Table 1 Analysis of monomeric catechins and oligomeric proanthocyanidins in leaf, stem and root of tea plant

From: Analysis of accumulation patterns and preliminary study on the condensation mechanism of proanthocyanidins in the tea plant [Camellia sinensis]

Peak/no.

tR (min)

[M – H]+/[M - H]− (m/z)

MS/MS (m/z)

UV λmax (nm)

identification

Leaf

Stem

Root

1

11.060

−/609.11332

−/125,305,423

272

GC-GC

+

+

—

2

14.166

−/305.06385

−/125, 165,179,219

275

gallocatechina

+

+

—

3

16.292

−/593.15606

−/289,305, 407,423

270

C-GC

+

+

—

4

16.765

−/425.03299

−/169,273

274

epiafzelechin gallate

+

+

—

5

18.587

−/305.06517

−/125,137,179, 219

275

epigallocatechina

+

+

—

6

20.343

−/761.12183

−/125,305,423,591

275

EGC-EGCG

+

+

—

7

20.630

−/289.06836

−/109,125,203,245

278

catechina

+

+

—

8

23.668

−/577.12389

−/125,289,407,425,451

273

EC-EC dimer

+

+

—

9

25.018

−/577.12284

−/125,289,407,425,451

273

Procyanidin B2a

+

+

++

10

26.621

−/745.12819

−/169,407,423,593

278

ECG-EGC

+

+

—

11

27.330

−/289.07148

−/109,125,203,245

278

epicatechina

+

+

+

12

30.993

−/457.09664

−/125,169,305

278

epigallocatechin gallatea

+

+

—

13

34.908

−/865.18022

−/125,407

278

EC-EC-EC PAs trimer

+

+

++

14

35.280

−/729.13377

−/125,245,407,577

278

EC-ECG

+

+

—

15

35.823

−/897.15219

−/−

278

ECG-EGCG or EGC-EGC-EC

+

+

—

16

36.596

−/273.07432

−/97,229

275

epiafzelechin

+

+

—

17

38.132

−/729.17308

−/289,407, 441,559

278

EC-ECG

+

+

—

18

50.200

−/441.10108

−/125,169, 271,289

278

epicatechin gallatea

+

+

—

19

52.896

−/1153

−/−

278

tetrameric procyanidin

—

—

+

20

57.201

−/1441

−/−

278

pentameric procyanidin

—

—

+

  1. Notes: aCompounds positively identified by direct comparison with the standard; other compounds were approximately identified qualitatively by comparing the wavelengths of maximum absorbance, protonated and deprotonated molecules ([M - H]+/[M - H]-) and fragment ions (PI/NI) from the published literature; tR (min) was the retention time in Figure 2. [M - H]+/[M - H]- (m/z) of compounds were detected by LC-TOF-MS; MS/MS (m/z) of compounds were detected by UPLC-TOF-MS/MS. —, not detected; +, detected; ++, signal was stronger.