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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19851 - 19875 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000198513a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#5JsmolC[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@@H](O[Si](C)(C)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)(C)C)[C@@]21CTBDMS766.5419Semi standard non polar3964.7705
RI000198523a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#6JsmolC[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@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS766.5419Semi standard non polar4058.6501
RI000198533a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#7JsmolC[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@@H](O[Si](C)(C)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)(C)C)[C@@]21CTBDMS766.5419Semi standard non polar3979.0557
RI000198543a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#8JsmolC[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@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS766.5419Semi standard non polar4021.8962
RI000198553a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS766.5419Semi standard non polar3979.6082
RI000198563a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#10JsmolC[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@@H](O[Si](C)(C)C(C)(C)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@@]21CTBDMS766.5419Semi standard non polar3961.0156
RI000198573a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,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@@H](O[Si](C)(C)C(C)(C)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@@]21CTBDMS880.6284Semi standard non polar4152.4575
RI000198583a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#2JsmolC[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@@H](O[Si](C)(C)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)(C)C)[C@@]21CTBDMS880.6284Semi standard non polar4168.4536
RI000198593a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#3JsmolC[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@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS880.6284Semi standard non polar4199.697
RI000198603a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#4JsmolC[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@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS880.6284Semi standard non polar4161.292
RI000198613a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#5JsmolC[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@@H](O[Si](C)(C)C(C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS880.6284Semi standard non polar4197.9062
RI000198623a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)[C@@H](O)[C@]2([H])C[C@H](O)CC[C@]12CUnderivatized424.2825Standard polar4156.788
RI000198633a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)[C@@H](O)[C@]2([H])C[C@H](O)CC[C@]12CUnderivatized424.2825Standard non polar3604.812
RI000198643a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)[C@@H](O)[C@]2([H])C[C@H](O)CC[C@]12CUnderivatized424.2825Semi standard non polar3817.7827
RI000198653,7-Dihydroxy-12-oxocholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3OTMS478.3115Semi standard non polar3458.3826
RI000198663,7-Dihydroxy-12-oxocholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS478.3115Semi standard non polar3385.2815
RI000198673,7-Dihydroxy-12-oxocholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS478.3115Semi standard non polar3454.657
RI000198683,7-Dihydroxy-12-oxocholanoic 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)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C)[C@@]21CTMS478.3115Semi standard non polar3327.4448
RI000198693,7-Dihydroxy-12-oxocholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS550.351Semi standard non polar3424.0674
RI000198703,7-Dihydroxy-12-oxocholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS550.351Semi standard non polar3342.021
RI000198713,7-Dihydroxy-12-oxocholanoic 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(O[Si](C)(C)C)[C@@]21CTMS550.351Semi standard non polar3309.1272
RI000198723,7-Dihydroxy-12-oxocholanoic acid,2TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS550.351Semi standard non polar3350.1204
RI000198733,7-Dihydroxy-12-oxocholanoic acid,2TMS,isomer#5JsmolC[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(O[Si](C)(C)C)[C@@]21CTMS550.351Semi standard non polar3244.7485
RI000198743,7-Dihydroxy-12-oxocholanoic acid,2TMS,isomer#6JsmolC[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(O[Si](C)(C)C)[C@@]21CTMS550.351Semi standard non polar3272.482
RI000198753,7-Dihydroxy-12-oxocholanoic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC(=O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS622.3905Semi standard non polar3344.7427
Displaying retention index compounds 19851 - 19875 of 1722868 in total