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crops is put into a 500 ml flask along with a solution made up of 150 ml ethyl alcohol, 150 ml water, and 100 grams KOH. Next, 15 ml of hydrazine hydrate is added. This hydrazine should be the monohydrate, which is 64% hydrazine. If a weaker variety has been scrounged up, this can be made to work by adding more, and using less water. Now the flask should be fitted with a condenser, and flushed with nitrogen. Then heat the flask in an oil bath to gentle boiling for 4 hours. A slow stream of nitrogen to the flask during the reflux averts the danger from hydrazine. The flask is next cooled, and the contents poured into a sep funnel of at least 1000 ml capacity. The batch is then extracted with 600 ml ether, followed by 600 ml of an 85-15% mix of ether and alcohol. Finally, one more extraction with 600 ml of 85-15% ether-alcohol is done. All of the desired product should now be extracted into the solvent, and out of the water. This fact should be checked using a black light to look for the characteristic blue fluorescence. The combined solvent extracts should now be lowered to a pH of about 2 using HC1. At this point, a precipitate should form, and it should be filtered out. The precipitate should be washed free of entrained product with 4-1 ether-alcohol, and the washing added to the rest of the filtered solvent. Now 2750 ml of water should be added to the solvent, and the mixture placed in a gallon and a half glass jug or 5000 ml beaker. To this should be added 3 portions of cation exchange resin in H* cycle. Cation exchange resin is a common item of commerce used in deionized water systems. Check the yellow pages under "water" and see which of the local Culligan men offer deionized water systems. The deionizers come in two-tank systems with one tank packed with cation exchange resin to remove calcium, magnesium and sodium from the water. The other tank has an anion exchange resin to remove chlorides, sulfates, and so on. It is no great task to buy cation exchange resin from these outlets. The resin consists of tiny plastic beads coated with the exchanger. In the case of the cation exchangers, Practical LSD Manufacture 44 this is generally a sulfonate. "In H* cycle" means that the resin is charged up and ready to go. This is generally done by soaking the resin in 20% sulfuric acid in water for a while, then rinsing with distilled water. Check the directions on the container of resin. Steer clear of mixed resins that contain both anion and cation exchangers. If the Culligan man is too stupid to know the difference, or doesn't know what he has, keep looking until you find one who knows his business. The treatment with three portions of cation exchange resin in H* cycle should be done as follows: Each portion of resin should weigh about 15 grams. The first portion is added, and then the mixture should be stirred strongly or shaken for about 10 minutes. The product will come out of the liquid, and stick Very Very (Trichocereus Skin (Trichocereus Torch – Very Peruvianus) Plants Liquid Preparation Ayahuasca The best range of legal highs, herbal ecstasy and party pills on the Internet Ayahuasca Ayahuasca Plants Liquid 4-aco-dmt vendor


there is decent drainage. Cacti tend to grow mostly during spring and autumn, to send down roots in the summer, and to rest through winter. Although cactus cuttings may be planted anytime of the year they stand the best chance if planted in the late spring. They should be watered thoroughly once or twice a week depending upon how rapidly moisture is lost. The soil an inch below the surface should always contain some moisture. Watering can be cut back to less than half during the winter. INCREASING THE POTENCY OF PSYCHOACTIVE CACTI There are several factors which influence production of mescaline and related alkaloids in cacti. Presence of a wide variety of trace minerals is important. Occasional watering with Hoagland A-Z trace mineral concentrate provides these minerals. Combine 1 part concentrate with 9 parts water and water cacti with this once every two months. Experiments conducted by Rosenberg, Mclaughlin and Paul at the University of of Michigan, Ann Arbor in 1966 demonstrated that dopamine is a precursor of mescaline in the peyote cactus. Tyramine and dopa were also found to be mescaline precursors, but not as immediate and efficient as dopamine. It appears that in the plant tyosine breaks down to become tyramine and dopa. These then recombine to form dopamine which is converted to nor-mescaline and finally to mescaline. One can take advantage to this sequence by inject-ing each peyote plant with dopamine 4 weeks prior to harvesting. Much of the dopamine will convert to mescaline during this time, giving a considerable increase in the alkaloid of the plant. Prepare a saturated solution of free base dopamine in a .05 N solution of hydrochloric acid and inject 1-2 cc into the root of each plant and the same amount into the green portion above the root. Let the needle penetrate to the center of the plant, inject slowly and allow the needle to remain in place a few seconds after injection. It is best to deprive the plant of water for 1-2 weeks before injection. This makes the plant tissues take up the injection fluids more readily. If dopamine is not available, a mixture of tyramine and dopa can be used instead 6 weeks before harvesting for comparable results. San Pedro and other mescaline-bearing cacti can be similarly treated for increased mescaline production. Inject at the base of the plant and again every 3-4 inches following a spiral pattern up the length of the plant. A series of booster injections can be given to any of these cacti every 6-8 weeks and once again 4 weeks before harvesting for greater mescaline accumulation. It is also possible to increase the macromerine and nor-macromerine content of Doñana cacti using tyramine or DL-norepinephrine as precursors. Injections should be given 20-25 days before harvesting. Series of injections can be given 45 days apart for higher alkaloid accumulation. EXTRACTING PURE MESCALINE FROM PEYOTE OR SAN PEDRO CACTUS The isolation of mescaline from cacti ayahuasca preparation Plants Liquid Buyayahuasca Peruvian Torch Skin Cuts (Trichocereus Peruvianus) – Very strong wnward through the alumina, two zones that fluoresce blue can be spotted by illumination with a black light. The faster-moving zone contains LSD, while the slower-moving zone is iso-LSD. When the zone containing LSD reaches the spigot of the burette, it should be collected in a separate flask. About 3000 ml of the 3-1 benzene-chloroform is required to get the LSD moved down the chromatography column, and finally eluted. The iso-LSD is then flushed from the column by switching the solvent being fed into the top of the column to chloroform. This material is collected in a separate flask, and the solvent removed under a vacuum. The residue is iso-LSD, and should be stored in the freezer until conversion to LSD is undertaken. Directions for this are also given in this chapter. For the fraction containing the LSD, conversion to LSD tartrate must be done to make it water soluble, improve its keeping characteristics, and to allow crystallization. Tartaric acid has the ability to react with two molecules of LSD. Use, then, of a 50% excess of tartaric acid dictates the use of about 1 gram of tartaric acid to 3 grams of LSD. The three grams of LSD would be expected from a well-done batch out of a total 3.5 LSD/iso-LSD mix. The crystalline tartrate is made by dissolving one gram of tartaric acid in a few mis of methanol, and adding this acid solution to the benzene-chloroform elute from the chromatography column. Evaporation of the solvent to a low volume under a vacuum gives crystalline LSD tartrate. Crystals are often difficult to obtain. Instead, an oil may result due to the presence of impurities. This is not cause for alarm; the oil is still likely 90%+ pure. It should be bottled up in dark glass, preferably under a nitrogen atmosphere, and kept in a freezer until moved. If chromatography reveals that one's chosen cooking method produces little of the iso products, then the production of the tartrate salt and crystallization is simplified. The residue obtained at the end Practical LSD Manufacture 32 of the batch is dissolved in a minimum amount of methanol. To this is then added tartaric acid. The same amount is added as above: one gram tartaric acid to three grams LSD. Next, ether is slowly added with vigorous stirring until a precipitate begins to form. The stoppered flask is then put in the freezer overnight to complete the precipitation. After filtering or centrifuging to isolate the product, it is transferred to a dark bottle, preferably under nitrogen, and kept in the freezer until moved. LSD from (so-LSD Two variations on this procedure will be presented here. The first is the method of Smith and Timmis from The Journal of the Chemistry Society Volume 139, H pages 1168-1169 (1936). The other is found in US patent 2,736,728. Both use the action of a strong hydroxide solution to convert iso material into a mixture that contains active and iso material. At equilibrium, the mixture contains about 2/3 Plants Liquid Caapi) Caapi Vine Ourinhos Ourinhos

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