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| Clinical data | |
|---|---|
| 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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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]
See also
- DOx (psychedelics)
- Ganesha (3-methyl-DOM)
- DOTMA (Julia; 3,6-dimethyl-DOM)
- 2-Methylmescaline
References
- ^ a b c d e f g h Shulgin A, Shulgin A (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. "And there is the 6-hydrogen atom [of DOM] which can become a 6-methyl group to produce a compound called JUNO, who is pretty much a lady’s lady, or should I say a woman’s woman." [...] "And, finally, JUNO (3,6-dimethoxy-2,4-dimethylamphetamine) has been made (from 2,5-dimethoxy-m-xylene, which was reacted with POCl3 and N-methylformanilide to the benzaldehyde, mp 53–54 °C, and to the nitrostyrene with nitroethane, mp 73–74 °C from cyclohexane, and to the final amine hydrochloride with LAH in THF). Rather amazingly, I have had JUNO on the shelf for almost 14 years and have not yet gotten around to tasting it."
- ^ a b c d e Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. ISBN 978-3-03788-700-4. OCLC 858805226. Archived from the original on 21 August 2025.
- ^ a b c Ger A, Ger D (April 2011). "Triple Goddess of the Night". British Neuroscience Association Bulletin. 63: 28–30.
External links
- JUNO - Isomer Design
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