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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21151 - 21175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0002115116,17-Epiestriol,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C[C@@H]12TBDMS516.3455Semi standard non polar3391.3965
RI0002115216,17-Epiestriol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]12TBDMS630.432Semi standard non polar3664.8398
RI0002115316,17-EpiestriolJsmol[H][C@@]12C[C@H](O)[C@@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized288.1725Standard polar3943.9067
RI0002115416,17-EpiestriolJsmol[H][C@@]12C[C@H](O)[C@@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized288.1725Standard non polar2917.311
RI0002115516,17-EpiestriolJsmol[H][C@@]12C[C@H](O)[C@@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized288.1725Semi standard non polar2941.945
RI000211563a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS480.3271Semi standard non polar3395.4204
RI000211573a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS480.3271Semi standard non polar3422.1797
RI000211583a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS480.3271Semi standard non polar3367.0347
RI000211593a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS480.3271Semi standard non polar3442.5322
RI000211603a,7b,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS552.3666Semi standard non polar3314.0388
RI000211613a,7b,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS552.3666Semi standard non polar3385.428
RI000211623a,7b,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3379.4204
RI000211633a,7b,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3337.051
RI000211643a,7b,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3372.2803
RI000211653a,7b,12a-Trihydroxy-5a-Cholanoic acid,2TMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS552.3666Semi standard non polar3336.18
RI000211663a,7b,12a-Trihydroxy-5a-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](O[Si](C)(C)C)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS624.4062Semi standard non polar3321.5957
RI000211673a,7b,12a-Trihydroxy-5a-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](O[Si](C)(C)C)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS624.4062Semi standard non polar3329.1436
RI000211683a,7b,12a-Trihydroxy-5a-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](O)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS624.4062Semi standard non polar3343.2441
RI000211693a,7b,12a-Trihydroxy-5a-Cholanoic acid,3TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS624.4062Semi standard non polar3336.5137
RI000211703a,7b,12a-Trihydroxy-5a-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](O[Si](C)(C)C)C[C@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS696.4457Semi standard non polar3341.1428
RI000211713a,7b,12a-Trihydroxy-5a-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](O)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3642.791
RI000211723a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS522.3741Semi standard non polar3636.3823
RI000211733a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3578.9705
RI000211743a,7b,12a-Trihydroxy-5a-Cholanoic acid,1TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3656.766
RI000211753a,7b,12a-Trihydroxy-5a-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](O[Si](C)(C)C(C)(C)C)C[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3752.9692
Displaying retention index compounds 21151 - 21175 of 1722868 in total