Dave Woodmont
Bluelighter
HBr -- Shulgin mentions 6-hydroxydopamine in PiHKAL, under #168, TMPEA. He says:
"The simple compound that results from the stripping of all three of the O-methyl groups from TMPEA is the extremely potent neurotoxin, 6-hydroxydopamine. When it is ad-ministered to an otherwise intact experimental animal, it produces sympathectomy, effectively destroying the sympathetic nervous system. And some of the methyl groups of TMPEA are known to be stripped off through the normal metabolic processes that occur in the liver. There are many fascinating psychedelics that have a signature of methoxyl groups para to one-another. It is known that they, too, can lose a methyl group or two. It would be intriguing to see if there was some biochemical overlap between the metabolism of some of these centrally active drugs and the metabolic fate of 6-hydroxydopamine. But in a test animal, of course, rather than in man."
I did a quick Medline search awhile back to try to see what its mechanism of neurotoxicity is, but only found articles that discussed using it as a way of sympathectomizing lab animals in order to do further studies. Apparently using it for that sort of thing is standard procedure, so the original papers determining how it works must be pretty old. An afternoon at the library could resolve this, but that's just not doable for me these days. Anyone who knows or can find out, please report back....
So you saw this in a chem supply site? Needless to say, this stuff shouldn't be sold like candy to ravers alongside the 2C-I. Neither should 2C-I .... but damn, this material is over the top dangerous, and I wonder how many "psychonauts" browsing the site you saw realized this? "Hey, let's try this new RC." Yikes.
peace,
Dave
"The simple compound that results from the stripping of all three of the O-methyl groups from TMPEA is the extremely potent neurotoxin, 6-hydroxydopamine. When it is ad-ministered to an otherwise intact experimental animal, it produces sympathectomy, effectively destroying the sympathetic nervous system. And some of the methyl groups of TMPEA are known to be stripped off through the normal metabolic processes that occur in the liver. There are many fascinating psychedelics that have a signature of methoxyl groups para to one-another. It is known that they, too, can lose a methyl group or two. It would be intriguing to see if there was some biochemical overlap between the metabolism of some of these centrally active drugs and the metabolic fate of 6-hydroxydopamine. But in a test animal, of course, rather than in man."
I did a quick Medline search awhile back to try to see what its mechanism of neurotoxicity is, but only found articles that discussed using it as a way of sympathectomizing lab animals in order to do further studies. Apparently using it for that sort of thing is standard procedure, so the original papers determining how it works must be pretty old. An afternoon at the library could resolve this, but that's just not doable for me these days. Anyone who knows or can find out, please report back....
So you saw this in a chem supply site? Needless to say, this stuff shouldn't be sold like candy to ravers alongside the 2C-I. Neither should 2C-I .... but damn, this material is over the top dangerous, and I wonder how many "psychonauts" browsing the site you saw realized this? "Hey, let's try this new RC." Yikes.
peace,
Dave