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. 2017 Aug 4;36(1):51–60. doi: 10.1007/s11419-017-0378-5

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© The Author(s) 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Fig. 3 — Extracted ion chromatograms of a AB-FUBINACA 2-fluorobenzyl isomer at m/z 369.1721 (Δ = ±0.5 mDa), b EMB-FUBINACA at m/z 398.1874 (Δ = ±0.5 mDa), c 5F-EMB-FUBINACA at m/z 378.2187 (Δ = ±0.5 mDa), d APP-CHMINACA at m/z 405.2285 (Δ = ±0.5 mDa), and e MDMB-FUBICA at m/z 397.1922 (Δ = ±0.5 mDa), as a function of enantiomers, obtained by liquid chromatography–high-resolution mass spectrometry

Fig. 3 — Extracted ion chromatograms of a AB-FUBINACA 2-fluorobenzyl isomer at m/z 369.1721 (Δ = ±0.5 mDa), b EMB-FUBINACA at m/z 398.1874 (Δ = ±0.5 mDa), c 5F-EMB-FUBINACA at m/z 378.2187 (Δ = ±0.5 mDa), d APP-CHMINACA at m/z 405.2285 (Δ = ±0.5 mDa), and e MDMB-FUBICA at m/z 397.1922 (Δ = ±0.5 mDa), as a function of enantiomers, obtained by liquid chromatography–high-resolution mass spectrometry