5-Methoxy-N,N-diisopropyltryptamine

Base Information

• Chemical Name: 5-Methoxy-N,N-diisopropyltryptamine
• CAS No.: 4021-34-5
• Molecular Formula: C₁₇H₂₆N₂O
• Molecular Weight: 274.406
• Hs Code.: 2933990090
• UNII: 12D06G8W8E
• DSSTox Substance ID: DTXSID00193209
• Nikkaji Number: J1.975.785D
• Wikipedia: 5-Methoxy-N,N-diisopropyltryptamine,Diisopropyltryptamine
• Wikidata: Q2983762
• Metabolomics Workbench ID: 56925
• ChEMBL ID: CHEMBL2140942
• Mol file: 4021-34-5.mol

Synonyms:5-methoxy-N,N-diisopropyltryptamine;5-methoxy-N,N-diisopropyltryptamine monohydrochloride

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of 5-Methoxy-N,N-diisopropyltryptamine

Chemical Property:

• Appearance/Colour: crystalline powder
• Vapor Pressure: 5.65E-07mmHg at 25°C
• Melting Point: 181 °C
• Refractive Index: 1.562
• Boiling Point: 411.3 °C at 760 mmHg
• PKA: 16.93±0.30(Predicted)
• Flash Point: 202.5 °C
• PSA: 28.26000
• Density: 1.032 g/cm³
• LogP: 3.83780
• Storage Temp.: Room temp
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 274.204513457
• Heavy Atom Count: 20
• Complexity: 285

Purity/Quality:

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)N(CCC1=CNC2=C1C=C(C=C2)OC)C(C)C
• Use Description: 5-Methoxy-N,N-diisopropyltryptamine, often abbreviated as 5-MeO-DiPT, is a chemical compound with various applications across different fields. In the field of pharmacology and neuroscience, it is used as a research chemical to study its effects on the central nervous system. Researchers investigate its interactions with neurotransmitter systems and receptor sites to gain insights into brain function and potentially discover new therapeutic applications. In the recreational and psychedelic community, 5-MeO-DiPT is sometimes used as a hallucinogenic substance due to its psychedelic properties, contributing to altered perceptions, sensory experiences, and expanded consciousness. However, its use in this context is often controversial and subject to legal restrictions in many places. Overall, 5-MeO-DiPT plays a pivotal role in advancing scientific understanding of the brain and has recreational applications, but its use is subject to legal and ethical considerations in various jurisdictions.

Technology Process of 5-Methoxy-N,N-diisopropyltryptamine

There total 1 articles about 5-Methoxy-N,N-diisopropyltryptamine 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:

→ 5-Methoxy-N,N-diisopropyltryptamine (4021-34-5)

Guidance literature:

<5-Methoxy-indol-3-yl>-glyoxylsaeure-diisopropylamid, LiAlH4, Tetrahydrofuran;

Reference yield: 44.0%

5-Methoxy-N,N-diisopropyltryptamine (4021-34-5) → 5-Hydroxy-N,N-diisopropyltryptamine (36288-76-3)

Guidance literature:

With boron tribromide; In dichloromethane; at -12 ℃; for 3h;

DOI:10.1016/j.bcp.2006.01.015

Reference yield:

5-Methoxy-N,N-diisopropyltryptamine (4021-34-5) → 6-hydroxy-5-methoxy-N,N-diisopropyltryptamine + 5-Hydroxy-N,N-diisopropyltryptamine (36288-76-3) + 5-Methoxy-N-isopropyltryptamine (109921-55-3)

Guidance literature:

With potassium phosphate buffer; α-D-glucose 6-phosphate; NADPH; rat recombinant cytochrome P₄₅₀ 1A₁; at 37 ℃; for 0.0833333h; Further Variations:; Catalysts; Enzyme kinetics;

DOI:10.1016/j.bcp.2007.09.019

Downstream raw materials:

5-Hydroxy-N,N-diisopropyltryptamine

5-Methoxy-N-isopropyltryptamine