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Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
| DOET | |
|---|---|
| Chemical name | 1-(2,5-dimethoxy-4-ethylphenyl)propan-2-amine |
| Chemical formula | C13H21NO2 |
| Molecular mass | 223.32 |
| Melting point | 194-195 °C hydrochloride |
| CAS numbers | 22004-32-6 |
| SMILES | COc1cc(CC)c(cc1CC(C)N)OC |
| |
DOET, HECATE, or 2,5-dimethoxy-4-ethylamphetamine is an analogue of DOM, and is the three-carbon chain homologue to 2C-E. It produces hallucinogenic, psychedelic, and entheogenic effects.
Chemistry[]
DOET is in a class of compounds commonly known as alpha-methyl phenethylamines, or amphetamines and the full chemical name is 4-Ethyl-2,5-dimethoxy-alpha-methylbenzeneethanamine, or 1-(2,5-dimethoxy-4-ethylphenyl)propan-2-amine. It has an active stereocenter and (R)-DOET is the more active isomer.
Effects[]
DOET produces psychedelic and entheogenic effects that last up 14-20 hours. In his book PiHKAL, Alexander Shulgin lists a dosage of DOET as being 2-7 mg orally, with 6-7mg being the dosage for full, desired effects.
Pharmacology[]
The mechanism that produces the hallucinogenic and entheogenic effects of DOET is thought to result from its action as an agonist at the 5-HT2A serotonin receptor.
Dangers[]
The toxicity of DOET is not known.
Legality[]
DOET is classified as a Schedule 1 substance in the United States, and is similarly controlled in other parts of the world. Internationally, DOET is a Schedule I drug under the Convention on Psychotropic Substances[1].
See also[]
External links[]
Categorization[]
Psychedelic phenethylamines
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