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5-MEO-MIPT, also known as 5-Methoxy-N-methyl-N-isopropyltryptamine, is a synthetic psychedelic tryptamine that is structurally related to N-methyl-N-isopropyltryptamine (MIPT). It is known for its potent inhibition of monoamine re-uptake, particularly serotonin and norepinephrine, without affecting dopamine re-uptake. 5-MEO-MIPT does not influence the release of monoamines from rat brain synaptosomes. 5-MEO-MIPT is primarily intended for forensic and research applications.

96096-55-8

96096-55-8 Suppliers

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96096-55-8 Usage

Uses

Used in Forensic Applications:
5-MEO-MIPT is used as a forensic tool for the detection and analysis of this synthetic compound in various samples, such as biological fluids and tissues. Its identification is crucial for legal and investigative purposes, as well as for understanding the prevalence and impact of its use in society.
Used in Research Applications:
In the field of research, 5-MEO-MIPT serves as a valuable compound for studying the effects of psychedelic tryptamines on the human brain and nervous system. It is used as a research chemical to investigate the mechanisms underlying its potent inhibition of serotonin and norepinephrine re-uptake, which can provide insights into the development of potential therapeutic agents for various neurological and psychiatric disorders.
Used in Pharmaceutical Research:
5-MEO-MIPT is utilized in pharmaceutical research to explore its potential as a lead compound for the development of new medications. Its unique action on monoamine re-uptake and lack of effect on dopamine release make it an interesting candidate for the treatment of conditions such as depression, anxiety, and other mood disorders.
Used in Neurobiological Studies:
5-MEO-MIPT is employed in neurobiological studies to better understand the role of monoamines in cognitive function, mood regulation, and other brain processes. By examining the effects of 5-MEO-MIPT on neurotransmitter systems, researchers can gain a deeper understanding of the complex interactions between various neurochemicals and their impact on behavior and mental health.

Check Digit Verification of cas no

The CAS Registry Mumber 96096-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,9 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96096-55:
(7*9)+(6*6)+(5*0)+(4*9)+(3*6)+(2*5)+(1*5)=168
168 % 10 = 8
So 96096-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N2O/c1-11(2)17(3)8-7-12-10-16-15-6-5-13(18-4)9-14(12)15/h5-6,9-11,16H,7-8H2,1-4H3

96096-55-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-methylpropan-2-amine

1.2 Other means of identification

Product number -
Other names Moxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:96096-55-8 SDS

96096-55-8Downstream Products

96096-55-8Relevant academic research and scientific papers

Psychotomimetic N-Methyl-N-isopropyltryptamines. Effects of Variation of Aromatic Oxygen Substituents

Repke, David B.,Grotjahn, Douglas B.,Shulgin, Alexander T.

, p. 892 - 896 (2007/10/02)

Eight N-methyl-N-isopropyltryptamines (MIPTs) possessing various aromatic oxygen substituents were prepared, characterized, and evaluated for hallucinogenic activity in man.In at least two instances (the Ar H and the Ar 5-OCH3, 1 and 4) the unsymmetrical nitrogen substitution led to a substantial increase in potency as well as oral activity when compared to the symmetrical dimethyl homologues.Qualitatively, 4-hydroxy-N-methyl-N-isopropyltryptamine (2) was the most interesting in overall effect, producing a classic hallucinogenic profile.The 5-methoxy congeger 4 resulted in a state characterized by heightened conceptual stimulation lacking in visual phenomena.Other members of the series exhibited diminished effects.