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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 68326 - 68350 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00068326Coproporphyrinogen III,2TBDMS,isomer#14JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(CCC(=O)O)C(C)=C(CC5=C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(C)=C(CC(=C1CCC(=O)O[Si](C)(C)C(C)(C)C)[NH]2)[NH]5)[NH]4)[NH]3TBDMS888.4889Semi standard non polar6220.992
RI00068327Coproporphyrinogen III,2TBDMS,isomer#15JsmolCC1=C2CC3=C(CCC(=O)O)C(C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O[Si](C)(C)C(C)(C)C)[NH]2)[NH]5)[NH]4)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6248.4116
RI00068328Coproporphyrinogen III,2TBDMS,isomer#16JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(C)C(CCC(=O)O[Si](C)(C)C(C)(C)C)=C(CC5=C(C)C(CCC(=O)O)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6247.873
RI00068329Coproporphyrinogen III,2TBDMS,isomer#17JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(CCC(=O)O)C(C)=C(CC5=C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(C)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6250.6323
RI00068330Coproporphyrinogen III,2TBDMS,isomer#18JsmolCC1=C2CC3=C(CCC(=O)O)C(C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O[Si](C)(C)C(C)(C)C)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6243.64
RI00068331Coproporphyrinogen III,2TBDMS,isomer#19JsmolCC1=C2CC3=C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)[NH]4)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6241.407
RI00068332Coproporphyrinogen III,2TBDMS,isomer#20JsmolCC1=C2CC3=C(C)C(CCC(=O)O[Si](C)(C)C(C)(C)C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(C)C(CCC(=O)O)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6255.3945
RI00068333Coproporphyrinogen III,2TBDMS,isomer#21JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(CCC(=O)O)C(C)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O[Si](C)(C)C(C)(C)C)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6250.2593
RI00068334Coproporphyrinogen III,2TBDMS,isomer#22JsmolCC1=C2CC3=C(CCC(=O)O[Si](C)(C)C(C)(C)C)C(C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6243.3325
RI00068335Coproporphyrinogen III,2TBDMS,isomer#23JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(C)C(CCC(=O)O)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6340.8257
RI00068336Coproporphyrinogen III,2TBDMS,isomer#24JsmolCC1=C2CC3=C(CCC(=O)O)C(C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)N5[Si](C)(C)C(C)(C)C)[NH]4)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6325.868
RI00068337Coproporphyrinogen III,2TBDMS,isomer#25JsmolCC1=C2CC3=C(CCC(=O)O)C(C)=C(CC4=C(C)C(CCC(=O)O)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6327.681
RI00068338Coproporphyrinogen III,2TBDMS,isomer#26JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(CCC(=O)O)C(C)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)N5[Si](C)(C)C(C)(C)C)[NH]4)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6325.507
RI00068339Coproporphyrinogen III,2TBDMS,isomer#27JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(CCC(=O)O)C(C)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)N5[Si](C)(C)C(C)(C)C)N4[Si](C)(C)C(C)(C)C)[NH]3TBDMS888.4889Semi standard non polar6341.11
RI00068340Coproporphyrinogen III,2TBDMS,isomer#28JsmolCC1=C2CC3=C(C)C(CCC(=O)O)=C(CC4=C(CCC(=O)O)C(C)=C(CC5=C(CCC(=O)O)C(C)=C(CC(=C1CCC(=O)O)[NH]2)[NH]5)N4[Si](C)(C)C(C)(C)C)N3[Si](C)(C)C(C)(C)CTBDMS888.4889Semi standard non polar6345.822
RI00068341Coproporphyrinogen IIIJsmolCC1=C2CC3=C(C)C(CCC(O)=O)=C(CC4=C(CCC(O)=O)C(C)=C(CC5=C(CCC(O)=O)C(C)=C(CC(N2)=C1CCC(O)=O)N5)N4)N3Underivatized660.3159Standard polar5811.878
RI00068342Coproporphyrinogen IIIJsmolCC1=C2CC3=C(C)C(CCC(O)=O)=C(CC4=C(CCC(O)=O)C(C)=C(CC5=C(CCC(O)=O)C(C)=C(CC(N2)=C1CCC(O)=O)N5)N4)N3Underivatized660.3159Standard non polar4642.6167
RI00068343Coproporphyrinogen IIIJsmolCC1=C2CC3=C(C)C(CCC(O)=O)=C(CC4=C(CCC(O)=O)C(C)=C(CC5=C(CCC(O)=O)C(C)=C(CC(N2)=C1CCC(O)=O)N5)N4)N3Underivatized660.3159Semi standard non polar6292.819
RI00068344Maltotriose,1TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)OC(O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1OTMS576.2086Semi standard non polar3929.3906
RI00068345Maltotriose,1TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@@H](O)[C@@H](O[C@@H]2[C@@H](CO)OC(O)[C@H](O)[C@H]2O)O[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1OTMS576.2086Semi standard non polar3932.3127
RI00068346Maltotriose,1TMS,isomer#3JsmolC[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1OTMS576.2086Semi standard non polar3932.4285
RI00068347Maltotriose,1TMS,isomer#4JsmolC[Si](C)(C)O[C@@H]1[C@@H](O)C(O)O[C@H](CO)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1OTMS576.2086Semi standard non polar3940.0771
RI00068348Maltotriose,1TMS,isomer#5JsmolC[Si](C)(C)O[C@H]1C(O)O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@@H]1OTMS576.2086Semi standard non polar3966.875
RI00068349Maltotriose,1TMS,isomer#6JsmolC[Si](C)(C)OC1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1OTMS576.2086Semi standard non polar3982.737
RI00068350Maltotriose,1TMS,isomer#7JsmolC[Si](C)(C)OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1OTMS576.2086Semi standard non polar3937.6902
Displaying retention index compounds 68326 - 68350 of 1722868 in total