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Displaying retention index compounds 17976 - 18000 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
3a,4b,7a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3OTMS480.3271Semi standard non polar3438.2698
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3OTMS552.3666Semi standard non polar3401.7554
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS552.3666Semi standard non polar3362.2493
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3339.7373
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3334.7026
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#5JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3321.56
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS552.3666Semi standard non polar3359.769
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS624.4062Semi standard non polar3342.3145
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS624.4062Semi standard non polar3330.5112
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS624.4062Semi standard non polar3306.9048
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[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)CTMS624.4062Semi standard non polar3328.5332
3a,4b,7a-Trihydroxy-5b-cholanoic acid,4TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[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)CTMS696.4457Semi standard non polar3332.612
3a,4b,7a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTBDMS522.3741Semi standard non polar3700.308
3a,4b,7a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS522.3741Semi standard non polar3607.8481
3a,4b,7a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS522.3741Semi standard non polar3633.882
3a,4b,7a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3OTBDMS522.3741Semi standard non polar3653.3938
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3OTBDMS636.4605Semi standard non polar3856.5952
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS636.4605Semi standard non polar3821.304
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS636.4605Semi standard non polar3797.7031
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS636.4605Semi standard non polar3756.988
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#5JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS636.4605Semi standard non polar3737.7598
3a,4b,7a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS636.4605Semi standard non polar3795.3887
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS750.547Semi standard non polar3984.7092
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS750.547Semi standard non polar3948.2986
3a,4b,7a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS750.547Semi standard non polar3921.835
Displaying retention index compounds 17976 - 18000 of 1722868 in total