5-MeO-MiPT HCl
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Common names: 5-methoxy MiPT, Foxy Methoxy, Moxy
The synthesis and pharmacology of 5-MeO-MiPT was first reported in 1985 by David Repke and Alexander Shulgin.[1] It is a lesser-known psychedelic substance of the tryptamine class. 5-MeO-MiPT is chemically related to tryptamines like 5-MeO-DMT and 5-MeO-DiPT.
5-MeO-MiPT is a psychedelic chemical that has structural and pharmacodynamic properties similar to the drugs 5-MeO-DiPT, DiPT, and MiPT. It is commonly used as a “substitute” for 5-MeO-DiPT because of the very similar structure and effects.
5-MeO-MiPT is a synthetic indole alkaloid molecule, in a class of compounds commonly known as tryptamines, Tryptamines share a core structure comprised of a bicylic indole heterocycle attached at R3 to an amino group via an ethyl side chain. 5-MeO-MiPT is substituted at R5 of its indole heterocycle with a methoxy (MeO) functional group CH3O−; it also contains a methyl group and an isopropyl chain bound to the terminal amine RN of its tryptamine backbone (MiPT).
5-MeO-MiPT is the N-substituted isopropyl homologue of 5-MeO-DMT.[2]
The full name of the chemical is 5-methoxy-N-methyl-N-isopropyltryptamine.
5-MeO-MiPT causes the ehrlich reagent to turn purple then fade to faint blue. It causes the marquis reagent to go yellow through to black.[1]
Chemical Name: 5-methoxy-N-isopropyl-N-methyltryptamine
Form: HCl
Molecular Formula: C15H22N2O
Molar Mass: 282.80 g/mol
IUPAC: 3-[2-(isopropylmethylamino)ethyl]-5-methoxyindole hydrochloride
CAS Number: 96096-55-8
| QUANTITY | 1000mg, 100mg, 2500mg, 250mg, 500mg |
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