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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19701 - 19725 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000197013-Hydroxytetradecanedioic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)CC(O)CCCCCCCCCCC(=O)OTBDMS388.2645Semi standard non polar2616.4666
RI000197023-Hydroxytetradecanedioic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCCCCCCCCCC(CC(=O)O)O[Si](C)(C)C(C)(C)CTBDMS502.351Semi standard non polar2920.9944
RI000197033-Hydroxytetradecanedioic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)CC(CCCCCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)CTBDMS502.351Semi standard non polar2881.21
RI000197043-Hydroxytetradecanedioic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)CCCCCCCCCCC(O)CC(=O)O[Si](C)(C)C(C)(C)CTBDMS502.351Semi standard non polar2912.3364
RI000197053-Hydroxytetradecanedioic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCCCCCCCCCC(CC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS616.4375Semi standard non polar3153.0713
RI000197063-Hydroxytetradecanedioic acidJsmolOC(CCCCCCCCCCC(O)=O)CC(O)=OUnderivatized274.178Standard polar3564.359
RI000197073-Hydroxytetradecanedioic acidJsmolOC(CCCCCCCCCCC(O)=O)CC(O)=OUnderivatized274.178Standard non polar1987.0527
RI000197083-Hydroxytetradecanedioic acidJsmolOC(CCCCCCCCCCC(O)=O)CC(O)=OUnderivatized274.178Semi standard non polar2296.175
RI000197093b,7b,12a-Trihydroxy-5b-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
RI000197103b,7b,12a-Trihydroxy-5b-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
RI000197113b,7b,12a-Trihydroxy-5b-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
RI000197123b,7b,12a-Trihydroxy-5b-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
RI000197133b,7b,12a-Trihydroxy-5b-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
RI000197143b,7b,12a-Trihydroxy-5b-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
RI000197153b,7b,12a-Trihydroxy-5b-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
RI000197163b,7b,12a-Trihydroxy-5b-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
RI000197173b,7b,12a-Trihydroxy-5b-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
RI000197183b,7b,12a-Trihydroxy-5b-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
RI000197193b,7b,12a-Trihydroxy-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](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
RI000197203b,7b,12a-Trihydroxy-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](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
RI000197213b,7b,12a-Trihydroxy-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](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
RI000197223b,7b,12a-Trihydroxy-5b-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
RI000197233b,7b,12a-Trihydroxy-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](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
RI000197243b,7b,12a-Trihydroxy-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](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
RI000197253b,7b,12a-Trihydroxy-5b-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
Displaying retention index compounds 19701 - 19725 of 1722868 in total