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{{SubstanceBox/MDAI}}
{{SubstanceBox/MDAI}}
'''MDAI''' ('''5,6-Methylenedioxy-2-aminoindane''') is a drug developed in the 1990s by a team led by [[David E. Nichols]] at Purdue University. It acts as a non-neurotoxic and highly selective [[serotonin]] [[releasing agent]] (SSRA) in vitro and produces [[entactogen]] effects in humans similar to that of [[MDMA]].
'''MDAI''' ('''5,6-Methylenedioxy-2-aminoindane''') is a drug developed in the 1990s by a team led by [[David E. Nichols]] at Purdue University. It acts as a non-neurotoxic and highly selective [[serotonin]] [[releasing agent]] (SSRA) in vitro and produces [[entactogen]] effects in humans similar to that of [[MDMA]].



Revision as of 21:38, 29 July 2014

This article is a stub.

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MDAI
Chemical Nomenclature
Common names MDAI
Substitutive name 5,6-Methylenedioxy-2-aminoindane
Systematic name 6,7-Dihydro-5H-cyclopenta[f][1,3]benzodioxol-6-amine
Class Membership
Psychoactive class Entactogen
Chemical class Aminoindane / MDxx
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold 40 mg
Light 40 - 100 mg
Common 100 - 175 mg
Strong 175 - 300 mg
Heavy 300 mg +
Duration
Total 4 - 6 hours
Onset 20 - 40 minutes
Come up 30 - 60 minutes
Peak 2 - 2.5 hours
Offset 1 - 2 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions
MAOIs
Serotonin releasers
SSRIs
5-HTP


MDAI (5,6-Methylenedioxy-2-aminoindane) is a drug developed in the 1990s by a team led by David E. Nichols at Purdue University. It acts as a non-neurotoxic and highly selective serotonin releasing agent (SSRA) in vitro and produces entactogen effects in humans similar to that of MDMA.

Chemistry

The chemical structure of MDAI is indirectly derived from that of the illicit drug MDA, but the alpha-methyl group of the alkylamino amphetamine side chain has been bound back to the benzene nucleus to form an indane ring system, which changes its pharmacological properties substantially.[1]

Pharmacology

The chemical structure of MDAI is indirectly derived from that of the illicit drug MDA, but the alpha-methyl group of the alkyl]]amino amphetamine side chain has been bound back to the benzene nucleus to form an indane ring system, which changes its pharmacological properties substantially.[1]

Subjective effects

Toxicity and Harm Potential

Lethal dosage

Tolerance and addition potential

See Also

References

  1. Monte AP, Marona-Lewicka D, Cozzi NV, Nichols DE. Synthesis and pharmacological examination of benzofuran, indan, and tetralin analogues of 3,4-(methylenedioxy)amphetamine. Journal of Medicinal Chemistry. 1993 Nov 12;36(23):3700-6. Template:DOI PMID 8246240