT Virola shoots & flowers

0.44% NN-DMT Desmanthus illinoensis root (bark)

0.34% NN-DMT Pilocarpus organensis

1.06%

5-MeODMT

Phalaris tuberosa

0.10% NN-DMT 5-MeO0.022% DMT 5-OH0.005% DMT Phalaris arundinacea

(‗net gossip) 0.060% NN-DMT 5-MeO?? DMT

Psychotria species (averaged,

from

Jonathan Ott) 0.200% NN-DMT

N,N-DMT

5-MeO-DMT

5-OH-DMT

MAOI

DMT (N,N-dimethyltryptamine) is one of the most hallucinogenic compounds known. DMT is not active orally (unless in the form of an ayahuasca brew), but must be smoked in it‘s freebase form to experience its effects. (DMT can be taken orally when mixed with a MAOIs, but this is not recommended for the first time user.) The body quickly builds a tolerance for the drug. Your DMT dose must be taken within 60 seconds. Any more of the drug after this first minute will not enhance the experience. It is recommended to give at least one hour before attempting another DMT trip. Effects of 5-MeO-DMT are psychedelic without the visual distortions found in NN-DMT. 5-MeO-DMT is taken at 1/4 the dose of NN-DMT and will overpower the NN-DMT. (Bufotenine) can cause severe physical discomfort including circulatory distress, nausea, psychological distress (panic and fear), severe skin flushing, and has the possibility of being fatal. (Monoamine Oxidase Inhibitors) will intensify and prolong the effects of NN-DMT, however this is never recommended. Foolish combinations of MAOIs and other drugs can lead to serious health problems and even death. The tryptamines are normally metabolized by an MAO in the body. MAO metabolizes serotonin, norepinephrine, and dopamine. By inhibiting this, MAOIs increase levels of those neurotransmitters. Tyramine will not be metabolized and will cause an increase in tyramine levels in the blood.

Extraction Procedure For our experiment we will be using Mimosa hostilis root-bark to provide a very pure product of NN-DMT without the over powering influence of 5-MeO-DMT or the negative side effects of 5-OH-DMT. For a solvent we will be using common naphtha. Notes on adaptations for chemicals and other variations of this process are described as well. The following is a list of materials:

It helps to test all non glass materials with solvents to make sure there aren‘t any adverse reactions. (30g suggested starting amount 1. Mimosa hostilis root-bark – $45/100g) 2. Muratic acid (pool acid – $4/gallon) 3. pH papers (litmus papers – $3/100 tests) 4. Lye (Red Devil Brand – $5) 5. Naphtha (Zippo lighter fluid – $5) 6. Coffee filters and cotton swabs/cloth ( – $2) 7. Funnel ( – $2) 8. 3 labeled glass jars with lids (thick canning jars (labeled Jar A , Jar B, and Jar work best, but pickle jars will do) C – $3) 9. Evaporating dish (glass baking pan – $10) 10. Glass pipette (turkey baster – $4) 11. Goggles and gloves ( – $10) 12. Distilled water ( – $2) Total = ~$100.00 STATEMENT OF HAZARDS: Methylene Chloride Suspect cancer hazard. Risk of cancer depends on duration and level of contact. Harmful if swallowed. Causes skin and eye irritation. Causes respiratory tract irritation. May affect blood cells. May affect the central nervous system. May cause blindness. Avoid breathing vapor or mist. Handle with caution. Keep in mind these risks whenever substituting DCM for any other solvent. STATEMENT OF HAZARDS: Muratic Acid STEP 1 Preparing Plant Material

Grind the plant material to a fine powder. The finer ground the material the better your yields will be. The best technique to pulverize and rupture the cell structure of any plant material is to repeatedly freeze and thaw it over and over again. An example of a plant requiring this treatment is Phalaris arundinacea, a strong and limber grass. Mimosa hostilis rootbark is easily pulverized to a fine powder in Above photo credit to Jim DeKorne a blender, releasing a pink haze.

First place the grass clippings in A. the freezer over night. B. Remove them and place the frozen clippings into a Mimosa hostilis root-bark blender. Try and © 2000 Erowid liquefy the clippings as much as possible while they are frozen. C. Repeat this process of freezing, thawing, and blending with the plant material several times for best results. STEP 2 Acidify Water to pH 2

Take two pickle jars (about 20 ounces each) and wash them in the dishwasher to help sterilize and clean them. Label the jars A and B. Fill Jar A 2/3 way full with distilled water (~15 ounces, or ~500ml filtered preferable.) Pour 1/2 teaspoon (~2ml) of acid into Jar A . Test the pH of the water in Jar A . The pH of the water should read 2 If not, add more distilled water to dilute (5% acidity). There are many sources of acid: (Always add acid into water, not water into acid. Use distilled water to avoid any adulterates.) electronic pH meter in jar

A. Distilled white vinegar (5% acidity, ~2 cups, or 500ml for every 50g root- bark) or lemon juice. B. Muratic acid from pool shop (10ml 30% HCl to 1 liter water is recommended.) C. Reagent grade hydrochloric and sulfuric acid (overpoweringly potent without dilution.) Figure 1 Add powdered root-bark to Jar B. Lab Notes: Proper method of testing pH with pH papers; Use a glass stirring rod (or something that won‘t corrode with acid) to stir the acidic solution. Dab the pH paper with the stirring rod lightly. To save pH paper, you can cut only a small section of strip for a single test. If a pH meter or pH papers are unavailable there are certain organic sources that produce antocyanines which change color with different pH ranges. Red beats or red cabbage may be used to produce a rough estimate of pH range. This is not always recommended, but it works. To create the indicator solution, blend or grind either red beats or red cabbage. Strain off the juice from the pulp and filter out any remaining plant material. If not enough pigment is found, try extracting more with water from the mushy pulp. If there is too much pigment, simply dilute solution with water. Indicator solution produced has a short shelf life but can be stored in a refrigerator for several weeks. Below is a rough pH chart for reference: (litmus paper comes with its own pH chart)

STEP 3 Convert Alkaloids to Salts

Using a pipette (or turkey baster) transfer enough acidified water from Jar A into Jar B to cover the root-bark in the bottom of Jar B (~8 ounces, or 250ml acidified water into Jar B.) When the acid reacts with the root-bark, it converts the alkaloids (elf-spice) into salts. To help facilitate this process we can: A Periodically . shake the contents of the jar. This helps more root-bark come in contact with the acid. B The weaker . the acid, the longer it should be heated for. Do not allow evaporation of the liquid inside. Do not boil. Maintai n temperature below 50° C or 122° F. Since we are using pickle jars, and not pyrex, they can shatter easily if

Figure 2

heated or cooled too quickly. It is recommend ed using a double boiler with hot (not boiling) water to warm the solution. To cool, simply turn off the heat source and allow the solution to slowly return to room temperature. When using muratic 1 acid, . heat the jar for 15-30 minutes. When using weaker acids, 2 simmer . the contents overnigh t. Allow the contents of the jar 24 hours to react the first time. The alkaloids (tryptamines) are converted into salts and become water soluble. Our elf-spice is now contained in the aqueous solution. STEP 4 Filtration

Plug the bottom of the funnel with cotton balls or cotton cloth to create a cotton-filter. Pour the contents of Jar B through the funnel and into Jar C. Squeeze the root-bark contents inside the filter to press out the remaining juices. Save the root-bark that has been caught by the filter and place it back into Jar B. Lab Notes: Whether filtering material through a cotton-filter or a coffee filter it helps if the thinner parts of the solution are filtered first, followed by the mushy and more bulky components (which may clog the pores of your filters as you strain.) The better your filtration, the more rapid and efficient your emulsions, also resulting in a cleaner product. Cot ton must be specifically used. Other fibers have the potential to react with our solvents. A tea strainer (wire strain)

Figure 3

can be a simple way to separate bulk ruffage. Ano ther way to improve this method is to use a vacuum filter. There are several varieties, the most affordable being a water vacuum filter that attaches to a household faucet. Thes e cost about $30.00 and are very quick, useful and effective. STEP 5 Collect 3 Extractions

The initial extraction is most important. For best results, allow the contents of the jar more time to react during the remaining two extractions. Shake Jar B, 4 times a day, for 1 week before filtering each time through a cotton-filter. Collect the acidic contents in Jar C each time. After these initial 3 cotton-filtration cycles, clean Jar A and Jar B, and dispose of remaining root-bark. Repeat the process outlined in STEPS 2, 3, and 4, two more times.

After all 3 extraction phases, filter the contents of Jar C again, this time using a paper coffee-filter instead of a cotton filter. Place several paperfilters A (coffee . filters) in the bottom of the funnel. Strain content s of Jar C through B the . paperfilters and into Jar B. When finishe C d, . clean Jar C. Repeat this process as necessary to remove as many of the particulates from our solution as possible.

Lab Notes: The majority of the alkaloids we are searching for will convert to salts in the first

Figure 4

extraction phase. The second and third extraction phases take place over a longer period of time. This will ensure that we will be able to extract as many alkaloids as possible from our material. The third phase can be reduced to 1-2 days but will not produce the best yields. Remember, these measurements are all crude estimates. STEP 6 Defatting

Next we defat the solution. This is part of standard lab procedure whenever extracting alkaloids of this sort. This process removes the oils, fats, and other unwanted substances from our aqueous solution and also helps with yields. All DMT salts are insoluble in non-polar solvents — with the exception of DMT acetate — which is soluble in chlorinated non-polar solvents such as chloroform and DCM. Thus if you are using white vinegar (acetic acid) as your acid, you will need to use naptha or ether to defat as chloroform or DCM would extract the DMT acetate along with the oils and fats, defeating the purpose of this step.When using mimosa hostilis root-bark you may find this step unnecessary, however, any plant material foliage containing chlorophyl it is strongly recommended. To do this we add an organic (nonpolar) solvent to the acidic solution. Before using any solvents test a significant amount (~500ml) of the solvent by evaporating it in a dish. This will verify that there are no residues or orders left when evaporation is complete (commonly found in many over-thecounter solvents.) Later in the procedure (STEP 10) you will be evaporating this solvent to leave a smokable form of DMT. Anything your solvent contributes, you may be smoking in the final product. Below are listed several more common organic nonpolar solvents. A. Naphtha: Coleman fuel, VM&P naphtha, Zippo, or lighter fluid. Evaporate a small amount in a dish and inspect the residue if you are unsure of it‘s contaminants. If used for the extraction phase instead of the defatting phase, warm Figure 5 naphtha will extract alkaloids much better than cool naphtha. Naphtha is considered more selective for catching these alkaloids than DCM. Naphtha rises to the top of the jar.

B. Methylene Chloride: Also known as DCM or dichloromethane. Often used as an adhesive solvent for acrylics. Pure DCM can be found in craft stores. DCM must be distilled first from all non-flammable paint strippers beforehand (they contain a paste that holds several unwanted substances.) The paint stripper may also contain methanol (most marine grade paint strippers are 80-90% DCM.) Methanol is also an organic solvent. DCM distills at 41° C or 106° F. Pure DCM is best. May cause cancer and blindness. Take necessary precautions. Methylene chloride sinks to the bottom of the jar . Naphtha C. Ether: Contained in engine-starting fluid purchased at automotive stores. To remove liquid ether from an engine-starting aerosol can, spray the contents of the can down a 12 inch (~30cm) length of 3/4 inch PVC pipe. The ether will condense on the sides of the pipe and fall into the jar, while the inert propellant will be released into the air. Ether is extremely volatile. Ether floats to the top of the jar. D. Chloroform: Chloroform (CH2C12) can be purchased over the internet from arts and crafts warehouses. It has Defatting process a tendency to be harsh on organics and has a boiling range of 35-65°C (95-149° F). Chloroform sinks to the bottom of the jar. It is important to remember what type of organic solvent you use. For our defatting process we will use naphtha. Add to Jar B ~50-100ml (~2-3.5 ounces) naphtha. (Only 10-15% the volume of our acidic solution is enough naphtha for this step. Visualize what 10% of the total of the solution is and add that amount of naphtha into the jar.) Cap the lid on Jar B and shake the contents vigorously for 20 minutes. Set Jar B aside and allow for emulsion (foam, bubbles, solutions, particles, etc.) to separate into two distinct layers (much like oil and water will separate.) This may take ~24 hours (48 in some cases.) The oils and fats will migrate into the nonpolar solvent layer leaving our alkaloids in the aqueous solution. Since we are using naphtha, the

Seperatory Funnel in Jar

solvent layer will rise to the top of Jar B. Using a pipette (or turkey baster) remove the solvent layer and discard. Repeat defatting process 2 times.

Lab Notes: A separatory funnel is very handy for dividing and eliminating layers of solutions. This device consists of a single chamber with a tapered bottom. On the bottom is a closed faucet. The container is filled with the two solutions and they are mixed. After mixing, the apparatus is set aside until both fluids separate into two distinct layers. The lower fraction of the fluids can be drained via the bottom faucet and into a container for preservation or to discard. A quick separatory funnel can be made by filling a Ziplock plastic baggie with your mixtures, and hanging it from one corner. When the layers have separated, the bottom corner of the bag is pinched and then cut for drainage. It is suggested to test the baggie to make sure your solvents will not melt it.

STEP 7 Prepare to Basify

In this step we will be preparing the solution for the alkaloids migration using a common organic non-polar solvent. For our solvent we will use warm naphtha (other solvents are identified in STEP 6.) Add to Jar B 100ml (~3 ounces) warm naphtha. Shake the jar for 5 minutes. STEP 8 Basify to pH 9

Now we must basify our solution. By doing this we will ―unhook‖ the salt and transform the alkaloid into its ―free base‖ form. The alkaloids will no longer be a salt, nor will they be soluble in water. This allows us to extract them with the organic solvent added in STEP 7. Ammonium hydroxide is normally used, but for our experiment we will be using NaOH found in household lye crystals (Red Devil drain cleaner) and purchased at hardware stores. Lye is very caustic and can react violently. Take the proper precautions when using lye. A good mixture for basifying is 5g (~0.2 ounces) lye mixed with 95g (~3 ounces) distilled water. The reason we dilute the base is to prevent localized pH spikes which will destroy the alkaloids in the area that we are adding the concentrated base. Create a basic mixture as follows: A. Fill Jar A 95ml (~3 ounces) full with water. Slowly add 5g (~1 teaspoon) of lye to B. water. Shake and mix contents thoroughly. C. Test to make sure pH is ~12. Now using a pipette transfer small amounts of solution in Jar A into Jar B. Stir and check the pH of contents in Jar B A. after each transfer of lye solution until the solution in Jar B reaches a pH of ~9-11. Shake the jar but be careful of pressure that will build up inside the jar. Release the lid and vent often! The solution will change a gray color as the alkaloids are turned B. from acid salts to free base. It may Figure 6 resemble a thick gel. Then the solution will turn black and slippery as you add more base. The jar will heat up during this process.

Approximate Basification Color You have now formed the free base alkaloids that are soluble in non-polar solvents. According to the Merck Index the pKa (natural pH) of DMT is 8.68 (which would make this the ideal pH to extract at.) In many experiments the average pH of the final basified solution in STEP 8 was ~10, which gave satisfactory results everytime. STEP 9 Emulsions

As these alkaloids dissolve in non-polar solvent added in STEP 7 , an emulsion will form. The strength of emulsion formed is directly proportional to the strength of stirring. Heavy, rapid stirring produces a thick emulsion that takes up to 4 days to settle out. Light, slow stirring over a longer period of time produces and emulsion that separates quickly without affecting the yield. Let the jar sit overnight until the emulsion has separated into two distinct layers. If emulsion has not cleared in 48 hours, try the following: A. Sometimes adding a lot of salt and gentle stirring will make the polar layer more polar and help with emulsions. B. Add more organic solvent. C. Filter solutions again through a cotton filter several times. A

Figure 7

Thick emulsion

paper filter will not work. D. Test and increase the pH. E. In most cases the solvent layer will have slight tint or may sometimes appear completely clear. If you want an early test of your extraction simply evaporate a small amount in a glass dish. The residue left should smell a bit synthetic (a smell like plastic.) This smell is a trait of your tryptamine.

The naphtha will create a thick orange/pink emulsion with small bubbles that sometimes takes over 48 hours to separate. Always wait a few days before trying other methods to break down the emulsion. Keeping the naphtha warm will increase the amount of alkaloids it carries with it during each extraction. To help keep the jar warm, place it in a pot surrounded by warm water. Naphtha floats. If DCM is used for our extraction solvent in STEP 7, we will have a faster resolving emulsion than naphtha (less than an hour in some cases.) The solvent may turn a slightly darker color, usually only a tint of reddish-brown or yellow. DCM sinks. Allow a minimum of 24 hours for the contents of the jar to react completely. If using methanol allow a minimum of 4 days warmed to roomtemperature for reactions to complete. Using a pipette remove the corresponding solvent layer from Jar B and save it in Jar A. STEP 10 Final Alkaloid Extraction and Evaporation Repeat STEP 7 and STEP 9 (in that order) 2 times.

solution and into our solvent.

Our elf-spice falls from the basified aqueous

The combined solvent fractions from our solvent extractions should now be in Jar A. Pour contents of Jar A into a glass baking dish. Allow for the solvent to evaporate. Evaporation may take up to one week (depending on your solvent.) During this time keep dish with solvent away from heat or open flame. The remaining substance may resemble anything from a sticky orangish goo to white or pale-orange crystals, depending on how well you followed the procedure. Scrape up this substance from the baking pan with a razor. About 25mg is a good starting amount (try about the size of a pea.) Assuming best yields you could get 5-6 doses (275mg) from 30g mimosa hostilis root-bark. You will know when DMT is in the final product by the smell. DMT has a distinct synthetic smell, almost like some manufactured plastics. “Don’t worry about weighing it. Smoke it ’til your high, then save the rest for next time. Remember the flame should never touch the dmt, just the glass that’s holding the dmt. Just heat up the “bulb” and gets to toking. Slow & steady, deep inhalation, hold the smoke ’til you burst. If nothing after 1st hit, huge toke again, etc. The 3rd toke will usually be the one.”

Lab Notes: After DCM has evaporated your product may contain trace amounts of hydroxide. Some find hydroxide to be unpleasant in the final product. To help reduce this try washing the DMT crystals in water, and letting the water evaporate. Water can be added to the solvent evaporating dish to help carry off hydroxide.