N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)

Base Information

• Chemical Name: N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)
• CAS No.: 96096-52-5
• Molecular Formula: C₁₄H₂₀N₂
• Molecular Weight: 216.326
• Mol file: 96096-52-5.mol

Synonyms:N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)

Chemical Property of N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)

Chemical Property:

• Vapor Pressure: 3.52E-05mmHg at 25°C
• Refractive Index: 1.589
• Boiling Point: 353.7°Cat760mmHg
• PKA: 17.39±0.30(Predicted)
• Flash Point: 167.7°C
• PSA: 19.03000
• Density: 1.038g/cm³
• LogP: 3.05060

Purity/Quality:

99% ^*data from raw suppliers

N-Methyl-N-(1-methylethyl)-1H-indole-3-ethanamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Description: MiPT is the methyl isopropyl tryptamine base for a series of psychedelic designer drugs, including 5-methoxy MiPT and 4-hydroxy MiPT . Screening for this and related compounds by LC-MS/MS has been reported. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
• Uses: MiPT is the methyl isopropyl tryptamine base for a series of psychedelic designer drugs, including 5-methoxy MiPT and 4-hydroxy MiPT.

Technology Process of N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)

There total 3 articles about N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

[2-(1H-indol-3-yl)-ethyl]-methylamine (61-49-4) + acetone (67-64-1) → N-methyl-N-isopropyltryptamine (96096-52-5)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol; for 15h; under 2585.7 Torr; Yield given;

DOI:10.1021/jm00145a007

Reference yield:

tryptamine (61-54-1) → N-methyl-N-isopropyltryptamine (96096-52-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 85 percent / K₂CO₃ / H₂O; toluene / 15 h / Ambient temperature

2: lithium aluminum hydride / tetrahydrofuran / 0.5 h / Heating

3: H₂ / 10 percent Pd/C / ethanol / 15 h / 2585.7 Torr

With lithium aluminium tetrahydride; hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol; water; toluene;

DOI:10.1021/jm00145a007

Reference yield:

(2-indol-3-yl-ethyl)-carbamic acid benzyl ester (38750-13-9) → N-methyl-N-isopropyltryptamine (96096-52-5)

Guidance literature:

Multi-step reaction with 2 steps

1: lithium aluminum hydride / tetrahydrofuran / 0.5 h / Heating

2: H₂ / 10 percent Pd/C / ethanol / 15 h / 2585.7 Torr

With lithium aluminium tetrahydride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol;

DOI:10.1021/jm00145a007

upstream raw materials:

[2-(1H-indol-3-yl)-ethyl]-methylamine

acetone

tryptamine

(2-indol-3-yl-ethyl)-carbamic acid benzyl ester

Refernces