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. 2017 Jan 9;54(1):114–129. doi: 10.1007/s13197-016-2442-2

Table 1.

Groups of phenolic compounds identified by LC/MS in the analyzed puree, juices and smoothies

Compounds R t (min) λmax (nm) MS [M-H] (m/z) MS/MS [M-H] (m/z)b SCP AJ SCP [%] ÷ AJ [%] PJ SCP [%] ÷ PJ [%]
80÷20 50÷50 20÷80 80÷20 50÷50 20÷80
Anthocyanins
 Cyjanidyno-3-O-sophoroside 3.428 515 611.162+a 287.055 x nd x x x nd x x x
 Cyjanidyno-3-O-glucosylo-rutinoside 3.583 517 757.219+ 611.162/287.055 x nd x x x nd x x x
 Cyjanidyno-3-O-glucoside 3.774 516 449.109+ 287.055 x nd x x nd nd x x nd 
 Cyjanidyno-3-O-rutinoside 3.929 517 595.166+ 287.055 x nd x x x nd x x x
 Peonidyno-3-O-rutinoside 4.513 517 609.183+ 463.785/301.884 x nd x x nd nd x x nd 
Hydroxycinnamic acids
 Neochlorogenic acid 3.081 323 353.094 191.057 x nd x x x x x x x
 3-p-coumarylquinc acid 3.619 310 337.091 191.057/183.087 x x x x x nd x x x
 Chlorogenic acid 4.135 324 353.094 191.057 x x x x x x x x x
 4-O-caffeoylquinic acid 5.221 320 353.086 191.057 x x x x x x x x x
 3,5-dicaffeoylquinic acid 7.650 320 515.140 353.069/191.055 x nd nd nd nd nd x x x
Flavan-3-ols
 (+)-catechin 3.360 278 289.073 x nd x x x x x x x
 Procyanidin B1 3.670 278 577.133 289.073 nd nd nd nd nd x nd nd x
 (−)-epicatechin 4.823 278 289.073 nd x x x x x nd x x
 Procyanidin B2 6.649 278 577.133 289.073 nd x nd nd x x nd nd x
Flavonols
 Quercetin-3-O-rutinoside-glucoside 5.530 337 771.196 301.028 x nd x x x nd x x x
 Quercetin-3-O-rutinoside 6.494 353 609.148 577.241/301.029 x x x x x x x x x
 Quercetin-3-O-galactoside 6.737 350 463.091 301.036 x nd x nd nd nd x x x
 Kaempferol-3-O-rutinoside 7.017 352 593.151 285.039 x x x x x x x x x
 Isorhamnetin-3-O-rutinoside 7.148 352 623.156 315.047 x nd x x x nd x x x
 Isorhamnetin-3-glucoside-7-rhamnoside 7.303 350 623.156 315.047 nd nd nd nd nd nd nd nd nd
Dihydrochalcone
 Phloretin-2`xylo-glucoside 7.701 280 567.169 273.076 nd x nd x x nd nd nd nd
Compounds QJ SCP [%] ÷ QJ [%] FQJ SCP [%] ÷ FQJ [%]
80÷20 50÷50 20÷80 80÷20 50÷50 20÷80
Anthocyanins
 Cyjanidyno-3-O-sophoroside nd x x x nd x x x
 Cyjanidyno-3-O-glucosylo-rutinoside nd x x x nd x x x
 Cyjanidyno-3-O-glucoside nd x x x nd x x x
 Cyjanidyno-3-O-rutinoside nd x x x nd x x x
 Peonidyno-3-O-rutinoside nd x x x nd x x x
Hydroxycinnamic acids
 Neochlorogenic acid x x x x nd x x x
 3-p-coumarylquinc acid x x x x x x x x
 Chlorogenic acid x x x x x x x x
 4-O-caffeoylquinic acid x x x x x x x x
 3,5-dicaffeoylquinic acid x x x x x x x x
Flavan-3-ols
 (+)-catechin x x x x x x x x
 Procyanidin B1 x nd x x x x x x
 (−)-epicatechin x nd nd x x x x x
 Procyanidin B2 x nd nd x x x x x
Flavonols
 Quercetin-3-O-rutinoside-glucoside nd x x nd nd x x x
 Quercetin-3-O-rutinoside nd x x x nd x x x
 Quercetin-3-O-galactoside nd x x x x x x x
 Kaempferol-3-O-rutinoside nd x x x x x x x
 Isorhamnetin-3-O-rutinoside nd x x x x x x x
 Isorhamnetin-3-glucoside-7-rhamnoside nd nd nd nd x x x x
Dihydrochalcone
 Phloretin-2`xylo-glucoside nd nd nd nd nd nd nd nd

SCP sour cherry puree, AJ apple juice, PJ pear juice, QJ quince juice, FQJ flowering quince juice. [M + H] (m/z) for anthocyanins were obtained in the positive ion mode. The m/z values of the predominant ions are given in bold type