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5-MeO-DIPT

From Wikipedia, the free encyclopedia

5-MeO-DIPT chemical structure
5-MeO-DIPT
Systematic (IUPAC) name
5-methoxy-N,N-diisopropyltryptamine
Identifiers
CAS number 2426-63-3
ATC code  ?
PubChem  ?
Chemical data
Formula C17H26N2O
Mol. weight 274.4
Physical data
Melt. point 181 °C (358 °F)
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

?

Legal status

Schedule I (USA)

Routes  ?
Indicated for:
  • ?

Recreational uses:

  • ?
  • ?

Unethical uses:

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Other uses:

  • ?
Contraindications:
  • ?
Side effects:

Severe:

  • ?

Atypical sensations:

  • ?

Cardiovascular:

  • ?

Ear, nose, and throat:

  • ?

Endocrinal:

  • ?

Eye:

  • ?

Gastrointestinal:

  • Nausea (often severe), primarily during first hour after consumption

Hematological:

  • ?

Musculoskeletal:

  • ?

Neurological:

  • Insomnia (for 6-8 hours after primary effects of drug wear off)

Psychological:

  • Many users report a combination of ecstasy-like "warm/positive" feelings, and psychedelic like "trippy" effects, including aural and visual distortions

Respiratory:

  • ?

Skin:

  • ?

Urogenital and reproductive:

  • Male impotence (while under effect of drug)

Miscellaneous:

  • ?

5-MeO-DiPT is a tryptamine also known as Foxy Methoxy or just foxy due to its supposed aphrodisiac-like effects, although it is primarily used recreationally as a psychedelic. 5-MeO-DiPT is orally active, and dosages between 6–20 mg are commonly reported. Many users note an unpleasant body load accompanies higher dosages. 5-MeO-DiPT is also taken by insufflation, or sometimes it is smoked or injected. Some users also report sound distortion, also noted with the related drug, DIPT.

On April 4, 2003, the United States DEA added both 5-MeO-DiPT and AMT to Schedule I of the Controlled Substances Act under "emergency scheduling" procedures. The drugs were officially placed into Schedule I on September 29, 2004.

Prior to its prohibition, 5-MeO-DIPT was sold on many US websites alongside psychoactive analogues like DIPT, DPT, and 5-MeO-DMT, none of which have yet been expressly outlawed. However, in July 2004, Operation Web Tryp was concluded, confirming that U.S. Federal law enforcement intends to prosecute sale of these analogs of 5-MeO-DIPT. Previous prosecutions under the Federal Analog Act have met on occasion with failure given some court rulings regarding possible unconstitutional vagueness regarding what substances are properly considered 'analogs' and such issues will be addressed on appeal.

5-MeO-DIPT has also been illegal in Germany since September 1999 and in Japan since April 2005.

[edit] See also

[edit] External links


Psychedelic tryptamines edit

4-Acetoxy-DET, 4-Acetoxy-DIPT, α-ET, α-MT, Baeocystin, Bufotenin, DET, DIPT, DMT, DPT, EIPT, Ethocin, Ethocybin, Iprocin, MET, MIPT, 5-MeO-α-ET, 5-MeO-α-MT, 5-MeO-DALT, 5-MeO-DET, 5-MeO-DIPT, 5-MeO-DMT, 5-MeO-DPT, 5-MeO-MIPT, Miprocin, Norbaeocystin, Psilocin, Psilocybin

Tryptamines - edit

4-Acetoxy-DET | 4-Acetoxy-DIPT | 4-Acetylpsilocin | 4-HO-DIPT | 5-MeO-α-ET | 5-MeO-α-MT | 5-MeO-DALT | 5-MeO-DET | 5-MeO-DIPT | 5-MeO-DMT | 5-MeO-DPT | 5-MeO-MIPT | α-ET | α-MT | Baeocystin | Bufotenin | DET | DIPT | DMT | DPT | Ethocybin | EIPT | Ethocin | Ibogaine | Iprocin | MET | MIPT | Miprocin | Melatonin | NMT | Norbaeocystin | Psilocin | Psilocybin | Rizatriptan | Serotonin | Sumatriptan | Tryptamine | Tryptophan

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