Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a25281efcc6f5c4f

Jump to content

// Workers AI · dad joke modeDoes 3,4-Methylenedioxy-N-methoxyamphetamine have a nickname? Meth-od to its madness.

From Wikipedia, the free encyclopedia
MDMEO
Clinical data
Other names3,4-Methylenedioxy-N-methoxyamphetamine; MDMEO; MDMEOA; MDMeOA; N-Methoxy-MDA
Routes of
administration
Oral[1]
ATC code
  • None
Pharmacokinetic data
Duration of actionUnknown[1]
Identifiers
  • 1-(2H-1,3-benzodioxol-5-yl)-N-methoxypropan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC11H15NO3
Molar mass209.245 g·mol−1
3D model (JSmol)
  • CC(NOC)Cc1ccc2OCOc2c1
  • InChI=1S/C11H15NO3/c1-8(12-13-2)5-9-3-4-10-11(6-9)15-7-14-10/h3-4,6,8,12H,5,7H2,1-2H3 checkY
  • Key:MTIKJUJMCMDSGM-UHFFFAOYSA-N checkY
  (verify)

MDMEO, also known as 3,4-methylenedioxy-N-methoxyamphetamine or as N-methoxy-MDA, is a psychoactive drug of the phenethylamine, amphetamine, and MDxx families.[1][2] It is the N-methoxy derivative of MDA.[1][2]

Use and effects

[edit]

In his book PiHKAL (Phenethylamines I Have Known and Loved, Alexander Shulgin lists MDMEO's dose as greater than 180 mg orally and its duration as unknown.[1][2] It produced few or no effects at tested doses.[1]

Chemistry

[edit]

Properties

[edit]

MDMEO may be found as white crystals.[1]

Synthesis

[edit]

The chemical synthesis of MDMEO has been described.[1]

Society and culture

[edit]
[edit]

United Kingdom

[edit]

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[3]

See also

[edit]

References

[edit]
  1. 1 2 3 4 5 6 7 8 Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
  2. 1 2 3 Shulgin AT (2003). "Basic Pharmacology and Effects". In Laing RR (ed.). Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137. ISBN 978-0-12-433951-4. Archived from the original on 13 July 2025.
  3. "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived from the original on 22 October 2017. Retrieved 12 March 2014.
[edit]