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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20376 - 20400 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703801(5alpha)-campestan-3-one,1TMS,isomer#2JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS472.41Standard polar3405.6094
RI01703800(5alpha)-campestan-3-one,1TMS,isomer#1JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC12CTMS472.41Standard polar3411.8618
RI01703799(5alpha)-campestan-3-one,1TBDMS,isomer#2JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4C=C(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12CTBDMS514.457Semi standard non polar3491.1917
RI01703798(5alpha)-campestan-3-one,1TBDMS,isomer#1JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)=CCC4(C)C3CCC12CTBDMS514.457Semi standard non polar3481.8088
RI01703797(5alpha)-campestan-3-one,1TMS,isomer#2JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS472.41Semi standard non polar3276.9746
RI01703796(5alpha)-campestan-3-one,1TMS,isomer#1JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC12CTMS472.41Semi standard non polar3264.5176
RI01703795(5alpha)-campestan-3-one,1TBDMS,isomer#2JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4C=C(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12CTBDMS514.457Standard non polar3400.8208
RI01703794(5alpha)-campestan-3-one,1TBDMS,isomer#1JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)=CCC4(C)C3CCC12CTBDMS514.457Standard non polar3340.5369
RI01703793(5alpha)-campestan-3-one,1TMS,isomer#2JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS472.41Standard non polar3195.5054
RI01703792(5alpha)-campestan-3-one,1TMS,isomer#1JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC12CTMS472.41Standard non polar3145.0654
RI01703791(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 polar3227.6174
RI01703790(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 polar3212.487
RI01703789(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 polar3545.587
RI01703788(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 polar3493.7139
RI01703787(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 polar3222.6653
RI01703786(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 polar3258.0522
RI01703785(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 polar3204.6687
RI01703784(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 polar3067.8777
RI01703783(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 polar3046.13
RI01703782(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 polar3460.35
RI01703781(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 polar3401.3108
RI01703780(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 polar3121.2095
RI01703779(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)CTMS493.2811Standard polar3164.9448
RI01703778(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)CTMS493.2811Standard polar3096.0295
RI01703777(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)CTBDMS691.4615Semi standard non polar3626.0151
Displaying retention index compounds 20376 - 20400 of 1722868 in total