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Displaying retention index compounds 17851 - 17875 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
18-Hydroxycorticosterone,2TMS,isomer#8JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO)CC[C@@H]12TMS506.2884Semi standard non polar3274.6997
18-Hydroxycorticosterone,2TMS,isomer#9JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3289.4683
18-Hydroxycorticosterone,2TMS,isomer#10JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3273.313
18-Hydroxycorticosterone,2TMS,isomer#11JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=O)CO)CC[C@@H]12TMS506.2884Semi standard non polar3240.469
18-Hydroxycorticosterone,2TMS,isomer#12JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3255.3352
18-Hydroxycorticosterone,2TMS,isomer#13JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3289.5957
18-Hydroxycorticosterone,2TMS,isomer#14JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3250.8105
18-Hydroxycorticosterone,3TMS,isomer#1JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3278.8647
18-Hydroxycorticosterone,3TMS,isomer#2JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)C(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3268.5356
18-Hydroxycorticosterone,3TMS,isomer#3JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3216.5413
18-Hydroxycorticosterone,3TMS,isomer#4JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3295.3186
18-Hydroxycorticosterone,3TMS,isomer#5JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)C(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3316.7812
18-Hydroxycorticosterone,3TMS,isomer#6JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3248.8481
18-Hydroxycorticosterone,3TMS,isomer#7JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3352.677
18-Hydroxycorticosterone,3TMS,isomer#8JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)C(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3267.6482
18-Hydroxycorticosterone,3TMS,isomer#9JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3271.2834
18-Hydroxycorticosterone,3TMS,isomer#10JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO[Si](C)(C)C)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3230.8645
18-Hydroxycorticosterone,3TMS,isomer#11JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO)CC[C@@H]12TMS578.3279Semi standard non polar3183.503
18-Hydroxycorticosterone,3TMS,isomer#12JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3173.4468
18-Hydroxycorticosterone,3TMS,isomer#13JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3264.8384
18-Hydroxycorticosterone,3TMS,isomer#14JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3197.0127
18-Hydroxycorticosterone,3TMS,isomer#15JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3193.9685
18-Hydroxycorticosterone,3TMS,isomer#16JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS578.3279Semi standard non polar3134.2114
18-Hydroxycorticosterone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12COTBDMS476.2958Semi standard non polar3716.3774
18-Hydroxycorticosterone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)COTBDMS476.2958Semi standard non polar3633.2722
Displaying retention index compounds 17851 - 17875 of 1722868 in total