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Preferred IUPAC name
2-(2,4,5-Trimethoxyphenyl)ethan-1-amine | |
Other names
2C-O; 2C-OMe; 2,4,5-TMPEA
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Identifiers | |
3D model (
JSmol)
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ChEMBL | |
ChemSpider | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C11H17NO3 | |
Molar mass | 211.261 g·mol−1 |
Melting point | 187 to 188 °C (369 to 370 °F; 460 to 461 K) |
Pharmacology | |
Legal status |
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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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2,4,5-Trimethoxyphenethylamine (2C-O or 2C-OMe) or is a phenethylamine of the 2C family and was first synthesized by Jansen in 1931. [1] It is a positional isomer of the drug mescaline (3,4,5-tri methoxy).
2C-O is a member of a class of chemical compounds commonly known as phenethylamines. Its full chemical name is 2-(2,4,5-trimethoxyphenyl)ethanamine; it is also known as 2,4,5-trimethoxyphenethylamine and 2,4,5-TMPEA.
Although not centrally active itself, 2C-O appeared to potentiate the action of mescaline when employed as pretreatment 45 minutes prior to the administration of mescaline. [2]
The toxicity of 2C-O is not known.
As of October 31, 2016, 2C-O is a controlled substance (Schedule III) in Canada. [3]
2C-O is a Schedule I substance, as a positional isomer of mescaline.
2C-O and all other compounds featured in PiHKAL are Class A drugs in the United Kingdom.