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2c-o-4

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Title: 2c-o-4  
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Subject: 2C (psychedelics), 2C-D, 2C-T-16, DESOXY, HOT-17
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2c-o-4

2C-O-4
Names
IUPAC name
2-(4-Isopropoxy-2,5-dimethoxyphenyl)ethanamine
Identifiers
 N
ChemSpider  Y
Jmol-3D images Image
Properties
C13H21NO3
Molar mass 239.31 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 N  (: Y/N?)

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 1
  • Effects 2
  • Pharmacology 3
  • Dangers 4
  • Legality 5
  • See also 6
  • References 7
  • External links 8

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

  1. ^  

External links

  • 2C-O-4 Entry in PiHKAL
  • 2C-O-4 Entry in PiHKAL • info
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