| SpectraBase Compound ID | 348rFSfkQ8B |
|---|---|
| InChI | InChI=1S/C75H126O6/c1-4-7-10-13-16-19-22-24-26-28-30-32-33-34-35-36-37-38-39-40-41-43-44-46-48-50-53-56-59-62-65-68-74(77)80-71-72(70-79-73(76)67-64-61-58-55-52-21-18-15-12-9-6-3)81-75(78)69-66-63-60-57-54-51-49-47-45-42-31-29-27-25-23-20-17-14-11-8-5-2/h7,10,16,19,24,26,29-32,34-35,37-38,40-41,44,46,50,53,72H,4-6,8-9,11-15,17-18,20-23,25,27-28,33,36,39,42-43,45,47-49,51-52,54-71H2,1-3H3/b10-7-,19-16-,26-24-,31-29-,32-30-,35-34-,38-37-,41-40-,46-44-,53-50- |
| InChIKey | AUSGXPXXBHPCJH-VUZNZCAVNA-N |
| Mol Weight | 1123.8 g/mol |
| Molecular Formula | C75H126O6 |
| Exact Mass | 1122.955442 g/mol |
Mass Spectrum (LC)
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| SpectraBase Spectrum ID | Co4sPE42Hbh |
|---|---|
| Name | TG 14:0_24:1_34:9 |
| Classification | Glycerolipids [GL] |
| Comments | Triacylglyceride |
| Copyright | Copyright © 2025 John Wiley & Sons, Inc. All Rights Reserved. |
| Exact Mass | 1122.955441771 u |
| Formula | C75H126O6 |
| InChI | InChI=1S/C75H126O6/c1-4-7-10-13-16-19-22-24-26-28-30-32-33-34-35-36-37-38-39-40-41-43-44-46-48-50-53-56-59-62-65-68-74(77)80-71-72(70-79-73(76)67-64-61-58-55-52-21-18-15-12-9-6-3)81-75(78)69-66-63-60-57-54-51-49-47-45-42-31-29-27-25-23-20-17-14-11-8-5-2/h7,10,16,19,24,26,29-32,34-35,37-38,40-41,44,46,50,53,72H,4-6,8-9,11-15,17-18,20-23,25,27-28,33,36,39,42-43,45,47-49,51-52,54-71H2,1-3H3/b10-7-,19-16-,26-24-,31-29-,32-30-,35-34-,38-37-,41-40-,46-44-,53-50- |
| InChIKey | AUSGXPXXBHPCJH-VUZNZCAVNA-N |
| Ion Polarity | P |
| 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+Na]+ |
| SMILES | CCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCCCCC\C=C/CCCCCCCCCC |
| Sample Comments | theoretical MS2 created from the information of SCIEX 5600 and 6600 with 45CE +-15CES |