N-Ethylbuphedrone

N-Ethylbuphedrone (also known as NEB) is a stimulant of the cathinone class that has been sold as a designer drug.[1][2][3][4] It is the β-ketone analogue of N,alpha-diethylphenylethylamine.

N-Ethylbuphedrone
Legal status
Legal status
  • DE: Anlage I (Authorized scientific use only)
  • UK: Class B
Identifiers
IUPAC name
  • 2-(Ethylamino)-1-phenylbutan-1-one
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC12H17NO
Molar mass191.274 g·mol−1
3D model (JSmol)
SMILES
  • CCNC(CC)C(=O)c1ccccc1
InChI
  • InChI=1S/C12H17NO/c1-3-11(13-4-2)12(14)10-8-6-5-7-9-10/h5-9,11,13H,3-4H2,1-2H3
  • Key:HEPVRDHGUWFXJS-UHFFFAOYSA-N

As of October 2015 NEB is a controlled substance in China.[5]

See also

References

  1. Lanza M, Acton WJ, Jürschik S, Sulzer P, Breiev K, Jordan A, et al. (September 2013). "Distinguishing two isomeric mephedrone substitutes with selective reagent ionisation mass spectrometry (SRI-MS)". Journal of Mass Spectrometry. 48 (9): 1015–1018. Bibcode:2013JMSp...48.1015L. doi:10.1002/jms.3253. PMID 24078242.
  2. Acton WJ, Lanza M, Agarwal B, Jürschik S, Sulzer P, Breiev K, et al. (March 2014). "Headspace analysis of new psychoactive substances using a Selective Reagent Ionisation-Time of Flight-Mass Spectrometer". International Journal of Mass Spectrometry. 360: 28–38. Bibcode:2014IJMSp.360...28A. doi:10.1016/j.ijms.2013.12.009. PMC 4375562. PMID 25844048.
  3. Uralets V, Rana S, Morgan S, Ross W (June 2014). "Testing for designer stimulants: metabolic profiles of 16 synthetic cathinones excreted free in human urine". Journal of Analytical Toxicology. 38 (5): 233–241. doi:10.1093/jat/bku021. PMID 24668489.
  4. Pieprzyca E, Skowronek R, Czekaj P (November 2021). "Toxicological Analysis of Cases of Mixed Poisonings with Synthetic Cathinones and other Drugs of Abuse". Journal of Analytical Toxicology. doi:10.1093/jat/bkab119. PMID 34849994.
  5. "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
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