2C-T-16

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A psychedelic phenethylamine of the 2C family



2C-T-16 is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin and is known for its psychoactive effects.

Chemical structure

2C-T-16 is chemically classified as a phenethylamine. Its structure is characterized by a phenyl ring bound to an amino group through an ethyl chain, with a thioether group attached to the phenyl ring. The chemical formula is C12H19NO2S.

Chemical structure of 2C-T-16

Pharmacology

2C-T-16 acts as a serotonin receptor agonist, primarily affecting the 5-HT2A receptor. This interaction is responsible for its psychedelic effects, which can include altered perception, mood, and cognition. The exact mechanism of action is similar to other compounds in the 2C family, which are known to modulate the activity of serotonin in the brain.

Effects

The effects of 2C-T-16 are similar to other psychedelics in the 2C series. Users report visual and auditory hallucinations, changes in thought patterns, and an altered sense of time. The intensity and duration of these effects can vary based on dosage and individual sensitivity.

Synthesis

2C-T-16 is synthesized from 2,5-dimethoxybenzaldehyde, which undergoes a series of chemical reactions including the addition of a thioether group. The synthesis process requires advanced knowledge of organic chemistry and access to specialized laboratory equipment.

Legal status

The legal status of 2C-T-16 varies by country. In some jurisdictions, it is classified as a controlled substance, making its manufacture, sale, or possession illegal. In others, it may be unregulated or fall under analog laws that restrict substances similar to known controlled drugs.

Related compounds

2C-T-16 is part of the 2C family of psychedelics, which includes other compounds such as 2C-B, 2C-I, and 2C-T-7. These compounds share a similar chemical structure and mechanism of action but differ in their potency and effects.

See also

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