96096-52-5 Usage
Description
N-METHYL-N-ISOPROPYLTRYPTAMINE (MIPT) is a chemical compound that serves as the base for a series of psychedelic designer drugs, such as 5-methoxy MIPT and 4-hydroxy MIPT. It is primarily used for forensic and research applications, and its physiological and toxicological properties are not well understood.
Uses
Used in Forensic Applications:
N-METHYL-N-ISOPROPYLTRYPTAMINE (MIPT) is used as a forensic tool for the detection and analysis of this compound and related substances in various samples. The use of LC-MS/MS has been reported for screening purposes, aiding in the identification and quantification of MIPT in cases related to drug abuse or criminal investigations.
Used in Research Applications:
In the field of research, N-METHYL-N-ISOPROPYLTRYPTAMINE (MIPT) is utilized for studying the effects and mechanisms of action of psychedelic designer drugs. This helps scientists and researchers to better understand the properties, potential therapeutic uses, and risks associated with these compounds, ultimately contributing to the development of new treatments and policies surrounding their use.
Check Digit Verification of cas no
The CAS Registry Mumber 96096-52-5 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 96096-52:
(7*9)+(6*6)+(5*0)+(4*9)+(3*6)+(2*5)+(1*2)=165
165 % 10 = 5
So 96096-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2/c1-11(2)16(3)9-8-12-10-15-14-7-5-4-6-13(12)14/h4-7,10-11,15H,8-9H2,1-3H3
96096-52-5Relevant articles and documents
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.
