2C-O-4
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| Names | |
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| IUPAC name
2-(4-Isopropoxy-2,5-dimethoxyphenyl)ethanamine
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| Identifiers | |
15394-83-9  |
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| ChemSpider | 21106225  |
| Jmol 3D model | Interactive image |
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| Properties | |
| C13H21NO3 | |
| Molar mass | 239.31 g/mol |
| Vapor pressure | {{{value}}} |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
2C-O-4 or 4-isopropoxy-2,5-dimethoxyphenethylamine is a phenethylamine of the 2C family. It is also a positional isomer of isoproscaline and was probably first synthesized by Alexander Shulgin. It produces hallucinogenic, psychedelic, and entheogenic effects. Because of the low potency of 2C-O-4, and the inactivity of 2C-O, Shulgin felt that the 2C-O series would not be an exciting area for research, and did not pursue any further analogues.
Contents
Chemistry
2C-O-4 is in a class of compounds commonly known as phenethylamines, and the full chemical name is 2-(4-isopropoxy-2,5-dimethoxyphenyl)ethanamine.
Effects
Little is known about the psychopharmacological effects of 2C-O-4. Based on the one report available in his book PiHKAL (Phenethylamines i Have Known And Loved), Shulgin lists the dosage of 2C-O-4 as being >60 mg.[1]
Pharmacology
The mechanism that produces the hallucinogenic and entheogenic effects of 2C-O-4 is unknown.
Dangers
The toxicity of 2C-O-4 is not known.
Legality
2C-O-4 is unscheduled and unregulated in the United States, however because of its close similarity in structure and effects to mescaline and 2C-T-7, possession and sale of 2C-O-4 may be subject to prosecution under the Federal Analog Act.
See also
References
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