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Table 2 Molecular ion peaks obtained from infusion experiments of mixtures of synthetic analogues of piperine (M 2–18 ) and Piperine (M 1 ) and the product ions obtained during the MS/MS (MS 2 ) measurements of the cross dimeric ionic peaks

From: Concentration dependent Electrospray Ionisation Mass Spectrometry and Tandem Mass Spectrometry (MS/MS ) studies on (E,E)-1-[5-(1,3-benzodioxol-5yl)-1-oxo-2,4-pentadienyl]- piperidine (Piperine) and its analogues

Mixture of 1 with

Molecular ion (m/z) peaks formed from the mixtures of Piperine (M1) with its synthetic analogues(M2-18)

Precursor ion (m/z) selected for MS2studies

Product ions(m/z) formed from the fragmentation of the parent ions

[2Mn + Na]+n =1,2,38

2

593 [2 M1 + Na]+, 601[2 M2+ Na]+ , 597[M1 + M2 + Na]+

597

312, 308.

3

593 [2 M1 + Na]+, 565[2 M 3+ Na]+ , 579[M1 + M3 + Na]+

579

294, 308

4

593 [2 M 1 + Na]+, 517[2 M 4+ Na]+ , 555[M1 + M4 + Na]+

555

270, 308

5

593 2[M 1 + Na]+, 597[2 M 5+ Na]+ , 595[M1+ M5 + Na]+

595

310, 308

6

593 [2 M 1 + Na]+, 565[2 M6+ Na]+ , 579[M1 + M6 + Na]+

579

294, 308

7

593 [2 M 1 + Na]+, 621[2 M 7 + Na]+ , 607[M1 + M7 + Na]+

607

322, 308

8

593 [2 M 1 + Na]+ or [2 M8 + Na]+

593

308

9

593 [2 M 1 + Na]+, 605[2 M 9+ Na]+ , 599[M1 + M9 + Na]+

599

314,, 308

10

593 [2 M 1 + Na]+, 541[2 M 10+ Na]+ , 567[M1+ M10 + Na]+

567

282, 308

11

593 [2 M1 + Na]+, 569[2 M 11+ Na]+ , 581[M1 + M11 + Na]+

581

296, 308

12

593 [2 M 1 + Na]+, 605[2 M12 + Na]+ , 599[M1 + M12 + Na]+

599

314, 308

13

593 [2 M 1 + Na]+, 625[2 M 13+ Na]+ , 609[M1 + M 13 + Na]+

609

324, 308

14

593 [2 M1 + Na]+, 577[2 M14+ Na]+ , 585[M1 + M14 + Na]+

585

300, 308

15

593 [2 M1 + Na]+, 633[2 M15+ Na]+ , 613[M1+ M15 + Na]+

613

328, 308

16

593 [2 M1 + Na]+, 573[2 M16+ Na]+ , 583[M1 + M16 + Na]+

583

298, 308

17

593 [2 M1 + Na]+, 565[2 M17+ Na]+ , 579[M1+ M17 + Na]+

579

294, 308

18

593 [2 M 1 + Na]+, 685[2 M 18+ Na]+ , 639[M1 + M18 + Na]+

639

354, 308