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

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 13476 - 13500 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00013476Tetrahydrocorticosterone,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
RI00013477Tetrahydrocorticosterone,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@]2(C)[C@H]3[C@@H](O)C[C@]4(C)[C@@H](C(=O)CO)CC[C@H]4[C@@H]3CC[C@@H]2C1TBDMS464.3322Semi standard non polar3378.7063
RI00013478Tetrahydrocorticosterone,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
RI00013479Tetrahydrocorticosterone,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
RI00013480Tetrahydrocorticosterone,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
RI00013481Tetrahydrocorticosterone,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
RI00013482Tetrahydrocorticosterone,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
RI00013483Tetrahydrocorticosterone,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
RI00013484Tetrahydrocorticosterone,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
RI00013485Tetrahydrocorticosterone,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
RI00013486Tetrahydrocorticosterone,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
RI00013487Tetrahydrocorticosterone,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
RI00013488Tetrahydrocorticosterone,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
RI00013489Tetrahydrocorticosterone,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
RI00013490Tetrahydrocorticosterone,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
RI00013491Tetrahydrocorticosterone,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
RI00013492Tetrahydrocorticosterone,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
RI00013493Tetrahydrocorticosterone,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
RI00013494Tetrahydrocorticosterone,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
RI00013495Tetrahydrocorticosterone,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
RI00013496TetrahydrocorticosteroneJsmol[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
RI00013497Tetrahydrocorticosterone,4TMS,isomer#1JsmolC[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@]34C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Standard non polar3183.8916
RI00013498Tetrahydrocorticosterone,4TMS,isomer#2JsmolC[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@]34C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS638.4038Standard non polar3083.4695
RI00013499Tetrahydrocorticosterone,4TBDMS,isomer#1JsmolCC(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[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Standard non polar3984.0261
RI00013500Tetrahydrocorticosterone,4TBDMS,isomer#2JsmolCC(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[Si](C)(C)C(C)(C)C)C[C@]12CTBDMS806.5916Standard non polar3858.9104
Displaying retention index compounds 13476 - 13500 of 1722868 in total