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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, Alexander;Ann Shulgin (September 1991).PiHKAL: A Chemical Love Story.Berkeley, California: Transform Press.ISBN 0-9630096-0-5.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, Hennessey JJ, Bock HA, Anderson EI, Sherwood AM, Morris H, de Klein R, Klein AK, Cuccurazzu B, Gamrat J, Fannana T, Zauhar R, Halberstadt AL, McCorvy JD (December 2023)."Identification of 5-HT2A receptor signaling pathways associated with psychedelic potential".Nat Commun.14 (1) 8221.Bibcode:2023NatCo..14.8221W.doi:10.1038/s41467-023-44016-1.PMC 10724237.PMID 38102107.

External links

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