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Displaying retention index compounds 18926 - 18950 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Epiandrosterone,1TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CCC4C[C@@H](O)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)CTMS362.2641Semi standard non polar2578.9614
Epiandrosterone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]32)C1TBDMS404.3111Semi standard non polar2818.4294
Epiandrosterone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS404.3111Semi standard non polar2849.604
EpiandrosteroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2C[C@@H](O)CC[C@]12CUnderivatized290.2246Standard polar2280.7334
Epiandrosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)CTMS434.3036Standard non polar2511.5203
Epiandrosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS518.3975Standard non polar2771.4558
EpiandrosteroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2C[C@@H](O)CC[C@]12CUnderivatized290.2246Standard non polar2441.4653
EpiandrosteroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2C[C@@H](O)CC[C@]12CUnderivatized290.2246Semi standard non polar2637.905
Epiandrosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)CTMS434.3036Semi standard non polar2602.6362
Epiandrosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS518.3975Semi standard non polar3134.5164
Epiandrosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)CTMS434.3036Standard polar2920.417
Epiandrosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS518.3975Standard polar3166.998
2-Deoxyribonic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC[C@@H](O)[C@@H](O)CC(=O)OTMS222.0924Semi standard non polar1459.54
2-Deoxyribonic acid,1TMS,isomer#2JsmolC[Si](C)(C)O[C@H](CO)[C@@H](O)CC(=O)OTMS222.0924Semi standard non polar1463.09
2-Deoxyribonic acid,1TMS,isomer#3JsmolC[Si](C)(C)O[C@@H](CC(=O)O)[C@H](O)COTMS222.0924Semi standard non polar1468.6759
2-Deoxyribonic acid,1TMS,isomer#4JsmolC[Si](C)(C)OC(=O)C[C@H](O)[C@H](O)COTMS222.0924Semi standard non polar1491.4973
2-Deoxyribonic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC[C@@H](O[Si](C)(C)C)[C@@H](O)CC(=O)OTMS294.1319Semi standard non polar1543.7672
2-Deoxyribonic acid,2TMS,isomer#2JsmolC[Si](C)(C)OC[C@@H](O)[C@H](CC(=O)O)O[Si](C)(C)CTMS294.1319Semi standard non polar1541.5162
2-Deoxyribonic acid,2TMS,isomer#3JsmolC[Si](C)(C)OC[C@@H](O)[C@@H](O)CC(=O)O[Si](C)(C)CTMS294.1319Semi standard non polar1568.956
2-Deoxyribonic acid,2TMS,isomer#4JsmolC[Si](C)(C)O[C@@H](CC(=O)O)[C@@H](CO)O[Si](C)(C)CTMS294.1319Semi standard non polar1539.4587
2-Deoxyribonic acid,2TMS,isomer#5JsmolC[Si](C)(C)OC(=O)C[C@H](O)[C@@H](CO)O[Si](C)(C)CTMS294.1319Semi standard non polar1546.4847
2-Deoxyribonic acid,2TMS,isomer#6JsmolC[Si](C)(C)OC(=O)C[C@H](O[Si](C)(C)C)[C@H](O)COTMS294.1319Semi standard non polar1538.4624
2-Deoxyribonic acid,3TMS,isomer#1JsmolC[Si](C)(C)OC[C@@H](O[Si](C)(C)C)[C@H](CC(=O)O)O[Si](C)(C)CTMS366.1714Semi standard non polar1629.6592
2-Deoxyribonic acid,3TMS,isomer#2JsmolC[Si](C)(C)OC[C@@H](O[Si](C)(C)C)[C@@H](O)CC(=O)O[Si](C)(C)CTMS366.1714Semi standard non polar1635.5728
2-Deoxyribonic acid,3TMS,isomer#3JsmolC[Si](C)(C)OC[C@@H](O)[C@H](CC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS366.1714Semi standard non polar1624.6655
Displaying retention index compounds 18926 - 18950 of 1722868 in total