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Drug synthesis guide. acquired at the darknet with sturdy suggestions, no longer verified.

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Hydroxy methylenedioxyphenethylamine has been stated to be a truly friendly excessive. 4-BROMO-2,5-DIMETHOXYPHENYLETHYLAMINE JCS, two hundred (1953) this is often in a different way to make a similar drug within the above formulation. The formulation less than is designed to take your already made pace and position the bromine atom within the right position within the molecule. this actual formulation is exemplified for phenylethylamine, that's approximately ten occasions weaker than phenylisopropylamine. the variation among the 2 is that phenylethylamine is made through the use of nitromethane because the nitrating agent and phenylisopropylamine is nitrated with nitroethane. Nitroethane is lots costlier and much more suspicious to the DEA while ordered, however it makes a stronger drug; you can find its synthesis within the precursor part. either the nitrating brokers are so alike, that they are utilized in formulation as analogs (if you don't have nitroethane round you could replacement an equimolar volume of nitromethane and get a sym- Amphetamines forty five pathomimetic drug and vice versa). Likewise, medicinal drugs made up of both of the nitrating brokers are typically universally utilized with good fortune in any formulation requiring one or the opposite, i. e. , the formulation that follows, the methylating, and so forth. The dose for the drug as made lower than (4-bromo-2,5dimethoxyphenylethylamine) is ready five mg and the dose for the drug as made above (4-bromo2,5-dimethoxyamphetamine, also known as 4-bromo-2,5-dimethoxyphenylisopropylamine) is zero. five (%) mg. the consequences of the drug made both method are a similar, MDA-like, simply the dosage turns out to alter. To a cooled resolution of 3,4-dimethoxyphenylethylamine five. four g in 20 cc of acetic acid, four. eight g of bromine in 15 cc of acetic acid is slowly additional with stirring. Separation of the product will start swiftly, and after atmosphere in a single day the crystals will be accumulated and recrystallized from ethanol. Addition of sodium hydroxide to an aqueous answer will precipitate the unfastened base as white plates. Yield: 7 g, mp: 202-204°. word: The microfiche I bought this formulation from used to be so abused that i couldn't learn the directions for making the precursors. it can be attention-grabbing to determine what results this bromination may have on 3,4-methylenedioxyamphetamine and different ring substituted amphetamines. 2,5-DIMETHOXY-4-METHYLAMPHETAMINE (DOM, STP) and ANALOGS JMC, thirteen, 134 (1970) This drug, recognized in laboratories as DOM and in the street as STP, is particularly effective and has one of many longest periods of motion of any pace; a minimal dose to get you excessive (5 mg) will preserve you excessive for a minimum of 24 hours. when you are so courageous as to do a virtually deadly dose, you can be not able to devour or sleep for every week or extra. therefore the drug won a nasty recognition with a few legislations officers and drug clients. besides the fact that, i believe that DOM represents a good price because it is simple to synthesize, it truly is reasonably cheap, it truly is strong and it lasts decades. 2,5-Dimethoxy-4-methyl-B-nitrostyrene. (This formulation is exemplified for the analog of DOM and is three-fourths as robust as DOM. in case you wish to make the particular DOM, then replacement nitroethane rather than nitromethane; it will produce nitropropene rather than nitrostyrene.

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