MiPT

MiPT

MiPT

Psychoactive Research chemicals are new synthetic substances that are structurally similar to the original drug, while being functional analogs. Research on the effects of, and treatment for, abuse of these drugs is limited due to the fact that they’re fairly new and have avoided mainstream notice. Research chemicals do not have a lot of human consumption data, and thus harm-reduction and special care should be taken if choosing to ingest them.

Psychedelics are drugs which cause profound changes in a one’s perceptions of reality, otherwise known as hallucinations. While under the influence of hallucinogens, users might see images, hear sounds or feel sensations. These chemicals offer some of the most intense psychological experiences and care should be taken when ingesting them.

Experimental drugs have extremely limited human consumption data. There is not enough reliable information about this substance. This is most likely because the substance is is not very old. Information on these substances is limite and incomplete. Please be cautioned. Always practice harm reduction.

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Description

MiPT

Also known as:

  • 1H-Indole-3-ethanamine, N-methyl-N-(1-methylethyl)-[ACD/Index Name]
  • MIPT
  • N-[2-(1H-Indol-3-yl)ethyl]-N-methyl-2-propanamin[German][ACD/IUPAC Name]
  • N-[2-(1H-Indol-3-yl)ethyl]-N-methyl-2-propanamine[ACD/IUPAC Name]
  • N-[2-(1H-Indol-3-yl)éthyl]-N-méthyl-2-propanamine[French][ACD/IUPAC Name]
  • N-[2-(1H-Indol-3-yl)ethyl]-N-methylpropan-2-amine
  • N-Methyl-N-isopropyltryptamine
  • N-Methyl-N-Isopropyltryptamine(MIPT)
  • [2-(1H-INDOL-3-YL)ETHYL](METHYL)(PROPAN-2-YL)AMINE
  • [2-(1H-Indol-3-yl)-ethyl]-isopropyl-methyl-amine
  • METHYLISOPROPYLTRYPTAMINE
  • MFCD09033203[MDL number]
  • N,N-Methylisopropyltryptamine
  • N-Methyl-N-(1-methylethyl)-1H-indole-3-ethanamine

N-Methyl-N-isopropyltryptamine, a tryptamine analogue of DMT, a very uncommon drug with very few reports of human use. Described as ‘more psychedelic than hallucinogenic’ users report only mild visuals with some stimulation and cognitive effects. One of the more stable tryptamines.

Summary

It is structurally related to tryptamines like DMT, DiPT, and MET, although it is reported to produce qualitatively different effects. Its effects are generally described as mild, indistinct, and highly variable between users. In contrast to many related tryptamines, it is able to be taken orally.

MiPT was first synthesized and investigated by Alexander Shulgin and described in his book TiHKAL (“Tryptamines I Have Known and Loved”). In the commentary, Shulgin notes that “there is almost a total lack of visual phenomena. .

. no wave-forms, color distortion or object shape changes, and no eyes-closed imagery, unlike most N,N-disubstituted tryptamines. " Today, MiPT remains relatively uncommon and is either used as a recreational or an entheogenic substance.

It has been distributed online as a research chemical. Very little data exists about the pharmacological properties, metabolism, and toxicity of MiPT in humans, and it has little history of human usage.

History

Chemistry

MiPT

MiPT

Common NameN-Methyl-N-Isopropyltryptamine(MIPT)
Systematic nameN-Methyl-N-Isopropyltryptamine(MIPT)
FormulaC_{14}H_{20}N_{2}
SMILESCC(C)N(C)CCc1c[nH]c2c1cccc2
Std. InChiInChI=1S/C14H20N2/c1-11(2)16(3)9-8-12-10-15-14-7-5-4-6-13(12)14/h4-7,10-11,15H,8-9H2,1-3H3
Std. InChiKeyKTQJVAJLJZIKKD-UHFFFAOYSA-N
Avg. Mass216.322 Da
Molecular Weight216.322
Monoisotopic Mass216.162643 Da
Nominal Mass216
ChemSpider ID21106353

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Dosing Guide

Oral
Light5-10mg
Common10-15mg
Strong15-25mg+
Insufflated
Light5-10mg
Common10-15mg
Strong15-20mg+
Vapourized
Light3-5mg
Common5-15mg
Strong15-20mg+

Duration

Oral
Onset30-45 minutes
Duration2-5 hours
After-effects1-6 hours

Interactions and Synergies

There are no existing interaction or synergy data for this drug.

General Information

Experiences
Oral
Vaporization
Come up
Dosage
EffectsEuphoria, empathy, insight, brightened colour, Closed/Open eye visuals, enhanced tactile sensation, mental/physical stimulation, decreased appetite, pupil dilation, restlessness, change in perception, ego softening, sweating/chills, muscle tension, confusion, insomnia.
After Effects
Avoid
Warning
Risks
Test Kits
Marguis Test Result
Tolerance
Detection
Half-life
Advice
Note
Note 2:
Note 3:

Effects

Pharmacological Effects

Like with most psychedelic tryptamines, MiPT is thought to act principally as a 5-HT2A partial agonist. The psychedelic effects are believed to come from MiPT’s binding efficacy at the 5-HT2A receptors. However, the role of these interactions and how it results in the psychedelic experience continues to remain elusive.

Subjective Effects

The sensory effects of MiPT are said to be similar to those of DiPT but with less intensity at the same dose, and without the same bias towards producing auditory distortions.

Physical Effects

Psychological Effects

The cognitive effects of MiPT are reported to be mild for a psychedelic. Rather than producing distinct perceptual distortions, it is reported instead to act as a mild sensory amplifier.

Visual Effects

Enhancements

Distortions

Auditory Effects

Sensory Effects

Transpersonal Effects

Legal Status

Due to its relative obscurity, the possession and sale of MiPT is unscheduled in most countries.

  • Germany: MiPT is controlled under the NpSG (New Psychoactive Substances Act) as of July 18, 2019. Production and import with the aim to place it on the market, administration to another person and trading is punishable. Possession is illegal but not penalized.
  • United Kingdom: MiPT is a Class A controlled substance in the United Kingdom as a result of the tryptamine catch-all clause.
  • United States: MiPT is unscheduled in the United States. It may be considered an analogue of DMT, which is a Schedule I compound under the Controlled Substances Act. As such, the sale for human consumption or the use for illicit non-medical or industrial intents and purposes could be prosecuted as crimes under the Federal Analogue Act.

  • References

    1. Shulgin, Alexander; Shulgin, Ann (1997). "#47. MIPT". TiHKAL: The Continuation. United States: Transform Press.  0-9630096-9-9. OCLC 38503252.
    2. "Anlage NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz [Federal Ministry of Justice and Consumer Protection]. Retrieved December 10, 2019.
    3. "Verordnung zur Änderung der Anlage des Neue-psychoaktive-Stoffe-Gesetzes und von Anlagen des Betäubungsmittelgesetzes" (PDF). Bundesgesetzblatt Jahrgang 2019 Teil I Nr. 27 (in German). Bundesanzeiger Verlag. July 17, 2019. pp. 1083–1094. Retrieved January 1, 2020.
    4. "§ 4 NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz [Federal Ministry of Justice and Consumer Protection]. Retrieved December 10, 2019.
    5. "Part I: Class A Drugs". "Misuse of Drugs Act 1971". UK Government. Retrieved January 7, 2020.

    Sources

    Information made possible with:

    1. PsychonautWiki is a community-driven online encyclopedia that aims to document the field of psychonautics in a comprehensive, scientifically-grounded manner.
    2. Erowid is a non-profit educational & harm-reduction resource with 60 thousand pages of online information about psychoactive drugs
    3. PubChem National Center for Bio Informatics
    4. Chemspider is a free chemical structure database providing fast access to over 34 million structures, properties and associated information.
    5. Wikipedia

    Additional APIs were used to construct this information. Thanks for ChemSpider, NCBI, PubChem etc.

    Data is constantly updated so please check back later to see if there is any more available information on this substance.