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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 About Angustifolia Hallucinogenic Ourinhos Caapi Vine (Banisteriopsis caapi) ing in the cold before then adding 25 ml of diethylamine. Stir for an additional 10 minutes, then pour the batch into a 2000 ml sep funnel. Now to the sep funnel add 800 ml of water. Mix this in thoroughly, then add 400 ml of saturated salt solution in water. Mix this in, then extract out the LSD by repeated extraction with 250 ml portions of ethylene dichloride. Check with a blacklight for complete extraction. 6 LSD From Lysergic Acid And SO3 55 The combined ethylene dichloride extracts should be evaporated under a vacuum as above, and the residue of LSD and iso-LSD should be separated and treated as above. 7 LSD From Lysergic Acid And Trifluoroacetic Anhydride 51 1 LSD From Lysergic Acid And Trifluoroacetic Anhydride This method is a little bit lame, but it may be the method of choice if trifluoroacetic anhydride or trifluoroacetic acid should happen to fall from the sky into one's hands. The reason why this method is a bit lame is threefold. Anhydrous lysergic acid is required for this reaction. To obtain anhydrous lysergic acid, the lysergic acid hydrate yielded by the methods in Chapter 5 must be baked under high vacuum for a couple hours. This is obviously not good for such a delicate molecule. The water molecule will be shed by a baking temperature of 120° C at a vacuum of 1 mm Hg, 140° C at 2 mm Hg, and still higher temperatures at less perfect vacuums. A MacLeod gauge is the only instrument that I know of which is capable of accurately measuring such high vacuums. Another reason why this method is lacking is that the yields are not so good as those achieved by the other synthetic routes presented in this book. It is possible to recover the unreacted lysergic acid at the end of the process, but this does not make up for the initial lower yield, not to mention the added hassle of recovering and redrying the lysergic acid. Strike number three for this route is its propensity to give byproducts that are difficult to separate from the desired product. I am Practical LSD Manufacture 58 not talking here about the large amount of iso-LSD that this method makes. That molecular jumbling is inconsequential, because the lysergic acid used is itself an isomeric mixture. Rather, what can occur here is the production of LSD and other by-products. The mechanics of this reaction are similar to the reaction with SOs, in that two molecules of the anhydride react with the lysergic acid molecule to form the mixed anhydride. In this reaction, there is no need to first react the lysergic acid with hydroxide to form the metal salt. Also, the need to follow exact stoichiometric quantities of reactants is not as pressing as in the SO$ method. To do the reaction, into a 1000 ml flask (carefully dried and equipped with a magnetic stirring bar) place 16 grams of lysergic acid and 375 ml of acetonitrile. The lysergic acid will not dissolve. Stopper the flask and place it in the freezer to cool the contents to -20f Premium Mimosa Hostilis Root Bark Angustifolia Hallucinogenic ayahuasca yage

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The plants build up alkaloids during dry seasons and draw upon them for growth when the rains come. If the plants are harvested during or after a wet spell, the alkaloid content may have dropped below 50 percent. If you have a soil test kit, you can get a good indication of the potency of cacti growing wild. If the soil is rich in nitrogen, the plants are likely to be rich in alkaloids. When harvesting peyote, many people uproot the entire plant. This is unnecessary and wasteful. The roots contain no mescaline. Some of these plants have taken a long time to reach their size. A cactus three inches in diameter may be more than 20 years old. To collect peyote properly the button should be cleanly decapitated slightly above ground level. When the roots are left intact new buds will form where the old was removed. These will eventually develop into full-size buttons which may be harvested as before. Faulty harvesting method have seriously depleted populations of this cactus. Because of the presence of several phenolic alkaloids peyote cacti do not spoil easily and may be kept in their fresh form for several weeks after harvesting. If they are to be kept longer than this they must be refrigerated, frozen, or dried. The enzymes which cause the harvested plant to eventually decompose also destroy the mescaline and other alkaloids. To dry peyote buttons lay them out in the hot sun or in an oven at 250 degrees F until completely devoid of moisture. OTHER PEYOTE-TYPE CACTI OF CENTRAL MEXICO There are several cacti which are used by the Tarahumares and other tribes of central Mexico as substitutes for peyote. Many of these cacti are now under investigation for their alkaloidal content and sychopharmacological activity. Progress is somewhat retarded in the studies of the effects of these plants because almost all experimentation has been conducted on laboratory animals rather than humans. Some of these cacti have been found to contain mescaline and other related alkaloids with known sympathomimetic properties. Much further research is needed on these plants and their activity. However, we will attempt to bring the reader up to date on what is known about them at this time. PEYOTILLO: This small cactus is botanically called PELECYPHORA ASELLIFORMIS. It is also known sometimes as the hatchet cactus because of its oddly flattened tubercules. It is often found growing in the state of San Louis Potosi in central Mexico. The plant contains traces of mescaline too minute to have any effect. It also contains small amounts of anhalidine, anhaladine, hordenine, Nmethylmescaline, pellotine, 3-demethyltrichocereine, B-phenethylamine, Nmethyl- B-phenethylamine, 3,4-dimethoxy-B-pheneththyl-amine, N-methyl-3,4- dimethoxy-B-phenethylamine, and 4-methoxy-B-phenethy- lamine. Most of these are found in peyote but in much larger quantities. TSUWIRI: The botanical name of this cactus is ARIOCARPUS RETUSUS. The Huichol name tsuwiri means F Gallery Angustifolia Hallucinogenic Hash Seed Peruvian Torch Skin Cuts (Trichocereus Peruvianus) – Very strong 1 Grams Digital Scales - UPTO 400 Gram / 0 Powdered SUPER Premium Kratom (Mitragyna speciosa) Angustifolia Hallucinogenic

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