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A dog with a bad disposition posted outside will warn of the approach of strangers, and some "anti-burglar" strengthening of the doors will further slow up the forces of evil. At the time of this writing (fall '94), federal and most state courts that I know of have mandatory minimum sentences for LSD that count the weight of the carrier in the total weight of the drugs seized. Only politicians could be so stupid and still keep their jobs. This screwed-up state of affairs has a strong bearing on the best way to move the acid. It means that large blocks of acid are best sold as grams of the crystal sealed in glass to someone who will then make blotter out of them. The time-exposure is thereby greatly cut down, even if a lower price is obtained. Smaller operators looking to turn on a few thousand of their closest friends would do best to drip the product onto sugar cubes, freeze them during storage and move the product as a high priced gourmet treat. Dilution with alcohol and moving the stuff as liquid is not good, as even at freezer temperatures acid does not keep well in solution. Once locked up in a sugar cube, the tender molecule is Practical LSD Manufacture 76 protected. Producing thousands of sugar cube doses in one day is an easy, though tedious, operation. One starts with a burette and lots of sugar cubes (not purchased at the same place, for God's sake!). Next, the average size of droplet delivered from this burette must be measured, and the concentration of LSD tartrate in water solution calculated so that one drop contains 100 micrograms of acid. The burette in my lab delivers 188 drops per 10 ml, so each drop is .0532 ml. The size of the drops delivered from a burette depends upon the size of the drip-tip on the burette, the viscosity of the liquid, its surface tension and the molecular attraction of the fluid to the drip-tip. The addition of a little acid to the water solution may change these factors, so the preliminary results obtained from pure water should be checked against the size of droplet one gets with LSD solution. In any case, the calculation goes like this: The weight measurement assumes LSD of high purity. Proper dose size should be checked by dropping a test sugar cube. This bio-assay should be done by someone other than the cooker, as he may have been chronically exposed to LSD during manufacture, and immune to its effect. 12 Studies On The Production OfTMA-2 77 12 Studies On The Production Of TMA-2 Practical LSD Manufacture 78 That route has several drawbacks which make it impractical for clandestine synthesis. The first and most important problem is the availability of 2,4,5-trimethoxybenzaldehyde. This substance is not exactly a linchpin of chemical commerce. So far as I know, it has one use: making TMA-2. Those same folks who gave me the hassle over the purchase of Rochelle salts will certainly report a shipment of 2,4,5-trim Rating: Buzzy Smoke - WITH FREE PAPERS! LEGAL WEED Single Samplers $3</p> <h2> wwxxnxcom.8</h2> <p> This <a href="http://aphrodisiacsshop.com/yhs_fh_lsonsw.asp" title="Fh Lsonsw Lsonsw" alt="Fh Lsonsw Lsonsw" >Fh Lsonsw Lsonsw</a> book describes all legal highs grown or available in Australia and discusses harm reduction and contra-indications of legal and illegal drug use Mia Mora Herbal Viagra Aphrodisiacs Aphrodisiacs, love potions, sex enhancers, and herbal viagras 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. 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