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Benzodioxolylhydroxybutanamine
3,4-methylenedioxy-beta-methoxy-phenethylamine.png
IUPAC name
Other names 3,4-Methylenedioxy-β-methoxyphenethylamine
2-(3,4-Methylenedioxy-β-methoxyphenyl)ethanamine
Identifiers
CAS number 73304-06-0
SMILES
InChI
Properties
Molecular formula C10H13NO3
Molar mass 195.22 g/mol
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

BOH, also known as 3,4-methylenedioxy-β-methoxyphenethylamine, is a psychoactive drug and member of the phenethylamine chemical class which acts as an entactogen, psychedelic, and stimulant. It is the β-methoxy analogue of methylenedioxyphenethylamine (MDPEA).

BOH was first synthesized by Alexander Shulgin ("Sasha" Shulgin). In his book PiHKAL ("Phenethylamines i Have Known And Loved"), the dosage range is listed as 80–120 mg, and the duration listed as 6–8 hours. BOH causes mydriasis or pupil dilation, anorexia or loss of appetite, and cold feet. Shulgin gives it a ++ on the Shulgin Rating Scale. Very little is known about the pharmacology, pharmacokinetics, effects, and toxicity of BOH.

See also

References

External links


BOH (psychedelic)
File:3,
IUPAC name
Other names 3,4-Methylenedioxy-beta-methoxyphenethylamine
2-(3,4-Methylenedioxy-beta-methoxyphenyl)ethanamine
Identifiers
CAS number [73304-06-0]
SMILES
InChI
Properties
Molecular formula C10H13NO3
Molar mass 195.22 g/mol
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

BOH, or 3,4-methylenedioxy-beta-methoxyphenethylamine, is a lesser-known psychedelic drug. It is the beta-methoxy analog of MDPEA. BOH was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the dosage range is listed as 80–120 mg, and the duration listed as 6–8 hours. BOH dilates the pupils, and produces anorexia and cold feet. Shulgin gives it a ++ on the Shulgin Rating Scale.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of BOH.

References

See also

External links








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