2C-T-13
A psychedelic phenethylamine of the 2C family
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2C-T-13 is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin and is known for its psychoactive effects.
Chemical structure[edit | edit source]
2C-T-13 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 structure of 2C-T-13 includes a methoxyethylthio group attached to the 4-position of the phenyl ring, and two methoxy groups at the 2- and 5-positions.
Pharmacology[edit | edit source]
2C-T-13 acts as a serotonin receptor agonist, primarily affecting the 5-HT2A receptor. This interaction is believed to be responsible for its psychedelic effects. The compound is part of the 2C family, which are known for their ability to alter perception, mood, and cognitive processes.
Effects[edit | edit source]
The effects of 2C-T-13 are similar to other psychedelics in the 2C family. Users report altered visual and auditory perceptions, 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[edit | edit source]
2C-T-13 was first synthesized by Alexander Shulgin, a renowned chemist known for his work with psychedelic compounds. The synthesis involves the reaction of 2,5-dimethoxy-4-methylthiophenethylamine with methoxyethyl chloride, resulting in the formation of 2C-T-13.
Legal status[edit | edit source]
The legal status of 2C-T-13 varies by country. In some jurisdictions, it is classified as a controlled substance, while in others it may be legal or unregulated. Users should be aware of the legal implications of possessing or using 2C-T-13 in their region.
Related pages[edit | edit source]
Gallery[edit | edit source]
Chemical structure of 2C-T-13
3D model of 2C-T-13
2C-T-13[edit | edit source]
Chemical structure of 2C-T-13
3D stick model of 2C-T-13
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