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Here we will explain the purpose of our organization. We may also include our mission statement on this page.

Organization Purpose

Name: MDMA
Drug class: Designer, amphetamine
Legal status: DEA classified
Chemical composition: 3-4,metylenedioxymetamphetamine
Common street names: X, Ecstacy, XTC, E, rolls, candy

Tips for Ecstacy users:
Drink lots of water to replenish body fluids. From time to time, stop moving, take deep breaths and relax. Maintain a healthy lifestyle: eat a balanced diet, take vitamins, and get plenty of sleep. Remember: less is more. Large or frequent doses can increase the side effects without adding to the experiance. Much of what is sold as Ecstasy is not pure MDMA. Be cautious of what you buy and who you buy from. Impurities may include amphetamine, LSD, or PCP. Alcohol can reduce or change the effects of Ecstasy, and the combination can cause undesired effects. Integrate what you've learned. Think about your thougths and feelings and try to apply them to real life.

1. Health: Check your physical condition. MDMA puts serious strain on the body. Before taking it try to be healthy and rested. Your heart, liver, and kidneys all have to work harder. Avoid taking MDMA if you are on anti-depressants. Your mental health is important also. If you feel that you are uneasy about taking it and not comfortable with being that open with yourself, and having your image stripped from you then don't do it or wait.
2. Situation: Find a situation you feel comfortable and safe in large parties or raves seem to be of the favourite places to take, and if you feel as if your bugging out find someone that is SOBER to talk you down or someone with a somewhat level head on them. E is ideal to take with a lover you are sure about. It gives you the ability to explore your relationship and each other. E at home would be ideal in a spacious room where you feel secure and can let yourself go without arousing the neighbours. It is also nice to take E outside in warm weather and pleasant and familiar surroundings. It is important to feel free to express yourself without inhibition or interruption.
3. Looking After Yourself: If you are feeling doubts or anxieties about taking E but still want to take it nonetheless take a small dose, and then wait a little over an hour to take the next bit. Drink as much water as you like, but avoid alcohol and other drugs, and if you are DANCING, realise that you may be dangerously overheated even without feeling uncomfortable. Taking vitamin C and E may help reduce exhaustion. Get good sleep afterwards.
4. Guide: If you are at home choose someone to guide you that you feel comfortable with and have no reason to feel emberassed about showing your feelings to.
5. Preparations: At home make sure that you will not be disturbed, by the phone door etc. Make sure they have comfortable places to sit or lie down. AT HOME AND AT THE RAVE MAKE SURE YOU HAVE PLENTY OF FRUIT JUICE AND WATER ON HAND TO DRINK AND CHEWING GUM OR SOOTHER TO PREVENT JAW CLENCHING. Wear LOOSE, LIGHT CLOTHING but have extra clothes and a downy blanket on hand in case you need to warm up. Bring personal objects that you are fond of----things to handle and look at or perhaps some photographs of people you are fond of. Have pleasant things to look at, smell and touch---flowers, essential oils and silks. Just let it happen and go with it. Do what your urges tell you.
6.Timing: The full effect of MDMA lasts about 3-4 hours, but set aside a good 8 hours to a whole weekend to recoperate and go over what has occurred. This is a learning experience also.

MDMA (also commonly known as Ecstacy, X, E, XTC, Adam, etc.) is a semi-synthetic chemical compound. In its pure form, it is a white crystalline powder. It usually seen in capsule form, in pressed pills, or as loose powder. Average cost ranges from - (U.S.) a dose. Common routes of administration are swallowing or snorting, although it can be smoked or injected as well. Currently, MDMA is on the U.S. Schedule I of controlled substances, and is illegal to manufacture, possess, or sell in the United States. Most other countries have similar laws.

Dosing: Usual doses of MDMA range from around 80 to160 milligrams (orally), though monks have used lower doses (40-60 mg) to assist meditation, and therapists have sometimes taken similarly low doses to become more in tune with clients. A benchmark standard dose is often considered to be 2 mg of MDMA per kilogram of body weight (though response to the drug is not strictly proportional to body weight). When MDMA is taken by mouth, the effects manifest about 30-45 minutes later; snorting, smoking or injecting produces much quicker onset. The primary effects usually reach a plateau at T+1:00 (one hour after taking the dose) to T+1:30, stay there for some two hours, then start tapering gradually. The primary effects are pretty much over by T+4:00 to T+6:00. Secondary effects (afterglow) may be felt for days, and tertiary psychological effects (e.g. improved outlook) may last indefinitely. Supplemental dosing: If you have taken an ordinary dose of MDMA (say 2 mg/kg), you like where you are at about T+1:30 (you will have reached plateau by then), and would like to prolong your stay there, take a supplement equal to about 1/3 to 1/2 the initial dose. Taking much more than this is likely to induce or increase unwanted side effects without providing additional benefit in return.

Contraindications and overdose information: MDMA causes an increase in blood pressure and pulse rate, modest in most people, similar to moderate exercise. Because of this, and because a few people may have a more pronounced cardiac response to MDMA, people with a history of high blood pressure, heart trouble, or stroke are advised not to use MDMA, or at the very least are advised to start with a much lower than average dose. The same warning applies to people who are hypersensitive to drugs. Liver or kidney problems may also contraindicate MDMA use. It is, of course, desirable to hear from your physician that you're in good overall health before ingesting any powerful substance. Deaths have been reported of some MDMA users who were also taking Monoamine Oxidase Inhibitors (MAOIs are often prescribed as antidepressants). MDMA is *not* recommended to anyone taking any MAOI. Ask your doctor or pharmacist if you're unsure whether a drug you are taking is an MAOI. Also be aware that some antidepressants (e.g. Prozac and Zoloft) may inhibit some of the effects of MDMA. MDMA is thought by many to be a fairly safe drug, as long as you keep track of what your body is telling you. The euphoria that it induces can make it easy to ignore bodily distress signals, so be watchful for things like dehydration (drink lots of water or fruit juices!), muscle cramping, dizziness, exhaustion or overexertion. Several reports from England tell of dosed ravers dancing themselves into severe dehydration and heat exhaustion that required hospitalization and in a few cases resulted in death. An MDMA overdose is characterized by high pulse or blood pressure, faintness, muscle cramping, or panic attacks. If you experience any of these symptoms, sit down, rest, and drink some fruit juice, water, or a gatorade-type sports drink. In the unlikely event someone has a more severe reaction, e.g. loss of consciousness or seizures, get medical help as soon as possible.

Effects: The physical effects of usual doses of MDMA are subtle and variable: some users report dryness of mouth, jaw clenching, teeth grinding, nystagmus (eye wiggles), sweating, or nausea. Others report feelings of profound physical relaxation. At higher doses (overdoses), the physical effects of MDMA resemble those of amphetamines: fast or pounding heartbeat, sweating, dizziness, restlessness, etc. The psychological effects are a bit more difficult.



    How to make MDMA (x)

    The following synthesis is not meant to be carried out by a novice chemist, although it is not terribly difficult. For descriptions of how to carry out the procedures, you should buy a standard lab procedures reference manual (or preferably you should take college organic chemistry).


    Method 1
    To a well stirred, cooled mixture of 34g of 30% H202 (hydrogen peroxide) in 150g 80% HCO2H (formic acid) there was added, dropwise, a solution of 32.4g isosafrole in 120ml acetone at a rate that kept the reaction mixture from exceeding 40 deg C. This required a bit over 1 hour, and external cooling was used as necessary. Stirring was continued for 16 hours, and care was taken that the slow exothermic reaction did not cause excess heating. An external bath with running water worked well. During this time the solution progressed from an orange color to a deep red. All volatile components were removed under vacuum which yielded some 60g of a very deep residue. This was dissolved in 60ml of MeOH (methyl alcohol -- methanol), treated with 360ml of 15% H2SO4 (sulfuric acid), and heated for 3 hours on the steam bath. After cooling the mixture was extracted with 3x75ml Et2O (diethyl ether) or C6H6 (benzene). Its recommended that, the pooled extracts can washed -- first with H2O and then with dilute NaOH (sodium hydroxide). Then the solvent is removed under vacuum to afford 20.6g 3,4-methylenedioxyphenylacetone (3,4-methylenedioxybenzyl methyl ketone). The final residue may be distilled at 2.0mm/108-112 deg C, or at about 160 deg C at the water pump.


    Add 23g 3,4-methylenedioxyphenylacetone to 65g HCONH2 (formamide) and heat at 190 deg for five hours. Cool, add 100ml H20, extract with C6H6 (benzene) and evaporate in vacuum the extract. Add 8ml MeOH (methyl alcohol -- methanol) and 75ml 15% HCl to residue, heat on water bath two hours and extract in vacuum (or basify with KOH and extract the oil with benzene and dry, evaporate in vacuum) to get 11.7 g 3,4-methylenedioxyamphetamine (MDA).
    To produce MDMA substitute N-methylformamide for formamide in the above synthesis.






    Method 2

    This is a less yealding method usually producing only MDA. It is a two step procedure first reacting safrole with hydrobromic acid to give 3,4-methylenedi- oxyphenyl-2-bromopropane, and then taking this material and reacting it with either ammonia or methylamine to yield MDA or MDMA respectively. This procedure has the advantages of not being at all sensitive to batch size, nor is it likely to "run away" and produce a tarry mess. It shares with the Ritter reaction the advantage of using cheap, simple, and easily available chemicals.



    The sole disadvantage of this method is the need to do the final reaction with ammonia or methylamine inside a sealed pipe. This is because the reaction must be done in the temperature range of 120- 140 C, and the only way to reach this temperature is to seal the reactants up inside of a bomb. This is not particularly dangerous, and is quite safe if some simple precautions are taken.



    The first stage of the conversion, the reaction with hydrobromic acid, is quite simple, and produces almost a 100% yield of the bromi- nated product. See the Journal of Biological Chemistry, Volume 108 page 619. The author is H.E. Carter. Also see Chemical Abstracts 1961, column 14350. The following reaction takes place:



    To do the reaction, 200 ml of glacial acetic acid is poured into a champagne bottle nestled in ice. Once the acetic acid has cooled down, 300 grams (200 ml) of 48% hydrobromic acid is slowly added with swirling. Once this mixture has cooled down, 100 grarns of safrole is slowly added with swirling. Once the safrole is added, the cheap plastic stopper of the champagne bottle is wired back into place, and the mixture is slowly allowed to come to room temperature with occasional shaking. After about 12 hours the original two layers will merge into a clear red solution. In 24 hours, the reaction is done. The chemist carefully removes the stopper from the bottle, wearing eye protection. Some acid mist may escape from around the stopper.



    The reaction mixture is now poured onto about 500 grams of crushed ice in a 1000 or 2000 ml beaker. Once the ice has melted, the red layer of product is separated, and the water is extracted with about l00 ml of petroleum ether or regular ethyl ether. The ether extract is added to the product, and the combined product is washed first with water, and then with a solution of sodium carbonate in water. The purpose of these washings is to remove HBr from the product. One can be sure that all the acid is removed from the product when some fresh carbonate solution does not fizz in contact with the product.



    Once all the acid in the product is removed, the ether must be removed from it. This is important because if the ether were allowed to remain in it, too much pressure would be generated in the next stage inside of the bomb. Also, it would interfere with the formation of a solution between the product and methylamine or ammonia. It is not necessary to distill the product because with a yield of over 90%, the crude product is pure enough to feed into the next stage. To remove the ether from the product, the crude product is poured into a flask, and a vacuum is applied to it. This causes the ether to boil off. Some gentle heating with hot water is quite helpful to this process. The yield of crude product is in the neighborhood of 200 grams.



    With the bromo compound in hand, it is time to move onto the next step which gives MDA or MDMA. The bromo compound reacts with ammonia or methylamine to give MDA or MDMA.




    To do the reaction, 50 grams of the bromo compound is poured into a beaker, and 200 ml of concentrated ammonium hydroxide (28% NH3) or 40% methylamine is added. Next, isopropyl alcohol is added with stirring until a nice smooth solution is formed. It is not good to add too much alcohol because a more dilute solution reacts slower. Now the mixture is poured into a pipe "bomb." This pipe should be made of stainless steel, and have fine threads on both ends. Stainless steel is preferred because the HBr given off in the reaction will rust regular steel. Both ends of the pipe are securely tightened down. The bottom may even be welded into place. Then the pipe is placed into cooking oil heated to around 130 C. This temperature is maintained for about 3 hours or so, then it is allowed to cool. Once the pipe is merely warm, it is cooled down some more in ice, and the cap unscrewed.


    The reaction mixture is poured into a distilling flask, the glass- ware rigged for simple distillation, and the isopropyl alcohol and excess ammonia or methylamine is distilled off. When this is done, the residue inside the flask is made acid with hydrochloric acid. If indicating pH paper is available, a pH of about 3 should be aimed for. This converts the MDA to the hydrochloride which is water soluble. Good strong shaking of the mixture ensures that this conversion is complete. The first stage of the purification is to recover unreacted bromo compound. To do this, 200 to 300 ml of ether is added. After some shaking, the ether layer is separated. It contains close to 20 grams of bromo compound which may be used again in later batches.

    Now the acid solution containing the MDA is made strongly basic with lye solution. The mixture is shaken for a few minutes to ensure that the MDA is converted to the free base. Upon sitting for a few minutes, the MDA floats on top of the water as a dark colored oily layer. This layer is separated and placed into a distilling flask. Next, the water layer is extracted with some toluene to get out the remaining MDA free base. The toluene is combined with the free base layer, and the toluene is distilled off. Then a vacuum is applied, and the mixture is fractionally distilled. A good aspirator with cold water will bring the MDA off at a temperature of 150 to 160 C. The free base should be clear to pale yellow, and give a yield of about 20 ml. This free base is made into the crystalline hydrochloride by dissolving it in ether and bubbling dry HCl gas through it.



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