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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17526 - 17550 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000175263b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,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)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3414.2004
RI000175273b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#8JsmolC[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)[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3360.215
RI000175283b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#9JsmolC[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@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3336.8577
RI000175293b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,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]3OTMS568.3615Semi standard non polar3373.1875
RI000175303b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,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)[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3387.312
RI000175313b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,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)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3347.4333
RI000175323b,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,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)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3369.127
RI000175333b,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
RI000175343b,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
RI000175353b,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
RI000175363b,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
RI000175373b,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
RI000175383b,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
RI000175393b,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
RI000175403b,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
RI000175413b,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
RI000175423b,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
RI000175433b,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
RI000175443b,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
RI000175453b,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
RI000175463b,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
RI000175473b,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
RI000175483b,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
RI000175493b,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
RI000175503b,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
Displaying retention index compounds 17526 - 17550 of 1722868 in total