Wikimore

MMDMA
Clinical data
Other names	5-MeO-MDMA;3-methoxy-4,5-methylenedioxy-N-methylamphetamine
Routes of; administration	Oral
ATC code	NoneCategory:Drugs not assigned an ATC code;
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)Category:Drugs with non-standard legal status#S;
Identifiers
	IUPAC name (2-RS)-6-methoxy-7,8-methylenedioxy-propan-2-(N-methylamine);
CAS Number	172518-52-4 ;
PubChem CID	547094;
ChemSpider	476196;
UNII	GR5ZT8ZV9F;
CompTox Dashboard (EPA)	DTXSID701027670 ;
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;

Category:Articles with short description Category:Short description is different from Wikidata Category:Articles with topics of unclear notability from November 2015 Category:All articles with topics of unclear notability Category:Articles with short description Category:Short description is different from Wikidata Category:Articles without EBI source#*Category:Chemical pages without DrugBank identifier#*Category:Articles without KEGG source#*Category:Articles without InChI source#*Category:Articles containing unverified chemical infoboxes#*

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

References

1 2 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.

External links

MMDMA - Isomer Design

Category:Methamphetamines Category:Methylenedioxyphenethylamines Category:Phenol ethers

[BaileyByLegault1976-1] 1 2 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.

[ClarkDeruiterNoggle1996-2] 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]

[2]

Clinical data

Other names	5-MeO-MDMA;3-methoxy-4,5-methylenedioxy-N-methylamphetamine^[1]
Routes of administration	Oral
ATC code	NoneCategory:Drugs not assigned an ATC code
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)Category:Drugs with non-standard legal status#S
Identifiers
IUPAC name (2-RS)-6-methoxy-7,8-methylenedioxy-propan-2-(N-methylamine)
CAS Number	172518-52-4^Y
PubChem CID	547094
ChemSpider	476196
UNII	GR5ZT8ZV9F
CompTox Dashboard (EPA)	DTXSID701027670
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