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Changing short description from "organic compound, 2-methoxy-4,5-diethoxyamphetamine" to "Amphetamine drug"
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| CASNo = 23693-35-8 |
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| UNII = ZD2KJL8HG7 |
| UNII = ZD2KJL8HG7 |
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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) |
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| Names | |
|---|---|
| Preferred IUPAC name
1-(4,5-Diethoxy-2-methoxyphenyl)propan-2-amine | |
| Other names
2-Methoxy-4,5-diethoxyphenethylamine | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| 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.
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