5-Methoxy-N-isopropyltryptamine

Base Information

Chemical Name:5-Methoxy-N-isopropyltryptamine
CAS No.:109921-55-3
Molecular Formula:C₁₄H₂₀N₂O
Molecular Weight:232.326
Hs Code.:2933990090
UNII:CEP4J0P21U
DSSTox Substance ID:DTXSID00351701
Nikkaji Number:J397.912A
Wikidata:Q72490145
Mol file:109921-55-3.mol

Synonyms:5-methoxy-N-isopropyltryptamine

Suppliers and Price of 5-Methoxy-N-isopropyltryptamine

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
5-Methoxy-N-isopropylTryptamine
50mg
$ 165.00

American Custom Chemicals Corporation
N-ISOPROPYL-5-METHOXYTRYPTAMINE 95.00%
500MG
$ 1963.50

American Custom Chemicals Corporation
N-ISOPROPYL-5-METHOXYTRYPTAMINE 95.00%
50MG
$ 750.75

Total 14 raw suppliers

Chemical Property of 5-Methoxy-N-isopropyltryptamine

Chemical Property:

Vapor Pressure:5.74E-06mmHg at 25°C
Refractive Index:1.559
Boiling Point:391.5 °C at 760 mmHg
Flash Point:190.6 °C
PSA：37.05000
Density:1.068 g/cm³
LogP:3.10790
XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:232.157563266
Heavy Atom Count:17
Complexity:232

Purity/Quality:

99% ^*data from raw suppliers

5-Methoxy-N-isopropylTryptamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NCCC1=CNC2=C1C=C(C=C2)OC
Uses A metabolite of 5-Methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT) (M262470) in human, a psychotomimetic tryptamine derivative.

Technology Process of 5-Methoxy-N-isopropyltryptamine

There total 5 articles about 5-Methoxy-N-isopropyltryptamine 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: 76.0%

: 608-07-1
2-(5-methoxyindol-3-yl)ethylamine

: 67-64-1
acetone

: 109921-55-3
5-Methoxy-N-isopropyltryptamine

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol; at 20 ℃; for 73h;
DOI:10.1016/j.bcp.2006.01.015

Reference yield:

: 92292-22-3
C₁₄H₁₈N₂O

: 109921-55-3
5-Methoxy-N-isopropyltryptamine

Guidance literature:: With sodium tetrahydroborate; In methanol; at 0 ℃;
DOI:10.1016/j.bmcl.2007.05.070

Reference yield:

: 608-07-1
2-(5-methoxyindol-3-yl)ethylamine

: 109921-55-3
5-Methoxy-N-isopropyltryptamine

Guidance literature:: Multi-step reaction with 2 steps

1: methanol / 20 °C

2: NaBH₄ / methanol / 0 °C

With sodium tetrahydroborate; In methanol;
DOI:10.1016/j.bmcl.2007.05.070