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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17901 - 17925 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001790118-Hydroxycorticosterone,3TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[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@]12COTBDMS704.4688Semi standard non polar4007.9187
RI0001790218-Hydroxycorticosterone,3TBDMS,isomer#9JsmolCC(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[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12COTBDMS704.4688Semi standard non polar3962.8384
RI0001790318-Hydroxycorticosterone,3TBDMS,isomer#10JsmolCC(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]1CCC2=C(CO)O[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar3953.8196
RI0001790418-Hydroxycorticosterone,3TBDMS,isomer#11JsmolCC(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@@H]2C(=O)COTBDMS704.4688Semi standard non polar3836.6685
RI0001790518-Hydroxycorticosterone,3TBDMS,isomer#12JsmolCC(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(=CO)O[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar3888.8057
RI0001790618-Hydroxycorticosterone,3TBDMS,isomer#13JsmolCC(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]1CCC2=C(CO)O[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar3976.162
RI0001790718-Hydroxycorticosterone,3TBDMS,isomer#14JsmolCC(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(=CO)O[Si](C)(C)C(C)(C)CTBDMS704.4688Semi standard non polar3904.3884
RI0001790818-Hydroxycorticosterone,3TBDMS,isomer#15JsmolCC(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(=C(CO)O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS704.4688Semi standard non polar3864.6753
RI0001790918-Hydroxycorticosterone,3TBDMS,isomer#16JsmolCC(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(=CO)O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS704.4688Semi standard non polar3824.2402
RI0001791018-HydroxycorticosteroneJsmol[H][C@@]12CC[C@H](C(=O)CO)[C@@]1(CO)C[C@H](O)[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized362.2093Standard polar3689.9475
RI0001791118-Hydroxycorticosterone,4TMS,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(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3342.4353
RI0001791218-Hydroxycorticosterone,4TMS,isomer#2JsmolC[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[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3396.6594
RI0001791318-Hydroxycorticosterone,4TMS,isomer#3JsmolC[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[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3277.7097
RI0001791418-Hydroxycorticosterone,4TMS,isomer#4JsmolC[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[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3418.0364
RI0001791518-Hydroxycorticosterone,4TMS,isomer#5JsmolC[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[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3355.7249
RI0001791618-Hydroxycorticosterone,4TMS,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(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3485.459
RI0001791718-Hydroxycorticosterone,4TMS,isomer#7JsmolC[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[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3442.237
RI0001791818-Hydroxycorticosterone,4TMS,isomer#8JsmolC[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(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3394.0696
RI0001791918-Hydroxycorticosterone,4TMS,isomer#9JsmolC[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(=CO)O[Si](C)(C)C)CC[C@@H]12TMS650.3674Standard non polar3335.9307
RI0001792018-Hydroxycorticosterone,5TMS,isomer#1JsmolC[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(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS722.407Standard non polar3447.0747
RI0001792118-Hydroxycorticosterone,5TMS,isomer#2JsmolC[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(=CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS722.407Standard non polar3389.044
RI0001792218-Hydroxycorticosterone,4TBDMS,isomer#1JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS818.5552Standard non polar4199.6724
RI0001792318-Hydroxycorticosterone,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]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)CTBDMS818.5552Standard non polar4105.444
RI0001792418-Hydroxycorticosterone,4TBDMS,isomer#3JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS818.5552Standard non polar4118.052
RI0001792518-Hydroxycorticosterone,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[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@]12COTBDMS818.5552Standard non polar4117.48
Displaying retention index compounds 17901 - 17925 of 1722868 in total