Ariadne (psychedelic)
| Ariadne (psychedelic) | |
|---|---|
| File:Ariadne.svg | |
| 1-(2,5-Dimethoxy-4-methyl-benzyl)-propylamine | |
| Other names 4-Methyl-2,5-dimethoxy-alpha-ethylphenethylamine 2-(4-Methyl-2,5-dimethoxyphenyl)ethan-alpha-ethylamine | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 52842-59-8 |
| PubChem | 169886 |
| ChemSpider | 2300980 |
| SMILES | Script error: No such module "collapsible list". |
| InChI | Script error: No such module "collapsible list". |
| InChI key | MLYCFWZIAJAIGW-LLVKDONJBY |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C13H21NO2 |
| Molar mass | 223.31 g/mol |
| Exact mass | 223.157229 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Ariadne (Dimoxamine, α-Et-DOM), or 4-methyl-2,5-dimethoxy-alpha-ethylphenethylamine, is a lesser-known psychedelic drug. It is a homologue of 2C-D and DOM. Ariadne was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), Shulgin reported testing Ariadne up to a dose of 32 mg, and reported that it produces psychedelia and a bare threshold.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of Ariadne in humans apart from Shulgin's limited testing.
However, in more recent animal studies, α-Et-DOM was shown to produce stimulus generalisation in rats trained to respond to the drug MDMA.[2] This suggests that while α-Et-DOM may lack hallucinogenic effects, it might potentially produce empathogenic effects similar to those of MDMA if used at higher dose ranges, beyond those trialled by Shulgin (the potency of α-Et-DOM in this study was similar to that of MDMA, 1.5 mg/kg, which would equate to a dose of ~100 mg in a human).
References
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External links
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