Methylenedioxymethoxyethylamphetamine

MDMEOET
Clinical data
Other names	3,4-Methylenedioxy-N-methoxyethylamphetamine; MDMEOET; MDMEOETA; N-Methoxyethyl-MDA
Routes of; administration	Oral
ATC code	None;
Pharmacokinetic data
Duration of action	Unknown
Identifiers
	IUPAC name 1-(2H-1,3-benzodioxol-5-yl)-N-(2-methoxyethyl)propan-2-amine;
CAS Number	74698-44-5 ;
PubChem CID	44719584;
ChemSpider	21106334 ;
UNII	YPA4B5U3U8;
CompTox Dashboard (EPA)	DTXSID401348154 DTXSID10660371, DTXSID401348154 ;
Chemical and physical data
Formula	C13H19NO3
Molar mass	237.299 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC(Cc1ccc2c(c1)OCO2)NCCOC;
	InChI InChI=1S/C13H19NO3/c1-10(14-5-6-15-2)7-11-3-4-12-13(8-11)17-9-16-12/h3-4,8,10,14H,5-7,9H2,1-2H3 ; Key:LOZJEWOZOKSOKA-UHFFFAOYSA-N ;
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MDMEOET, also known as 3,4-methylenedioxy-N-methoxyethylamphetamine or as N-methoxyethyl-MDA, is a psychoactive drug of the phenethylamine, amphetamine, and MDxx families.^[1] It is the N-methoxyethyl derivative of MDA.^[1]

Use and effects

In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists MDMEOET's dose as greater than 180 mg orally and its duration as unknown.^[1] It prdouced few or no effects at tested doses.^[1]

Chemistry

Synthesis

The chemical synthesis of MDMEOET has been described.^[1]

Society and culture

Legal status

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.^[2]

References

^ ^a ^b ^c ^d ^e ^f ^g Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived from the original on 22 October 2017. Retrieved 12 March 2014.

External links

[PiHKAL-1] ^ ^a ^b ^c ^d ^e ^f ^g Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.

[2] "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived from the original on 22 October 2017. Retrieved 12 March 2014.

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