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Displaying retention index compounds 18026 - 18050 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
16-Oxoandrostenediol,1TMS,isomer#4JsmolC[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@@]43C)C1C=C(O[Si](C)(C)C)[C@@H]2OTMS376.2434Semi standard non polar2723.174
16-Oxoandrostenediol,2TMS,isomer#1JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1CC(=O)[C@@H]2O[Si](C)(C)CTMS448.2829Semi standard non polar2842.5452
16-Oxoandrostenediol,2TMS,isomer#2JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1CC(O[Si](C)(C)C)=C2OTMS448.2829Semi standard non polar2755.7903
16-Oxoandrostenediol,2TMS,isomer#3JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1C=C(O[Si](C)(C)C)[C@@H]2OTMS448.2829Semi standard non polar2731.166
16-Oxoandrostenediol,2TMS,isomer#4JsmolC[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@@]43C)C1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS448.2829Semi standard non polar2821.291
16-Oxoandrostenediol,2TMS,isomer#5JsmolC[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@@]43C)C1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS448.2829Semi standard non polar2793.5947
16-Oxoandrostenediol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(=CCC3C4CC(=O)[C@H](O)[C@@]4(C)CCC32)C1TBDMS418.2903Semi standard non polar3063.751
16-Oxoandrostenediol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1C(=O)CC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@@]21CTBDMS418.2903Semi standard non polar3103.362
16-Oxoandrostenediol,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C(O)[C@@]2(C)CCC3C(CC=C4C[C@@H](O)CC[C@@]43C)C2C1TBDMS418.2903Semi standard non polar3027.445
16-Oxoandrostenediol,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@]2(C)[C@H]1OTBDMS418.2903Semi standard non polar3010.5024
16-Oxoandrostenediol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(=CCC3C4CC(=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@]4(C)CCC32)C1TBDMS532.3768Semi standard non polar3339.2388
16-Oxoandrostenediol,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C(O)[C@@]2(C)CCC3C(CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@]43C)C2C1TBDMS532.3768Semi standard non polar3243.7383
16-Oxoandrostenediol,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC2C3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3CC[C@]2(C)[C@H]1OTBDMS532.3768Semi standard non polar3225.5547
16-Oxoandrostenediol,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CCC3C(CC=C4C[C@@H](O)CC[C@@]43C)C2C1TBDMS532.3768Semi standard non polar3352.1035
16-Oxoandrostenediol,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC1=CC2C3CC=C4C[C@@H](O)CC[C@]4(C)C3CC[C@]2(C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS532.3768Semi standard non polar3322.1877
16-OxoandrostenediolJsmolC[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@]34C)C1CC(=O)[C@@H]2OUnderivatized304.2038Standard polar2821.9963
16-Oxoandrostenediol,3TMS,isomer#1JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS520.3224Standard non polar2783.4219
16-Oxoandrostenediol,3TMS,isomer#2JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS520.3224Standard non polar2776.5903
16-Oxoandrostenediol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CCC3C(CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@]43C)C2C1TBDMS646.4633Standard non polar3381.6345
16-Oxoandrostenediol,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC2C3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3CC[C@]2(C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS646.4633Standard non polar3300.2668
16-OxoandrostenediolJsmolC[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@]34C)C1CC(=O)[C@@H]2OUnderivatized304.2038Standard non polar2636.0454
16-OxoandrostenediolJsmolC[C@]12CCC3C(CC=C4C[C@@H](O)CC[C@]34C)C1CC(=O)[C@@H]2OUnderivatized304.2038Semi standard non polar2701.5706
16-Oxoandrostenediol,3TMS,isomer#1JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS520.3224Semi standard non polar2800.1536
16-Oxoandrostenediol,3TMS,isomer#2JsmolC[C@]12CCC3C(CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)C1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS520.3224Semi standard non polar2781.4907
16-Oxoandrostenediol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CCC3C(CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@]43C)C2C1TBDMS646.4633Semi standard non polar3490.8196
Displaying retention index compounds 18026 - 18050 of 1722868 in total