2C-O-4

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2C-O-4
Chemical name 2-(4-isopropoxy-2,5-dimethoxyphenyl)ethanamine
Chemical formula C13H21NO3
Molecular mass 239.31 g/mol
Melting point  ??
CAS numbers  ?
SMILES COc1cc(OC)c(cc1OC)CCN
Chemical structure of 2C-O-4

2C-O-4 (or 4-(i)-propoxy-2,5-dimethoxyphenethylamine) is 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, and did not pursue any further analogues.

Contents

[edit] 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.

[edit] Effects

Little is known about the psychopharmacological effects of 2C-O-4. Based on the one report available in his book PiHKAL, Shulgin lists the dosage of 2C-O-4 as being >60 mg.

[edit] Pharmacology

The mechanism that produces the hallucinogenic and entheogenic effects of 2C-O-4 is unknown.

[edit] Dangers

The toxicity of 2C-O is not known.

[edit] 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.

[edit] See also

[edit] External links

[edit] Categorization


Hallucinogenic phenethylamines edit

2C-B, 2C-B-FLY, 2C-C, 2C-D, 2C-E, 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-21, 2C-TFM, 3C-E, 3C-P, Br-DFLY, DESOXY, DMMDA-2, DOB, DOC, DOET, DOI, DOM, DON, Escaline, Isoproscaline, Lophophine, MDA, MMDA, Macromerine, Mescaline, Proscaline, TMA