EEM  |
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| Names |
| IUPAC name 2-(2,4-Diethoxy-5-methoxy-phenyl)-1-methyl-ethylamine |
| Identifiers |
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3D model (JSmol) | |
| ChemSpider | |
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InChI=1S/C14H23NO3/c1-5-17-12-9-14(18-6-2)13(16-4)8-11(12)7-10(3)15/h8-10H,5-7,15H2,1-4H3  Key: SAFDWWQYGOOGMX-UHFFFAOYSA-N InChI=1/C14H23NO3/c1-5-17-12-9-14(18-6-2)13(16-4)8-11(12)7-10(3)15/h8-10H,5-7,15H2,1-4H3 Key: SAFDWWQYGOOGMX-UHFFFAOYAW
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SMILES CCOc1cc(OCC)c(cc1OC)CC(C)N
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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). |
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EEM (2,4-diethoxy-5-methoxyamphetamine) is a lesser-known substituted amphetamine. It is a diethoxy-methoxy analog of trimethoxyamphetamine (TMA-2). EEM was first synthesized by Alexander Shulgin. In his book PiHKAL, both the dosage and duration are unknown.[1] EEM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EEM.
See also
References
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