RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17751 - 17775 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000177512b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#5JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3464.4634
RI000177522b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3497.4187
RI000177532b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#7JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3451.0815
RI000177542b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#8JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3472.456
RI000177552b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#9JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3457.6638
RI000177562b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#10JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3461.399
RI000177572b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS712.4406Semi standard non polar3394.9097
RI000177582b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3424.3315
RI000177592b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3458.5962
RI000177602b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3465.727
RI000177612b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TMS,isomer#5JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS712.4406Semi standard non polar3409.3372
RI000177622b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,5TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS784.4801Semi standard non polar3419.9592
RI000177632b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3837.5107
RI000177642b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3876.9106
RI000177652b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3850.2583
RI000177662b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS538.369Semi standard non polar3852.603
RI000177672b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TBDMS,isomer#5JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3OTBDMS538.369Semi standard non polar3868.7488
RI000177682b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3990.839
RI000177692b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3949.1108
RI000177702b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3986.628
RI000177712b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3983.6665
RI000177722b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#5JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar4034.026
RI000177732b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3996.3604
RI000177742b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#7JsmolC[C@@H](CCC(=O)O)C1CCC2C3C(C[C@H](O)[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3986.85
RI000177752b,3a,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#8JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3C(C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)C[C@H](O)[C@@H](O)C[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar4032.6956
Displaying retention index compounds 17751 - 17775 of 1722868 in total