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| Name = MEE |
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| verifiedrevid = 400293834 |
| verifiedrevid = 400293834 |
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| ImageFile = MEE.png |
| ImageFile = MEE.png |
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|Section2={{Chembox Properties |
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| C=14 |
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| Formula = C<sub>14</sub>H<sub>23</sub>NO<sub>3</sub> |
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| H=23 |
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| MolarMass = 253.34 |
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| N=1 |
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| O=3 |
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'''MEE''' |
'''MEE''' ('''2-methoxy-4,5-diethoxyamphetamine''') is a lesser-known [[Psychedelics, dissociatives and deliriants|psychedelic drug]] of the [[substituted amphetamine|amphetamine class]]. It is a diethoxy-methoxy [[analog (chemistry)|analog]] of [[Trimethoxyamphetamine|TMA-2]]. MEE was first synthesized by [[Alexander Shulgin]]. In his book ''[[PiHKAL]]'', both the dosage and duration are unknown.<ref>[http://www.erowid.org/library/books_online/pihkal/pihkal121.shtml MEE entry in ''PiHKAL'']</ref> MEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MEE. |
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== See also == |
== See also == |
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* [[Psychedelics, dissociatives and deliriants]] |
* [[Psychedelics, dissociatives and deliriants]] |
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== |
== References== |
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{{reflist}} |
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* [http://www.erowid.org/library/books_online/pihkal/pihkal121.shtml MEE entry in ''PiHKAL''] |
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* [http://pihkal.info/read.php?domain=pk&id=121 MEE entry in PiHKAL • info] |
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{{PiHKAL}} |
{{PiHKAL}} |
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 |
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Names | |
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IUPAC name
2-(4,5-Diethoxy-2-methoxy-phenyl)-1-methyl-ethylamine | |
Other names
2-Methoxy-4,5-diethoxyphenethylamine | |
Identifiers | |
3D model (JSmol) |
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ChemSpider |
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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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