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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18776 - 18800 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001877617-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
RI0001877717-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
RI0001877817-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
RI000187793alpha,7alpha-Dihydroxycoprostanic acid,1TMS,isomer#1JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C)C(=O)OTMS506.3791Semi standard non polar3582.0186
RI000187803alpha,7alpha-Dihydroxycoprostanic acid,1TMS,isomer#2JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O)C(=O)OTMS506.3791Semi standard non polar3629.0012
RI000187813alpha,7alpha-Dihydroxycoprostanic acid,1TMS,isomer#3JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O)C(=O)O[Si](C)(C)CTMS506.3791Semi standard non polar3539.4375
RI000187823alpha,7alpha-Dihydroxycoprostanic acid,2TMS,isomer#1JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C)C(=O)OTMS578.4187Semi standard non polar3511.6135
RI000187833alpha,7alpha-Dihydroxycoprostanic acid,2TMS,isomer#2JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS578.4187Semi standard non polar3459.4053
RI000187843alpha,7alpha-Dihydroxycoprostanic acid,2TMS,isomer#3JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O)C(=O)O[Si](C)(C)CTMS578.4187Semi standard non polar3535.8684
RI000187853alpha,7alpha-Dihydroxycoprostanic acid,3TMS,isomer#1JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS650.4582Semi standard non polar3438.2026
RI000187863alpha,7alpha-Dihydroxycoprostanic acid,1TBDMS,isomer#1JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS548.4261Semi standard non polar3799.8787
RI000187873alpha,7alpha-Dihydroxycoprostanic acid,1TBDMS,isomer#2JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O)C(=O)OTBDMS548.4261Semi standard non polar3847.8384
RI000187883alpha,7alpha-Dihydroxycoprostanic acid,1TBDMS,isomer#3JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS548.4261Semi standard non polar3801.3135
RI000187893alpha,7alpha-Dihydroxycoprostanic acid,2TBDMS,isomer#1JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS662.5126Semi standard non polar3935.2852
RI000187903alpha,7alpha-Dihydroxycoprostanic acid,2TBDMS,isomer#2JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS662.5126Semi standard non polar3932.4133
RI000187913alpha,7alpha-Dihydroxycoprostanic acid,2TBDMS,isomer#3JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS662.5126Semi standard non polar4022.2166
RI000187923alpha,7alpha-Dihydroxycoprostanic acid,3TBDMS,isomer#1JsmolCC(CCC[C@@H](C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS776.599Semi standard non polar4139.293
RI000187933alpha,7alpha-Dihydroxycoprostanic acidJsmol[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C(O)=OUnderivatized434.3396Standard polar3711.5098
RI000187943alpha,7alpha-Dihydroxycoprostanic acidJsmol[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C(O)=OUnderivatized434.3396Standard non polar3535.337
RI000187953alpha,7alpha-Dihydroxycoprostanic acidJsmol[H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C(O)=OUnderivatized434.3396Semi standard non polar3716.613
RI000187962,4-Dihydroxybutanoic acid,1TMS,isomer#1JsmolC[Si](C)(C)OCCC(O)C(=O)OTMS192.0818Semi standard non polar1277.9636
RI000187972,4-Dihydroxybutanoic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC(CCO)C(=O)OTMS192.0818Semi standard non polar1286.2496
RI000187982,4-Dihydroxybutanoic acid,1TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C(O)CCOTMS192.0818Semi standard non polar1220.4576
RI000187992,4-Dihydroxybutanoic acid,2TMS,isomer#1JsmolC[Si](C)(C)OCCC(O[Si](C)(C)C)C(=O)OTMS264.1213Semi standard non polar1384.6646
RI000188002,4-Dihydroxybutanoic acid,2TMS,isomer#2JsmolC[Si](C)(C)OCCC(O)C(=O)O[Si](C)(C)CTMS264.1213Semi standard non polar1330.1002
Displaying retention index compounds 18776 - 18800 of 1722868 in total