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Displaying retention index compounds 20351 - 20375 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
18-Hydroxycortisol,2TMS,isomer#3JsmolC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C)(C(=O)CO)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS522.2833Semi standard non polar3400.1665
18-Hydroxycortisol,2TMS,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)[C@@]3(CO)C[C@H](O)[C@@H]12TMS522.2833Semi standard non polar3402.6694
18-Hydroxycortisol,2TMS,isomer#5JsmolC[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)C[C@H](O)[C@@H]12TMS522.2833Semi standard non polar3427.7346
18-Hydroxycortisol,2TMS,isomer#6JsmolC[C@]12CCC(=O)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)[C@@H]12TMS522.2833Semi standard non polar3432.2515
18-Hydroxycortisol,2TMS,isomer#7JsmolC[C@]12CCC(=O)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]12TMS522.2833Semi standard non polar3434.9277
18-Hydroxycortisol,2TMS,isomer#8JsmolC[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)[C@@H]12TMS522.2833Semi standard non polar3424.8726
18-Hydroxycortisol,2TMS,isomer#9JsmolC[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)[C@@H]12TMS522.2833Semi standard non polar3468.9507
18-Hydroxycortisol,2TMS,isomer#10JsmolC[C@]12CCC(=O)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]12TMS522.2833Semi standard non polar3355.8599
18-Hydroxycortisol,2TMS,isomer#11JsmolC[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)[C@@H]12TMS522.2833Semi standard non polar3357.729
18-Hydroxycortisol,2TMS,isomer#12JsmolC[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)[C@@H]12TMS522.2833Semi standard non polar3369.6663
18-Hydroxycortisol,2TMS,isomer#13JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@H]1[C@@H]3CC[C@@](O)(C(=O)CO)[C@@]3(CO)C[C@H](O[Si](C)(C)C)[C@@H]12TMS522.2833Semi standard non polar3346.4521
18-Hydroxycortisol,2TMS,isomer#14JsmolC[C@]12CCC(=O)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]12TMS522.2833Semi standard non polar3354.6611
18-Hydroxycortisol,2TMS,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)C[C@H](O)[C@@H]12TMS522.2833Semi standard non polar3355.556
18-Hydroxycortisol,3TMS,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)[C@@H]12TMS594.3228Semi standard non polar3489.8147
18-Hydroxycortisol,3TMS,isomer#2JsmolC[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)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3411.3042
18-Hydroxycortisol,3TMS,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(=O)CO[Si](C)(C)C)[C@@]3(CO)C[C@H](O)[C@@H]12TMS594.3228Semi standard non polar3395.6675
18-Hydroxycortisol,3TMS,isomer#4JsmolC[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)[C@@H]12TMS594.3228Semi standard non polar3432.5098
18-Hydroxycortisol,3TMS,isomer#5JsmolC[C@]12CCC(=O)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]12TMS594.3228Semi standard non polar3362.7583
18-Hydroxycortisol,3TMS,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(=O)CO)[C@@]3(CO[Si](C)(C)C)C[C@H](O)[C@@H]12TMS594.3228Semi standard non polar3370.022
18-Hydroxycortisol,3TMS,isomer#7JsmolC[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)[C@@H]12TMS594.3228Semi standard non polar3384.1016
18-Hydroxycortisol,3TMS,isomer#8JsmolC[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)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3295.3513
18-Hydroxycortisol,3TMS,isomer#9JsmolC[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)C[C@H](O[Si](C)(C)C)[C@@H]12TMS594.3228Semi standard non polar3306.0847
18-Hydroxycortisol,3TMS,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)[C@@H]12TMS594.3228Semi standard non polar3323.8245
18-Hydroxycortisol,3TMS,isomer#11JsmolC[C@]12CCC(=O)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]12TMS594.3228Semi standard non polar3320.9724
18-Hydroxycortisol,3TMS,isomer#12JsmolC[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)[C@@H]12TMS594.3228Semi standard non polar3318.3145
Displaying retention index compounds 20351 - 20375 of 1722868 in total