2C-T-17

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A psychedelic phenethylamine of the 2C family




2C-T-17 is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin and is known for its psychoactive effects.

Chemical structure and properties[edit | edit source]

2C-T-17 is chemically classified as a phenethylamine, which is a compound containing a phenyl ring and an amino group connected by a two-carbon chain. The chemical structure of 2C-T-17 is characterized by the presence of a thioether group, which is a sulfur atom bonded to two carbon atoms. This structural feature is shared with other compounds in the 2C-T series.

2D structure of 2C-T-17
3D stick model of 2C-T-17

Pharmacology[edit | edit source]

2C-T-17 acts primarily as a serotonin receptor agonist, particularly at the 5-HT2A receptor, which is believed to be responsible for its psychedelic effects. The compound's interaction with these receptors leads to alterations in perception, mood, and cognition.

Effects[edit | edit source]

The effects of 2C-T-17 are similar to those of other psychedelics in the 2C family. Users report visual hallucinations, altered sensory perception, and changes in thought processes. The intensity and duration of these effects can vary depending on the dose and individual sensitivity.

Synthesis[edit | edit source]

The synthesis of 2C-T-17 involves the reaction of 2,5-dimethoxybenzaldehyde with a thioether precursor, followed by a series of chemical transformations to produce the final compound. The synthesis process requires advanced knowledge of organic chemistry and access to specialized laboratory equipment.

Legal status[edit | edit source]

The legal status of 2C-T-17 varies by country. In some jurisdictions, it is classified as a controlled substance, making its manufacture, distribution, and possession illegal. In other areas, it may not be specifically regulated, although it could still be subject to general drug laws.

Related pages[edit | edit source]

Gallery[edit | edit source]

2C-T-17[edit | edit source]

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Contributors: Prab R. Tumpati, MD