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Desoxy (psychedelic)

From Wikipedia, the free encyclopedia
(Redirected fromDESOXY)
Not to be confused withdesoxy- orDesoxyn.

Pharmaceutical compound
Desoxy
Clinical data
Other names4-Methyl-3,5-dimethoxyphenethylamine; 3,5-Dimethoxy-4-methylphenethylamine
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action6–8 hours[1]
Identifiers
  • 2-(3,5-dimethoxy-4-methylphenyl)ethan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H17NO2
Molar mass195.262 g·mol−1
3D model (JSmol)
  • Cc1c(cc(cc1OC)CCN)OC
  • InChI=1S/C11H17NO2/c1-8-10(13-2)6-9(4-5-12)7-11(8)14-3/h6-7H,4-5,12H2,1-3H3 checkY
  • Key:LLHRMWHYJGLIEV-UHFFFAOYSA-N checkY
  (verify)

Desoxy, orDESOXY, also known as4-desoxymescaline or as4-methyl-3,5-dimethoxyphenethylamine, is apsychedelic drug of thephenethylamine andscaline families related tomescaline (3,4,5-trimethoxyphenethylamine).[1][2] It is theanalogue of mescaline in which themethoxy group at the 4 position has been replaced with amethyl group, hence anoxygen has been removed and the name "desoxy".[1][2] The drug was first described in thescientific literature by F. Benington and colleagues in 1960.[3] Subsequently, it was described in greater detail byAlexander Shulgin in his 1991 bookPiHKAL (Phenethylamines I Have Known and Loved) and other publications.[1][2]

Use and effects

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A typical dose is within the range of 40 to 120 mgorally and lasts 6 to 8 hours.[1] The effects of DESOXY vary significantly frommescaline, despite their chemical similarity.[1] Its effects includedclosed-eye imagery but noopen-eye visuals.[1]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

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Pharmacodynamics

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DESOXY acts as aserotonin5-HT2 receptoragonist.[4]

Society and culture

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Legal status

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United States

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In 1970 theControlled Substances Act placedmescaline intoSchedule I in theUnited States. It is similarly controlled in other nations. Depending on whether or not it is intended for human consumption, 4-desoxymescaline could be considered ananalogue ofmescaline, under theFederal Analogue Act and similar bills in other countries, making it illegal to manufacture, buy, possess, or distribute without a DEA or related license. DESOXY is also an isomer of2C-D which makes it a schedule 1 drug in the United States.

See also

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References

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  1. ^abcdefghShulgin A, Shulgin A (September 1991).PiHKAL: A Chemical Love Story.Berkeley, California: Transform Press.ISBN 978-0-9630096-0-9.OCLC 25627628.
  2. ^abcShulgin A, Manning T, Daley P (2011).The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley:Transform Press. pp. 46–47.ISBN 978-0-9630096-3-0. Retrieved2 November 2024.
  3. ^Benington F, Morin R, Clark Jr L (1960)."Notes- Mescaline Analogs. X. 3,4-Dimethyl-, 3,4-Dichloro- and 3,5-Dimethoxy-4-methyl-β-phenethylamines".The Journal of Organic Chemistry.25 (11):2066–2067.doi:10.1021/jo01081a626.ISSN 0022-3263. Retrieved23 November 2025.
  4. ^Wallach J, Cao AB, Calkins MM, Heim AJ, Lanham JK, Bonniwell EM, et al. (December 2023)."Identification of 5-HT2A receptor signaling pathways associated with psychedelic potential".Nature Communications.14 (1) 8221.Bibcode:2023NatCo..14.8221W.doi:10.1038/s41467-023-44016-1.PMC 10724237.PMID 38102107.

External links

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