NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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[2-(5-methoxy-1H-indol-3-yl)ethyl]bis(propan-2-yl)amine
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IUPAC Traditional name
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Synonyms
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5-methoxy-N,N-bis(1-methylethyl)-1H-Indole-3-ethanamine
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5-MeO-DIPT
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Foxy methoxy
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Foxy
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5-Methoxy-N,N-diisopropyltryptamine
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Diisopropyl-[2-(5-methoxy-1H-indol-3-yl)-ethyl]-amine
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CAS Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
ALOGPS 2.1
Acid pKa
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17.440752
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H Acceptors
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2
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H Donor
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1
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LogD (pH = 5.5)
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0.19873744
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LogD (pH = 7.4)
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0.6141407
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Log P
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3.6911604
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Molar Refractivity
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85.2402 cm3
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Polarizability
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34.30691 Å3
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Polar Surface Area
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28.26 Å2
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Rotatable Bonds
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6
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Lipinski's Rule of Five
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true
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Log P
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4.35
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LOG S
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-3.61
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Solubility (Water)
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6.73e-02 g/l
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PROPERTIES
PROPERTIES
Product Information
Bioassay(PubChem)
Purity
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98%
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Show
data source
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DETAILS
DETAILS
DrugBank
DrugBank -
DB01441
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Item |
Information |
Drug Groups
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illicit; experimental |
Description
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5-methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT) is a tryptamine derivative and shares many similarities with schedule I tryptamine hallucinogens such as alpha-ethyltryptamine, N,N-dimethyltryptamine, N,N-diethyltryptamine, bufotenine, psilocybin and psilocin. Since 1999, there has been a growing popularity of 5-MeO-DIPT among drug abusers. This substance is abused for its hallucinogenic effects. |
Pharmacology |
5-methoxy-diisopropyltryptamine, also known as 5-methoxy-N,N-diisopropyltryptamine, 5-MeO-DiPT, foxy methoxy, or just foxy, is a tryptamine that is used recreationally as a psychedelic. 5-MeO-DiPT is orally active, and dosages between 6–20 mg are commonly reported. Many users note an unpleasant body load accompanies higher dosages. 5-MeO-DiPT is also taken by insufflation, or sometimes it is smoked or injected. Some users also report sound distortion, also noted with the related drug, DiPT. |
Affected Organisms |
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Humans and other mammals |
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Absorption |
5-MeO-DIPT produces effects with an onset of 20 to 30 minutes and with peak effects occurring between 1 to 1.5 hours after administration. |
References |
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External Links |
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PATENTS
PATENTS
PubChem Patent
Google Patent