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MDAI
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.
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 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
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.
All entactogens, All serotonergic stimulants
Harm Potential
Addiction & Dependence
Psychological
LowMDAI 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
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
| Species | Route | Value |
|---|---|---|
| Rat | Subcutaneous | 28 mg/kg |
In animals, MDAI produces substantially less serotonergic neurotoxicity than MDMA, but weak serotonergic neurotoxicity has been reported with MDAI alone, including during chronic use.
Very high doses of MDAI caused fatal disruption of thermoregulation in rats, with 50% mortality after subcutaneous administration of 28 mg/kg.
MDAI increased blood pressure without increasing heart rate.7
MDAI increased cortisol and prolactin levels.7
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
References
Source Pages
Citations
Further Reading
Article Status
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