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Details

Stereochemistry ACHIRAL
Molecular Formula C17H26N2O.ClH
Molecular Weight 310.862
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5-METHOXY-N,N-DIISOPROPYLTRYPTAMINE HYDROCHLORIDE

SMILES

Cl.COC1=CC=C2NC=C(CCN(C(C)C)C(C)C)C2=C1

InChI

InChIKey=QEBJXWFHKCUFLS-UHFFFAOYSA-N
InChI=1S/C17H26N2O.ClH/c1-12(2)19(13(3)4)9-8-14-11-18-17-7-6-15(20-5)10-16(14)17;/h6-7,10-13,18H,8-9H2,1-5H3;1H

HIDE SMILES / InChI

Molecular Formula C17H26N2O
Molecular Weight 274.4011
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Schedules of controlled substances: temporary placement of alpha-methyltryptamine and 5-methoxy-N,N-diisopropyltryptamine into Schedule I. Final rule.
2003 Apr 4
[Latest cases of acute poisoning in clinical practice--5MeO-DIPT and GHB precursor].
2004 Jul
Analytical chemistry of synthetic routes to psychoactive tryptamines. Part I. Characterisation of the Speeter and Anthony synthetic route to 5-methoxy-N,N-diisopropyltryptamine using ESI-MS-MS and ESI-TOF-MS.
2004 Nov
A general screening and confirmation approach to the analysis of designer tryptamines and phenethylamines in blood and urine using GC-EI-MS and HPLC-electrospray-MS.
2004 Sep
Schedules of controlled substances: placement of alpha-methyltryptamine and 5-methoxy-N,N-diisopropyltryptamine into schedule I of the Controlled Substances Act. Final rule.
2004 Sep 29
Sensitive determination of alpha-methyltryptamine (AMT) and 5-methoxy-N,N-diisopropyltryptamine (5MeO-DIPT) in whole blood and urine using gas chromatography-mass spectrometry.
2005 Aug 25
A foxy intoxication.
2005 Feb 10
Analysis of hallucinogenic constituents in Amanita mushrooms circulated in Japan.
2006 Dec 20
Metabolism of the psychotomimetic tryptamine derivative 5-methoxy-N,N-diisopropyltryptamine in humans: identification and quantification of its urinary metabolites.
2006 Feb
Hallucinogen-like actions of 5-methoxy-N,N-diisopropyltryptamine in mice and rats.
2006 Jan
A fatal poisoning with 5-methoxy-N,N-diisopropyltryptamine, Foxy.
2006 Nov 10
Acute confusional state after designer tryptamine abuse.
2007 Apr
5-Methoxy-N,N-diisopropyltryptamine (Foxy), a selective and high affinity inhibitor of serotonin transporter.
2007 Apr 5
Neuropsychotoxicity of abused drugs: molecular and neural mechanisms of neuropsychotoxicity induced by methamphetamine, 3,4-methylenedioxymethamphetamine (ecstasy), and 5-methoxy-N,N-diisopropyltryptamine (foxy).
2008 Jan
A general approach to the screening and confirmation of tryptamines and phenethylamines by mass spectral fragmentation.
2008 Jan 15
Comparison of time-dependent effects of (+)-methamphetamine or forced swim on monoamines, corticosterone, glucose, creatine, and creatinine in rats.
2008 May 30
Comparison of the developmental effects of 5-methoxy-N,N-diisopropyltryptamine (Foxy) to (+/-)-3,4-methylenedioxymethamphetamine (ecstasy) in rats.
2009 Jun
Tinnitus psychopharmacology: A comprehensive review of its pathomechanisms and management.
2010 Jun 24
The hallucinogenic world of tryptamines: an updated review.
2015 Aug
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:54:12 GMT 2023
Edited
by admin
on Sat Dec 16 08:54:12 GMT 2023
Record UNII
SJ048VQB9S
Record Status Validated (UNII)
Record Version
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Name Type Language
5-METHOXY-N,N-DIISOPROPYLTRYPTAMINE HYDROCHLORIDE
MI  
Systematic Name English
1H-INDOLE-3-ETHANAMINE, 5-METHOXY-N,N-BIS(1-METHYLETHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
5-METHOXY-N,N-BIS(1-METHYLETHYL)-1H-INDOLE-3-ETHANAMINE HYDROCHLORIDE
Systematic Name English
5-METHOXY-N,N-DIISOPROPYLTRYPTAMINE HYDROCHLORIDE [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m7332
Created by admin on Sat Dec 16 08:54:12 GMT 2023 , Edited by admin on Sat Dec 16 08:54:12 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID7048900
Created by admin on Sat Dec 16 08:54:12 GMT 2023 , Edited by admin on Sat Dec 16 08:54:12 GMT 2023
PRIMARY
FDA UNII
SJ048VQB9S
Created by admin on Sat Dec 16 08:54:12 GMT 2023 , Edited by admin on Sat Dec 16 08:54:12 GMT 2023
PRIMARY
PUBCHEM
24802109
Created by admin on Sat Dec 16 08:54:12 GMT 2023 , Edited by admin on Sat Dec 16 08:54:12 GMT 2023
PRIMARY
CAS
2426-63-3
Created by admin on Sat Dec 16 08:54:12 GMT 2023 , Edited by admin on Sat Dec 16 08:54:12 GMT 2023
PRIMARY
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