Eutylone
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Formula | C13H17NO3 |
Molar mass | 235.283 g·mol−1 |
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β-Keto-1,3-benzodioxolyl-N-ethylbutanamine (Eutylone, bk-EBDB, N-Ethylbutylone) is a stimulant and empathogenic compound developed in the 1960s,[1][2] which has been reported as a novel designer drug,[3] first being reported to the EMCDDA in 2014 but becoming widespread internationally in 2019-2020 following bans on the related compound ephylone.[4][5][6]
Legal status
Sweden's public health agency suggested classifying Eutylone as a hazardous substance, on September 25, 2019.[7]
See also
- 5-Methylethylone
- Butylone
- Ethyl-J
- Ethylone
- Ephylone
- N-Ethylhexedrone
- N-Ethylhexylone
- N-Ethylheptylone
References
- ↑ Substituted phenyl-α-amino ketones. British Patent GB 1085135 (1969).
- ↑ Glatfelter GC, Walther D, Evans-Brown M, Baumann MH. Eutylone and Its Structural Isomers Interact with Monoamine Transporters and Induce Locomotor Stimulation. ACS Chem Neurosci. 2021 Apr 7;12(7):1170-1177. doi:10.1021/acschemneuro.0c00797 PMID 33689284
- ↑ "Eutylone". New Synthetic Drugs Database.
- ↑ Bade R, White JM, Nguyen L, Tscharke BJ, Mueller JF, O'Brien JW, et al. (August 2020). "Determining changes in new psychoactive substance use in Australia by wastewater analysis". The Science of the Total Environment. 731: 139209. Bibcode:2020ScTEn.731m9209B. doi:10.1016/j.scitotenv.2020.139209. PMID 32417485. S2CID 218680033.
- ↑ Krotulski AJ, Papsun DM, Chronister CW, Homan J, Crosby MM, Hoyer J, et al. (August 2020). "Eutylone Intoxications-An Emerging Synthetic Stimulant in Forensic Investigations". Journal of Analytical Toxicology. 45 (1): 8–20. doi:10.1093/jat/bkaa113. PMID 33325503.
- ↑ Chen HY, Chien WC, Huang MN, Fang CC, Weng TI (January 2021). "Analytically confirmed eutylone (bk-EBDB) exposure in emergency department patients". Clinical Toxicology. 59 (9): 846–848. doi:10.1080/15563650.2020.1868491. PMID 33448882. S2CID 231611658.
- ↑ "Tretton ämnen föreslås klassas som narkotika eller hälsofarlig vara" (in Swedish). Folkhälsomyndigheten. 25 September 2019.
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