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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20626 - 20650 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017035515-ethyl-4-hydroxy-2-methyl-3(2H)-furanone,2TMS,isomer#1JsmolCCC1=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(C)O1TMS286.142Semi standard non polar1339.1274
RI017035505-ethyl-4-hydroxy-2-methyl-3(2H)-furanone,2TBDMS,isomer#1JsmolCCC1=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C(C)O1TBDMS370.2359Standard non polar1842.0387
RI017035495-ethyl-4-hydroxy-2-methyl-3(2H)-furanone,2TMS,isomer#1JsmolCCC1=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(C)O1TMS286.142Standard non polar1434.6
RI01703548Methyl dihydroepijasmonate,1TBDMS,isomer#2JsmolCCCCC[C@@H]1C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]1CC(=O)OCTBDMS340.2434Standard polar2312.5808
RI01703547Methyl dihydroepijasmonate,1TBDMS,isomer#1JsmolCCCCCC1=C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1CC(=O)OCTBDMS340.2434Standard polar2292.0793
RI01703546Methyl dihydroepijasmonate,1TMS,isomer#2JsmolCCCCC[C@@H]1C(O[Si](C)(C)C)=CC[C@@H]1CC(=O)OCTMS298.1964Standard polar2186.4634
RI01703545Methyl dihydroepijasmonate,1TMS,isomer#1JsmolCCCCCC1=C(O[Si](C)(C)C)CC[C@@H]1CC(=O)OCTMS298.1964Standard polar2147.8225
RI01703544Methyl dihydroepijasmonate,1TBDMS,isomer#2JsmolCCCCC[C@@H]1C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]1CC(=O)OCTBDMS340.2434Semi standard non polar1965.5619
RI01703543Methyl dihydroepijasmonate,1TBDMS,isomer#1JsmolCCCCCC1=C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1CC(=O)OCTBDMS340.2434Semi standard non polar2000.7526
RI01703542Methyl dihydroepijasmonate,1TMS,isomer#2JsmolCCCCC[C@@H]1C(O[Si](C)(C)C)=CC[C@@H]1CC(=O)OCTMS298.1964Semi standard non polar1763.4061
RI01703541Methyl dihydroepijasmonate,1TMS,isomer#1JsmolCCCCCC1=C(O[Si](C)(C)C)CC[C@@H]1CC(=O)OCTMS298.1964Semi standard non polar1781.7913
RI01703540Methyl dihydroepijasmonate,1TBDMS,isomer#2JsmolCCCCC[C@@H]1C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]1CC(=O)OCTBDMS340.2434Standard non polar1913.518
RI01703539Methyl dihydroepijasmonate,1TBDMS,isomer#1JsmolCCCCCC1=C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1CC(=O)OCTBDMS340.2434Standard non polar1956.4619
RI01703538Methyl dihydroepijasmonate,1TMS,isomer#2JsmolCCCCC[C@@H]1C(O[Si](C)(C)C)=CC[C@@H]1CC(=O)OCTMS298.1964Standard non polar1791.506
RI01703537Methyl dihydroepijasmonate,1TMS,isomer#1JsmolCCCCCC1=C(O[Si](C)(C)C)CC[C@@H]1CC(=O)OCTMS298.1964Standard non polar1778.845
RI01703536(E)-3-oxo-beta-ionone,2TBDMS,isomer#1JsmolC=C(/C=C/C1=C(C)C(O[Si](C)(C)C(C)(C)C)=CCC1(C)C)O[Si](C)(C)C(C)(C)CTBDMS434.3036Standard polar2245.4338
RI01703535(E)-3-oxo-beta-ionone,1TBDMS,isomer#2JsmolC=C(/C=C/C1=C(C)C(=O)CCC1(C)C)O[Si](C)(C)C(C)(C)CTBDMS320.2172Standard polar2130.2358
RI01703534(E)-3-oxo-beta-ionone,1TBDMS,isomer#1JsmolCC(=O)/C=C/C1=C(C)C(O[Si](C)(C)C(C)(C)C)=CCC1(C)CTBDMS320.2172Standard polar2113.5652
RI01703533(E)-3-oxo-beta-ionone,2TMS,isomer#1JsmolC=C(/C=C/C1=C(C)C(O[Si](C)(C)C)=CCC1(C)C)O[Si](C)(C)CTMS350.2097Standard polar2006.4425
RI01703532(E)-3-oxo-beta-ionone,1TMS,isomer#2JsmolC=C(/C=C/C1=C(C)C(=O)CCC1(C)C)O[Si](C)(C)CTMS278.1702Standard polar1981.475
RI01703531(E)-3-oxo-beta-ionone,1TMS,isomer#1JsmolCC(=O)/C=C/C1=C(C)C(O[Si](C)(C)C)=CCC1(C)CTMS278.1702Standard polar1975.3264
RI01703530(E)-3-oxo-beta-ionone,2TBDMS,isomer#1JsmolC=C(/C=C/C1=C(C)C(O[Si](C)(C)C(C)(C)C)=CCC1(C)C)O[Si](C)(C)C(C)(C)CTBDMS434.3036Semi standard non polar2397.2952
RI01703529(E)-3-oxo-beta-ionone,1TBDMS,isomer#2JsmolC=C(/C=C/C1=C(C)C(=O)CCC1(C)C)O[Si](C)(C)C(C)(C)CTBDMS320.2172Semi standard non polar2037.948
RI01703528(E)-3-oxo-beta-ionone,1TBDMS,isomer#1JsmolCC(=O)/C=C/C1=C(C)C(O[Si](C)(C)C(C)(C)C)=CCC1(C)CTBDMS320.2172Semi standard non polar2083.2668
RI01703527(E)-3-oxo-beta-ionone,2TMS,isomer#1JsmolC=C(/C=C/C1=C(C)C(O[Si](C)(C)C)=CCC1(C)C)O[Si](C)(C)CTMS350.2097Semi standard non polar1919.5554
Displaying retention index compounds 20626 - 20650 of 1722868 in total