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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18526 - 18550 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000185262-Hydroxyestrone,1TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC(O[Si](C)(C)C)=C(O)C=C4CC[C@H]3[C@@H]1CCC2=OTMS358.1964Semi standard non polar2818.938
RI000185272-Hydroxyestrone,1TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC(O)=C(O)C=C4CC[C@H]3[C@@H]1CC=C2O[Si](C)(C)CTMS358.1964Semi standard non polar2770.838
RI000185282-Hydroxyestrone,2TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CCC2=OTMS430.2359Semi standard non polar2866.8079
RI000185292-Hydroxyestrone,2TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC(O)=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC=C2O[Si](C)(C)CTMS430.2359Semi standard non polar2772.7852
RI000185302-Hydroxyestrone,2TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC(O[Si](C)(C)C)=C(O)C=C4CC[C@H]3[C@@H]1CC=C2O[Si](C)(C)CTMS430.2359Semi standard non polar2743.0857
RI000185312-Hydroxyestrone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)[C@H]1CC[C@]3(C)C(=O)CC[C@H]3[C@@H]1CC2TBDMS400.2434Semi standard non polar3108.3513
RI000185322-Hydroxyestrone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12TBDMS400.2434Semi standard non polar3100.681
RI000185332-Hydroxyestrone,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4=CC(O)=C(O)C=C4[C@H]3CC[C@]12CTBDMS400.2434Semi standard non polar3045.835
RI000185342-Hydroxyestrone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@]3(C)C(=O)CC[C@H]3[C@@H]1CC2TBDMS514.3298Semi standard non polar3393.662
RI000185352-Hydroxyestrone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4[C@H]3CC[C@]12CTBDMS514.3298Semi standard non polar3270.5466
RI000185362-Hydroxyestrone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4[C@H]3CC[C@]12CTBDMS514.3298Semi standard non polar3241.9182
RI000185372-HydroxyestroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(O)=C3Underivatized286.1569Standard polar3682.178
RI000185382-Hydroxyestrone,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC=C2O[Si](C)(C)CTMS502.2755Standard non polar2726.3252
RI000185392-Hydroxyestrone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4[C@H]3CC[C@]12CTBDMS628.4163Standard non polar3306.1086
RI000185402-HydroxyestroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(O)=C3Underivatized286.1569Standard non polar2797.2043
RI000185412-HydroxyestroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(O)=C3Underivatized286.1569Semi standard non polar2996.7148
RI000185422-Hydroxyestrone,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC=C2O[Si](C)(C)CTMS502.2755Semi standard non polar2752.215
RI000185432-Hydroxyestrone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4[C@H]3CC[C@]12CTBDMS628.4163Semi standard non polar3410.373
RI000185442-Hydroxyestrone,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC=C2O[Si](C)(C)CTMS502.2755Standard polar2953.2317
RI000185452-Hydroxyestrone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4[C@H]3CC[C@]12CTBDMS628.4163Standard polar3282.1616
RI000185462-Methoxyestradiol-3-methylether,1TMS,isomer#1JsmolCOC1=CC2=C(C=C1OC)[C@H]1CC[C@]3(C)[C@@H](O[Si](C)(C)C)CC[C@H]3[C@@H]1CC2TMS388.2434Semi standard non polar2768.225
RI000185472-Methoxyestradiol-3-methylether,1TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1OC)[C@H]1CC[C@]3(C)[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@H]3[C@@H]1CC2TBDMS430.2903Semi standard non polar3048.9497
RI000185482-Methoxyestradiol-3-methyletherJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OC)C(OC)=C3Underivatized316.2038Standard polar3397.7864
RI000185492-Methoxyestradiol-3-methyletherJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OC)C(OC)=C3Underivatized316.2038Standard non polar2580.5042
RI000185502-Methoxyestradiol-3-methyletherJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OC)C(OC)=C3Underivatized316.2038Semi standard non polar2792.2793
Displaying retention index compounds 18526 - 18550 of 1722868 in total