what if I buy 4-AcO DMT powder online today, what basic information should I know concerning this drug
4-Acetoxy-N, N-dimethyltryptamine (also known as 4-AcO-DMT, 4-Acetoxy-DMT, O-Acetylpsilocin, psilacetin, and “synthetic mushrooms”) is a novel psychedelic substance of the tryptamine class. It is a structural analog of psilocybin, the active ingredient in psilocybin mushrooms (magic mushrooms). Like psilocybin, it is thought to produce its effects primarily by binding to serotonin receptors in the brain; however, the precise mechanism is not fully understood.
The synthesis of the 4-AcO-DMT chemical was first reported in 1963 by Albert Hofmann and Franz Troxler as part of an investigation into psilocin analogs. However, its pharmacology and subjective effects were not explored. A paper authored by David E.
Nichols in 1999 proposed it as a potentially useful alternative to psilocybin for pharmacological research due to the lower cost of synthesis. Reports of recreational use began to surface shortly after its appearance on the online research chemical market in the 2010s
4-AcO chemical formulae and properties | buy 4-AcO DMT near me without getting caught
Relevant identified uses: For research use only, not for human or veterinary use
4-Acetoxy-N,N-dimethyltryptamine Fumarate / O-Acetylpsilocin Fumarate
Molecular Formula: C14H18N2O2
Molecular Weight: 246.3049 g/mol
Form: fumarate salt
IUPAC: 3-[2-(Dimethylamino)ethyl]-1H-indol-4-yl acetate
Material Data Safety Sheet: Available upon request
NMR: Available upon request
What is there to know about the history and chemistry of 4-AcO chemical powder?
O-Acetylpsilocin (psilacetin) and several other esters of psilocin were patented on January 16, 1963, by Sandoz Ltd via Albert Hofmann & Franz Troxler. Despite this, psilacetin remains a psychedelic compound with a limited history of use.
It is theorized to be a prodrug of psilocin, as is psilocybin, which occurs naturally in many species of hallucinogenic mushrooms. Psilacetin is O-acetylated psilocin, whereas psilocybin is O-phosphorylated. This is because the aromatic acetyl moiety on the 4th position of the indole ring system is subject to deacetylation in acidic conditions such as those found in the stomach.
O-Acetylpsilocin is more resistant than psilocin to oxidation under basic conditions due to its acetoxy group. It is, therefore, a semi-synthetic compound. It is believed to be a prodrug of psilocin; however, speculation exists that psilacetin itself also may be psychoactive.
O-Acetylpsilocin can be obtained by acetylation of psilocin under alkaline or strongly acidic conditions. While O-acetylpsilocin is not well researched (sometimes viewed negatively as a research chemical, as opposed to psilocin and psilocybin), it is not as difficult as psilocybin to synthesize.
Due to their similar proposed mechanisms of action, this factor may provide further support for the proposition that O-acetylpsilocin might serve as an appropriate substitute for psilocybin in research of the application of psychedelic compounds in medicine.