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Displaying retention index compounds 18701 - 18725 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
(2S,3R)-3-Hydroxy-2-methylbutanoic acidJsmolC[C@@H](O)[C@H](C)C(O)=OUnderivatized118.063Semi standard non polar1040.2854
16a-Hydroxydehydroisoandrosterone,1TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@]43C)[C@@H]1C[C@@H](O[Si](C)(C)C)C2=OTMS376.2434Semi standard non polar2802.305
16a-Hydroxydehydroisoandrosterone,1TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1C[C@@H](O)C2=OTMS376.2434Semi standard non polar2769.5457
16a-Hydroxydehydroisoandrosterone,1TMS,isomer#3JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@]43C)[C@@H]1CC(O)=C2O[Si](C)(C)CTMS376.2434Semi standard non polar2759.1052
16a-Hydroxydehydroisoandrosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1C[C@@H](O[Si](C)(C)C)C2=OTMS448.2829Semi standard non polar2828.383
16a-Hydroxydehydroisoandrosterone,2TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@]43C)[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS448.2829Semi standard non polar2833.7637
16a-Hydroxydehydroisoandrosterone,2TMS,isomer#3JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC(O)=C2O[Si](C)(C)CTMS448.2829Semi standard non polar2765.2012
16a-Hydroxydehydroisoandrosterone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1C[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]2(C)C1=OTBDMS418.2903Semi standard non polar3073.1123
16a-Hydroxydehydroisoandrosterone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4C[C@@H](O)C(=O)[C@@]4(C)CC[C@@H]32)C1TBDMS418.2903Semi standard non polar3042.5715
16a-Hydroxydehydroisoandrosterone,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C(O)C[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS418.2903Semi standard non polar3042.9072
16a-Hydroxydehydroisoandrosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)C(=O)[C@@]4(C)CC[C@@H]32)C1TBDMS532.3768Semi standard non polar3359.602
16a-Hydroxydehydroisoandrosterone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@H]3[C@@H](CC=C4C[C@@H](O)CC[C@@]43C)[C@@H]2C1TBDMS532.3768Semi standard non polar3384.4893
16a-Hydroxydehydroisoandrosterone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C(O)C[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS532.3768Semi standard non polar3308.7676
16a-HydroxydehydroisoandrosteroneJsmol[H][C@@]12C[C@@H](O)C(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12CUnderivatized304.2038Standard polar2709.4602
16a-Hydroxydehydroisoandrosterone,3TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS520.3224Standard non polar2812.9424
16a-Hydroxydehydroisoandrosterone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@]43C)[C@@H]2C1TBDMS646.4633Standard non polar3382.2966
16a-HydroxydehydroisoandrosteroneJsmol[H][C@@]12C[C@@H](O)C(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12CUnderivatized304.2038Standard non polar2602.4563
16a-HydroxydehydroisoandrosteroneJsmol[H][C@@]12C[C@@H](O)C(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12CUnderivatized304.2038Semi standard non polar2716.8223
16a-Hydroxydehydroisoandrosterone,3TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS520.3224Semi standard non polar2825.8792
16a-Hydroxydehydroisoandrosterone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@]43C)[C@@H]2C1TBDMS646.4633Semi standard non polar3579.3643
16a-Hydroxydehydroisoandrosterone,3TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS520.3224Standard polar3081.8206
16a-Hydroxydehydroisoandrosterone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@H]3[C@@H](CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@]43C)[C@@H]2C1TBDMS646.4633Standard polar3374.327
3b,15b,17a-Trihydroxy-pregnenone,1TMS,isomer#1JsmolCC[C@@]1(O)C[C@@H](O[Si](C)(C)C)[C@H]2[C@@H]3CCC4CC(O)=CC(=O)[C@]4(C)[C@H]3CC[C@@]21CTMS420.2696Semi standard non polar3032.8086
3b,15b,17a-Trihydroxy-pregnenone,1TMS,isomer#2JsmolCC[C@@]1(O[Si](C)(C)C)C[C@@H](O)[C@H]2[C@@H]3CCC4CC(O)=CC(=O)[C@]4(C)[C@H]3CC[C@@]21CTMS420.2696Semi standard non polar3053.73
3b,15b,17a-Trihydroxy-pregnenone,1TMS,isomer#3JsmolCC[C@@]1(O)C[C@@H](O)[C@H]2[C@@H]3CCC4CC(O[Si](C)(C)C)=CC(=O)[C@]4(C)[C@H]3CC[C@@]21CTMS420.2696Semi standard non polar3081.711
Displaying retention index compounds 18701 - 18725 of 1722868 in total