Eutylone

Source: Wikipedia, the free encyclopedia.
Eutylone
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • (±)-1-(1,3-benzodioxol-5-yl)-2-(ethylamino)butan-1-one
JSmol)
  • CCC(C(=O)C1=CC2=C(C=C1)OCO2)NCC
  • InChI=1S/C13H17NO3/c1-3-10(14-4-2)13(15)9-5-6-11-12(7-9)17-8-16-11/h5-7,10,14H,3-4,8H2,1-2H3 ☒N
  • Key:YERSNXHEOIYEGX-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Eutylone (also known as β-keto-1,3-benzodioxolyl-N-ethylbutanamine, bk-EBDB, and N-ethylbutylone) is a

ephylone.[6][7][8][9] It is not a natural, but a synthetic cathinone.[9] In 2021, eutylone was the most common cathinone identified by the Drug Enforcement Administration in the United States.[10]

Legal status

Sweden's public health agency suggested classifying eutylone as a hazardous substance, on September 25, 2019.[11]

In the United States Eutylone is considered a schedule 1 controlled substance as a positional isomer of Pentylone.[12][13]

See also

References

  1. ^ Anvisa (2023-07-24). "RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-07-25). Archived from the original on 2023-08-27. Retrieved 2023-08-27.
  2. ^ "Substance Details Eutylone". Retrieved 2024-01-22.
  3. ^ GB 108513, "Aryl-α-aminoketone derivatives", published 1967-09-27, assigned to Boehringer Ingelheim 
  4. S2CID 232192447
    .
  5. ^ "Eutylone". New Synthetic Drugs Database. 12 November 2023.
  6. S2CID 218680033
    .
  7. .
  8. .
  9. ^ .
  10. ^ "Emerging Threat Report" (PDF). 2021.
  11. ^ "Tretton ämnen föreslås klassas som narkotika eller hälsofarlig vara" (in Swedish). Folkhälsomyndigheten. 25 September 2019. Archived from the original on 31 October 2019. Retrieved 11 November 2019.
  12. ^ Lists of: Scheduling Actions. Controlled Substances. Regulated Chemicals
  13. ^ "Federal Register :: Request Access".