5,N-Dimethyl-N-isopropyltryptamine

5,N-Dimethyl-N-isopropyltryptamine (also known as 5-MeO-DiPT or Foxy Methoxy) is a psychedelic and hallucinogenic drug. It is part of the tryptamine family, a group of compounds naturally found in a variety of plant species and the brains of mammals.

Chemistry[edit | edit source]

5-MeO-DiPT is a synthetic compound of the tryptamine class. 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-DiPT 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 (DiPT).

Pharmacology[edit | edit source]

The pharmacology of 5-MeO-DiPT is not fully understood. It is thought to act as a serotonin agonist, meaning it binds to and activates serotonin receptors in the brain. This action on the serotonin system is believed to be responsible for its psychedelic effects.

Effects[edit | edit source]

The effects of 5-MeO-DiPT are often compared to those of other psychedelic tryptamines such as DMT, psilocybin, and LSD. Users report intense visual hallucinations, altered perception of time, and heightened sensory experiences. However, the drug also has a unique profile of physical effects, including tactile enhancement, spontaneous bodily sensations, and physical euphoria.

Legality[edit | edit source]

5-MeO-DiPT is illegal in many countries, including the United States, where it is classified as a Schedule I drug under the Controlled Substances Act. It is also controlled in the United Kingdom under the Misuse of Drugs Act.

Health Risks[edit | edit source]

Like other psychedelic drugs, 5-MeO-DiPT can cause a range of adverse psychological effects, including anxiety, paranoia, and psychosis. There have also been reports of physical health risks, including heart palpitations, increased blood pressure, and nausea.