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. 2016 Jun 13;34:372–385. doi: 10.1007/s11419-016-0324-y

Table 2.

Chromatographic data for the synthetic cathinones present in the different samples using the Chiralpak® AS-H chiral stationary phase

Cathinone Sample k 1 k 2 α Rs
Flephedrone Blast A2 1.93 3.72 1.93 6.33
Pentedrone Standard 0.82 1.42 1.79 8.63
Kick A12 0.79 1.47 1.87 9.30
Bloom A1 0.75 1.45 1.95 10.52
4-MEC Standard 1.16 1.47 1.27 2.54
Blow A11 1.09 1.47 1.35 3.24
Blow A10 1.08 1.48 1.37 3.38
3,4-DMMC Cyclop A5 1.89 6.77 3.59 10.34
Crabby A4 1.86 6.75 3.62 9.46
Methedrone Bliss A7 6.08 10.39 1.71 6.79
Bliss A6 6.01 10.32 1.72 6.79
Bloom A1 5.70 9.79 1.72 5.39
Buphedrone Kick A13 0.94 2.23 2.36 7.54
Charlie A9 1.02 2.25 2.21 4.10
Charlie A8 1.01 2.24 2.21 6.14
Rush A3 0.97 2.27 2.34 7.62
Methylone Standard 7.58 13.45 1.77 7.39
Bliss A14 7.56 13.53 1.79 7.47
Ethcathinone Bloom A1 0.95 1.24 1.30 2.61
Charlie A9 1.02 1.27 1.25 1.25
Charlie A8 1.01 1.26 1.24 1.24

Mobile phase conditions: n-hexane (Hex)/2-propanol (2-PrOH)/triethylamine (TEA) (97:3:0.1,v/v/v), flow rate 0.5 mL/min

k retention factor, α separation factor, Rs resolution factor