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MDAI

MDAI molecule structureMDAI molecule structure
5,6-Methylenedioxy-2-aminoindane
Sparkle, MindyOpen in Piru
Psychoactive Class
Chemical Class

MDAI is a psychoactive substance in the aminoindane class1 that produces effects similar to MDMA2, described as largely non-stimulating. David E. Nichols and colleagues at Purdue University first described it in the scientific literature in 1989. In animals, MDAI shows substantially less serotonin-related neurotoxicity than MDMA3, but retains a weak capacity to cause neurotoxicity with chronic use or when combined 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
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Pharmacology

Pharmacodynamics

MDAI promotes serotonin and norepinephrine release with a well-balanced action on these two neurotransmitters, while its effect on dopamine release is approximately tenfold weaker.4 It also inhibits the reuptake of all three neurotransmitters.5 MDAI has significant binding affinity for α2-adrenergic receptors, while its affinity for serotonin receptors, including 5-HT2A and 5-HT2B, is very low.4

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
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Tolerance

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

Full Tolerance
Tolerance to many of MDAI's effects develops with prolonged, repeated use, with a pattern described as similar to MDMA. Increasingly larger doses may then be needed to produce the same effects.
Baseline Reset
Tolerance returns to baseline in approximately 1–2 weeks, provided no further MDAI is consumed.
Half Tolerance
Tolerance takes approximately 3–7 days to fall to half its previous level, provided no further MDAI is consumed.
Cross Tolerance

All entactogens, All serotonergic stimulants

Harm Potential

Addiction & Dependence

Psychological

Low

MDAI is somewhat habit-forming but has low abuse potential, with psychological dependence considered unlikely in most users. Cravings may occur after abrupt cessation if addiction has developed.

Physical

Withdrawal effects may occur after abrupt cessation if addiction has developed.

Toxicity

Lethal Dosage

The human lethal dose and exact toxic threshold are unknown; overdose is considered likely to cause serotonin syndrome. One death in the United Kingdom during 2011–2012 appeared to involve MDAI alone and included symptoms consistent with serotonin syndrome.

LD50 Data
SpeciesRouteValue
RatSubcutaneous28 mg/kg
Nervous system

In animals, MDAI produces substantially less serotonergic neurotoxicity than MDMA, but weak serotonergic neurotoxicity has been reported with MDAI alone, including during chronic use.

Thermoregulatory system

Very high doses of MDAI caused fatal disruption of thermoregulation in rats, with 50% mortality after subcutaneous administration of 28 mg/kg.

Cardiovascular system

MDAI increased blood pressure without increasing heart rate.7

Endocrine system

MDAI increased cortisol and prolactin levels.7

Fluid and electrolyte balance

Water intoxication has been reported in MDAI users who drank excessive amounts of water.

History & Culture

David E. Nichols and colleagues at Purdue University first described MDAI in the scientific literature in 1989. MDAI and related compounds were subsequently used widely in scientific research. Interest also developed in its potential medical applications, including drug-assisted psychotherapy and…

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. MDAI (5,6-methylenedioxy-2-aminoindane; 6,7-dihydro-5H-cyclopenta[f][1,3]benzodioxol-6-amine; ‘sparkle’; ‘mindy’) toxicity: a brief overview and update. Human Psychopharmacology (2013). https://doi.org/10.1002/hup.229812
  2. Acute psychotropic, autonomic, and endocrine effects of 5,6-methylenedioxy-2-aminoindane (MDAI) compared with 3,4-methylenedioxymethamphetamine (MDMA) in human volunteers: A self-administration study. Drug Testing and Analysis (2024). https://doi.org/10.1002/dta.36221
  3. Nonneurotoxic tetralin and indan analogues of 3,4-(methylenedioxy)amphetamine (MDA). Journal of Medicinal Chemistry (1990). https://doi.org/10.1021/jm00164a0371
  4. 2-Aminoindan and its Ring-Substituted Derivatives Interact with Plasma Membrane Monoamine Transporters and α2-Adrenergic Receptors. Psychopharmacology (2019). https://doi.org/10.1007/s00213-019-05207-11234
  5. [3H]monoamine releasing and uptake inhibition properties of 3,4-methylenedioxymethamphetamine and p-chloroamphetamine analogues. European Journal of Pharmacology (1991). https://doi.org/10.1016/0014-2999(91)90659-e1
  6. Pharmacological profiles of aminoindanes, piperazines, and pipradrol derivatives. University of Basel (2014). https://doi.org/10.1016/j.bcp.2014.01.0241
  7. Acute psychotropic, autonomic, and endocrine effects of 5,6-methylenedioxy-2-aminoindane (MDAI) compared with 3,4-methylenedioxymethamphetamine (MDMA) in human volunteers: A self-administration study. Drug Testing and Analysis (2024). https://doi.org/10.1002/dta.3622123
  8. 5,6-Methylenedioxy-2-aminoindane: from laboratory curiosity to 'legal high'. Human Psychopharmacology (2012). https://doi.org/10.1002/hup.12551
  9. 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
  10. 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

Further Reading

  1. Oeri (2021): Beyond ecstasy - Alternative entactogens to MDMA
  2. Release UK: MDAI Information
  3. Sainsbury et al. 2011 - Aminoindanes—the next wave of ‘legal highs’?
  4. Johnson et al. 1991 - Serotonin neurotoxicity in rats after combined treatment with a dopaminergic agent followed by a nonneurotoxic 3,4-methylenedioxymethamphetamine (MDMA) analogue

Article Status

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