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3C-AL

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
3C-AL
Clinical data
Other names4-Allyloxy-3,5-dimethoxyamphetamine; 3,5-Dimethoxy-4-allyloxyamphetamine; α-Methylallylescaline; 3C-Allylescaline
Routes of
administration
Oral[1][2]
Drug classSerotonin receptor modulator;Serotonin5-HT2A receptoragonist;Serotonergic psychedelic;Hallucinogen
Pharmacokinetic data
Duration of action8–12 hours[1][2]
Identifiers
  • 1-[3,5-dimethoxy-4-[(prop-2-en-1-yl)oxy]phenyl]propan-2-amine
CAS Number
PubChemCID
ChemSpider
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H21NO3
Molar mass251.326 g·mol−1
3D model (JSmol)
Melting point180 to 181 °C (356 to 358 °F)
  • C=CCOc1c(OC)cc(cc1OC)CC(N)C
  • InChI=1S/C14H21NO3/c1-5-6-18-14-12(16-3)8-11(7-10(2)15)9-13(14)17-4/h5,8-10H,1,6-7,15H2,2-4H3
  • Key:ROINMNZLTKSBPR-UHFFFAOYSA-N

3C-AL, also known as4-allyloxy-3,5-dimethoxyamphetamine or asα-methylallylescaline (3C-allylescaline), is apsychedelic drug of thephenethylamine,amphetamine, and3C families related to3,4,5-trimethoxyamphetamine (TMA).[3][1][2] It is the amphetamine (3C)analogue ofallylescaline.[3][1][2] The drug has a dose range of 15 to 30 mgorally and aduration of 8 to 12 hours.[1][2] Its effects have been described as morevisual than those of allylescaline.[1] The drug is apotentpartial agonist of theserotonin5-HT2A receptor and also interacts with otherserotonin receptors andtargets.[2] Thechemical synthesis of 3C-AL has been described.[3][4] 3C-AL was described byAlexander Shulgin in his 1991 bookPiHKAL (Phenethylamines I Have Known and Loved), but he did not synthesize or test 3C-AL.[3] Instead,Daniel Trachsel synthesized 3C-AL in 2002[4] and described its properties and effects in 2013.[1] Thepharmacology of 3C-AL was studied in greater detail in 2021.[2]

See also

[edit]

References

[edit]
  1. ^abcdefgTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 642–643,736–737.ISBN 978-3-03788-700-4.OCLC 858805226. Retrieved31 January 2025.
  2. ^abcdefgKolaczynska KE, Luethi D, Trachsel D, Hoener MC, Liechti ME (2021)."Receptor Interaction Profiles of 4-Alkoxy-3,5-Dimethoxy-Phenethylamines (Mescaline Derivatives) and Related Amphetamines".Front Pharmacol.12 794254.doi:10.3389/fphar.2021.794254.PMC 8865417.PMID 35222010.
  3. ^abcdShulgin A. "AL".PiHKAL.
  4. ^abTrachsel D (2002). "Synthesis of novel (phenylalkyl)amines for the investigation of structure-activity relationships. Part 1. Mescalin derivatives".Helvetica Chimica Acta.85 (9):3019–3026.doi:10.1002/1522-2675(200209)85:9<3019::AID-HLCA3019>3.0.CO;2-4.

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