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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20401 - 20425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703776(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TBDMS,isomer#1JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS691.4615Semi standard non polar3620.3772
RI01703775(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#5JsmolCCCCC=C(/C=C/[C@H]1[C@H](O)C=C(O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS577.375Semi standard non polar3371.606
RI01703774(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#4JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O)O[Si](C)(C)C(C)(C)CTBDMS577.375Semi standard non polar3440.5532
RI01703773(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#3JsmolCCCCCC(=O)/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-]TBDMS577.375Semi standard non polar3179.75
RI01703772(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CC(=O)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS577.375Semi standard non polar3357.404
RI01703771(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#1JsmolCCCCCC(=O)/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)CTBDMS577.375Semi standard non polar3201.3489
RI01703770(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)CTMS565.3206Semi standard non polar2906.636
RI01703769(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TMS,isomer#1JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)O[Si](C)(C)CTMS565.3206Semi standard non polar2940.2905
RI01703768(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#5JsmolCCCCC=C(/C=C/[C@H]1[C@H](O)C=C(O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)CTMS493.2811Semi standard non polar2891.5444
RI01703767(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#4JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C)C[C@H]1O)O[Si](C)(C)CTMS493.2811Semi standard non polar2966.4167
RI01703766(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#3JsmolCCCCCC(=O)/C=C/[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-]TMS493.2811Semi standard non polar2693.262
RI01703765(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C)CC(=O)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)CTMS493.2811Semi standard non polar2898.655
RI01703764(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#1JsmolCCCCCC(=O)/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)CTMS493.2811Semi standard non polar2739.7852
RI01703763(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TBDMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS691.4615Standard non polar3147.2183
RI01703762(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TBDMS,isomer#1JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS691.4615Standard non polar3344.872
RI01703761(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#5JsmolCCCCC=C(/C=C/[C@H]1[C@H](O)C=C(O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS577.375Standard non polar3043.3955
RI01703760(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#4JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O)O[Si](C)(C)C(C)(C)CTBDMS577.375Standard non polar3173.6172
RI01703759(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#3JsmolCCCCCC(=O)/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-]TBDMS577.375Standard non polar3031.545
RI01703758(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CC(=O)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS577.375Standard non polar3216.8591
RI01703757(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TBDMS,isomer#1JsmolCCCCCC(=O)/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C(C)(C)C)C[C@H]1O[Si](C)(C)C(C)(C)CTBDMS577.375Standard non polar3137.3816
RI01703756(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TMS,isomer#2JsmolCCCCC=C(/C=C/[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)CTMS565.3206Standard non polar2750.7063
RI01703755(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,3TMS,isomer#1JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)O[Si](C)(C)CTMS565.3206Standard non polar2832.0222
RI01703754(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#5JsmolCCCCC=C(/C=C/[C@H]1[C@H](O)C=C(O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-])O[Si](C)(C)CTMS493.2811Standard non polar2754.753
RI01703753(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#4JsmolCCCCC=C(/C=C/[C@@H]1C(C/C=C\CCCC(=O)[O-])=C(O[Si](C)(C)C)C[C@H]1O)O[Si](C)(C)CTMS493.2811Standard non polar2793.194
RI01703752(5Z)-(15S)-11-alpha-hydroxy-9,15-dioxoprosta-13-enoate,2TMS,isomer#3JsmolCCCCCC(=O)/C=C/[C@H]1[C@H](O[Si](C)(C)C)C=C(O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)[O-]TMS493.2811Standard non polar2716.5632
Displaying retention index compounds 20401 - 20425 of 1722868 in total