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Displaying retention index compounds 17876 - 17900 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
18-Hydroxycorticosterone,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@]2(CO)[C@@H](C(=O)CO)CC[C@H]2[C@@H]2CCC3=CC(=O)CC[C@]3(C)[C@@H]12TBDMS476.2958Semi standard non polar3624.8994
18-Hydroxycorticosterone,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12COTBDMS476.2958Semi standard non polar3658.2568
18-Hydroxycorticosterone,1TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC(=CO)[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 polar3595.3655
18-Hydroxycorticosterone,1TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=O)CO)CC[C@@H]12TBDMS476.2958Semi standard non polar3584.0583
18-Hydroxycorticosterone,2TBDMS,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[Si](C)(C)C(C)(C)C)C[C@]12COTBDMS590.3823Semi standard non polar3857.206
18-Hydroxycorticosterone,2TBDMS,isomer#2JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS590.3823Semi standard non polar3892.7156
18-Hydroxycorticosterone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12COTBDMS590.3823Semi standard non polar3918.2212
18-Hydroxycorticosterone,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]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12COTBDMS590.3823Semi standard non polar3860.0503
18-Hydroxycorticosterone,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[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@]12COTBDMS590.3823Semi standard non polar3814.1309
18-Hydroxycorticosterone,2TBDMS,isomer#6JsmolCC(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)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)COTBDMS590.3823Semi standard non polar3753.654
18-Hydroxycorticosterone,2TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)C(C)(C)CTBDMS590.3823Semi standard non polar3863.569
18-Hydroxycorticosterone,2TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)COTBDMS590.3823Semi standard non polar3744.4106
18-Hydroxycorticosterone,2TBDMS,isomer#9JsmolCC(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(=CO)O[Si](C)(C)C(C)(C)CTBDMS590.3823Semi standard non polar3771.6868
18-Hydroxycorticosterone,2TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)OC(CO)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12COTBDMS590.3823Semi standard non polar3789.0405
18-Hydroxycorticosterone,2TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)OC(=CO)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12COTBDMS590.3823Semi standard non polar3712.873
18-Hydroxycorticosterone,2TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]2(CO)[C@@H](C(=O)CO)CC[C@@H]12TBDMS590.3823Semi standard non polar3683.5005
18-Hydroxycorticosterone,2TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)C(=C(CO)O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS590.3823Semi standard non polar3806.0132
18-Hydroxycorticosterone,2TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=CO)O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS590.3823Semi standard non polar3743.6406
18-Hydroxycorticosterone,3TBDMS,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[Si](C)(C)C(C)(C)C)C[C@]12CO[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar4012.0315
18-Hydroxycorticosterone,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12COTBDMS704.4688Semi standard non polar3990.5637
18-Hydroxycorticosterone,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]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12COTBDMS704.4688Semi standard non polar3961.4756
18-Hydroxycorticosterone,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[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@]12COTBDMS704.4688Semi standard non polar3876.6401
18-Hydroxycorticosterone,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CO[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar4077.5198
18-Hydroxycorticosterone,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CO[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar4062.639
18-Hydroxycorticosterone,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[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@]12CO[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar3981.6675
Displaying retention index compounds 17876 - 17900 of 1722868 in total