For citations & permissions, please see: Citations & Permissions - Wiley Science Solutions*

*Links on SpectraBase are not permalinks.
CL 32:5_44:7
SpectraBase Compound ID HSXak1Vhwd1
InChI InChI=1S/C85H142O17P2/c1-5-9-13-17-21-25-29-32-35-37-39-41-44-47-51-54-58-62-66-70-83(88)96-76-81(102-85(90)72-68-64-60-56-52-48-45-42-40-38-36-33-30-26-22-18-14-10-6-2)78-100-104(93,94)98-74-79(86)73-97-103(91,92)99-77-80(101-84(89)71-67-63-59-55-49-28-24-20-16-12-8-4)75-95-82(87)69-65-61-57-53-50-46-43-34-31-27-23-19-15-11-7-3/h9,11,13,15,21-23,25-27,32-36,39-43,50,53,61,65,79-81,86H,5-8,10,12,14,16-20,24,28-31,37-38,44-49,51-52,54-60,62-64,66-78H2,1-4H3,(H,91,92)(H,93,94)/b13-9-,15-11-,25-21-,26-22-,27-23-,35-32-,36-33-,41-39-,42-40-,43-34-,53-50-,65-61-
InChIKey HZUGOEDXYXUHSV-WNDOAVCXNA-N
Mol Weight 1498.0 g/mol
Molecular Formula C85H142O17P2
Exact Mass 1496.972227 g/mol

Mass Spectrum (LC)

Mass Spectrum (LC)

View the Full Spectrum for FREE!

The full spectrum can only be viewed using a FREE account.

SpectraBase Spectrum ID 1CjKVxwkN2Q
Name CL 14:0_18:5_22:3_22:4
Classification Glycerophospholipids [GP]
Comments Cardiolipin
Copyright Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved.
Exact Mass 1496.972227091 u
Formula C85H142O17P2
InChI InChI=1S/C85H142O17P2/c1-5-9-13-17-21-25-29-32-35-37-39-41-44-47-51-54-58-62-66-70-83(88)96-76-81(102-85(90)72-68-64-60-56-52-48-45-42-40-38-36-33-30-26-22-18-14-10-6-2)78-100-104(93,94)98-74-79(86)73-97-103(91,92)99-77-80(101-84(89)71-67-63-59-55-49-28-24-20-16-12-8-4)75-95-82(87)69-65-61-57-53-50-46-43-34-31-27-23-19-15-11-7-3/h9,11,13,15,21-23,25-27,32-36,39-43,50,53,61,65,79-81,86H,5-8,10,12,14,16-20,24,28-31,37-38,44-49,51-52,54-60,62-64,66-78H2,1-4H3,(H,91,92)(H,93,94)/b13-9-,15-11-,25-21-,26-22-,27-23-,35-32-,36-33-,41-39-,42-40-,43-34-,53-50-,65-61-
InChIKey HZUGOEDXYXUHSV-WNDOAVCXNA-N
Ion Polarity N
Literature Reference Tsugawa, H.; Ikeda, K.; Takahashi, M.; Satoh, A.; Mori, Y.; Uchino, H.; Okahashi, N.; Yamada, Y.; Tada, I.; Bonini, P.; Higashi, Y.; Okazaki, Y.; Zhou, Z.; Zhu, Z.-J.; Koelmel, J.; Cajka, T.; Fiehn, O.; Saito, K.; Arita, M.; Arita, M. A Lipidome Atlas in MS-DIAL 4. Nature Biotechnology 2020, 38 (10), 1159–1163.
Literature Reference DOI https://doi.org/10.1038/s41587-020-0531-2
Precursor Ion [M-H]-
SMILES CCCCCCCCCCCCCC(=O)OC(COC(=O)C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)COP(O)(=O)OCC(O)COP(O)(=O)OCC(COC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCC\C=C/C\C=C/C\C=C/CCCCC
Sample Comments theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES