5-MeO-AET

5-MeO-AET
Legal status
Legal status	DE:NpSG(Industrial and scientific use only); UK:Class A;
Identifiers
	IUPAC name 1-(5-methoxy-1H-indol-3-yl)butan-2-amine;
CAS Number	4765-10-0;
ChemSpider	21106244;
UNII	QCQ6JFX5NL;
CompTox Dashboard(EPA)	DTXSID20894761;
Chemical and physical data
Formula	C13H18N2O
Molar mass	218.300g·mol−1
3D model (JSmol)	Interactive image;
Melting point	201 to 203 °C (394 to 397 °F)
	SMILES 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; Key:JHTPCKWBFLMJMQ-UHFFFAOYSA-N;
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5-Methoxy- Alpha -ethyltryptamine(5-MeO-α-ET) is apsychoactive drugand member of thetryptamine chemical class.It producespsychedelicandstimulanteffects.^[1]

Dosage[edit]

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

Effects[edit]

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

Dangers[edit]

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

Legality[edit]

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 theFederal Analog Actbecause of its structural similarities to α-ET andα-MT.

References[edit]

^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.

[Deluca_2012-1] 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.

[1]

v t e Empathogens/entactogens
Phenylalkyl- amines (other than cathinones)	Unfused benzene ring:3-CMA 4-CAB 4-FA 4-MA 4-MMA 4-FMA 4-MTA 4,4'-DMAR Ariadne Metaescaline MMA PMA PMEA PMMA mMMA Benzodioxine:EDMA Benzodioxoles:Phenethylamine: {Lophophine} Amphetamines: {2-Methyl-MDA 2,3-MDA 3,4-MDA (tenamfetamine) 5-Methyl-MDA 6-Methyl-MDA DFMDA DMMDA DMMDA-2 EIDA Lys-MDA MDEA MDMA (midomafetamine) MDMOH MDOH MMDA MMDA-2 MMDMA N-t-BOC-MDMA} 1-Phenylbutan-2-amines: {BDB EBDB MBDB} Phentermines: {MDMP MDPH} Benzofurans, dihydrobenzofurans and benzothiophenes:2-MAPB 5-APB 5-APDB 5-EAPB 5-MAPB 5-MAPDB 5-MAPBT 5-MBPB 6-APB 6-APDB 6-EAPB 6-MAPB 6-MAPDB IBF5MAP Indanes:5-APDI 5-MAPDI Indoles:5-IT 6-API Naphthalenes:Methamnetamine Naphthylaminopropane Tetralin:6-APT
Cyclized phenyl- alkylamines	Aminoindanes:5-IAI AMMI BFAI ETAI MDAI MDMAI MMAI MEAI NM-2-AI TAI Aminotetralins:6-CAT MDAT MDMAT
Cathinones	3-MMC 4-EMC BK-5-MAPB Brephedrone Butylone Dimethylone Ethylone Eutylone Flephedrone Mephedrone Methedrone Methylone TH-PVP
Tryptamines	4-Methyl-αET αET αMT
Chemical classes	Substituted amphetamine Sub. benzofuran Sub. cathinone Sub. MDPEA Sub. PEA Sub. tryptamine

Dosage[edit]

Effects[edit]

Dangers[edit]

Legality[edit]

See also[edit]

References[edit]