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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18626 - 18650 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000186263-Deoxyarabinohexonic acid,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS636.4093Semi standard non polar2691.6597
RI000186273-Deoxyarabinohexonic acid,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC[C@@H](O)[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS636.4093Semi standard non polar2685.8203
RI000186283-Deoxyarabinohexonic acid,4TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS636.4093Semi standard non polar2688.0627
RI000186293-Deoxyarabinohexonic acid,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS750.4958Semi standard non polar2901.5596
RI000186303-Deoxyarabinohexonic acidJsmolOC[C@@H](O)[C@@H](O)C[C@H](O)C(O)=OUnderivatized180.0634Standard polar3207.4255
RI000186313-Deoxyarabinohexonic acidJsmolOC[C@@H](O)[C@@H](O)C[C@H](O)C(O)=OUnderivatized180.0634Standard non polar1650.5728
RI000186323-Deoxyarabinohexonic acidJsmolOC[C@@H](O)[C@@H](O)C[C@H](O)C(O)=OUnderivatized180.0634Semi standard non polar1658.1837
RI0001863316b-Hydroxyestradiol,1TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@@H]2OTMS360.2121Semi standard non polar2789.2388
RI0001863416b-Hydroxyestradiol,1TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@H](O)[C@@H]2O[Si](C)(C)CTMS360.2121Semi standard non polar2794.0862
RI0001863516b-Hydroxyestradiol,1TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O)[C@@H]2OTMS360.2121Semi standard non polar2771.8933
RI0001863616b-Hydroxyestradiol,2TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@@H]2OTMS432.2516Semi standard non polar2842.8718
RI0001863716b-Hydroxyestradiol,2TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS432.2516Semi standard non polar2782.1436
RI0001863816b-Hydroxyestradiol,2TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O)[C@@H]2O[Si](C)(C)CTMS432.2516Semi standard non polar2842.8809
RI0001863916b-Hydroxyestradiol,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS504.2911Semi standard non polar2907.424
RI0001864016b-Hydroxyestradiol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@]2(C)[C@H]1OTBDMS402.259Semi standard non polar3065.0571
RI0001864116b-Hydroxyestradiol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@@]21CTBDMS402.259Semi standard non polar3081.2944
RI0001864216b-Hydroxyestradiol,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1C[C@H](O)[C@@H]2OTBDMS402.259Semi standard non polar3084.2534
RI0001864316b-Hydroxyestradiol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2OTBDMS516.3455Semi standard non polar3374.4844
RI0001864416b-Hydroxyestradiol,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@]2(C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS516.3455Semi standard non polar3303.1072
RI0001864516b-Hydroxyestradiol,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1C[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)CTBDMS516.3455Semi standard non polar3391.3965
RI0001864616b-Hydroxyestradiol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)CTBDMS630.432Semi standard non polar3664.8398
RI0001864716b-HydroxyestradiolJsmol[H][C@@]12C[C@H](O)[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized288.1725Standard polar3943.9067
RI0001864816b-HydroxyestradiolJsmol[H][C@@]12C[C@H](O)[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized288.1725Standard non polar2917.311
RI0001864916b-HydroxyestradiolJsmol[H][C@@]12C[C@H](O)[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized288.1725Semi standard non polar2941.945
RI000186503b,12a-Dihydroxy-5a-cholanoic acid,1TMS,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)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS464.3322Semi standard non polar3290.7327
Displaying retention index compounds 18626 - 18650 of 1722868 in total