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Displaying retention index compounds 20376 - 20400 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
18-Hydroxycortisol,3TMS,isomer#13JsmolC[C@]12CCC(=O)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)[C@@H]12TMS594.3228Semi standard non polar3370.3687
18-Hydroxycortisol,3TMS,isomer#14JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=O)CO[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3312.6963
18-Hydroxycortisol,3TMS,isomer#15JsmolC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO[Si](C)(C)C)O[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3347.3784
18-Hydroxycortisol,3TMS,isomer#16JsmolC[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)C[C@H](O)[C@@H]12TMS594.3228Semi standard non polar3344.3164
18-Hydroxycortisol,3TMS,isomer#17JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=O)CO)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3238.5132
18-Hydroxycortisol,3TMS,isomer#18JsmolC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3242.861
18-Hydroxycortisol,3TMS,isomer#19JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O)[C@@H]12TMS594.3228Semi standard non polar3271.2844
18-Hydroxycortisol,3TMS,isomer#20JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO)O[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3226.1602
18-Hydroxycortisol,4TMS,isomer#1JsmolC[C@]12CCC(=O)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]12TMS666.3623Semi standard non polar3399.53
18-Hydroxycortisol,4TMS,isomer#2JsmolC[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)[C@@H]12TMS666.3623Semi standard non polar3366.1316
18-Hydroxycortisol,4TMS,isomer#3JsmolC[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)[C@@H]12TMS666.3623Semi standard non polar3392.5938
18-Hydroxycortisol,4TMS,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(=O)CO[Si](C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3314.1177
18-Hydroxycortisol,4TMS,isomer#5JsmolC[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)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3328.7698
18-Hydroxycortisol,4TMS,isomer#6JsmolC[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)[C@@H]12TMS666.3623Semi standard non polar3305.8474
18-Hydroxycortisol,4TMS,isomer#7JsmolC[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)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3280.3325
18-Hydroxycortisol,4TMS,isomer#8JsmolC[C@]12CCC(=O)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]12TMS666.3623Semi standard non polar3269.9658
18-Hydroxycortisol,4TMS,isomer#9JsmolC[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)[C@@H]12TMS666.3623Semi standard non polar3291.6377
18-Hydroxycortisol,4TMS,isomer#10JsmolC[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)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3235.4087
18-Hydroxycortisol,4TMS,isomer#11JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=O)CO[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3216.7827
18-Hydroxycortisol,4TMS,isomer#12JsmolC[C@]12CCC(=O)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]12TMS666.3623Semi standard non polar3245.7551
18-Hydroxycortisol,4TMS,isomer#13JsmolC[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)[C@@H]12TMS666.3623Semi standard non polar3239.7415
18-Hydroxycortisol,4TMS,isomer#14JsmolC[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)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3241.128
18-Hydroxycortisol,4TMS,isomer#15JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO)O[Si](C)(C)C)[C@@]3(CO[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]12TMS666.3623Semi standard non polar3164.8635
18-Hydroxycortisol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@]1(C(=O)CO)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21COTBDMS492.2907Semi standard non polar3756.498
18-Hydroxycortisol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21COTBDMS492.2907Semi standard non polar3793.0957
Displaying retention index compounds 20376 - 20400 of 1722868 in total