Adverts

Open Access Articles- Top Results for MEE (psychedelic)

MEE (psychedelic)

MEE (psychedelic)
200px
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Names

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

IUPAC name
2-(4,5-Diethoxy-2-methoxy-phenyl)-1-methyl-ethylamine
Other names
2-Methoxy-4,5-diethoxyphenethylamine
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Identifiers#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-



23693-35-8 7pxY
ChemSpider 21106337 7pxY
Jmol-3D images Image
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Properties

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

C14H23NO3
Molar mass 253.34
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 14pxY verify (what is10pxY/10pxN?)
Infobox references

MEE, or 2-methoxy-4,5-diethoxyamphetamine, is a lesser-known psychedelic drug. It is a diethoxy-methoxy analog of TMA-2. MEE was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), both the dosage and duration are unknown. MEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MEE.

See also

External links

Lua error in package.lua at line 80: module 'Module:Buffer' not found.