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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
Chemical structure of DOET

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

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Smallwikipedialogo.png 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.

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