Roidipedia.Compound reference & reporting
05 AUG 2026
CompoundsResearch chemical MDAT
Research chemicalEntactogenSerotonin releaserAminotetralin

MDAT

Also known as 6,7-methylenedioxy-2-aminotetralin · MD-2-AT

MDAT (6,7-methylenedioxy-2-aminotetralin) is a conformationally restricted entactogen from the aminotetralin series, related to MDAI. Designed in academic research as a serotonin-selective, non-neurotoxic releaser, it produces MDMA-like emotional effects with minimal stimulation. Human data are essentially absent.

01 Overview

MDAT was synthesised in structure-activity work exploring rigid analogs of MDMA that release serotonin without the classic neurotoxic signature. Like its cousin MDAI, it is a serotonin-selective releaser expected to give gentle entactogenic effects.

There is little to no human pharmacology or safety data. Even serotonin-selective releasers carry serotonin-syndrome risk, and long-term safety is unknown. Likely covered by analog or psychoactive-substances legislation.

02 Mechanism

Selective serotonin-releasing agent at the serotonin transporter with minimal dopamine activity, based on a rigid aminotetralin scaffold intended to avoid MDMA-type neurotoxicity.

03 Dosing

TierDoseRouteNotes
Light50–100 mgOralEstimated; poorly defined potency
Common100–180 mgOralEstimated, high uncertainty

04 Effects

EffectMagnitudeEvidence
Gentle entactogenesisExpected MDMA-like openness with little stimulation, by analogy to MDAI.Presumed mild-moderateUnconfirmed
Minimal stimulationSerotonin-selective profile implies little energising effect.MinimalUnconfirmed

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
Serotonin syndromeSerotonin-selective releasers can still precipitate serotonin toxicity, especially in combination.Life-threateningRare, elevated with serotonergic drugsUnconfirmed
Unknown long-term safetyNo chronic toxicity data exist for this obscure compound.ModerateUncharacterisedUnconfirmed

07 References

Nichols DE et al. Nonneurotoxic serotonin releasers: aminoindanes and aminotetralinsJournal of Medicinal Chemistry, 1990

08 Discussion0 comments

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