Bufotenine

Bufotenine Basic information
Product Name:Bufotenine
Synonyms:BUFOTENINE;1H-Indol-5-ol, 3-[2-(dimethylamino)ethyl]-;3-(2-(dimethylamino)ethyl)-indol-5-o;3-(2-dimethylaminoethyl)-5-indolol;3-(beta-dimethylaminoethyl)-5-hydroxyindole;3-[2-(Dimethylamino)ethyl]-1H-indol-5-ol;3-[2-(Dimethylamino)ethyl]-5-indolol;3-[2-(Dimethylamino)ethyl]indol-5-ol
CAS:487-93-4
MF:C12H16N2O
MW:204.27
EINECS:207-667-9
Product Categories:Amines;Aromatics;Heterocycles
Mol File:487-93-4.mol
Bufotenine Structure
Bufotenine Chemical Properties
Melting point 62-64°C
Boiling point bp0.1 320°
density 1.0565 (rough estimate)
refractive index 1.6000 (estimate)
Fp 2℃
storage temp. Refrigerator, Under Inert Atmosphere
solubility Bufotenine is soluble in dilute acids and alkalis.
pka10.11±0.40(Predicted)
EPA Substance Registry System1H-Indol-5-ol, 3-[2-(dimethylamino)ethyl]- (487-93-4)
Safety Information
Hazard Codes F,Xn
Risk Statements 11-20/21/22-36
Safety Statements 16-36/37
RIDADR 1544
WGK Germany 2
HazardClass 6.1(b)
PackingGroup III
DEA Controlled SubstancesCSCN: 7433
CSA SCH: Schedule I
NARC: No

MSDS Information
Bufotenine Usage And Synthesis
Chemical PropertiesBufotenine is an indole alkaloid obtained from the seeds and leaves of Piptadenia peregrine and P. macrocarpa. It has also been isolated from the skin glands of toads (Bufo species). The base is typically seen as white crystalline powder and the oxalate hydrate as a lavender to brown powder. The oxalate hydrate is slightly soluble in chloroform and can be separated from chloroform insoluble material for analysis.
HistoryBufotenin was isolated from toad skin, and named by the Austrian chemist Handovsky at the University of Prague during World War I.The structure of bufotenine was confirmed in 1934 by Heinrich Wieland's laboratory in Munich, and the first reported synthesis of bufotenine was by Toshio Hoshino and Kenya Shimodaira in 1935.
UsesControlled 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.
DefinitionChEBI: Bufotenine is a tertiary amine that consists of N,N-dimethyltryptamine bearing an additional hydroxy substituent at position 5. It has a role as a hallucinogen and a coral metabolite. It is a tryptamine alkaloid and a tertiary amine. It derives from a N,N-dimethyltryptamine.
Bufotenine Preparation Products And Raw materials
Bufotenine 5-METHOXY-N,N-DIETHYLTRYPTAMINE(5-MEO-DET) BUFOTENINE, OXALATE SALT MONOHYDRATE Milipertine Alpertine spegatrine 5-METHOXY DMT OXALATE BUFOTENINE MONOOXALATE*METHANOL SOLUTION Bufotenine, O-methyl- IBOGAINE HYDROCHLORIDE--DEA*SCHEDULE I I TEM oxypertine SARPAGINE 2-[2-(5-METHOXY-1H-INDOL-3-YL)-ETHYL]-ISOINDOLE-1,3-DIONE VOACANGINE 5-BENZYLOXY-[3-(2-DIMETHYLAMINOETHYL)]INDOLE HYDROGENOXALATE Solypertine 3-(5-METHOXY-1H-INDOL-3-YL)-1-[3-(TRIFLUOROMETHYL)PHENYL]DIHYDRO-1H-PYRROLE-2,5-DIONE 5-HTQ IODIDE

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