5-MeO-NMT
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| Names | |
|---|---|
| Other names
5-methoxy-N-methyltryptamine | |
| Identifiers | |
2009-03-2 (freebase)  2426-68-8 (hydrochloride) | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:189635  |
| ChEMBL | ChEMBL58579 |
| ChemSpider | 15360 |
| PubChem | 16184 |
| UNII | YBO217L5YV (freebase) 3390M5391J (hydrochloride) |
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| Properties | |
| C12H16N2O | |
| Molar mass | 204.27 g/mol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
5-MeO-NMT, or 5-methoxy-N-methyltryptamine, is an organic chemical compound, being the 5-methoxy analog of N-methyltryptamine (NMT). It was first isolated from Phalaris arundinacea (reed canary grass)[1] and was also synthesized by Alexander Shulgin in his book TiHKAL (Tryptamines I Have Known and Loved). In contrast to other members of the N-methyltryptamine family of compounds 5-MeO-NMT is believed to produces few or no psychedelic effects, although very little data exists about its pharmacological properties or toxicity.
See also
External links
References
- ↑ Wilkinson, S. (1958). "428. 5-Methoxy-N-methyltryptamine: a new indole alkaloid from Phalaris arundinacea L.". Journal of the Chemical Society (Resumed): 2079. doi:10.1039/jr9580002079.
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