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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20101 - 20125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000201012b,3a,7a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS750.547Semi standard non polar3964.9429
RI000201022b,3a,7a-Trihydroxy-5b-cholanoic acid,4TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS864.6335Semi standard non polar4139.192
RI000201032b,3a,7a-Trihydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])C[C@H](O)[C@@H](O)C[C@]12CUnderivatized408.2876Standard polar4025.847
RI000201042b,3a,7a-Trihydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])C[C@H](O)[C@@H](O)C[C@]12CUnderivatized408.2876Standard non polar3507.126
RI000201052b,3a,7a-Trihydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])C[C@H](O)[C@@H](O)C[C@]12CUnderivatized408.2876Semi standard non polar3630.4336
RI000201062-Methoxyestradiol,1TMS,isomer#1JsmolCOC1=CC2=C(C=C1O)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O[Si](C)(C)C)CC[C@@H]12TMS374.2277Semi standard non polar2793.8188
RI000201072-Methoxyestradiol,1TMS,isomer#2JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)CC[C@@H]12TMS374.2277Semi standard non polar2781.2725
RI000201082-Methoxyestradiol,2TMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O[Si](C)(C)C)CC[C@@H]12TMS446.2672Semi standard non polar2778.1724
RI000201092-Methoxyestradiol,1TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS416.2747Semi standard non polar3082.5522
RI000201102-Methoxyestradiol,1TBDMS,isomer#2JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)CC[C@@H]12TBDMS416.2747Semi standard non polar3072.1912
RI000201112-Methoxyestradiol,2TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS530.3611Semi standard non polar3296.2139
RI000201122-MethoxyestradiolJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(OC)=C3Underivatized302.1882Standard polar3790.8298
RI000201132-MethoxyestradiolJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(OC)=C3Underivatized302.1882Standard non polar2605.1233
RI000201142-MethoxyestradiolJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(OC)=C3Underivatized302.1882Semi standard non polar2814.6199
RI0002011516-Ketoestradiol,1TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1CC(=O)[C@@H]2O[Si](C)(C)CTMS358.1964Semi standard non polar2832.5537
RI0002011616-Ketoestradiol,1TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC(=O)[C@@H]2OTMS358.1964Semi standard non polar2823.505
RI0002011716-Ketoestradiol,1TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1CC(O[Si](C)(C)C)=C2OTMS358.1964Semi standard non polar2764.095
RI0002011816-Ketoestradiol,1TMS,isomer#4JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C=C(O[Si](C)(C)C)[C@@H]2OTMS358.1964Semi standard non polar2734.4912
RI0002011916-Ketoestradiol,2TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC(=O)[C@@H]2O[Si](C)(C)CTMS430.2359Semi standard non polar2904.062
RI0002012016-Ketoestradiol,2TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS430.2359Semi standard non polar2779.4495
RI0002012116-Ketoestradiol,2TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS430.2359Semi standard non polar2749.8643
RI0002012216-Ketoestradiol,2TMS,isomer#4JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC(O[Si](C)(C)C)=C2OTMS430.2359Semi standard non polar2845.1572
RI0002012316-Ketoestradiol,2TMS,isomer#5JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C=C(O[Si](C)(C)C)[C@@H]2OTMS430.2359Semi standard non polar2762.2632
RI0002012416-Ketoestradiol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1C(=O)C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@@]21CTBDMS400.2434Semi standard non polar3108.1592
RI0002012516-Ketoestradiol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC(=O)[C@@H]2OTBDMS400.2434Semi standard non polar3110.7898
Displaying retention index compounds 20101 - 20125 of 1722868 in total