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3C-MAL

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
3C-MAL
Clinical data
Other names4-Methylallyloxy-3,5-dimethoxyamphetamine; 3,5-Dimethoxy-4-methylallyloxyamphetamine; α-Methylmethallylescaline; α-Methyl-MAL; 3C-Methallylescaline
Routes of
administration
Unknown[1]
Pharmacokinetic data
Duration of actionUnknown[1]
Identifiers
  • 1-[3,5-dimethoxy-4-(2-methylprop-2-enoxy)phenyl]propan-2-amine
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC15H23NO3
Molar mass265.353 g·mol−1
3D model (JSmol)
Melting point159 to 160 °C (318 to 320 °F)
  • CC(CC1=CC(=C(C(=C1)OC)OCC(=C)C)OC)N
  • InChI=1S/C15H23NO3/c1-10(2)9-19-15-13(17-4)7-12(6-11(3)16)8-14(15)18-5/h7-8,11H,1,6,9,16H2,2-5H3
  • Key:PUSUEDYGABXNSF-UHFFFAOYSA-N

3C-MAL, also known as4-methylallyloxy-3,5-dimethoxyamphetamine or asα-methylmethallylescaline (3C-methallylescaline), is achemical compound of thephenethylamine,amphetamine, and3C families related to thepsychedelic drug3,4,5-trimethoxyamphetamine (TMA).[1][2] It is the amphetamine (3C)analogue of the psychedelicmethallylescaline (MAL).[1][2] The compound does not appear to have been tested in humans, and its dose,duration, and effects are unknown.[1] Itschemical synthesis has been described.[2] 3C-MAL was first described in thescientific literature byDaniel Trachsel in 2002.[1][2]

See also

[edit]

References

[edit]
  1. ^abcdefTrachsel 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. p. 736.ISBN 978-3-03788-700-4.OCLC 858805226. Retrieved31 January 2025.
  2. ^abcdTrachsel 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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Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
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