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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17926 - 17950 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001792618-Hydroxycorticosterone,4TBDMS,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]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 polar4022.5938
RI0001792718-Hydroxycorticosterone,4TBDMS,isomer#6JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS818.5552Standard non polar4200.863
RI0001792818-Hydroxycorticosterone,4TBDMS,isomer#7JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS818.5552Standard non polar4122.7974
RI0001792918-Hydroxycorticosterone,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[Si](C)(C)C(C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)C(C)(C)CTBDMS818.5552Standard non polar4066.2427
RI0001793018-Hydroxycorticosterone,4TBDMS,isomer#9JsmolCC(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(=CO)O[Si](C)(C)C(C)(C)CTBDMS818.5552Standard non polar4010.2854
RI0001793118-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 non polar3189.5483
RI0001793218-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@]12CUnderivatized362.2093Semi standard non polar3625.6582
RI0001793318-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]12TMS650.3674Semi standard non polar3252.6606
RI0001793418-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]12TMS650.3674Semi standard non polar3195.361
RI0001793518-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]12TMS650.3674Semi standard non polar3284.8481
RI0001793618-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]12TMS650.3674Semi standard non polar3170.5164
RI0001793718-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]12TMS650.3674Semi standard non polar3195.1243
RI0001793818-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]12TMS650.3674Semi standard non polar3219.6973
RI0001793918-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]12TMS650.3674Semi standard non polar3240.7263
RI0001794018-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]12TMS650.3674Semi standard non polar3161.2844
RI0001794118-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]12TMS650.3674Semi standard non polar3116.466
RI0001794218-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]12TMS722.407Semi standard non polar3164.051
RI0001794318-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]12TMS722.407Semi standard non polar3205.5435
RI0001794418-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)CTBDMS818.5552Semi standard non polar4155.6846
RI0001794518-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)CTBDMS818.5552Semi standard non polar4163.162
RI0001794618-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)CTBDMS818.5552Semi standard non polar4071.5945
RI0001794718-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@]12COTBDMS818.5552Semi standard non polar4035.7664
RI0001794818-Hydroxycorticosterone,4TBDMS,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]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@]12COTBDMS818.5552Semi standard non polar4047.077
RI0001794918-Hydroxycorticosterone,4TBDMS,isomer#6JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS818.5552Semi standard non polar4161.6885
RI0001795018-Hydroxycorticosterone,4TBDMS,isomer#7JsmolCC(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@]12CO[Si](C)(C)C(C)(C)CTBDMS818.5552Semi standard non polar4134.061
Displaying retention index compounds 17926 - 17950 of 1722868 in total