4-AcO-MET

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4-AcO-MET
Clinical data
Other names4-Acetoxy-MET; Metacetin; 4-Acetoxy-N-methyl-N-ethyltryptamine
Identifiers
  • [3-[2-[ethyl(methyl)amino]ethyl]-1H-indol-4-yl] acetate
JSmol)
  • CCN(C)CCc1c[nH]c2c1c(ccc2)OC(=O)C
  • InChI=1S/C15H20N2O2/c1-4-17(3)9-8-12-10-16-13-6-5-7-14(15(12)13)19-11(2)18/h5-7,10,16H,4,8-9H2,1-3H3
  • Key:OMDKHOOGGJRLLX-UHFFFAOYSA-N

4-acetoxy-MET (4-acetoxy-N-

4-AcO-DMT. It is a novel compound with very little history of human use.[1] It is sometimes sold as a research chemical
by online retailers.

Due to its similarity to the psilocin prodrug 4-AcO-DMT, which is deacetylated to form psilocin in vivo,

serum esterases
, but human studies concerning the metabolic fate of this drug are lacking.

Legality

In the United States, 4-Acetoxy-MET is not scheduled. It may be considered an analogue of psilocin, a Schedule I drug under the Controlled Substances Act. As such, the sale for human consumption or the use for illicit non-medical purposes could be considered a crime under the Federal Analogue Act.[4]

In Switzerland, 4-Acetoxy-MET is a controlled substance under Verzeichnis E.[5]

In the United Kingdom, 4-Acetoxy-MET is a Class A drug in the UK because it is an ester of the drug 4-HO-MET, which is a Class A drug under the tryptamine catch-all clause.[6]

References

  1. ^ "New psychoactive substances reported to the EMCDDA and Europol for the first time in 2009 under the terms of Council Decision 2005/387/JHA" (PDF). www.emcdda.europa.eu. Retrieved 6 May 2022.
  2. S2CID 32044725
    .
  3. .
  4. ^ "21 U.S. Code § 841 - Prohibited acts A", LII / Legal Information Institute, retrieved 2016-08-02
  5. ^ "Fedlex". www.fedlex.admin.ch. Retrieved 2021-08-15.
  6. ^ "Misuse of Drugs Act 1971". 2021-08-15. Archived from the original on 2012-11-11.