5-MeO-AET

Chemical compound
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
Identifiers
  • 1-(5-methoxy-1H-indol-3-yl)butan-2-amine
CAS Number
  • 4765-10-0 ☒N
ChemSpider
  • 21106244 checkY
UNII
  • QCQ6JFX5NL
CompTox Dashboard (EPA)
  • DTXSID20894761 Edit this at Wikidata
Chemical and physical dataFormulaC13H18N2OMolar mass218.300 g·mol−13D model (JSmol)
  • Interactive image
Melting point201 to 203 °C (394 to 397 °F)
  • CCC(N)Cc2c[nH]c1ccc(cc12)OC
InChI
  • InChI=1S/C13H18N2O/c1-3-10(14)6-9-8-15-13-5-4-11(16-2)7-12(9)13/h4-5,7-8,10,15H,3,6,14H2,1-2H3 checkY
  • Key:JHTPCKWBFLMJMQ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

5-Methoxy-alpha-ethyltryptamine (5-MeO-α-ET) is a psychoactive drug and member of the tryptamine chemical class. It produces psychedelic and stimulant effects.[1]

Dosage

5-MeO-α-ET, when used recreationally, is usually taken orally at dosages of 50–75 mg.

Effects

5-MeO-α-ET produces entactogenic and stimulant effects that can last 4–6 hours. However, little information exists on the psychopharmacological effects of this compound, thus considerable variation with regard to dosage and effects can be expected.

Dangers

There have been no reported deaths or hospitalizations from 5-MeO-α-ET, but its safety profile is unknown.

Legality

5-MeO-α-ET is unscheduled and uncontrolled in the United States, but possession and sales of 5-MeO-α-ET could be prosecuted under the Federal Analog Act because of its structural similarities to α-ET and α-MT.

See also

References

  1. ^ Deluca P, Davey Z, Corazza O, Di Furia L, Farre M, Flesland LH, et al. (December 2012). "Identifying emerging trends in recreational drug use; outcomes from the Psychonaut Web Mapping Project". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 39 (2). Elsevier BV: 221–226. doi:10.1016/j.pnpbp.2012.07.011. PMID 22841965. S2CID 22296279.
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See also: Receptor/signaling modulators • Monoamine reuptake inhibitors • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins
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