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Displaying retention index compounds 20451 - 20475 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
18-Hydroxycortisol,4TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21CO[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4110.7114
18-Hydroxycortisol,4TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21COTBDMS834.5501Semi standard non polar4096.242
18-Hydroxycortisol,4TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21CO[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4168.277
18-Hydroxycortisol,4TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)OC[C@]12C[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@]2(O)C(=CO)O[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4040.5713
18-HydroxycortisolJsmol[H][C@@]12CC[C@@](O)(C(=O)CO)[C@@]1(CO)C[C@H](O)[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized378.2042Standard polar3366.5176
18-Hydroxycortisol,5TMS,isomer#1JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=O)CO[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard non polar3428.2964
18-Hydroxycortisol,5TMS,isomer#2JsmolC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard non polar3327.6003
18-Hydroxycortisol,5TMS,isomer#3JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O)[C@@H]12TMS738.4019Standard non polar3483.4949
18-Hydroxycortisol,5TMS,isomer#4JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard non polar3429.7102
18-Hydroxycortisol,5TMS,isomer#5JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard non polar3377.9622
18-Hydroxycortisol,5TMS,isomer#6JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard non polar3400.666
18-Hydroxycortisol,6TMS,isomer#1JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS810.4414Standard non polar3407.2905
18-HydroxycortisolJsmol[H][C@@]12CC[C@@](O)(C(=O)CO)[C@@]1(CO)C[C@H](O)[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized378.2042Standard non polar3269.7324
18-HydroxycortisolJsmol[H][C@@]12CC[C@@](O)(C(=O)CO)[C@@]1(CO)C[C@H](O)[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized378.2042Semi standard non polar3634.4497
18-Hydroxycortisol,5TMS,isomer#1JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=O)CO[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Semi standard non polar3287.8726
18-Hydroxycortisol,5TMS,isomer#2JsmolC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Semi standard non polar3296.5261
18-Hydroxycortisol,5TMS,isomer#3JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O)[C@@H]12TMS738.4019Semi standard non polar3276.613
18-Hydroxycortisol,5TMS,isomer#4JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Semi standard non polar3237.979
18-Hydroxycortisol,5TMS,isomer#5JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Semi standard non polar3224.3865
18-Hydroxycortisol,5TMS,isomer#6JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Semi standard non polar3171.1182
18-Hydroxycortisol,6TMS,isomer#1JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS810.4414Semi standard non polar3226.62
18-Hydroxycortisol,5TMS,isomer#1JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=O)CO[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard polar3585.4272
18-Hydroxycortisol,5TMS,isomer#2JsmolC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard polar3609.434
18-Hydroxycortisol,5TMS,isomer#3JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O)[C@@H]12TMS738.4019Standard polar3702.5085
18-Hydroxycortisol,5TMS,isomer#4JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS738.4019Standard polar3718.4526
Displaying retention index compounds 20451 - 20475 of 1722868 in total