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MMDMA
Clinical data
Other names	5-MeO-MDMA;3-methoxy-4,5-methylenedioxy-N-methylamphetamine
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
	IUPAC name (2-RS)-6-methoxy-7,8-methylenedioxy-propan-2-(N-methylamine);
CAS Number	172518-52-4 ;
ChemSpider	476196;
UNII	GR5ZT8ZV9F;
Chemical and physical data
Formula	C12H17NO3
Molar mass	223.272 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES COC1=CC(CC(C)NC)=CC2=C1OCO2;

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

References

^ 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.
^ 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.

[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] 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.

[1]

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