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3,4-Methylenedioxy-N-hydroxyamphetamine

From Wikipedia, the free encyclopedia
(Redirected fromMethylenedioxyhydroxyamphetamine)
Psychedelic and entactogen
Pharmaceutical compound
MDOH
Clinical data
Other namesMDOH; MDH;N-Hydroxy-MDA
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen;Entactogen
ATC code
  • None
Legal status
Legal status
Pharmacokinetic data
Duration of action3–6 hours[1]
Identifiers
  • 1-(1,3-Benzodioxol-5-yl)-N-hydroxypropan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC10H13NO3
Molar mass195.218 g·mol−1
3D model (JSmol)
  • CC(CC1=CC2=C(C=C1)OCO2)NO

3,4-Methylenedioxy-N-hydroxyamphetamine (MDOH,MDH), also known asN-hydroxy-MDA, is anentactogen,psychedelic, andstimulant of thephenethylamine andamphetaminechemical classes.[2] It is theN-hydroxyhomologue ofMDA, and theN-desmethyl homologue ofMDHMA.[1]

Use and effects

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In his bookPiHKAL (Phenethylamines I Have Known and Loved),Alexander Shulgin listed the dose range as 100 to 160 mgorally and itsduration as approximately 3 to 6 hours.[1] He describes MDOH as being very psychedelic and producing increased pleasure in beauty and nature.[1] Shulgin also mentioned several negative side effects also seen withMDMA ("Ecstasy") such as difficulty urinating and internal dryness.[1] He has noted that the properties and effects of MDOH are very similar or near-identical to those of MDA and that MDOH might be converted into MDA in the body.[1]

Interactions

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See also:MDMA § Interactions,Psychedelic drug § Interactions,Trip killer § Serotonergic psychedelic antidotes,Trip killer § Antidotes of other hallucinogens, andMDMA/citalopram

See also

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References

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  1. ^abcdefgShulgin A,Shulgin A (September 1991).PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.
  2. ^de Boer D, Bosman I (April 2004). "A new trend in drugs-of-abuse; the 2C-series of phenethylamine designer drugs".Pharmacy World & Science.26 (2):110–113.doi:10.1023/b:phar.0000018600.03664.36.PMID 15085947.

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