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MDAI
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.
Duration
Subjective Effects
Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.
Effects vary widely by individual, dose, and context.
Physical
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.
Visual
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
Dangerous
Highest riskThese 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.
Tolerance
Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.
Entactogens, Serotonergic stimulants
Harm Potential
Addiction & Dependence
Psychological
LowMDAI 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
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
| Species | Route | Value |
|---|---|---|
| rat | subcutaneous | 28 mg/kg |
In animals, MDAI has substantially lower serotonergic neurotoxicity than MDMA but retains a weak capacity for serotonergic neurotoxicity during chronic use.
MDAI increased blood pressure, cortisol, and prolactin, while no increase in heart rate or body temperature was observed.
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
References
Source Pages
Citations
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
Article Status
Step 1 · Automated synthesisAn autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.
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Recent changes7 human edits · latest
Times are UTCNewest first
24 January 2026
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more
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