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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 22751 - 22775 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01701426Isorhamnetin 3-sophoroside,2TMS,isomer#29JsmolCOC1=CC(C2=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OTMS784.243Standard non polar4911.4136
RI01701425Isorhamnetin 3-sophoroside,2TMS,isomer#28JsmolCOC1=CC(C2=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OTMS784.243Standard non polar4923.289
RI01701424Isorhamnetin 3-sophoroside,2TMS,isomer#25JsmolCOC1=CC(C2=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3OC3OC(CO)C(O)C(O)C3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)=CC=C1OTMS784.243Standard non polar4999.0605
RI01701423Isorhamnetin 3-sophoroside,2TMS,isomer#20JsmolCOC1=CC(C2=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3OC3OC(CO)C(O)C(O)C3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OTMS784.243Standard non polar4892.8486
RI01701422Isorhamnetin 3-sophoroside,1TMS,isomer#4JsmolCOC1=CC(C2=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3OC3OC(CO)C(O)C(O)C3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OTMS712.2035Standard non polar5011.937
RI01701421Procyanidin A1,2TBDMS,isomer#30JsmolCC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(O)C=C(O)C=C4OC(C4=CC=C(O)C(O)=C4)(O2)C3O[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS804.2997Standard polar6900.2993
RI01701420Procyanidin A1,2TBDMS,isomer#29JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(O)C=C(O)C=C4OC(C4=CC=C(O)C(O)=C4)(O2)C3O[Si](C)(C)C(C)(C)C)C=C1OTBDMS804.2997Standard polar6871.451
RI01701419Procyanidin A1,2TBDMS,isomer#28JsmolCC(C)(C)[Si](C)(C)OC1=CC(C23OC4=CC(O)=CC(O)=C4C(C4=C(C=C(O)C5=C4OC(C4=CC=C(O)C(O)=C4)C(O)C5)O2)C3O[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS804.2997Standard polar6930.0757
RI01701418Procyanidin A1,2TBDMS,isomer#27JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C23OC4=CC(O)=CC(O)=C4C(C4=C(C=C(O)C5=C4OC(C4=CC=C(O)C(O)=C4)C(O)C5)O2)C3O[Si](C)(C)C(C)(C)C)C=C1OTBDMS804.2997Standard polar6911.37
RI01701417Procyanidin A1,2TBDMS,isomer#26JsmolCC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C1C3=C(C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)OC(C3=CC=C(O)C(O)=C3)(O2)C1O[Si](C)(C)C(C)(C)CTBDMS804.2997Standard polar6839.026
RI01701416Procyanidin A1,2TBDMS,isomer#19JsmolCC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC1(C3=CC=C(O)C(O)=C3)OC3=CC(O)=C4CC(O)C(C5=CC=C(O)C(O)=C5)OC4=C3C2C1O[Si](C)(C)C(C)(C)CTBDMS804.2997Standard polar6870.0435
RI01701415Procyanidin A1,2TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)OC1=CC2=C(C3=C1CC(O)C(C1=CC=C(O)C(O)=C1)O3)C1C3=C(O)C=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)(O2)C1O[Si](C)(C)C(C)(C)CTBDMS804.2997Standard polar6805.735
RI01701414Procyanidin A1,2TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC1CC2=C(O)C=C3OC4(C5=CC=C(O)C(O)=C5)OC5=CC(O)=CC(O)=C5C(C3=C2OC1C1=CC=C(O)C(O)=C1)C4O[Si](C)(C)C(C)(C)CTBDMS804.2997Standard polar6918.9165
RI01701413Procyanidin A1,1TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC1C2C3=C(O)C=C(O)C=C3OC1(C1=CC=C(O)C(O)=C1)OC1=CC(O)=C3CC(O)C(C4=CC=C(O)C(O)=C4)OC3=C12TBDMS690.2133Standard polar7439.8516
RI01701412Procyanidin A1,4TMS,isomer#125JsmolC[Si](C)(C)OC1=CC(C23OC4=CC(O)=CC(O)=C4C(C4=C(C=C(O)C5=C4OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)C5)O2)C3O[Si](C)(C)C)=CC=C1OTMS864.2849Standard polar6289.8843
RI01701411Procyanidin A1,4TMS,isomer#124JsmolC[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(O)C=C(O)C=C4OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)(O2)C3O[Si](C)(C)C)=CC=C1OTMS864.2849Standard polar6283.3135
RI01701410Procyanidin A1,4TMS,isomer#123JsmolC[Si](C)(C)OC1=CC=C(C23OC4=CC(O)=CC(O)=C4C(C4=C(C=C(O)C5=C4OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)C5)O2)C3O[Si](C)(C)C)C=C1OTMS864.2849Standard polar6283.2085
RI01701409Procyanidin A1,4TMS,isomer#122JsmolC[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(O)C=C(O)C=C4OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)(O2)C3O[Si](C)(C)C)C=C1OTMS864.2849Standard polar6264.4565
RI01701408Procyanidin A1,4TMS,isomer#121JsmolC[Si](C)(C)OC1=CC=C(C23OC4=CC(O)=CC(O[Si](C)(C)C)=C4C(C4=C(C=C(O)C5=C4OC(C4=CC=C(O)C(O)=C4)C(O)C5)O2)C3O[Si](C)(C)C)C=C1O[Si](C)(C)CTMS864.2849Standard polar6207.317
RI01701407Procyanidin A1,4TMS,isomer#120JsmolC[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(C=C(O)C=C4O[Si](C)(C)C)OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)(O2)C3O[Si](C)(C)C)=CC=C1OTMS864.2849Standard polar6317.0225
RI01701406Procyanidin A1,4TMS,isomer#118JsmolC[Si](C)(C)OC1=CC=C(C23OC4=CC(O)=CC(O[Si](C)(C)C)=C4C(C4=C(C=C(O)C5=C4OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)C5)O2)C3O[Si](C)(C)C)C=C1OTMS864.2849Standard polar6317.8037
RI01701405Procyanidin A1,4TMS,isomer#117JsmolC[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(C=C(O)C=C4O[Si](C)(C)C)OC(C4=CC=C(O)C(O)=C4)(O2)C3O[Si](C)(C)C)C=C1O[Si](C)(C)CTMS864.2849Standard polar6193.9966
RI01701404Procyanidin A1,4TMS,isomer#115JsmolC[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(C=C(O)C=C4O[Si](C)(C)C)OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)(O2)C3O[Si](C)(C)C)C=C1OTMS864.2849Standard polar6296.6846
RI01701403Procyanidin A1,4TMS,isomer#113JsmolC[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC2=C3C3C4=C(C=C(O)C=C4O[Si](C)(C)C)OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)(O2)C3O[Si](C)(C)C)C=C1OTMS864.2849Standard polar6288.5894
RI01701402Procyanidin A1,4TMS,isomer#111JsmolC[Si](C)(C)OC1=CC(O)=C2C(=C1)OC1(C3=CC=C(O)C(O)=C3)OC3=CC(O)=C4CC(O)C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3C2C1O[Si](C)(C)CTMS864.2849Standard polar6229.2554
Displaying retention index compounds 22751 - 22775 of 1722868 in total