Recently I found this cool article..
In this article we see a 1% solution of diacetylmorphine will have a 90% conversion to 6-monoacetylmorphine (the remaining being leftover diacetylmorphine and morphine) if left to sit for exactly 12mos at room temperature. While the hydrolysis is easy the time it takes is longer than most would like to wait.
Here’s the reason why you really should give this a try… For a long time I’ve wondered on more precise pharmacological differences between DAM (heroin) and 6-MAM. Now in this article I’m getting a better picture. Go down to the morphine based alkaloids table for more info.
We see that 6-MAM has stronger pharmacological effects WHILE being less toxic than diacetylmorphine. Analgesia and “excitant effects” of 6-MAM are double that of DAM, with less convulsant effects and respiratory depression.
By simply leaving your heroin hcl (or other salt) at 1g per 100ml distilled water in a closet for a year, then pour it in a glass tray to dry. Scrape it up and you have 6-monoacetylmorphine.
-GC
In this article we see a 1% solution of diacetylmorphine will have a 90% conversion to 6-monoacetylmorphine (the remaining being leftover diacetylmorphine and morphine) if left to sit for exactly 12mos at room temperature. While the hydrolysis is easy the time it takes is longer than most would like to wait.
Here’s the reason why you really should give this a try… For a long time I’ve wondered on more precise pharmacological differences between DAM (heroin) and 6-MAM. Now in this article I’m getting a better picture. Go down to the morphine based alkaloids table for more info.
We see that 6-MAM has stronger pharmacological effects WHILE being less toxic than diacetylmorphine. Analgesia and “excitant effects” of 6-MAM are double that of DAM, with less convulsant effects and respiratory depression.
By simply leaving your heroin hcl (or other salt) at 1g per 100ml distilled water in a closet for a year, then pour it in a glass tray to dry. Scrape it up and you have 6-monoacetylmorphine.
-GC