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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19376 - 19400 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000193762-Hydroxyestradiol-3-methyl ether,1TMS,isomer#2JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)[C@H]1CC[C@]3(C)[C@@H](O)CC[C@H]3[C@@H]1CC2TMS374.2277Semi standard non polar2779.001
RI000193772-Hydroxyestradiol-3-methyl ether,2TMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)[C@H]1CC[C@]3(C)[C@@H](O[Si](C)(C)C)CC[C@H]3[C@@H]1CC2TMS446.2672Semi standard non polar2774.7463
RI000193782-Hydroxyestradiol-3-methyl ether,1TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O)[C@H]1CC[C@]3(C)[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@H]3[C@@H]1CC2TBDMS416.2747Semi standard non polar3106.9014
RI000193792-Hydroxyestradiol-3-methyl ether,1TBDMS,isomer#2JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@]3(C)[C@@H](O)CC[C@H]3[C@@H]1CC2TBDMS416.2747Semi standard non polar3074.3672
RI000193802-Hydroxyestradiol-3-methyl ether,2TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@]3(C)[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@H]3[C@@H]1CC2TBDMS530.3611Semi standard non polar3294.0095
RI000193812-Hydroxyestradiol-3-methyl etherJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OC)C(O)=C3Underivatized302.1882Standard polar3806.4578
RI000193822-Hydroxyestradiol-3-methyl etherJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OC)C(O)=C3Underivatized302.1882Standard non polar2610.3174
RI000193832-Hydroxyestradiol-3-methyl etherJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(OC)C(O)=C3Underivatized302.1882Semi standard non polar2819.1694
RI00019384Allolithocholic acid,1TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3CC[C@@]21CTMS448.3373Semi standard non polar3199.0635
RI00019385Allolithocholic acid,1TMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C)CC[C@]4(C)C3CC[C@@]21CTMS448.3373Semi standard non polar3303.541
RI00019386Allolithocholic acid,2TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C)CC[C@]4(C)C3CC[C@@]21CTMS520.3768Semi standard non polar3161.9492
RI00019387Allolithocholic acid,1TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3CC[C@@]21CTBDMS490.3842Semi standard non polar3456.0833
RI00019388Allolithocholic acid,1TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3CC[C@@]21CTBDMS490.3842Semi standard non polar3517.3525
RI00019389Allolithocholic acid,2TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3CC[C@@]21CTBDMS604.4707Semi standard non polar3646.067
RI00019390Allolithocholic acidJsmolC[C@@H](CCC(O)=O)C1CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3CC[C@]12CUnderivatized376.2977Standard polar3038.3242
RI00019391Allolithocholic acidJsmolC[C@@H](CCC(O)=O)C1CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3CC[C@]12CUnderivatized376.2977Standard non polar3035.7356
RI00019392Allolithocholic acidJsmolC[C@@H](CCC(O)=O)C1CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3CC[C@]12CUnderivatized376.2977Semi standard non polar3236.1658
RI000193933a,17a-Dihydroxy-5b-androstane,1TMS,isomer#1JsmolC[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2CC[C@@]2(C)C1CC[C@H]2OTMS364.2798Semi standard non polar2593.1262
RI000193943a,17a-Dihydroxy-5b-androstane,1TMS,isomer#2JsmolC[C@]12CC[C@@H](O)CC1CCC1C2CC[C@@]2(C)C1CC[C@H]2O[Si](C)(C)CTMS364.2798Semi standard non polar2591.0156
RI000193953a,17a-Dihydroxy-5b-androstane,2TMS,isomer#1JsmolC[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2CC[C@@]2(C)C1CC[C@H]2O[Si](C)(C)CTMS436.3193Semi standard non polar2586.239
RI000193963a,17a-Dihydroxy-5b-androstane,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)C(CCC3C2CC[C@@]2(C)C3CC[C@H]2O)C1TBDMS406.3267Semi standard non polar2844.8738
RI000193973a,17a-Dihydroxy-5b-androstane,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3CC[C@@]21CTBDMS406.3267Semi standard non polar2864.8315
RI000193983a,17a-Dihydroxy-5b-androstane,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)C(CCC3C2CC[C@@]2(C)C3CC[C@H]2O[Si](C)(C)C(C)(C)C)C1TBDMS520.4132Semi standard non polar3106.9556
RI000193993a,17a-Dihydroxy-5b-androstaneJsmolC[C@]12CCC3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@H]2OUnderivatized292.2402Standard polar2344.7349
RI000194003a,17a-Dihydroxy-5b-androstaneJsmolC[C@]12CCC3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@H]2OUnderivatized292.2402Standard non polar2441.963
Displaying retention index compounds 19376 - 19400 of 1722868 in total