RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18651 - 18675 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000186513b,12a-Dihydroxy-5a-cholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS464.3322Semi standard non polar3366.5308
RI000186523b,12a-Dihydroxy-5a-cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS464.3322Semi standard non polar3376.256
RI000186533b,12a-Dihydroxy-5a-cholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS536.3717Semi standard non polar3307.6038
RI000186543b,12a-Dihydroxy-5a-cholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS536.3717Semi standard non polar3285.4995
RI000186553b,12a-Dihydroxy-5a-cholanoic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS536.3717Semi standard non polar3308.271
RI000186563b,12a-Dihydroxy-5a-cholanoic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS608.4112Semi standard non polar3270.3984
RI000186573b,12a-Dihydroxy-5a-cholanoic acid,1TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS506.3791Semi standard non polar3553.3845
RI000186583b,12a-Dihydroxy-5a-cholanoic acid,1TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS506.3791Semi standard non polar3585.1748
RI000186593b,12a-Dihydroxy-5a-cholanoic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS506.3791Semi standard non polar3592.5366
RI000186603b,12a-Dihydroxy-5a-cholanoic acid,2TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS620.4656Semi standard non polar3785.22
RI000186613b,12a-Dihydroxy-5a-cholanoic acid,2TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS620.4656Semi standard non polar3775.7417
RI000186623b,12a-Dihydroxy-5a-cholanoic acid,2TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS620.4656Semi standard non polar3758.63
RI000186633b,12a-Dihydroxy-5a-cholanoic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS734.5521Semi standard non polar3984.1072
RI000186643b,12a-Dihydroxy-5a-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized392.2927Standard polar3905.3838
RI000186653b,12a-Dihydroxy-5a-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized392.2927Standard non polar3315.4275
RI000186663b,12a-Dihydroxy-5a-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized392.2927Semi standard non polar3477.9966
RI00018667Erythrono-1,4-lactone,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1COC(=O)[C@@H]1OTMS190.0661Semi standard non polar1296.684
RI00018668Erythrono-1,4-lactone,1TMS,isomer#2JsmolC[Si](C)(C)O[C@H]1C(=O)OC[C@H]1OTMS190.0661Semi standard non polar1275.9707
RI00018669Erythrono-1,4-lactone,2TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1COC(=O)[C@@H]1O[Si](C)(C)CTMS262.1057Semi standard non polar1410.0176
RI00018670Erythrono-1,4-lactone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1COC(=O)[C@@H]1OTBDMS232.1131Semi standard non polar1506.0682
RI00018671Erythrono-1,4-lactone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1C(=O)OC[C@H]1OTBDMS232.1131Semi standard non polar1519.207
RI00018672Erythrono-1,4-lactone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1COC(=O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS346.1996Semi standard non polar1834.6362
RI00018673Erythrono-1,4-lactoneJsmolO[C@@H]1COC(=O)[C@@H]1OUnderivatized118.0266Standard polar2308.9346
RI00018674Erythrono-1,4-lactoneJsmolO[C@@H]1COC(=O)[C@@H]1OUnderivatized118.0266Standard non polar1156.6611
RI00018675Erythrono-1,4-lactoneJsmolO[C@@H]1COC(=O)[C@@H]1OUnderivatized118.0266Semi standard non polar1289.0726
Displaying retention index compounds 18651 - 18675 of 1722868 in total