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4-AcO-MiPT Also known as:

  • 1H-Indol-4-ol, 3-[2-[methyl(1-methylethyl)amino]ethyl]-, acetate (ester)[ACD/Index Name]
  • 3-{2-[Isopropyl(methyl)amino]ethyl}-1H-indol-4-yl acetate[ACD/IUPAC Name]
  • 3-{2-[Isopropyl(methyl)amino]ethyl}-1H-indol-4-yl-acetat[German][ACD/IUPAC Name]
  • Acétate de 3-{2-[isopropyl(méthyl)amino]éthyl}-1H-indol-4-yle[French][ACD/IUPAC Name]
  • SS93IMV779
  • [3-[2-[Isopropyl(methyl)amine]ethyl]-1H-indol-4-yl] acetate[ACD/IUPAC Name]
  • [3-[2-[methyl(propan-2-yl)amino]ethyl]-1H-indol-4-yl] acetate
  • 3-(2-(Isopropyl(methyl)amino)ethyl)-1H-indol-4-yl acetate
  • 3-{2-[Methyl(propan-2-yl)amino]ethyl}-1H-indol-4-yl acetate
  • 4-Acetate 3-[2-[methyl(1-methylethyl)amino]ethyl]-1H-indol-4-ol
  • 4-Acetoxy-N,N-Methylisopropyltryptamine
  • 4-Acetoxy-N-isopropyl-N-methyltryptamine
  • 4-AcOMIPT
  • 4-AcO-N,N-MIPT
  • MFCD16293750[MDL number]
  • UNII:SS93IMV779

A quite potent tryptamine that has be related to having “shroom-like” visuals. Yet without much bodyload. Very hydroscopic. Seems to be quite safe in dosing. Similar to the likes of 2C-B.


It is the acetylated form of 4-HO-MiPT (also known as miprocin) and is a higher homolog of 4-AcO-DMT, 4-AcO-MET and 4-AcO-DET. These substances are commonly hypothesized to act primarily as prodrugs for their respective hydroxylated counterparts (e. g.

4-HO-DMT, 4-HO-MET and 4-HO-DET), although there is on-going debate as to whether they possess their own innate activity. There is very little information on the human pharmacology or toxicity of 4-AcO-MiPT, although analytical methods have been developed for its detection. Today it is either used recreationally or as an entheogenic substance and is typically acquired through the use of online research chemical vendors.

It remains relatively uncommon and has very little history of human usage.


Tryptamines share a core structure comprised of a bicylic indole heterocycle attached at R3 to an amino group via an ethyl side chain.

4-AcO-MiPT is substituted at R4 of its indole heterocycle with an acetoxy (AcO) functional group CH3COO−.

It also contains isopropyl and methyl chains bound to the terminal amine RN of its tryptamine backbone (MiPT). 4-AcO-MiPT is the N-substituted methisopropyl homologue of 4-HO-DMT (psilocin).

4-AcO-MiPT is the acetate ester analog of MiPT and the N-substituted methisopropyl analog of 4-AcO-DMT.

Systematic nameMIPRACETIN
Std. InChiInChI=1S/C16H22N2O2/c1-11(2)18(4)9-8-13-10-17-14-6-5-7-15(16(13)14)20-12(3)19/h5-7,10-11,17H,8-9H2,1-4H3
Avg. Mass274.3581 Da
Molecular Weight274.3581
Monoisotopic Mass274.168121 Da
Nominal Mass274
ChemSpider ID23976075

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Dose Chart


Duration Chart

Onset15-45 minutes
Duration4-9 hours

Legal Status

Due to its relative obscurity, the possession and sale of 4-AcO-MiPT is unscheduled in most countries.

  • Germany: 4-AcO-MiPT is controlled under the NpSG (New Psychoactive Substances Act) as of July 18, 2019. Production and import with the aim to place it on the market, administration to another person and trading is punishable. Possession is illegal but not penalized.
  • Sweden: 4-AcO-MiPT is classified as "health hazard" under the act "Lagen om förbud mot vissa hälsofarliga varor" (translated to the "Act on the Prohibition of Certain Goods Dangerous to Health"). The drug is listed in their regulation SFS 2005:733, making it illegal to sell or possess.
  • United Kingdom: 4-AcO-MiPT is a Class A drug in the UK as it is an ester of the drug 4-HO-MiPT., which is a Class A drug as a result of the tryptamine catch-all clause.
  • United States: 4-AcO-MiPT is unscheduled in the United States. It may be considered an analogue of psilocin (4-HO-DMT) which is a Schedule I drug under the Controlled Substances Act. As such, the sale for human consumption or the use for illicit non-medical or industrial intents and purposes could be prosecuted as crimes under the Federal Analogue Act.
  • Sources


    3. 4-Acetoxy-MiPT - PubChem |
    4. Talaie, H.; Panahandeh, R.; Fayaznouri, M. R.; Asadi, Z.; Abdollahi, M. (2009). "Dose-independent occurrence of seizure with tramadol". Journal of Medical Toxicology. 5 (2): 63–67. :10.1007/BF03161089.  1556-9039.
    5. "Verordnung zur Änderung der Anlage des Neue-psychoaktive-Stoffe-Gesetzes und von Anlagen des Betäubungsmittelgesetzes" (PDF) (in German). Bundesanzeiger Verlag. Retrieved December 10, 2019.
    6. "Anlage NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz. Retrieved December 10, 2019.
    7. "§ 4 NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz. Retrieved December 10, 2019.
    9. Misuse of Drugs Act 1971 ( |
    10. Misuse of Drugs Act 1971 ( |

    Information made possible with:

    1. PsychonautWiki is a community-driven online encyclopedia that aims to document the field of psychonautics in a comprehensive, scientifically-grounded manner.
    2. Erowid is a non-profit educational & harm-reduction resource with 60 thousand pages of online information about psychoactive drugs
    3. PubChem National Center for Bio Informatics
    4. Chemspider is a free chemical structure database providing fast access to over 34 million structures, properties and associated information.
    5. Wikipedia

    Additional APIs were used to construct this information. Thanks to ChemSpider, NCBI, PubChem etc.

    Data is constantly updated so please check back later to see if there is any more available information on this substance.