para-Methoxy-N-ethylamphetamine

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PMEA
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Legal status
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Identifiers
  • N-ethyl-1-(4-methoxyphenyl)propan-2-amine
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Chemical and physical data
FormulaC12H19NO
Molar mass193.290 g·mol−1
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  • O(c1ccc(cc1)CC(NCC)C)C
  • InChI=1S/C12H19NO/c1-4-13-10(2)9-11-5-7-12(14-3)8-6-11/h5-8,10,13H,4,9H2,1-3H3
  • Key:USBWBBAUWVUJLA-UHFFFAOYSA-N
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para-Methoxyethylamphetamine (PMEA) is a stimulant drug related to PMA.[1] PMEA reputedly produces similar effects to PMA, but is considerably less potent[2] and seems to have slightly less tendency to produce severe hyperthermia, at least at low doses. At higher doses however the side effects and danger of death approach those of PMA itself, and PMEA should still be considered a potentially dangerous drug. Investigation of a drug-related death in Japan in 2005 showed PMEA to be present in the body and was thought to be responsible for the death.[1][3]

It is formed as a minor metabolite by mebeverine, which can result in false positives on drug tests for "ecstasy".[1][4]

See also

References

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  1. ^ a b c Page Module:Citation/CS1/styles.css has no content."PMEA (пара-Метоксиэтиламфетамин)". АИПСИН (in русский). 1 January 2007. Retrieved 2 January 2026.
  2. ^ Page Module:Citation/CS1/styles.css has no content.Bustamante D, Díaz-Véliz G, Paeile C, Zapata-Torres G, Cassels BK (October 2004). "Analgesic and behavioral effects of amphetamine enantiomers, p-methoxyamphetamine and n-alkyl-p-methoxyamphetamine derivatives". Pharmacology, Biochemistry, and Behavior. 79 (2): 199–212. doi:10.1016/j.pbb.2004.06.017. PMID 15501295. S2CID 594578.
  3. ^ Page Module:Citation/CS1/styles.css has no content.Zaitsu K, Katagi M, Kamata T, Kamata H, Shima N, Tsuchihashi H, et al. (May 2008). "Determination of a newly encountered designer drug "p-methoxyethylamphetamine" and its metabolites in human urine and blood". Forensic Science International. 177 (1): 77–84. doi:10.1016/j.forsciint.2007.11.001. PMID 18155375.
  4. ^ Page Module:Citation/CS1/styles.css has no content."Мебеверин (Mebeverine)". АИПСИН (in русский). Retrieved 2 January 2026.

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