25H-NBOH
A detailed overview of the chemical compound 25H-NBOH
25H-NBOH is a chemical compound that belongs to the class of phenethylamines. It is a derivative of the 2C family of psychedelic phenethylamines and is closely related to 25I-NBOH and 25C-NBOH.
Chemical Structure and Properties[edit | edit source]
25H-NBOH is chemically known as 2-(2,5-Dimethoxyphenyl)-N-(2-hydroxybenzyl)ethanamine. It features a phenethylamine core with a methoxy group at the 2 and 5 positions of the benzene ring, and a hydroxybenzyl group attached to the nitrogen atom.
Molecular Formula: C₁₇H₂₁NO₃
Molecular Weight: 287.35 g/mol
Pharmacology[edit | edit source]
25H-NBOH acts as a partial agonist at the 5-HT2A receptor, which is the primary target for psychedelic effects. The compound is known to produce hallucinogenic effects similar to other members of the 2C family, although its potency and duration of action can vary.
Synthesis[edit | edit source]
The synthesis of 25H-NBOH involves the reaction of 2,5-dimethoxyphenethylamine with 2-hydroxybenzaldehyde under reductive amination conditions. This process typically requires the use of a reducing agent such as sodium borohydride.
Effects[edit | edit source]
The effects of 25H-NBOH are similar to those of other psychedelic phenethylamines, including altered perception of time and space, visual hallucinations, and changes in mood and thought patterns. The onset of effects typically occurs within 30 to 60 minutes after administration, with a duration of action lasting 6 to 10 hours.
Legal Status[edit | edit source]
As of the current date, 25H-NBOH is not specifically controlled under international drug control treaties. However, its legal status may vary by country, and it may be subject to analogue laws in jurisdictions where similar compounds are controlled.
Safety and Toxicity[edit | edit source]
There is limited data on the safety and toxicity of 25H-NBOH in humans. As with other research chemicals, caution is advised, and it should only be used in a controlled research setting.
Also see[edit | edit source]
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