DOM-2,5-DiEtO
| Clinical data | |
|---|---|
| Other names | DOM-DiEtO; DOM-Di-EtO; DOM-DIETO; DOM-DI-ETO; 2,5-Diethoxy-4-methylamphetamine; 4-Methyl-2,5-diethoxyamphetamine |
| Routes of administration | Unknown[1][2] |
| Drug class | Possible stimulant[1][2] |
| ATC code |
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| Pharmacokinetic data | |
| Duration of action | Unknown[1][2] |
| Identifiers | |
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| Chemical and physical data | |
| 3D model (JSmol) | |
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DOM-2,5-DiEtO, also known as 2,5-diethoxy-4-methylamphetamine, is a drug of the phenethylamine, amphetamine, and DOx families related to the psychedelic drug DOM.[1][3] It is the derivative of DOM in which the methoxy groups at the 2 and 5 positions have been replaced with ethoxy groups.[1] The properties and effects of DOM-2,5-DiEtO in humans do not appear to be known.[1][2] Similarly to DOM and DOET however, DOM-2,5-DiEtO has been reported to produce stimulant-like effects in rabbits.[3] The drug was patented by Alexander Shulgin as a potential "CNS stimulant" in 1970.[1][3] The chemical synthesis of DOM-2,5-DiEtO has been described.[1][3] Close analogues of DOM-2,5-DiEtO, besides DOM, include Florence (DOM-2-EtO) and Iris (DOM-5-EtO), as well as 2CD-2,5-DiEtO.[2][1]
See also
References
- ^ a b c d e f g h i Shulgin A, Manning T, Daley PF (2011). The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley: Transform Press. ISBN 978-0-9630096-3-0.
- ^ a b c d e Shulgin A, Shulgin A (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
- ^ a b c d US 3547999A, Shulgin AT, "4-alkyl-dialkoxy-alpha-methyl-phenethylamines and their pharmacologically-acceptable salts", issued 15 December 1970, assigned to Dow Chemical Co.