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. 2021 Aug 20;10(8):1312. doi: 10.3390/antiox10081312

Table 3.

Phenolic compounds putatively identified in the fresh, oven-dried, and freeze-dried extracts from S. ramosissima.

Peak tr (min.) a λmax (nm) Precursor Ion
[M-H] m/z
Product Ion
m/z
Tentative Identification Extracts b References
1 7.14 301 215 191, 179 quinic acid derivative FH [69,70]
2 8.58 275 133 133, 115, 113, 71 malic acid OD [70,71,87]
3 9.36 260 191 111, 87, 85 quinic acid FH, OD, FD [69,70]
4 29.03 300,325 353 191, 179, 135 neochlorogenic acid FH, OD, FD [71,72,88]
5 32.77 280,317 285 153, 152, 108, 109 protocatechuic-acid-arabinoside FH [69,89]
6 33.83 275 305 305, 225, 97, 59 gallocatechin FH, FD [90]
7 34.85 284,318 355 137, 93 salicylic acid derivative FH, OD [91]
8 35.38 281,332 355 273, 253, 191, 173 hydrocaffeoylquinic acid FD [15]
9 35.63 274, 310 163 119 p-coumaric acid FH, FD [78,92]
10 36.58 300,327 353 191, 179 chlorogenic acid * FH, OD, FD [71,72,88]
11 38.63 267,345 193 134, 161, 178 ferulic acid FH, OD, FD [69,88]
12 40.26 269,332 355 193, 178, 161, 134 ferulic acid-glucoside FH, OD, FD [69,87,88]
13 40.69 268,337 303 303, 97 dihydroquercetin (taxifolin) FH, OD, FD [93,94]
14 42.40 312 337 191, 173, 163 p-coumaroylquinic acid (isomer 1) FH, OD, FD [95,96]
15 43.88 - 371 249, 121, 113 saccharide FH, OD, FD [97]
16 44.60 311 337 215, 191, 173, 163 p-coumaroylquinic acid (isomer 2) OD [95,96]
17 45.49 256,336 319 295, 294, 187, 97 n.i. FH, FD
18 46.34 270,354 609 301, 151 quercetin-rhamnosyl-hexoside FH, OD, FD [98]
19 46.50 300 449 253, 118 p-coumaric acid benzyl ester derivative OD [99]
20 47.10 274,335 519 315, 301, 300, 299 quercetin-methyl-ether derivative (isomer 1) FH, FD [100]
21 47.64 255,352 463 463, 301, 300 quercetin 3-glucoside* FH, OD, FD [15,71,78]
22 48.18 284,329 517 517, 355, 179, 135 caffeic acid-glucuronide-glucoside (isomer 1) FD [88,101]
23 48.62 251,358 549 505, 463, 301, 300 quercetin-malonyglucoside FH, OD, FD [71,84,102]
24 49.37 302,332 515 353, 325, 191, 179 3,5-dicaffeoylquinic acid FH, OD, FD [70,96]
25 50.38 302,329 515 479, 353, 191, 179, 173 4,5-dicaffeoylquinic acid FH, OD, FD [70,78,96]
26 50.94 266,331 517 355, 179, 135 caffeoyl-hydrocaffeoylquinic acid FH, OD, FD [15]
27 51.66 268,346 519 519, 350, 315, 300 quercetin-methyl-ether derivative (isomer 2) FH, OD, FD [100]
28 52.33 328 563 503, 473, 459, 443, 383, 353 apigenin-6-arabinosyl-8-glucoside (isoschaftoside) FH [94,103]
29 59.90 287 953 953, 767, 575, 285 kaempferol derivative FH, FD [71,104]

a Mean value for retention times obtained from the analysis of fresh, oven-dried and freeze-dried S. ramosissima extracts. b Extracts: FH, fresh; OD, oven-dried; and FD, freeze-dried. * Phenolic compound identified with standard. n.i. means not identified.The phenolic composition of S. ramosissima samples was in compliance with the literature [15,105]. The occurrence of quinic acid, p-coumaric and ferulic acid, 3-O-caffeoylquinic acid, and quercetin-3-O-glucoside in aqueous extracts [105], and quercetin-glucoside, hydrocaffeoylquinic, caffeoylquinic, dihydrocaffeoyl quinic, caffeoyl-hydrocaffeoylquinic acid, and dicaffeoyl quinic acids in an ethyl acetate fraction isolated from S. ramosissima were already described [15]. Quercetin-glucoside, caffeoylquinic acid, and other hydroxycinnamic acid derivatives were also reported in other Salicornia species [19,106,107].