4-HO-MiPT

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"Miprocin" redirects here. It is not to be confused with Mupirocin.
4-HO-MiPT
Miprocin.png 4-HO-MiPT-3d-sticks.png
Clinical data
Routes of
administration
Oral, intranasal, rectal, IV, IM
ATC code None
Legal status
Legal status
Identifiers
Synonyms 4-hydroxy-N-methyl-N-isopropyltryptamine
CAS Number 77872-43-6 N
PubChem (CID) 10082683
ChemSpider 8258221 YesY
UNII 4GAJ9OJ8YZ N
ChEMBL CHEMBL171419 YesY
Chemical and physical data
Formula C14H20N2O
Molar mass 232.32 g/mol
3D model (Jmol) Interactive image
Melting point 123 to 125 °C (253 to 257 °F)
 NYesY (what is this?)  (verify)

4-HO-MiPT (miprocin, 4-hydroxy-N-methyl-N-isopropyltryptamine) is a synthetic substituted aromatic compound and a lesser-known psychedelic tryptamine. It is thought to be a serotonergic psychedelic, similar to magic mushrooms, LSD and mescaline.[citation needed] Its molecular structure and pharmacological effects resemble those of the tryptamine psilocin, which is the primary psychoactive chemical in magic mushrooms.

History[edit]

4-HO-MiPT was presumably first synthesized by Alexander Shulgin. Its synthesis is described in his book TiHKAL along with reports by people who had ingested the compound. Shulgin's trials and other anecdotal information suggest that 4-HO-MiPT is a synthetic psychedelic similar in activity to psilocin. It is relatively uncommon and has only a short history of human use.

Chemistry[edit]

Miprocin is the 4-hydroxyl analog of the chemical N-methyl-N-isopropyltryptamine as well as the isopropyl homolog and possible structural analog of 4-HO-DMT.

Pharmacology[edit]

4-HO-MiPT is thought to be a serotonergic psychedelic.[citation needed] Like other serotonergic psychedelics, its method of action is believed to result from its partial agonism of 5-HT2A and 5-HT1A serotonin receptors.[citation needed]

Toxicity[edit]

Very little is known about the toxicity of 4-HO-MiPT. Its chemical structure and pharmacological activity are very similar to psilocin, a compound which isn't associated with compulsive use or physical dependence. However, because very little research has been done on 4-HO-MiPT, it cannot be definitively concluded that its pharmacological actions in the human body do not differ from those of psilocin. To date, there have been no reported deaths from 4-HO-MiPT.[citation needed]

Duration[edit]

Onset of action is 3 to 10 seconds; the duration of action is one half-hour to two hours when injected IV.[citation needed]

Drug prohibition laws[edit]

Sweden[edit]

Sveriges riksdags health ministry Statens folkhälsoinstitut classified 4-HO-MiPT as "health hazard" under the act Lagen om förbud mot vissa hälsofarliga varor (translated Act on the Prohibition of Certain Goods Dangerous to Health) as of Nov 1, 2005, in regulation SFS 2005:733 listed as "4-hydroxi-N,N-metylisopropyltryptamin (4-HO-MIPT)", making it illegal to sell or possess.[1]

UK[edit]

The substance could also be considered illegal in the UK under the Misuse of Drugs Act 1971.

USA[edit]

4-HO-MiPT is an unscheduled drug in the United States. However, it is an analog of psilocin, which could lead to prosecution under the Federal Analog Act.

Russia[edit]

4-HO-MiPT is in Shedule 1 in Russia as an analog of 4-hydroxytryptamine.

See also[edit]

References[edit]

External links[edit]