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
Hs Code.:
Mol file:96096-52-5.mol

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

Suppliers and Price of N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N-Methyl-N-(1-methylethyl)-1H-indole-3-ethanamine
100mg
$ 1200.00

Cayman Chemical
MiPT ≥98%
5mg
$ 221.00

Cayman Chemical
MiPT ≥98%
1mg
$ 59.00

Cayman Chemical
MiPT ≥98%
50mg
$ 1180.00

American Custom Chemicals Corporation
MIPT 95.00%
5MG
$ 496.57

AK Scientific
n-Methyl-n-isopropyltryptamine
5mg
$ 398.00

Total 40 raw suppliers

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 N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT) 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:

: 61-49-4
[2-(1H-indol-3-yl)-ethyl]-methylamine

: 67-64-1
acetone

: 96096-52-5
N-methyl-N-isopropyltryptamine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 15h; under 2585.7 Torr; Yield given;
DOI:10.1021/jm00145a007

Reference yield:

: 61-54-1
tryptamine

: 96096-52-5
N-methyl-N-isopropyltryptamine

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:

: 38750-13-9
(2-indol-3-yl-ethyl)-carbamic acid benzyl ester

: 96096-52-5
N-methyl-N-isopropyltryptamine

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