5-Methyl-MDA

Chemical compound From Wikipedia, the free encyclopedia

5-Methyl-MDA, also known as 5-methyl-3,4-methylenedioxyamphetamine, is an entactogen and psychedelic designer drug of the amphetamine class. It is a ring-methylated homologue of MDA and a structural isomer of MDMA.[1]

ATC code
  • None
Legal status
CAS Number
Quick facts Clinical data, Routes ofadministration ...
5-Methyl-MDA
Clinical data
Routes of
administration
Oral
ATC code
  • None
Legal status
Legal status
Identifiers
  • 1-(7-methyl-1,3-benzodioxol-5-yl)propan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC11H15NO2
Molar mass193.246 g·mol−1
3D model (JSmol)
  • O2COc1c2cc(CC(N)C)cc1C
  • InChI=1S/C11H15NO2/c1-7-3-9(4-8(2)12)5-10-11(7)14-6-13-10/h3,5,8H,4,6,12H2,1-2H3 checkY
  • Key:OLENSVFSNAULML-UHFFFAOYSA-N checkY
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Pharmacology

5-Methyl-MDA acts as a selective serotonin releasing agent (SSRA) with IC50 values of 107nM, 11,600nM, and 1,494nM for serotonin, dopamine, and norepinephrine release, respectively.[1]

2-methyl-MDA and 5-methyl-MDA have been used to help guide computer modelling of the serotonin transporter complex.[2]

Society and culture

International

5-Methyl-MDA is not scheduled by the United Nations' Convention on Psychotropic Substances.[3]

Canada

As per the Safe Streets and Communities Act, 5-methyl-MDA, along with all other amphetamines, is a Schedule I controlled substance under the Controlled Drugs and Substances Act.

United States

5-Methyl-MDA is not explicitly scheduled at the federal level in the United States,[4] however 5-Methyl-MDA is a structural isomer of MDMA, and so sales or possession could potentially be prosecuted under the Federal Analogue Act.[5]

See also

References

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