RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Displaying retention index compounds 21851 - 21875 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
5a-Tetrahydrocorticosterone,3TMS,isomer#5JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3097.9797
5a-Tetrahydrocorticosterone,3TMS,isomer#6JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS566.3643Semi standard non polar3000.276
5a-Tetrahydrocorticosterone,3TMS,isomer#7JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS566.3643Semi standard non polar2965.7844
5a-Tetrahydrocorticosterone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS464.3322Semi standard non polar3416.346
5a-Tetrahydrocorticosterone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@]2(C)[C@@H](C(=O)CO)CC[C@H]2[C@@H]2CC[C@H]3C[C@H](O)CC[C@]3(C)[C@@H]12TBDMS464.3322Semi standard non polar3315.1218
5a-Tetrahydrocorticosterone,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CC[C@H](C(=O)CO)[C@@]4(C)C[C@H](O)[C@@H]32)C1TBDMS464.3322Semi standard non polar3378.7063
5a-Tetrahydrocorticosterone,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS464.3322Semi standard non polar3382.4646
5a-Tetrahydrocorticosterone,1TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS464.3322Semi standard non polar3319.3154
5a-Tetrahydrocorticosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS578.4187Semi standard non polar3620.8882
5a-Tetrahydrocorticosterone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS578.4187Semi standard non polar3520.11
5a-Tetrahydrocorticosterone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS578.4187Semi standard non polar3652.5994
5a-Tetrahydrocorticosterone,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS578.4187Semi standard non polar3565.2153
5a-Tetrahydrocorticosterone,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@]2(C)[C@@H](C(=O)CO)CC[C@H]2[C@@H]2CC[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]3(C)[C@@H]12TBDMS578.4187Semi standard non polar3460.7664
5a-Tetrahydrocorticosterone,2TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS578.4187Semi standard non polar3501.1396
5a-Tetrahydrocorticosterone,2TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS578.4187Semi standard non polar3423.457
5a-Tetrahydrocorticosterone,2TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS578.4187Semi standard non polar3620.1145
5a-Tetrahydrocorticosterone,2TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS578.4187Semi standard non polar3524.2766
5a-Tetrahydrocorticosterone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](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@]12CTBDMS692.5051Semi standard non polar3686.1074
5a-Tetrahydrocorticosterone,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS692.5051Semi standard non polar3847.5686
5a-Tetrahydrocorticosterone,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS692.5051Semi standard non polar3770.952
5a-Tetrahydrocorticosterone,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS692.5051Semi standard non polar3690.8052
5a-Tetrahydrocorticosterone,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS692.5051Semi standard non polar3678.7893
5a-Tetrahydrocorticosterone,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](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@]12CTBDMS692.5051Semi standard non polar3663.2947
5a-Tetrahydrocorticosterone,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](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@]12CTBDMS692.5051Semi standard non polar3618.6401
5a-TetrahydrocorticosteroneJsmol[H][C@@]12CC[C@H](C(=O)CO)[C@@]1(C)C[C@H](O)[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@H](O)CC[C@]12CUnderivatized350.2457Standard polar2505.8977
Displaying retention index compounds 21851 - 21875 of 1722868 in total