“…Consequently, their derivatives will exhibit corresponding characteristic aglycone ions by losing glycoside moiety, e.g., pentosyl (132 Da), glucosyl (162 Da), hexosyl (162 Da), rhamnosyl (146 Da) or rutinosyl (308 Da). Under negative ion mode, flavonoids will exhibit typical losses of CO, CO 2 , C 3 O 2 , and C 2 H 2 O. Flavones are more likely to produce ions at 1,3 A − and 1,3 B − , and flavonols are easier to get fragment ions at 1,2 A − and 1,2 B − [ 36 , 37 ]. In addition, when the glycosidic bond is bonded to the 3-OH position of aglycone, Y 0 − and [Y 0 − H] − fragments will occur, but the intensity of [Y 0 − H] − is customarily higher than that of Y 0 − [ 38 ].…”