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Displaying retention index compounds 17426 - 17450 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
1beta-Hydroxycholic acid,3TMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3386.4429
1beta-Hydroxycholic acid,3TMS,isomer#7JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)[C@H](O)C[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3426.8198
1beta-Hydroxycholic acid,3TMS,isomer#8JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS640.4011Semi standard non polar3389.524
1beta-Hydroxycholic acid,3TMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS640.4011Semi standard non polar3402.5068
1beta-Hydroxycholic acid,3TMS,isomer#10JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS640.4011Semi standard non polar3411.047
1beta-Hydroxycholic acid,4TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3385.1755
1beta-Hydroxycholic acid,4TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3388.476
1beta-Hydroxycholic acid,4TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3369.0195
1beta-Hydroxycholic acid,4TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3402.1165
1beta-Hydroxycholic acid,4TMS,isomer#5JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS712.4406Semi standard non polar3380.8987
1beta-Hydroxycholic acid,5TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS784.4801Semi standard non polar3392.2434
1beta-Hydroxycholic acid,1TBDMS,isomer#1JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS538.369Semi standard non polar3710.6453
1beta-Hydroxycholic acid,1TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)[C@H](O)C[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3768.6448
1beta-Hydroxycholic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C(C)(C)C)C[C@H]3OTBDMS538.369Semi standard non polar3719.4
1beta-Hydroxycholic acid,1TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3OTBDMS538.369Semi standard non polar3768.2883
1beta-Hydroxycholic acid,1TBDMS,isomer#5JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3OTBDMS538.369Semi standard non polar3787.605
1beta-Hydroxycholic acid,2TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3863.4895
1beta-Hydroxycholic acid,2TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3886.5647
1beta-Hydroxycholic acid,2TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]1O)C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3861.292
1beta-Hydroxycholic acid,2TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C(C)(C)C)C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3839.67
1beta-Hydroxycholic acid,2TBDMS,isomer#5JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)[C@H](O)C[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3938.586
1beta-Hydroxycholic acid,2TBDMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)[C@H](O)C[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3904.576
1beta-Hydroxycholic acid,2TBDMS,isomer#7JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C)C[C@H]3OTBDMS652.4554Semi standard non polar3862.268
1beta-Hydroxycholic acid,2TBDMS,isomer#8JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C(C)(C)C)C[C@H]3OTBDMS652.4554Semi standard non polar3887.9365
1beta-Hydroxycholic acid,2TBDMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C(C)(C)C)C[C@H]3OTBDMS652.4554Semi standard non polar3878.6816
Displaying retention index compounds 17426 - 17450 of 1722868 in total