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| pregnancy_category =
| pregnancy_category =
| legal_status = Uncontrolled
| legal_status = Uncontrolled
| legal_US =[[List of Schedule I drugs|Schedule I (isomer of MDOH)]]
| routes_of_administration = [[Mouth|Oral]]
| routes_of_administration = [[Mouth|Oral]]


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'''BOH''', also known as '''3,4-methylenedioxy-β-methoxyphenethylamine''', is a [[drug]] of the [[substituted phenethylamine|phenethylamine]] class.<ref name="isbn0-9630096-0-5">{{cite book | vauthors = Shulgin A, Shulgin A | title = Pihkal: A Chemical Love Story | publisher = Transform Press | year = 1991 | isbn = 0-9630096-0-5 | url = http://www.erowid.org/library/books_online/pihkal/pihkal015.shtml}}</ref> It is the β-[[methoxy]] [[structural analog|analog]] of [[methylenedioxyphenethylamine]] (MDPEA) and is also more distantly related to [[methylone]]. On account of its similarity to [[norepinephrine]], the effects of BOH may be of a purely [[adrenergic]] nature.<ref name="isbn0-9630096-0-5"/>
'''BOH''', also known as '''3,4-methylenedioxy-β-methoxyphenethylamine''', is a [[drug]] of the [[substituted phenethylamine|phenethylamine]] class.<ref name="isbn0-9630096-0-5">{{cite book | vauthors = Shulgin A, Shulgin A | title = Pihkal: A Chemical Love Story | publisher = Transform Press | year = 1991 | isbn = 0-9630096-0-5 | url = http://www.erowid.org/library/books_online/pihkal/pihkal015.shtml}}</ref> It is the β-[[methoxy]] [[structural analog|analog]] of [[methylenedioxyphenethylamine]] (MDPEA) and is also more distantly related to [[methylone]]. On account of its similarity to [[norepinephrine]], the effects of BOH may be of a purely [[adrenergic]] nature.<ref name="isbn0-9630096-0-5"/>


BOH was first [[Chemical synthesis|synthesized]] by [[Alexander Shulgin]].<ref name="isbn0-9630096-0-5"/> In his book [[PiHKAL]], the dosage range is listed as 80–120&nbsp;mg, and the duration listed as 6–8 hours. Shulgin reports that BOH causes slight [[hyperthermia|warmth]], [[mydriasis]], [[anorexia (symptom)|anorexia]], mild [[nausea]], and [[cold feet]], with no [[psychedelic drug|psychedelic]], [[entactogen]], or [[euphoriant]] effects.<ref name="isbn0-9630096-0-5"/> He gives it a ++ on the [[Shulgin Rating Scale]].<ref name="isbn0-9630096-0-5"/>
BOH was first [[Chemical synthesis|synthesized]] by [[Alexander Shulgin]].<ref name="isbn0-9630096-0-5"/> In his book [[PiHKAL]], the dosage range is listed as 80–120&nbsp;mg, and the duration listed as 6–8 hours. Shulgin reports that BOH causes slight [[hyperthermia|warmth]], [[mydriasis]], [[anorexia (symptom)|anorexia]], mild [[nausea]], and [[cold feet]], with no [[psychedelic drug|psychedelic]], [[entactogen]], or [[euphoriant]] effects.<ref name="isbn0-9630096-0-5"/> He gives it a ++ on the [[Shulgin Rating Scale]].<ref name="isbn0-9630096-0-5"/>


==Legality==
==Legality==

Latest revision as of 01:44, 11 January 2023

BOH
Clinical data
Other names3,4-methylenedioxy-β-methoxyphenethylamine
MedlinePlusa609035
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
Identifiers
  • 2-(1,3-Benzodioxol-5-yl)-2-methoxyethanamine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC10H13NO3
Molar mass195.218 g·mol−1
3D model (JSmol)
  • NCC(OC)c1ccc2OCOc2c1
  • InChI=1S/C10H13NO3/c1-12-10(5-11)7-2-3-8-9(4-7)14-6-13-8/h2-4,10H,5-6,11H2,1H3 checkY
  • Key:KUTKTMOZFCYDLZ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

BOH, also known as 3,4-methylenedioxy-β-methoxyphenethylamine, is a drug of the phenethylamine class.[1] It is the β-methoxy analog of methylenedioxyphenethylamine (MDPEA) and is also more distantly related to methylone. On account of its similarity to norepinephrine, the effects of BOH may be of a purely adrenergic nature.[1]

BOH was first synthesized by Alexander Shulgin.[1] In his book PiHKAL, the dosage range is listed as 80–120 mg, and the duration listed as 6–8 hours. Shulgin reports that BOH causes slight warmth, mydriasis, anorexia, mild nausea, and cold feet, with no psychedelic, entactogen, or euphoriant effects.[1] He gives it a ++ on the Shulgin Rating Scale.[1]

Legality

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United Kingdom

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This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[2]

See also

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References

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  1. ^ a b c d e Shulgin A, Shulgin A (1991). Pihkal: A Chemical Love Story. Transform Press. ISBN 0-9630096-0-5.
  2. ^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.