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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 Caupuri Caapi Vine (Banisteriopsis Caapi) Ayahuasca Black Negra San Pedro Cactus Trichocereus ayahuasca erature reading lesson to those who have made these claims. See Proceedings of the Royal Society of London, Series B, Volume 155, pages 26 to 54 (1961). Also see US Patent 3,219,545. You will note while reading these articles detailing how to get lysergic amide production in a culture medium that these guys had to scour the globe to find that rare strain of claviceps fungus that will cooperate in this manner. The vast majority of claviceps fungi just will not produce these alkaloids while being cultured. See the following articles to convince yourself of just how futile it is to collect a wild strain of claviceps and try to get it to produce lysergic acid amides in culture: Ann. Rep. Takeda Res. Lab Volume 10, page 73 (1951); and Farmco, Volume 1, page 1 (1946); also Arch. Pharm. Berl. Volume 273, page 348 (1935); also American Journal of Practical LSD Manufacture Botany, Volume 18, page 50 (1931); also Journal of the American Pharmacy Association Volume 40, page 434 (1951); also US patent 2,809,920; also Canadian Journal of Microbiology, Volume 3, page 55 (1957), and Volume 4, page 611 (1958) and Volume 6, page 355 (1960); also Journal of the American Pharmacy Society Volume 44, page 736 (1955). With this matter disposed of, it is time to move on to what actually are viable sources of lysergic acid amides for the production of LSD. This is the farming end of the acid business. It is only through raising ergot-infested rye, or growing morning glories and Hawaiian baby woodrose that the required feedstocks of lysergic compounds can be obtained without making a target of oneself. I have for years seen ads in High Times offering morning glory seeds and Hawaiian baby woodrose seeds for sale, but these are offered in small amounts at high prices. I would bet my bottom dollar that these outfits, if they are not front operations, will at least report to the heat any large orders they get. To avoid detection, the aspiring LSD manufacturer must be ready to get his hands dirty, and spend some time as a farmer. The most difficult farming choice, and as luck would have it, the one that gives the purest acid, is to grow a patch of ergot-infested rye. The reason why ergot is superior to growing morning glory seeds or woodrose seeds is that these seeds have a considerable amount of another type of alkaloid in them besides the ones that yield lysergic acid. These other alkaloids are of the clavine type, meaning that they have the lysergic-acid skeleton, but lack the carboxyl grouping. In its place will be a methyl grouping, an alcohol grouping, a methyl alcohol grouping or combinations of the above. These clavine alkaloids will likely be carried all the way through into the product, producing both the GIGO situation during the synthetic operations and a contaminated product when finished. I will present my ideas on how to remove them, but they are best avoided in the first place. Ergot is the name given to a dark brow Whole (Mitragyna (Mitragyna Kratom Strength (Mitragyna (Mitragyna Ayahuasca Black Negra San Pedro Cactus Trichocereus (Mitragyna Instant Kratom speciosa) speciosa) Instant

 Hawaiian Baby Woodrose

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

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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

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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 Plants Liquid 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 Ayahuasca Black Negra San Pedro Cactus Trichocereus Get drug Get drug To ayahuasca
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