N,N-Dipropyltryptamine

Base Information

• Chemical Name: N,N-Dipropyltryptamine
• CAS No.: 61-52-9
• Molecular Formula: C16H24N2
• Molecular Weight: 244.38
• Hs Code.: 2933990090
• UNII: S7272VWU50
• DSSTox Substance ID: DTXSID30209847
• Nikkaji Number: J53.646F
• Wikipedia: Dipropyltryptamine
• Wikidata: Q2723010
• ChEMBL ID: CHEMBL1779153
• Mol file: 61-52-9.mol

Synonyms:dipropyltryptamine;dipropyltryptamine hydrochloride

Chemical Property of N,N-Dipropyltryptamine

Chemical Property:

• Vapor Pressure: 3.3E-06mmHg at 25°C
• Melting Point: 174-178 °C
• Refractive Index: 1.574
• Boiling Point: 387.4 °C at 760 mmHg
• PKA: 17.30±0.30(Predicted)
• Flash Point: 188.1 °C
• PSA: 19.03000
• Density: 1.014 g/cm³
• LogP: 3.83240
• XLogP3: 4.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 244.193948774
• Heavy Atom Count: 18
• Complexity: 223

Purity/Quality:

98%,99%, ^*data from raw suppliers

DPT ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCN(CCC)CCC1=CNC2=CC=CC=C21
• Uses: N,N-Dipropyl-1H-indole-3-ethanamine is a tryptamine designer drug used in toxicology studies which was one of the findings in an analysis of street drugs in seized material without primary reference standards.

Technology Process of N,N-Dipropyltryptamine

There total 5 articles about N,N-Dipropyltryptamine 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: 94.0%

tryptamine (61-54-1) + propionaldehyde (123-38-6) → Dipropyltryptamine (61-52-9)

Guidance literature:

With sodium cyanoborohydride; acetic acid; In methanol; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1016/j.bmc.2011.04.004

Reference yield: 46.0%

tryptamine (61-54-1) + 1-iodo-propane (107-08-4) + N-ethyl-N,N-diisopropylamine (7087-68-5) → Dipropyltryptamine (61-52-9)

Guidance literature:

In diethyl ether; at 20 ℃; for 16h;

DOI:10.1159/000085649

Reference yield:

→ Dipropyltryptamine (61-52-9)

Guidance literature:

With tetrahydrofuran; lithium aluminium tetrahydride;

upstream raw materials:

3-(2-bromoethyl)-1H-indole

di-n-propylamine

tryptamine

1-iodo-propane

Refernces

• 1、 -. "Benzocarbazoles heterocyclic compound and its preparation and use (by machine translation)". Paragraph 0106; 0108. . Retrieved 2016/10/07.