2C-AL

From WikiMD's Food, Medicine & Wellness Encyclopedia

2C-AL is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin.

Chemistry[edit | edit source]

2C-AL, or 2,5-dimethoxy-4-allyloxyphenethylamine, is a substituted phenethylamine featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain. 2C-AL belongs to the 2C family of phenethylamines which contain methoxy groups on the 2 and 5 positions of the benzene ring.

Pharmacology[edit | edit source]

The exact mechanism of action of 2C-AL is not known, but it is believed to work, like other psychedelic phenethylamines, as a 5-HT2A receptor agonist. This means it binds to this receptor in the brain and induces a psychedelic effect.

Effects[edit | edit source]

The effects of 2C-AL are not well documented. As a psychedelic, it is assumed to produce effects similar to other drugs in the 2C family, such as 2C-B, 2C-I, and 2C-E. These effects can include open and closed-eye visuals, euphoria, time distortion, enhanced introspection, and increased empathy. However, the specific effects can vary greatly depending on the individual and the dose taken.

Toxicity and harm potential[edit | edit source]

The toxicity and long-term health effects of recreational 2C-AL use do not seem to have been studied in any scientific context and the exact toxic dose is unknown. As with all psychedelics, it is advised to use harm reduction practices if using this substance.

Legal status[edit | edit source]

2C-AL is unscheduled and uncontrolled in the United States. However, it could potentially be considered an analog of 2C-B, which could make its sale for human consumption subject to prosecution under the Federal Analog Act.

See also[edit | edit source]

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD