2,5-Dimethoxy-4-ethylamphetamine
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| 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.
Contents |
[edit] 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.
[edit] 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.
[edit] 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.
[edit] Dangers
The toxicity of DOET is not known.
[edit] 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].
[edit] See also
[edit] External links
[edit] Categorization
Psychedelic phenethylamines
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Aleph • 2C-B • 2C-B-FLY • 2C-C • 2C-D • 2C-E • 2C-F • 2C-G • 2C-I • 2C-N • 2C-O • 2C-O-4 • 2C-P • 2C-T • 2C-T-2 • 2C-T-4 • 2C-T-7 • 2C-T-8 • 2C-T-9 • 2C-T-13 • 2C-T-15 • 2C-T-17 • 2C-T-21 • 2C-TFM • 3C-E • 3C-P • Br-DFLY • DESOXY • DMMDA-2 • DOB • DOC • DOET • DOI • DOM • DON • Escaline • Ganesha • HOT-2 • HOT-7 • HOT-17 • Isoproscaline • Lophophine • MDA • MMDA • MMDA-2 • MMDA-3a • MMDMA • Macromerine • Mescaline • Proscaline • TMA |
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| This page uses content from the English-language version of Wikipedia. The original article was at 2,5-Dimethoxy-4-ethylamphetamine. The list of authors can be seen in the page history. As with Psychology Wiki, the text of Wikipedia is available under the GNU Free Documentation License. |

