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| Clinical data | |
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| Other names | IRIS; 2-Methoxy-5-ethoxy-4-methylamphetamine; DOM-5ETO; DOM-5EtO |
| Routes of administration | Oral [1] |
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| Pharmacokinetic data | |
| Duration of action | Unknown [1] |
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| Chemical and physical data | |
| Formula | C13H21NO2 |
| Molar mass | 223.316 g·mol−1 |
| 3D model (JSmol) | |
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Iris, also known as 2-methoxy-5-ethoxy-4-methylamphetamine or as DOM-5ETO, is a drug and a substituted amphetamine. [1] [2] [3] It is also the 5-ethoxy analogue of DOM. [1] [2] [3] The drug was first synthesized by Alexander Shulgin. [1] In his book PiHKAL (Phenethylamines I Have Known and Loved), the minimum dose is listed as 9 mg orally and the duration as unknown. [1] [2] Iris produces few to no effects. [1] [2] Very little data exists about the pharmacological properties, metabolism, and toxicity of IRIS. [1] The drug is one of Shulgin's "ten classic ladies", a series of methylated DOM derivatives. [1] [3] It is not an explicitly controlled substance in the United States, but may be considered scheduled as an isomer of DOET. [4] [5] Iris is a controlled substance in Canada due to phenethylamine blanket-ban language. [6]
