Anodyne

4-HO-DMT
Psilocin
Esters
[]
Psilocin benzoate
Psilocin benzoate
Molecular structure via molpic based on CDK
Physical properties
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204.27 g/mol [1]
Melting point174.5 °C [1]
2.1 [1]
Structural Identifiers
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C12H16N2[1]
3-[2-(dimethylamino)ethyl]-1H-indol-4-ol [1]
CN(C)CCC1=CNC2=C1C(=CC=C2)O [1]
InChI=1S/C12H16N2O/c1-14(2)7-6-9-8-13-10-4-3-5-11(15)12(9)10/h3-5,8,13,15H,6-7H2,1-2H3 [1]
InChIKeySPCIYGNTAMCTRO-UHFFFAOYSA-N [1]
Dosing
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Elimination half-lifeOral psilocybin: 2.3–3 hours (as psilocin) Intravenous injection psilocybin: 1.2 hours (as psilocin)

Psilocin

Psilocin (also known as Psilocine, Psilotsin, 4-Hydroxy-N,N-dimethyltryptamine, Psilocyn, 3-[2-(Dimethylamino)ethyl]-1H-indol-4-ol, 3-(2-(Dimethylamino)ethyl)indol-4-ol, N,N-Dimethyl-4-Hydroxytryptamine, CX-59, 3-(2-(Dimethylamino)ethyl)-1H-indol-4-ol or 4-OH-DMT) is a substance of the tryptamine class.

Chemistry

Esters []

Psilocin is typically found in the form of its ester.

 []

Psilocin is a achiral mixture

Legal status []

  • Australia: Psilocin is a S9 substance.
  • Brazil: Psilocin is a F2 substance.
  • Canada: Psilocin is a Schedule III substance.
  • United Kingdom: Psilocin is a Class A substance.
  • United States: Psilocin is a Schedule I substance.
  • New Zealand: Psilocin is a Class A substance.
  • Germany: Psilocin is a Anlage I substance.
  • United Nations: Psilocin is a Schedule I drug under the "Convention on Psychotropic Substances 1971".