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Also psilacetin, 4-acetoxy-DMT, or 4-AcO-DMT,O-Acetylpsilocin). It is a synthetically produced psychoactive drug. It is the acetylated form of the psilocybin mushroom. Alkaloid psilocin and is a lower homolog of 4-AcO-DET, 4-AcO-MiPT and 4-AcO-DiPT.

1 Product name 4-Aco-DMT
2 Full chemical name 3-[2-(Dimethylamino)ethyl]-1H-indol-4-yl acetate
3 Formal Name psilacetin, 4-acetoxy-DMT,O-Acetylpsilocin
4 CAS num 92292-84-7
5 Molecular Formula C14H18N2O2
6 Average mass 246.3049 g·mol−1
7 Purity ≥99.0%
8 Stability 2 years
9 Storage -20°C
10 Formulation A powder solid
11 λmax 221, 315 nm
12 Shipping Wet ice in continental US; may vary elsewhere
It is the acetylated form of the psilocybin mushroom alkaloid psilocin. 4-AcO-DET, 4-AcO-MiPT and 4-AcO-DiPT.
The compound has been suggest by David Nichols to be a potentially useful alternative to psilocybin. For pharmacological studies as they are both believe to be prodrugs of psilocin.
Its structural similarities to psilocin and psilocybin results in an identical subjective effect profile. The three compounds can feel indistinguishable from each other.
This allows 4-AcO-DMT to function as a perfect substitute for psilocybin mushrooms.

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Buy 4-Aco-DMT Online

Buy 4-Aco-DMT cheap Online because (O-Acetylpsilocin) Online is a novel psychedelic substance of the tryptamine class. Buy 4-Aco-DMT also online from trust supplier

4-ACO-DMT cheap, O-Acetylpsilocin is a synthetically produced psychoactive drug and has been suggested by David Nichols to be a potentially useful alternative to psilocybin for pharmacological studies, as they are both believed to be prodrugs of psilocin.

It is the acetylated form of the psilocybin mushroom alkaloid psilocin and is a lower homolog of 4-AcO-DET, 4-AcO-MiPT and 4-AcO-DiPT.

44-ACO-DMT and several other esters of psilocin were originally patented on January 16, 1963 by Sandoz Ltd. via Albert Hofmann & Franz Troxler.[2][3] Despite this fact, 4-AcO-DMT remains a psychedelic with a limited history of use prior to its release as a grey area compound on the online research chemical market.

However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive.

There are, however, claims of subjective differences in effect between the acetylated and non-acetylated forms of psilocin.[4] Some users report that it lasts slightly longer than. psilocin while others report that it lasts for a considerably shorter time. Many users report less body load and nausea compared to psilocin. Some users find that the visual distortions produced by 4-AcO-DMT more closely resemble those.

produced by DMT than those produced by psilocin. These differences could be possible if 4-AcO-DMT is active itself and not merely as a prodrug.

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Cathinone derivatives can easily pass through the brain–blood barrier and because of structural similarities with phenethylamine, they display psychoactive properties. The most important mechanism of action of
cathinones is inhibiting of protein-transporting monoamines (dopamine,
noradrenaline and serotonin) of the synaptic gap. The sympathomimetic syndrome dominates in a clinical picture [2,3].
Since then, further cathinones were synthesized and marketed, posing a real threat to public health [4,5].
Cathinones cause a number of side effects associated with the cardiovascular system (increased heart rate, arrhythmias, increased blood
pressure, myocardial ischemia with ECG changes and chest pain, myocarditis and sudden cardiac death), the coagulation system
(disseminated vascular coagulation syndrome and decrease in platelet count), the nervous system (sleep disturbances, headache, vision disorder, mydriasis, paresthesia, convulsions and hyperthermia), and the gastrointestinal tract (nausea, vomiting and abdominal pain).
These compounds also cause mental disorders and metabolic disorders (including metabolic acidosis, dehydration, electrolyte disorders and
nitrogen body retention). The most commonly reported adverse reactions for cathinones are cardiovascular, nervous, and psychiatric disorders (including acute psychoses).




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