25I-NBF
25I-NBF is a derivative of the phenethylamine hallucinogen 2C-I, which is used for its psychedelic effects. It is part of the 25x-NBx family and was first synthesized by the research team led by David E. Nichols at Purdue University.
History[edit | edit source]
25I-NBF was first synthesized by a research team at Purdue University led by David E. Nichols. It is part of the 25x-NBx family of psychedelic phenethylamines, specifically a derivative of 2C-I.
Chemistry[edit | edit source]
25I-NBF is a phenethylamine derivative and shares a common structure with other members of the 25x-NBx family. It is characterized by the substitution of an iodine atom at the 4 position of the phenyl ring.
Pharmacology[edit | edit source]
The pharmacology of 25I-NBF is not fully understood. It is known to act as a highly potent partial agonist for the 5-HT2A receptor, which is thought to be responsible for its psychedelic effects.
Effects[edit | edit source]
The effects of 25I-NBF are similar to those of other psychedelic phenethylamines. These can include open and closed eye visuals, euphoria, time distortion, and introspection. As with all psychedelics, the effects are highly subjective and can vary greatly between individuals.
Legal Status[edit | edit source]
The legal status of 25I-NBF varies by country. In the United States, it is a Schedule I controlled substance. In the United Kingdom, it is a Class A drug.
See Also[edit | edit source]
References[edit | edit source]
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