5-MeO-DMT Freebase
Common names: The God Molecule, Toad, Jaguar
The synthesis of 5-MeO-DMT was documented by Alexander Shulgin, in his 1997 book TiHKAL (“Tryptamines I Have Known and Loved”). It is a naturally-occurring psychedelic substance of the tryptamine class. It is structurally related to DMT and 5-HO-DMT (bufotenine)
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This research chemical is for educational, scientific, in-vitro laboratory research only. Not for human consumption or veterinarian use.
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Description
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Chemical Name: 5-methoxy-N,N-dimethyltryptamine
Form: Freebase
Molecular Formula: C13H18N2O
Molar Mass: 218.300 g/mol
IUPAC: 2-(5-Methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
CAS Number: 1019-45-0
5-MeO-DMT is a ring-substituted indole alkaloid molecule of the tryptamine class. Tryptamines share a core structure comprised of a bicylic indole heterocycle attached at R3 to a terminal amine group via an ethyl side chain. 5-MeO-DMT is substituted at R5 of its indole heterocycle with a methoxy (MeO) functional group CH3O−; it also contains two methyl groups CH3– bound to the terminal amine RN of its tryptamine backbone (DMT).
5-MeO-DMT is the N-substituted methyl homologue of 5-MeO-MiPT and 5-MeO-DiPT, although it radically differs in its effects.[2]
5-methoxy-N,N-dimethyltryptamine is an especially potent natural psychedelic that can be found in a variety of plant species and the Sonoran Desert Toad’s poisonous secretions. Real, also known as the River Toad of Colorado. It can also synthetically be produced in a laboratory, hence the 5-Methoxy-N, N-Dimethyltryptamine abbreviation. This research chemical stands out as one of the most effective currently available psychedelic drugs.
This has been provided for educational purposes only. Chemiverse will only sell 5-MeO-DMT Freebase for educational, scientific, in-vitro laboratory research. NOT for human consumption or veterinarian use!
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