MME  |
| Names |
| IUPAC name 1-(5-Ethoxy-2,4-dimethoxyphenyl)propan-2-amine |
| Other names 2,4-Dimethoxy-5-ethoxyamphetamine |
| Identifiers |
| | |
3D model (JSmol) | |
| ChEMBL | |
| ChemSpider | |
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| | |
InChI InChI=1S/C13H21NO3/c1-5-17-13-7-10(6-9(2)14)11(15-3)8-12(13)16-4/h7-9H,5-6,14H2,1-4H3  Key: NAMNXRTWJMASNT-UHFFFAOYSA-N InChI=1/C13H21NO3/c1-5-17-13-7-10(6-9(2)14)11(15-3)8-12(13)16-4/h7-9H,5-6,14H2,1-4H3 Key: NAMNXRTWJMASNT-UHFFFAOYAR
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SMILES COc1cc(OC)c(cc1OCC)CC(C)N
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| Properties |
Chemical formula | C13H21NO3 |
| Molar mass | 239.315 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
| | |
MME (2,4-dimethoxy-5-ethoxyamphetamine) is a lesser-known psychedelic drug. It is a dimethoxy-ethoxy analog of TMA-2. MME was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 40 mg, and the duration listed as 6–10 hours.[1] Shulgin gives MME a ++ on the Shulgin Rating Scale. Very little data exists about the pharmacological properties, metabolism, and toxicity of MME.
See also
References
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