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Displaying retention index compounds 21826 - 21850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Adipic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCCCC(=O)OTMS218.0974Semi standard non polar1425.8909
Adipic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCCCC(=O)O[Si](C)(C)CTMS290.137Semi standard non polar1512.1201
Adipic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCCCC(=O)OTBDMS260.1444Semi standard non polar1680.5669
Adipic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCCCC(=O)O[Si](C)(C)C(C)(C)CTBDMS374.2309Semi standard non polar1966.5647
Adipic acidJsmolOC(=O)CCCCC(O)=OUnderivatized146.0579Standard polar2157.3394
Adipic acidJsmolOC(=O)CCCCC(O)=OUnderivatized146.0579Standard non polar1136.3252
Adipic acidJsmolOC(=O)CCCCC(O)=OUnderivatized146.0579Semi standard non polar1369.9872
5a-Tetrahydrocorticosterone,1TMS,isomer#1JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS422.2852Semi standard non polar3123.7078
5a-Tetrahydrocorticosterone,1TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)COTMS422.2852Semi standard non polar3062.4902
5a-Tetrahydrocorticosterone,1TMS,isomer#3JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)COTMS422.2852Semi standard non polar3126.9385
5a-Tetrahydrocorticosterone,1TMS,isomer#4JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS422.2852Semi standard non polar3094.7007
5a-Tetrahydrocorticosterone,1TMS,isomer#5JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS422.2852Semi standard non polar3070.6309
5a-Tetrahydrocorticosterone,2TMS,isomer#1JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS494.3248Semi standard non polar3021.3162
5a-Tetrahydrocorticosterone,2TMS,isomer#2JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS494.3248Semi standard non polar3103.3186
5a-Tetrahydrocorticosterone,2TMS,isomer#3JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS494.3248Semi standard non polar3119.815
5a-Tetrahydrocorticosterone,2TMS,isomer#4JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS494.3248Semi standard non polar3101.76
5a-Tetrahydrocorticosterone,2TMS,isomer#5JsmolC[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@@]43C)[C@@H]1CC[C@@H]2C(=O)COTMS494.3248Semi standard non polar3004.3115
5a-Tetrahydrocorticosterone,2TMS,isomer#6JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS494.3248Semi standard non polar3018.212
5a-Tetrahydrocorticosterone,2TMS,isomer#7JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS494.3248Semi standard non polar2983.187
5a-Tetrahydrocorticosterone,2TMS,isomer#8JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS494.3248Semi standard non polar3106.857
5a-Tetrahydrocorticosterone,2TMS,isomer#9JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS494.3248Semi standard non polar3045.1929
5a-Tetrahydrocorticosterone,3TMS,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@@]43C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS566.3643Semi standard non polar3001.9082
5a-Tetrahydrocorticosterone,3TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3017.4521
5a-Tetrahydrocorticosterone,3TMS,isomer#3JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@H]4C[C@H](O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3034.392
5a-Tetrahydrocorticosterone,3TMS,isomer#4JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@H]4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3103.0684
Displaying retention index compounds 21826 - 21850 of 1722868 in total