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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17951 - 17975 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001795118-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)CTBDMS818.5552Semi standard non polar4032.98
RI0001795218-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)CTBDMS818.5552Semi standard non polar3999.9585
RI0001795318-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 polar3653.119
RI0001795418-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 polar3664.5479
RI0001795518-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 polar3703.5066
RI0001795618-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 polar3735.6497
RI0001795718-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 polar3781.3748
RI0001795818-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 polar3718.2227
RI0001795918-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 polar3756.6514
RI0001796018-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 polar3715.9836
RI0001796118-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 polar3752.8047
RI0001796218-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 polar3571.3123
RI0001796318-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 polar3635.5957
RI0001796418-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 polar3914.758
RI0001796518-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 polar3935.7632
RI0001796618-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 polar3917.0337
RI0001796718-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 polar3958.2097
RI0001796818-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 polar4000.352
RI0001796918-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 polar3972.9731
RI0001797018-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 polar4010.6594
RI0001797118-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 polar3946.687
RI0001797218-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 polar3968.798
RI000179733a,4b,7a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTMS480.3271Semi standard non polar3432.1526
RI000179743a,4b,7a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS480.3271Semi standard non polar3387.878
RI000179753a,4b,7a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS480.3271Semi standard non polar3408.5144
Displaying retention index compounds 17951 - 17975 of 1722868 in total