MMDMA

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MMDMA
Clinical data
Other names5-Methoxy-MDMA; 5-MeO-MDMA; 5-Methoxy-3,4-methylenedioxy-N-methylamphetamine; 3-Methoxy-4,5-methylenedioxy-N-methylamphetamine;[1]
Routes of
administration		Oral
ATC code
  • None
Legal status
Legal status
  • UK: Class A
  • US: Unscheduled(but possession or sale may be illegal under the Federal Analogue Act in the U.S., and under similar bills in other countries)
Identifiers
  • 1-(7-methoxy-1,3-benzodioxol-5-yl)-N-methylpropan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC12H17NO3
Molar mass223.272 g·mol−1
3D model (JSmol)
  • COC1=CC(CC(C)NC)=CC2=C1OCO2
  • InChI=1S/C12H17NO3/c1-8(13-2)4-9-5-10(14-3)12-11(6-9)15-7-16-12/h5-6,8,13H,4,7H2,1-3H3
  • Key:XEULPLUJSUSGMX-UHFFFAOYSA-N

5-Methoxy-3,4-methylenedioxymethamphetamine (MMDMA; 5-MeO-MDMA) is a designer drug of the substituted methylenedioxyphenethylamine (MDxx) class.[2][1][3] Little is known about its effects and it has not been formally studied in animals.

See also

References

  1. Bailey K, By A, Legault D, Verner D (1976). "Identification of the N-Methylated Analogs of the Hallucinogenic Amphetamines and Some Isomers". Journal of the Association of Official Analytical Chemists. 58 (1): 62–69. Archived from the original on 2022-03-30. Retrieved 2024-05-27.
  2. Shulgin A, Manning T, Daley P (2011). The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley: Transform Press. ISBN 978-0-9630096-3-0.
  3. Clark CR, Deruiter J, Noggle FT (1996). "Analysis of 1-(3-methoxy-4,5-methylenedioxyphenyl)-2-propanamine (MMDA) derivatives synthesized from nutmeg oil and 3-methoxy-4,5-methylenedioxybenzaldehyde". Journal of Chromatographic Science. 34 (1): 34–42. doi:10.1093/chromsci/34.1.34.