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N,N-Dimethyl-5-methoxytryptamine

Base Information Edit
  • Chemical Name:N,N-Dimethyl-5-methoxytryptamine
  • CAS No.:1019-45-0
  • Molecular Formula:C13H18N2O
  • Molecular Weight:218.299
  • Hs Code.:29339980
  • European Community (EC) Number:213-813-2
  • NSC Number:88624
  • UNII:X0MKX3GWU9
  • DSSTox Substance ID:DTXSID70144324
  • Nikkaji Number:J21.248B
  • Wikipedia:5-MeO-DMT
  • Wikidata:Q570757
  • NCI Thesaurus Code:C190495
  • Pharos Ligand ID:LDP39GMBMNCQ
  • Metabolomics Workbench ID:37968
  • ChEMBL ID:CHEMBL7257
  • Mol file:1019-45-0.mol
N,N-Dimethyl-5-methoxytryptamine

Synonyms:5 Methoxy N,N Dimethyltryptamine;5-Methoxy-N,N-Dimethyltryptamine;Methoxydimethyltryptamine;Methoxydimethyltryptamines;Methylbufotenin;N,N Dimethyl 5 Methoxytryptamine;N,N-Dimethyl-5-Methoxytryptamine

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

Chemical Property of N,N-Dimethyl-5-methoxytryptamine Edit
Chemical Property:
  • Appearance/Colour:off-white to slightly yellow crystalline powder 
  • Vapor Pressure:1.1E-05mmHg at 25°C 
  • Melting Point:68-71 °C 
  • Refractive Index:1.6450 (estimate) 
  • Boiling Point:370.5 °C at 760 mmHg 
  • PKA:16.94±0.30(Predicted) 
  • Flash Point:177.9 °C 
  • PSA:28.26000 
  • Density:1.097 g/cm3 
  • LogP:2.28060 
  • Storage Temp.:0-6°C 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • Water Solubility.:PRACTICALLY INSOLUBLE 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:218.141913202
  • Heavy Atom Count:16
  • Complexity:220
Purity/Quality:
Safty Information:
  • Pictogram(s): CorrosiveC,HarmfulXn 
  • Hazard Codes:C,Xn 
  • Statements: 20-34-43-21/22 
  • Safety Statements: 22-26-28A-36/37/39-45-36-24/25 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CN(C)CCC1=CNC2=C1C=C(C=C2)OC
  • Recent ClinicalTrials:Single Ascending Dose Study With 5-MeO-DMT in Healthy Subjects
  • Recent EU Clinical Trials:A randomized, double-blind, placebo-controlled, Phase 2b trial with an open-label extension to determine the safety and efficacy of GH001 in patients with treatment-resistant depression
  • Description Obtained from Desmodium pulchellum Benth ex Baker, and also from Phalaris tuberosa L., this indole alkaloid is best crystallized from Et20-light petroleum when it yields colourless rectangular plates. It is optically inactive and the ultraviolet spectrum has absorption maxima at 224, 277 and 296 mil. It forms a crystalline picrate as orange-yellow needles, m.p. 176-7°C and the methiodide, m.p. 181-2°C.
  • Uses Hallucinogen; non-selective serotonin receptor agonist 5-Methoxy-N,N-dimethyltryptamine is a tryptamine derivative and a full potent agonist used in the study of mammalian hormones to stimukate cAMP formation by colliculi neurons and mediate serotoninergic receptors. It is a natural hallucinogen component of Ayahuasca, an Amazonian beverage and is currently being made as a designer drug.
Technology Process of N,N-Dimethyl-5-methoxytryptamine

There total 23 articles about N,N-Dimethyl-5-methoxytryptamine 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:
Guidance literature:
With sodium cyanoborohydride; acetic acid; In methanol; at 0 - 25 ℃; for 2h;
Guidance literature:
With sodium; In tetrahydrofuran; ammonia; at -33 ℃; for 1.5h;
DOI:10.1021/jo0110597