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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21276 - 21300 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000212763a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#4JsmolC[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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3337.7908
RI000212773a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,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)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3338.106
RI000212783a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#6JsmolC[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)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3311.5752
RI000212793a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#7JsmolC[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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3361.9565
RI000212803a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#8JsmolC[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)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3391.471
RI000212813a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3364.391
RI000212823a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#10JsmolC[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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3345.4282
RI000212833a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS712.4406Semi standard non polar3343.1074
RI000212843a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3378.3362
RI000212853a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3349.083
RI000212863a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#4JsmolC[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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3335.282
RI000212873a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#5JsmolC[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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3385.0103
RI000212883a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS784.4801Semi standard non polar3368.8489
RI000212893a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,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)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3762.326
RI000212903a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,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)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3726.956
RI000212913a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS538.369Semi standard non polar3657.1968
RI000212923a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,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)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3666.0513
RI000212933a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,isomer#5JsmolC[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)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3700.916
RI000212943a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3913.7134
RI000212953a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#2JsmolC[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)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3879.5518
RI000212963a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#3JsmolC[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)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3828.9836
RI000212973a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#4JsmolC[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)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3826.4907
RI000212983a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#5JsmolC[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)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3844.1658
RI000212993a,4b,7a,12a-Tetrahydroxy-5b-cholanoic 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)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3810.378
RI000213003a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#7JsmolC[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)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3849.2078
Displaying retention index compounds 21276 - 21300 of 1722868 in total