Skip to main content
Lyrea avatar

Not yet reviewed — this article is pending editorial review by Lyrea.

Citation noticeOur citation system is being overhauled

References and citation markers may currently be incomplete, mismatched, or incorrect. This system is being rebuilt and reviewed before the full site launch.

MDAI

MDAI molecule structureMDAI molecule structure
5,6-Methylenedioxy-2-aminoindane
Sparkle, Mindy
Psychoactive Class
Chemical Class

MDAI is a synthetic aminoindane entactogen with MDMA-like subjective effects that are generally described as less stimulating. It was first reported by David E. Nichols and colleagues at Purdue University in 1989 and developed there during the 1990s. Its indane ring distinguishes it structurally from related amphetamines and substantially alters its properties. Animal findings indicate greatly reduced serotonergic neurotoxicity relative to MDMA, although weak neurotoxicity may occur with chronic use or combination with amphetamine.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold20-40 mg
Light40-100 mg
Moderate100-150 mg
Strong175-300 mg
Heavy150-300 mg

Duration

Onset20-40 minutes
Come Up30-60 minutes
Peak2-2.5 hours
Offset1-2 hours
Total4-6 hours

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

Effects vary widely by individual, dose, and context.

Physical

Physical euphoriaEnhancement of touch

Cognitive

The general head space of MDAI is described by many as one of euphoria and feelings of love or empathy. It contains a number of typical entactogenic cognitive effects.

Acceleration of thoughtMindfulness

Visual

Forked from Subjective Effect Documentation byJosie Kins August 2014.

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Marquis(MQ)
white → orange2 → orange3 → brown2
Mecke(ME)
white → brown3 → brown2
Mandelin(MD)
yellow2 → brown3
Liebermann(LB)
white → green3 → brown3
Powered by PROtestkit.eu

Pharmacology

Pharmacodynamics

MDAI acts primarily as a well-balanced serotonin and norepinephrine releasing agent, while its effect on dopamine release is approximately 10-fold lower. It also inhibits the reuptake of serotonin, norepinephrine, and dopamine, further increasing extracellular monoamine concentrations. MDAI has no appreciable affinity for serotonin receptors at tested concentrations, including 5-HT2A and 5-HT2B, but shows significant affinity for α2-adrenergic receptors.

Pharmacokinetics

Absorption & half-lifenot documented yetMetabolitesnone documented yet

Interactions

Dangerous

Highest risk

These combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.

5-HTPAlcoholCocaineDXMDissociativesMAOIsMDMAMXENBOMe compoundsSNRIsSSRIsSerotonin releasersStimulantsTramadol
Powered by TripSit

Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
Tolerance to many effects may develop with prolonged, repeated use, reportedly in a manner similar to MDMA, and may require increasingly large doses to produce the same effects.
Baseline Reset
In the absence of further consumption, tolerance is reported to return to baseline after approximately 1–2 weeks.
Half Tolerance
In the absence of further consumption, tolerance is reported to decrease by half after approximately 3–7 days.
Cross Tolerance

Entactogens, Serotonergic stimulants

Harm Potential

Addiction & Dependence

Psychological

Low

MDAI is considered somewhat habit-forming, with low abuse potential and psychological dependence unlikely among most users.

Physical

If addiction develops, abrupt discontinuation may cause cravings and withdrawal effects.

Toxicity

Lethal Dosage

The lethal dose and exact toxic dosage in humans are unknown. One reported UK death appeared attributable to MDAI alone and involved symptoms consistent with serotonin syndrome; overdose is expected to risk serotonin syndrome.

LD50 Data
SpeciesRouteValue
ratsubcutaneous28 mg/kg
Nervous system

In animals, MDAI has substantially lower serotonergic neurotoxicity than MDMA but retains a weak capacity for serotonergic neurotoxicity during chronic use.

Cardiovascular and endocrine systems

MDAI increased blood pressure, cortisol, and prolactin, while no increase in heart rate or body temperature was observed.

Thermoregulatory system

Very high subcutaneous doses were fatal in rats, with 50% mortality at 28 mg/kg.

History & Culture

Scientific origins

David E. Nichols and colleagues at Purdue University first described MDAI in the scientific literature in 1989. A team led by Nichols continued its development during the 1990s.

Legality

International

MDAI is not listed in the official current schedules under the 1961 or 1971 drug conventions or in the precursor tables to the 1988 Convention.

By Country

Illegal17
Brazil flagBrazilIllegal
Canada flagCanadaIllegal (analog/blanket ban)
Chile flagChileIllegal
China flagChinaIllegal
Czech Republic flagCzech RepublicIllegal
Denmark flagDenmarkIllegal
Germany flagGermanyIllegal
Ireland flagIrelandIllegal
Israel flagIsraelIllegal (analog/blanket ban)
Italy flagItalyIllegal
Netherlands flagNetherlandsIllegal (analog/blanket ban)
Poland flagPolandIllegal (analog/blanket ban)
Russia flagRussiaIllegal
Singapore flagSingaporeIllegal
Sweden flagSwedenIllegal
Switzerland flagSwitzerlandIllegal
Ukraine flagUkraineIllegal
Controlled / restricted5
Austria flagAustriaRestricted
Finland flagFinlandRestricted
Japan flagJapanRestricted
Portugal flagPortugalRestricted
United Kingdom flagUnited KingdomRestricted
Not scheduled2
United States flagUnited StatesNot scheduled
Norway flagNorwayNot scheduled

References

Source Pages

  1. Bluelight: The Big & Dandy MDAI Thread
  2. Disregard Everything I Say
  3. Drug Users Bible by Dominic Milton Trott
  4. Erowid
  5. Isomer Design (TiHKAL/PiHKAL)
  6. PsychonautWiki
  7. TripSit Factsheets
  8. Wikipedia

Citations

  1. Neue-Psychoaktive-Substanzen-Gesetz (NPSG) and Neue-Psychoaktive-Substanzen-Verordnung (NPSV). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/GeltendeFassung.wxe?Abfrage=Bundesnormen&Gesetzesnummer=200076421
  2. Neue-Psychoaktive-Substanzen-Gesetz (NPSG) and Neue-Psychoaktive-Substanzen-Verordnung (NPSV). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/eli/bgbl/ii/2011/468/ANL2/NOR402614411
  3. Neue-Psychoaktive-Substanzen-Gesetz (NPSG) and Neue-Psychoaktive-Substanzen-Verordnung (NPSV). ris.bka.gv.at (n.d.). https://www.ris.bka.gv.at/GeltendeFassung.wxe?Abfrage=Bundesnormen&Gesetzesnummer=200076051
  4. Portaria SVS/MS nº 344/1998, Anexo I (as updated by ANVISA). gov.br (n.d.). https://www.gov.br/anvisa/pt-br/assuntos/medicamentos/controlados/lista-substancias1
  5. Controlled Drugs and Substances Act. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/C-38.8/FullText.html1
  6. Decreto Supremo N.º 405 de 1983 del Ministerio de Salud, Reglamento de Productos Psicotrópicos, modificado por Decreto N.º 43 de 2022. diariooficial.interior.gob.cl (n.d.). https://www.diariooficial.interior.gob.cl/publicaciones/2022/01/06/43145/01/2067684.pdf1
  7. Decreto Supremo N.º 405 de 1983 del Ministerio de Salud, Reglamento de Productos Psicotrópicos, modificado por Decreto N.º 43 de 2022. bcn.cl (n.d.). https://www.bcn.cl/leychile/navegar?idNorma=1171005&idParte=10299514&idVersion=2022-01-061
  8. Decreto Supremo N.º 405 de 1983 del Ministerio de Salud, Reglamento de Productos Psicotrópicos, modificado por Decreto N.º 43 de 2022. bcn.cl (n.d.). https://www.bcn.cl/leychile/Navegar?idNorma=13066&idParte=9585433&idVersion=2022-04-011
  9. Catalogue of Non-medical Narcotic Drugs and Psychotropic Substances. ga.sz.gov.cn (n.d.). https://ga.sz.gov.cn/SZJDZX/SZBMFW/content/post_12898420.html1
  10. Government Regulation No. 463/2013 Coll., on lists of addictive substances, read with Act No. 167/1998 Coll., on addictive substances. e-sbirka.cz (n.d.). https://www.e-sbirka.cz/sb/2013/4631

Further Reading

  1. Angerer et al. (2024): Acute psychotropic, autonomic, and endocrine effects of MDAI compared with MDMA
  2. Corkery et al. (2013): MDAI toxicity - a brief overview and update
  3. Oeri (2021): Beyond ecstasy - Alternative entactogens to MDMA
  4. Release UK: MDAI Information

Article Status

  • Josie Kins avatar
    Step 1 · Automated synthesis

    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

  • Step 2 · First-pass reviewPending

    Not yet reviewed — this article is pending editorial review by Lyrea.

  • Step 3 · Citation reviewPending

    No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.

Recent changes7 human edits · latest

Times are UTCNewest first

24 January 2026

  1. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  2. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  3. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  4. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  5. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  6. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  7. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

All changes to this article · Site-wide recent changes

Suggest an edit

Spotted a mistake, an outdated claim, or something missing from the MDAI article? Send the editors a private note. Feedback lands in a moderation queue and is never shown on the site.

Wish to give generalised feedback? You can do so here.