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Displaying retention index compounds 7851 - 7875 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
EstradiolJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized272.1776Standard non polar2655.4216
EstradiolJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized272.1776Semi standard non polar2739.3735
Gentisic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OTMS226.0661Semi standard non polar1724.3672
Gentisic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC1=CC=C(O)C=C1C(=O)OTMS226.0661Semi standard non polar1744.3853
Gentisic acid,1TMS,isomer#3JsmolC[Si](C)(C)OC1=CC=C(O)C(C(=O)O)=C1TMS226.0661Semi standard non polar1736.0713
Gentisic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1OTMS298.1057Semi standard non polar1711.2635
Gentisic acid,2TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1=CC(O)=CC=C1O[Si](C)(C)CTMS298.1057Semi standard non polar1765.0758
Gentisic acid,2TMS,isomer#3JsmolC[Si](C)(C)OC1=CC=C(O[Si](C)(C)C)C(C(=O)O)=C1TMS298.1057Semi standard non polar1783.2026
Gentisic acid,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS370.1452Semi standard non polar1811.8302
Gentisic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1OTBDMS268.1131Semi standard non polar1986.1656
Gentisic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(O)C=C1C(=O)OTBDMS268.1131Semi standard non polar1995.7274
Gentisic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(O)C(C(=O)O)=C1TBDMS268.1131Semi standard non polar1995.802
Gentisic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS382.1996Semi standard non polar2180.3162
Gentisic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS382.1996Semi standard non polar2248.905
Gentisic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(O[Si](C)(C)C(C)(C)C)C(C(=O)O)=C1TBDMS382.1996Semi standard non polar2272.292
Gentisic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC=C1O[Si](C)(C)C(C)(C)CTBDMS496.286Semi standard non polar2451.4387
Gentisic acidJsmolOC(=O)C1=C(O)C=CC(O)=C1Underivatized154.0266Standard polar2929.7227
Gentisic acidJsmolOC(=O)C1=C(O)C=CC(O)=C1Underivatized154.0266Standard non polar1547.2797
Gentisic acidJsmolOC(=O)C1=C(O)C=CC(O)=C1Underivatized154.0266Semi standard non polar1504.9126
Estriol,1TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@@H](O[Si](C)(C)C)[C@@H]2OTMS360.2121Semi standard non polar2789.2388
Estriol,1TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@@H](O)[C@@H]2O[Si](C)(C)CTMS360.2121Semi standard non polar2794.0862
Estriol,1TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@@H](O)[C@@H]2OTMS360.2121Semi standard non polar2771.8933
Estriol,2TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@@H](O[Si](C)(C)C)[C@@H]2OTMS432.2516Semi standard non polar2842.8718
Estriol,2TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS432.2516Semi standard non polar2782.1436
Estriol,2TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@@H](O)[C@@H]2O[Si](C)(C)CTMS432.2516Semi standard non polar2842.8809
Displaying retention index compounds 7851 - 7875 of 1722868 in total