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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 8126 - 8150 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017160515-Hexen-2-one, 5-methyl-3-methylene,1TMS,isomer#1JsmolC=C(C)CC(=C)C(=C)O[Si](C)(C)CTMS196.1283Standard polar1256.2831
RI017160505-Hexen-2-one, 5-methyl-3-methylene,1TBDMS,isomer#1JsmolC=C(C)CC(=C)C(=C)O[Si](C)(C)C(C)(C)CTBDMS238.1753Semi standard non polar1293.373
RI017160495-Hexen-2-one, 5-methyl-3-methylene,1TMS,isomer#1JsmolC=C(C)CC(=C)C(=C)O[Si](C)(C)CTMS196.1283Semi standard non polar1081.8049
RI017160485-Hexen-2-one, 5-methyl-3-methylene,1TBDMS,isomer#1JsmolC=C(C)CC(=C)C(=C)O[Si](C)(C)C(C)(C)CTBDMS238.1753Standard non polar1296.8336
RI017160475-Hexen-2-one, 5-methyl-3-methylene,1TMS,isomer#1JsmolC=C(C)CC(=C)C(=C)O[Si](C)(C)CTMS196.1283Standard non polar1086.5789
RI01716046buddlenol E,4TBDMS,isomer#1JsmolC=C(/C=C/C1=CC(OC)=C(O[Si](C)(C)C(C)(C)C)C(C2=CC(/C=C/C(=O)O[Si](C)(C)C(C)(C)C)=CC(OC)=C2O[Si](C)(C)C(C)(C)C)=C1)O[Si](C)(C)C(C)(C)CTBDMS840.4668Standard polar4029.909
RI01716045buddlenol E,4TMS,isomer#1JsmolC=C(/C=C/C1=CC(OC)=C(O[Si](C)(C)C)C(C2=CC(/C=C/C(=O)O[Si](C)(C)C)=CC(OC)=C2O[Si](C)(C)C)=C1)O[Si](C)(C)CTMS672.279Standard polar3838.1443
RI01716044buddlenol E,4TBDMS,isomer#1JsmolC=C(/C=C/C1=CC(OC)=C(O[Si](C)(C)C(C)(C)C)C(C2=CC(/C=C/C(=O)O[Si](C)(C)C(C)(C)C)=CC(OC)=C2O[Si](C)(C)C(C)(C)C)=C1)O[Si](C)(C)C(C)(C)CTBDMS840.4668Semi standard non polar4206.745
RI01716043buddlenol E,4TMS,isomer#1JsmolC=C(/C=C/C1=CC(OC)=C(O[Si](C)(C)C)C(C2=CC(/C=C/C(=O)O[Si](C)(C)C)=CC(OC)=C2O[Si](C)(C)C)=C1)O[Si](C)(C)CTMS672.279Semi standard non polar3363.9434
RI01716042buddlenol E,4TBDMS,isomer#1JsmolC=C(/C=C/C1=CC(OC)=C(O[Si](C)(C)C(C)(C)C)C(C2=CC(/C=C/C(=O)O[Si](C)(C)C(C)(C)C)=CC(OC)=C2O[Si](C)(C)C(C)(C)C)=C1)O[Si](C)(C)C(C)(C)CTBDMS840.4668Standard non polar4433.2373
RI01716041buddlenol E,4TMS,isomer#1JsmolC=C(/C=C/C1=CC(OC)=C(O[Si](C)(C)C)C(C2=CC(/C=C/C(=O)O[Si](C)(C)C)=CC(OC)=C2O[Si](C)(C)C)=C1)O[Si](C)(C)CTMS672.279Standard non polar3687.9548
RI01716040hydroxymedioresinol,6TMS,isomer#1JsmolCOC1=CC(/C=C/C(=O)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS758.3373Standard polar3130.2185
RI01716039hydroxymedioresinol,6TMS,isomer#1JsmolCOC1=CC(/C=C/C(=O)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS758.3373Semi standard non polar3013.4438
RI01716038hydroxymedioresinol,6TMS,isomer#1JsmolCOC1=CC(/C=C/C(=O)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(CO[Si](C)(C)C)O[Si](C)(C)C)=CC=C1O[Si](C)(C)CTMS758.3373Standard non polar3028.0657
RI01716037rhamnetin 3-rhamninoside,6TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(=O)/C=C/C1=CC=C(O[Si](C)(C)C)C=C1TMS728.3268Standard polar2949.3618
RI01716036rhamnetin 3-rhamninoside,6TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(=O)/C=C/C1=CC=C(O[Si](C)(C)C)C=C1TMS728.3268Semi standard non polar2954.636
RI01716035rhamnetin 3-rhamninoside,6TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(=O)/C=C/C1=CC=C(O[Si](C)(C)C)C=C1TMS728.3268Standard non polar2909.9167
RI01716034formononetin methylated ,4TMS,isomer#204JsmolC[Si](C)(C)OC1[C@H](OC2O[C@@H](C3=C(O)C=C4OC(C5=CC=C(O)C(O)=C5)=CC(=O)C4=C3O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)OC(CO)[C@@H](O)[C@@H]1OTMS884.2958Standard polar6779.468
RI01716033formononetin methylated ,4TMS,isomer#138JsmolC[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1[C@@H]1OC(O[C@@H]3OC(CO)[C@@H](O)[C@H](O)C3O)[C@@H](O)[C@H](O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2TMS884.2958Standard polar6965.5728
RI01716032formononetin methylated ,4TMS,isomer#204JsmolC[Si](C)(C)OC1[C@H](OC2O[C@@H](C3=C(O)C=C4OC(C5=CC=C(O)C(O)=C5)=CC(=O)C4=C3O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)OC(CO)[C@@H](O)[C@@H]1OTMS884.2958Semi standard non polar5147.349
RI01716031formononetin methylated ,4TMS,isomer#138JsmolC[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1[C@@H]1OC(O[C@@H]3OC(CO)[C@@H](O)[C@H](O)C3O)[C@@H](O)[C@H](O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2TMS884.2958Semi standard non polar5133.321
RI01716030formononetin methylated ,4TMS,isomer#204JsmolC[Si](C)(C)OC1[C@H](OC2O[C@@H](C3=C(O)C=C4OC(C5=CC=C(O)C(O)=C5)=CC(=O)C4=C3O)C(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)OC(CO)[C@@H](O)[C@@H]1OTMS884.2958Standard non polar4826.5254
RI01716029formononetin methylated ,4TMS,isomer#138JsmolC[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1[C@@H]1OC(O[C@@H]3OC(CO)[C@@H](O)[C@H](O)C3O)[C@@H](O)[C@H](O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C=C(C1=CC=C(O)C(O)=C1)O2TMS884.2958Standard non polar4867.0654
RI01716028isoleucine betaine,2TBDMS,isomer#5JsmolC[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C4OC(C5=CC=C(O)C=C5)=CC(=O)C4=C3O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1OTBDMS806.3365Standard polar6848.5874
RI01716027isoleucine betaine,4TMS,isomer#55JsmolC[C@@H]1O[C@@H](O[C@H]2[C@H](C3=C(O)C=C4OC(C5=CC=C(O)C=C5)=CC(=O)C4=C3O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)CTMS866.3217Standard polar6014.8647
Displaying retention index compounds 8126 - 8150 of 1722868 in total