Juno (psychedelic)
Pharmaceutical compound
From Wikipedia, the free encyclopedia
Juno, also known as 4,6-dimethyl-2,5-dimethoxyamphetamine or as 6-methyl-DOM, is a possible psychedelic drug of the phenethylamine, amphetamine, and DOx families related to DOM.[1][2][3] It is the 6-methyl derivative of DOM and a positional isomer of Ganesha (3-methyl-DOM).[1][2][3] The drug is one of Alexander Shulgin's "ten classic ladies", a series of methylated DOM derivatives.[1][3] DOM, Ganesha, and DOTMA (Julia; 3,6-dimethyl-DOM) are all known to be active psychedelics, so Juno is expected to be an active psychedelic as well, but has not yet been tested.[1][2] Juno was first described by Shulgin in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).[1] He shared in PiHKAL that he had had Juno on a shelf in his lab for almost 14 years but had never gotten around to trying it.[1] It is a controlled substance in Canada under phenethylamine blanket-ban language.[4] The drug is not an explicitly controlled substance in the United States, but may be considered scheduled as an isomer of DOET.[5][6]
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| Clinical data | |
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| Other names | JUNO; 3,6-Dimethoxy-2,4-dimethylamphetamine; 4,6-Dimethyl-2,5-dimethoxyamphetamine; 6-Methyl-DOM; 6-Me-DOM |
| Routes of administration | Unknown[1][2] |
| Drug class | Serotonergic psychedelic; Hallucinogen |
| ATC code |
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| Pharmacokinetic data | |
| Duration of action | Unknown[1][2] |
| Identifiers | |
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| Chemical and physical data | |
| Formula | C13H21NO2 |
| Molar mass | 223.316 g·mol−1 |
| 3D model (JSmol) | |
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See also
- DOx (psychedelics)
- Ganesha (3-methyl-DOM)
- DOTMA (Julia; 3,6-dimethyl-DOM)
- 2-Methylmescaline
