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Displaying retention index compounds 20426 - 20450 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
18-Hydroxycortisol,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)CO)[C@@]3(CO)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]12TBDMS720.4637Semi standard non polar3974.331
18-Hydroxycortisol,3TBDMS,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@@]2(O[Si](C)(C)C(C)(C)C)C(=O)COTBDMS720.4637Semi standard non polar4085.0981
18-Hydroxycortisol,3TBDMS,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@@]2(O[Si](C)(C)C(C)(C)C)C(=CO)O[Si](C)(C)C(C)(C)CTBDMS720.4637Semi standard non polar4114.714
18-Hydroxycortisol,3TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C(C)(C)C)(C(=CO)O[Si](C)(C)C(C)(C)C)[C@@]3(CO)C[C@H](O)[C@@H]12TBDMS720.4637Semi standard non polar4041.1614
18-Hydroxycortisol,3TBDMS,isomer#11JsmolCC(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[Si](C)(C)C(C)(C)C)C[C@@]21CO[Si](C)(C)C(C)(C)CTBDMS720.4637Semi standard non polar4045.934
18-Hydroxycortisol,3TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O)CC[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@@]21COTBDMS720.4637Semi standard non polar4032.1243
18-Hydroxycortisol,3TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O)CC[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@@]21COTBDMS720.4637Semi standard non polar3995.9304
18-Hydroxycortisol,3TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21CO[Si](C)(C)C(C)(C)CTBDMS720.4637Semi standard non polar4088.6416
18-Hydroxycortisol,3TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O)CC[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@@]21CO[Si](C)(C)C(C)(C)CTBDMS720.4637Semi standard non polar4063.0088
18-Hydroxycortisol,3TBDMS,isomer#16JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O)CC[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@@]21COTBDMS720.4637Semi standard non polar4048.5935
18-Hydroxycortisol,3TBDMS,isomer#17JsmolCC(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[Si](C)(C)C(C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@]2(O)C(=O)COTBDMS720.4637Semi standard non polar3914.0315
18-Hydroxycortisol,3TBDMS,isomer#18JsmolCC(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@@]2(O)C(=CO)O[Si](C)(C)C(C)(C)CTBDMS720.4637Semi standard non polar3951.3157
18-Hydroxycortisol,3TBDMS,isomer#19JsmolCC(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@@]2(O)C(=CO)O[Si](C)(C)C(C)(C)CTBDMS720.4637Semi standard non polar3983.0254
18-Hydroxycortisol,3TBDMS,isomer#20JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@@](O)(C(=CO)O[Si](C)(C)C(C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]12TBDMS720.4637Semi standard non polar3921.0654
18-Hydroxycortisol,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O[Si](C)(C)C(C)(C)C)CC[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@@]21CO[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4303.405
18-Hydroxycortisol,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O[Si](C)(C)C(C)(C)C)CC[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@@]21COTBDMS834.5501Semi standard non polar4214.9487
18-Hydroxycortisol,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O[Si](C)(C)C(C)(C)C)CC[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@@]21COTBDMS834.5501Semi standard non polar4175.534
18-Hydroxycortisol,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@@]21CO[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4335.695
18-Hydroxycortisol,4TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@]1(O[Si](C)(C)C(C)(C)C)CC[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@@]21CO[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4304.6143
18-Hydroxycortisol,4TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O[Si](C)(C)C(C)(C)C)CC[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@@]21COTBDMS834.5501Semi standard non polar4241.1973
18-Hydroxycortisol,4TBDMS,isomer#7JsmolCC(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[Si](C)(C)C(C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@]2(O[Si](C)(C)C(C)(C)C)C(=O)COTBDMS834.5501Semi standard non polar4120.801
18-Hydroxycortisol,4TBDMS,isomer#8JsmolCC(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@@]2(O[Si](C)(C)C(C)(C)C)C(=CO)O[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4203.1885
18-Hydroxycortisol,4TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@@](O[Si](C)(C)C(C)(C)C)(C(=CO)O[Si](C)(C)C(C)(C)C)[C@@]3(CO)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]12TBDMS834.5501Semi standard non polar4106.748
18-Hydroxycortisol,4TBDMS,isomer#10JsmolCC(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@@]2(O[Si](C)(C)C(C)(C)C)C(=CO)O[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4210.3125
18-Hydroxycortisol,4TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@]1(O)CC[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@@]21CO[Si](C)(C)C(C)(C)CTBDMS834.5501Semi standard non polar4154.171
Displaying retention index compounds 20426 - 20450 of 1722868 in total