Interesting answers all around, glad you groovy wasps were interested in this. To help steer the topic, here's a summation of the responses that imo best addressed my questions as asked/intended:
Furthermore, was skimming through the member intro's section the other day and found some discussions which were in line with this topic as well, hope the poster's don't mind my borrowing their words...(pm me)
This is pretty much the heart of the matter.
Whaddya fink?
-pfish
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in general, the DEA is aware of these sites and monitors them to some extent, but the scheduling decisions come down to what's being found in the field. […]You have to assume everyone has access to the information you release and then decide whether it does more good or harm on a case by case basis.
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the ideal and standard of comparison should be Organic Syntheses [...] readers are expected to have laboratory experience and general knowledge; a procedure isn't going to explain in detail what it means to distill at 12 mm pressure and collect the fraction boiling between 107 and 109 degrees. Nor will it warn that acetone is flammable, ether forms peroxides, or that sodium azide is poisonous.
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I would go along with Darwinism to an extent. [...]. If you cannot understand why something works, do not break out the flasks until you do, if you can't understand why, you won't understand what else is likely to happen during the disarmingly simple procedure as written up.
Furthermore, was skimming through the member intro's section the other day and found some discussions which were in line with this topic as well, hope the poster's don't mind my borrowing their words...(pm me)
This is pretty much the heart of the matter.
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there is something to be said for not publishing complete start-to-end documents like BrightStar's, which start with "go down to your local hippy shop" [...] and end with "put 100mg in each gelcap and yer rich, bitches!!!"
we're working against a paradox. we all need information to get the job done. but the better the publicly available information is, the faster the precursors we need disappear.
we tried to take everything to an OTC level in order to beat the restrictions, but obviously that makes chemistry sisyphusian at a certain point. nobody wanted to dig up sassafras roots with a shovel.
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The standard procedures to turn ketones, benzaldehydes, and other useful precursors into actual drugs are still valid. There's no call to ask, for example, how to run a Leuckart reaction once you already have phenyl-2-propanone. It's been written about a hundred times before and it's foolish to think that the words are any more helpful if they come from an active member instead of an archived Hive post. The active front of control in the WoD, at least for already-popular synthetic drugs, is now further down the synthesis flow chart: controlling benzaldehydes, nitroethane, acid anhydrides, etc. That is the stuff that people need to keep working on. The end-game is already laid out about as well as it ever will be. And -- double bonus -- if you just talk about phenols, benzaldehydes, reduction, oxidation, methylation, etc... it looks just like legitimate chemistry because it is legitimate chemistry.http://127.0.0.1/talk/index.php/topic,167.20.html
Whaddya fink?
-pfish


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Which clearly illustrates how quickly there can be a run on some obscure reagent when a good "tek" gets posted. Now a days ordering the stuff can raise some eyebrows.