N-Ethylbuphedrone

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N-Ethylbuphedrone
N-Ethylbuphedrone.svg
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

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.

Legal status[]

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. 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. doi:10.1016/j.ijms.2013.12.009. 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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