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	218.300 g·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あるふぁ-ET) is a psychoactive drug and member of the tryptamine chemical class. It produces psychedelic and stimulant effects.^[1]

Dosage

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

Effects

5-MeO-αあるふぁ-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あるふぁ-ET, but its safety profile is unknown.

Legality

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

References

^ 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-αあるふぁET αあるふぁET αあるふぁMT
Chemical classes	Substituted amphetamine Sub. benzofuran Sub. cathinone Sub. MDPEA Sub. PEA Sub. tryptamine

Dosage

Effects

Dangers

Legality

See also

References