2C-O-4
| Clinical data | |
|---|---|
| Other names | 4-Isopropoxy-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-isopropoxyphenethylamine |
| Routes of administration | Oral[1] |
| ATC code |
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| Pharmacokinetic data | |
| Duration of action | A few hours[1] |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| E number | {{#property:P628}} |
| CompTox Dashboard (EPA) |
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| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C13H21NO3 |
| Molar mass | 239.315 g·mol−1 |
| 3D model (JSmol) | |
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| ☒check (what is this?) (verify) | |
2C-O-4, also known as 4-isopropoxy-2,5-dimethoxyphenethylamine, is a phenethylamine of the 2C family.[1] It is also a positional isomer of isoproscaline and was probably first synthesized by Alexander Shulgin.[1] It produces hallucinogenic or psychedelic effects.[1] 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.[1]
Use and effects
[edit | edit source]Little is known about the psychopharmacological effects of 2C-O-4.[1] Based on the one report available in his book PiHKAL, Shulgin lists the dose of 2C-O-4 as being >60 mg.[1] At 60 mg, threshold psychoactive effects occurred.[1] These included awareness of something in the front part of the head, yawning, physiological changes, and a general exhilaration and excitement.[1] The effects lasted a few hours and were rated as a +1 on the Shulgin Rating Scale.[1] The drug was regarded as remaining to be fully explored.[1]
Toxicity
[edit | edit source]The toxicity of 2C-O-4 is not known.
Pharmacology
[edit | edit source]The pharmacology of 2C-O-4 has been studied.[2]
Chemistry
[edit | edit source]2C-O-4 is in a class of compounds commonly known as phenethylamines, and the systematic chemical name is 2-(4-isopropoxy-2,5-dimethoxyphenyl)ethanamine.
Society and culture
[edit | edit source]Legal status
[edit | edit source]Canada
[edit | edit source]As of October 31, 2016, 2C-O-4 is a controlled substance (Schedule III) in Canada.[3]
United States
[edit | edit source]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
[edit | edit source]References
[edit | edit source]- ^ a b c d e f g h i j k l Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value). 2C-O-4 Entry in PiHKAL
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