Displaying retention index compounds 251 - 275 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
3-Oxo-5beta-cholanoic acid,1TMS,isomer#2JsmolCC(CCC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC12CTMS446.3216Standard non polar3036.0725
3-Oxo-5beta-cholanoic acid,1TMS,isomer#1JsmolCC(CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(=O)CCC4(C)C3CCC12CTMS446.3216Standard non polar3180.4268
Nordeoxycholic acid,3TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS720.5364Standard polar3697.6016
Nordeoxycholic acid,2TBDMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS606.45Standard polar3746.6414
Nordeoxycholic acid,2TBDMS,isomer#2JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS606.45Standard polar3755.207
Nordeoxycholic acid,2TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12CTBDMS606.45Standard polar3832.7573
Nordeoxycholic acid,1TBDMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS492.3635Standard polar3701.054
Nordeoxycholic acid,1TBDMS,isomer#2JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12CTBDMS492.3635Standard polar3776.2412
Nordeoxycholic acid,1TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12CTBDMS492.3635Standard polar3779.663
Nordeoxycholic acid,3TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS594.3956Standard polar3439.3943
Nordeoxycholic acid,2TMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS522.3561Standard polar3518.364
Nordeoxycholic acid,2TMS,isomer#2JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS522.3561Standard polar3531.0764
Nordeoxycholic acid,2TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12CTMS522.3561Standard polar3615.6084
Nordeoxycholic acid,1TMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS450.3165Standard polar3547.5674
Nordeoxycholic acid,1TMS,isomer#2JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12CTMS450.3165Standard polar3630.5513
Nordeoxycholic acid,1TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12CTMS450.3165Standard polar3641.5479
Nordeoxycholic acid,3TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS720.5364Semi standard non polar3878.833
Nordeoxycholic acid,2TBDMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS606.45Semi standard non polar3769.2612
Nordeoxycholic acid,2TBDMS,isomer#2JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS606.45Semi standard non polar3697.3357
Nordeoxycholic acid,2TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12CTBDMS606.45Semi standard non polar3785.7283
Nordeoxycholic acid,1TBDMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS492.3635Semi standard non polar3551.7812
Nordeoxycholic acid,1TBDMS,isomer#2JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12CTBDMS492.3635Semi standard non polar3594.5508
Nordeoxycholic acid,1TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12CTBDMS492.3635Semi standard non polar3554.5364
Nordeoxycholic acid,3TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS594.3956Semi standard non polar3200.9453
Nordeoxycholic acid,2TMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS522.3561Semi standard non polar3343.796
Displaying retention index compounds 251 - 275 of 1722868 in total