Bufotenine

Base Information Edit

Chemical Name:Bufotenine
CAS No.:487-93-4
Molecular Formula:C12H16 N2 O
Molecular Weight:204.272
Hs Code.:2933990090
European Community (EC) Number:207-667-9
NSC Number:89593
UNII:0A31347TZK
DSSTox Substance ID:DTXSID0048894
Nikkaji Number:J6.027E
Wikipedia:Bufotenin
Wikidata:Q408915
Pharos Ligand ID:R6CHYBZ99QM2
Metabolomics Workbench ID:49574
ChEMBL ID:CHEMBL416526
Mol file:487-93-4.mol

Synonyms:5 Hydroxy N,N dimethyltryptamine;5-Hydroxy-N,N-dimethyltryptamine;Bufotenin;Bufotenine;Dimethylserotonin;Mappin;Mappine;N,N Dimethyl 5 hydroxytryptamine;N,N-Dimethyl-5-hydroxytryptamine

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

Chemical Property of Bufotenine Edit

Chemical Property:

Vapor Pressure:9.89E-07mmHg at 25°C
Melting Point:62-64oC
Refractive Index:1.6000 (estimate)
Boiling Point:392.8°C at 760 mmHg
PKA:10.11±0.40(Predicted)
Flash Point:191.3°C
PSA：39.26000
Density:1.178g/cm³
LogP:1.97760
Storage Temp.:Refrigerator, Under Inert Atmosphere
Solubility.:Bufotenine is soluble in dilute acids and alkalis.
XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:204.126263138
Heavy Atom Count:15
Complexity:208

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:F,Xn
Statements: 11-20/21/22-36
Safety Statements: 16-36/37

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)CCC1=CNC2=C1C=C(C=C2)O
Uses Controlled substance (hallucinogen).Bufotenine is a hallucinogenic serotonin analog found in frog and toad skins, mushrooms, plants and some mammals (especially in the brains, plasma, and urine of schizophrenics). It is a potent hallucinogen used in its natural state by several shaman sects and in some drug abuse situations in the United States and Australia. It causes schizophrenia and other psychotic symptoms.

Technology Process of Bufotenine

There total 38 articles about Bufotenine 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: 100.0%

: 25390-67-4
5-Benzyloxy DMT

: 487-93-4
bufotenin

Guidance literature:: With palladium 10% on activated carbon; ammonium formate; In methanol; at 70 ℃; for 0.75h; Inert atmosphere;
DOI:10.1016/j.tet.2016.03.007

Reference yield: 85.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 153-98-0,21591-86-6
serotonin hydrochloride

: 487-93-4
bufotenin

Guidance literature:: With sodium methylate; sodium cyanoborohydride; acetic acid; In methanol; water; at 20 ℃; for 2h; pH=5 - 9; Inert atmosphere;