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. 2021 Feb 16;10(2):304. doi: 10.3390/antiox10020304

Table 1.

UHPLC-HRMS/MS data of detected compounds in “Ramata di Montoro” (M) and “Rossa di Tropea” (T) onion-dried skin extracts.

Compound Molecular Formula RT(UV)
(min)
Measured (m/z)
[M − H] (m/z)
Error (ppm) Product Ion
MS/MS
Measured (m/z)
[M + H]+ (m/z)
Error (ppm) Product Ion
MS/MS
Onion Cultivar
1 Protocatechuic acid C7H6O4 1.0 153.1235 1.6 / / / / M, T
2 2-(3,4-Dihydroxybenzoyl)-2,4,6-trihydroxy-3(2H)-benzofuranone (Qox) C15H10O8 6.0 317.0303 3.3 299; 191; 207; 273 / / / M, T
3 Cyanidin 3-glucoside (CyG) C21H21O11 6.2 / / / 449.1077 −0.3 287 T
4 Quercetin dihexoside C27H30O17 6.6 625.1405 0.9 463; 301 627.1557 0.3 465; 303 M, T
5 Cyanidin 3-laminaribioside C27H31O16 7.0 / / / 611.1609 0.3 287 T
6 Quercetin 3,4’-diglucoside (QdG) C27H30O17 7.4 625.1410 −0.3 463; 301 627.1559 0.6 465; 303 M, T
7 Isorhamnetin dihexoside C28H32O17 8.2 639.1571 0.04 477; 315 641.1716 0.5 317; 479 M, T
8 Cyanidin 3-malonilglucoside C24H23O14 10.5 / / / 535.1084 0.3 287 T
9 Cyanidin 3-malonillaminaribioside C30H33O19 11.4 / / / 697.1609 0.2 287 T
10 Quercetin-3-glucoside C21H20O12 11.6 463.0874 0.6 301 465.1027 −0.2 303 M, T
11 Quercetin-4’-glucoside (QG) C21H20O12 12.4 463.0873 0.8 301 465.1025 −0.6 303 M, T
12 Isorhamnetin-O-hexoside C22H22O12 13.3 477.1031 0.7 315 479.1186 0.5 317 M, T
13 Quercetin (Q) C15H10O7 14.3 301.0350 0.6 179; 151 303.0496 −1.0 285; 257; 229; M, T
14 Protocatecoyl quercetin C22H14O11 14.8 453.0454 0.4 299 455.0610 0.1 437; 301; M, T
15 Protocatecoyl quercetin C22H14O11 14.9 453.0455 0.6 299 455.00609 0.1 437; 301; M, T
16 Kaempferol C15H10O6 16.3 285.0399 2.1 / 287.0548 −0.6 / M, T
17 Isorhamnetin C16H12O7 16.9 315.0503 1.2 300; 257 317.0656 0.0 302, 285; 257 M, T
18 Quercetin dimer 4’-glucoside (Q2Ga) C36H28O19 17.2 763.1140 −0.2 611; 449; 765.1300 0.3 603; 451 M, T
19 Quercetin dimer 4’-glucoside (Q2Gb) C36H28O19 18.3 763.1139 −0.3 611; 600; 299 765.1298 0.1 603; 585 M, T
20 Quercetin dimer hexoside C36H28O19 18.8 763.1139 −0.2 611; 600; 299 765.1299 0.2 603; 585 M, T
21 Quercetin dimer (Q2) C30H18O14 19.4 601.0617 0.8 449; 299 603.0772 0.5 585; 313; 303 M, T
22 Quercetin trimer (Q3) C45H26O21 20.8 901.0881 −0.2 299; 449; 599; 601 903.1044 0.5 885; 751; 585; 613 M, T