This article relies largely or entirely on a single source. Relevant discussion may be found on the talk page. Please help improve this articlebyintroducing citations to additional sources.
Find sources: "MEE" psychedelic – news · newspapers · books · scholar · JSTOR (June 2019) |
Names | |
---|---|
Preferred IUPAC name
1-(4,5-Diethoxy-2-methoxyphenyl)propan-2-amine | |
Other names
2-Methoxy-4,5-diethoxyphenethylamine | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider |
|
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C14H23NO3 | |
Molar mass | 253.342 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
MEE (2-methoxy-4,5-diethoxyamphetamine) is a lesser-known psychedelic drug of the amphetamine class. It is a diethoxy-methoxy analogofTMA-2. MEE was first synthesized by Alexander Shulgin. In his book PiHKAL, both the dosage and duration are unknown.[1] MEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MEE.
This psychoactive drug-related article is a stub. You can help Wikipedia by expanding it. |