Bufotenine

Modify Date: 2024-01-01 19:24:35

Bufotenine Structure
Bufotenine structure
Common Name Bufotenine
CAS Number 487-93-4 Molecular Weight 204.26800
Density 1.178g/cm3 Boiling Point 392.8ºC at 760 mmHg
Molecular Formula C12H16N2O Melting Point 62-64ºC
MSDS N/A Flash Point 191.3ºC
Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Danger

 Names

Name bufotenin
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.178g/cm3
Boiling Point 392.8ºC at 760 mmHg
Melting Point 62-64ºC
Molecular Formula C12H16N2O
Molecular Weight 204.26800
Flash Point 191.3ºC
Exact Mass 204.12600
PSA 39.26000
LogP 1.97760
Vapour Pressure 9.89E-07mmHg at 25°C
Index of Refraction 1.646
Storage condition Refrigerator, Under Inert Atmosphere

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NM2800000
CHEMICAL NAME :
Indol-5-ol, 3-(2-(dimethylamino)ethyl)-
CAS REGISTRY NUMBER :
487-93-4
BEILSTEIN REFERENCE NO. :
0160628
LAST UPDATED :
199612
DATA ITEMS CITED :
4
MOLECULAR FORMULA :
C12-H16-N2-O
MOLECULAR WEIGHT :
204.30
WISWESSER LINE NOTATION :
T56 BMJ D2N1&1 GQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Human
DOSE/DURATION :
57 ug/kg
TOXIC EFFECTS :
Peripheral Nerve and Sensation - sensory change involving peripheral nerve Lungs, Thorax, or Respiration - other changes Gastrointestinal - other changes
REFERENCE :
SCIEAS Science. (American Assoc. for the Advancement of Science, 1333 H St., NW, Washington, DC 20005) V.1- 1895- Volume(issue)/page/year: 123,886,1956
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
290 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PSYPAG Psychopharmacologia (Berlin). (Berlin, Ger.) V.1-46, 1959-76. For publisher information, see PSCHDL. Volume(issue)/page/year: 16,385,1970
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
25 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
NYKZAU Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. (Nippon Yakuri Gakkai, c/o Kyoto Daigaku Igakubu Yakurigaku Kyoshitsu, Konoe-cho, Yoshida, Sakyo-ku, Kyoto 606, Japan) V.40- 1944- Volume(issue)/page/year: 64,144,1968
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Parenteral
SPECIES OBSERVED :
Amphibian - frog
DOSE/DURATION :
2500 mg/kg
TOXIC EFFECTS :
Cardiac - other changes
REFERENCE :
AEXPBL Archiv fuer Experimentelle Pathologie und Pharmakologie. (Leipzig, Ger. Dem. Rep.) V.1-109, 1873-1925. For publisher information, see NSAPCC. Volume(issue)/page/year: 86,138,1920

 Safety Information

Symbol GHS02 GHS07
GHS02, GHS07
Signal Word Danger
Hazard Statements H225-H302 + H312 + H332-H319
Precautionary Statements P210-P280-P305 + P351 + P338
Hazard Codes F,Xn
Risk Phrases 11-20/21/22-36
Safety Phrases 16-36/37
RIDADR UN 1544
Packaging Group III
Hazard Class 6.1(b)
HS Code 2933990090

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles25

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Psychedelic 5-methoxy-N,N-dimethyltryptamine: metabolism, pharmacokinetics, drug interactions, and pharmacological actions.

Curr. Drug Metab. 11(8) , 659-66, (2010)

5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT) belongs to a group of naturally-occurring psychoactive indolealkylamine drugs. It acts as a nonselective serotonin (5-HT) agonist and causes many physiolog...

Isolation of N,N-dimethyl and N-methylserotonin 5-O-β-glucosides from immature Zanthoxylum piperitum seeds.

Biosci. Biotechnol. Biochem. 74(9) , 1951-2, (2010)

Two serotonin derivatives, N,N-dimethylserotonin 5-O-β-glucoside (1a) and N-methylserotonin 5-O-β-glucoside (1b) were isolated from immature seeds of Zanthoxylum piperitum. Their structures were deter...

A critical review of reports of endogenous psychedelic N, N-dimethyltryptamines in humans: 1955-2010.

Drug Test. Anal. 4(7-8) , 617-35, (2012)

Three indole alkaloids that possess differing degrees of psychotropic/psychedelic activity have been reported as endogenous substances in humans; N,N-dimethyltryptamine (DMT), 5-hydroxy-DMT (bufotenin...

 Synonyms

Bufotenin
Cohoba
Mapine
Mappine
Mappin
Bufotenine
N,N-Dimethylserotonin
EINECS 207-667-9
3-[2-(dimethylamino)ethyl]-1H-indol-5-ol
Dimethylserotonin
5-hydroxy-N,N-dimethyltryptamine
N,N-Dimethyl-5-hydroxytryptamine