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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 10901 - 10925 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00010901Orotidylic acid,4TMS,isomer#11JsmolC[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1OTMS656.1838Standard polar3808.8079
RI00010902Orotidylic acid,5TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1=CC(=O)[NH]C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)CTMS728.2233Standard polar3474.3118
RI00010903Orotidylic acid,5TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)CTMS728.2233Standard polar3693.0854
RI00010904Orotidylic acid,5TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1OTMS728.2233Standard polar3522.1548
RI00010905Orotidylic acid,5TMS,isomer#4JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C(C(=O)O)=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1O[Si](C)(C)CTMS728.2233Standard polar3524.8916
RI00010906Orotidylic acid,5TMS,isomer#5JsmolC[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)CTMS728.2233Standard polar3551.1777
RI00010907Orotidylic acid,6TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)CTMS800.2629Standard polar3380.8113
RI00010908Orotidylic acid,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)[NH]C(=O)N1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS824.3716Standard polar4050.5735
RI00010909Orotidylic acid,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C(C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS824.3716Standard polar4254.926
RI00010910Orotidylic acid,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)[NH]C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1OTBDMS824.3716Standard polar3913.6538
RI00010911Orotidylic acid,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C(C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1OTBDMS824.3716Standard polar4092.964
RI00010912Orotidylic acid,4TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C(C(=O)O)=CC(=O)[NH]C2=O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS824.3716Standard polar3901.378
RI00010913Orotidylic acid,4TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C(C(=O)O)=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS824.3716Standard polar4104.3022
RI00010914Orotidylic acid,4TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C(C(=O)O)=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OTBDMS824.3716Standard polar3961.689
RI00010915Orotidylic acid,4TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)[NH]C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS824.3716Standard polar3942.109
RI00010916Orotidylic acid,4TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C(C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS824.3716Standard polar4108.072
RI00010917Orotidylic acid,4TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C(C(=O)O)=CC(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS824.3716Standard polar3991.3196
RI00010918Orotidylic acid,4TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(=O)N([Si](C)(C)C(C)(C)C)C(=O)N1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1OTBDMS824.3716Standard polar4020.873
RI00010919Palmitic acid,1TMS,isomer#1JsmolCCCCCCCCCCCCCCCC(=O)O[Si](C)(C)CTMS328.2798Semi standard non polar2044.7003
RI00010920Palmitic acid,1TBDMS,isomer#1JsmolCCCCCCCCCCCCCCCC(=O)O[Si](C)(C)C(C)(C)CTBDMS370.3267Semi standard non polar2291.2058
RI00010921Palmitic acidJsmolCCCCCCCCCCCCCCCC(O)=OUnderivatized256.2402Standard polar2904.2034
RI00010922Palmitic acidJsmolCCCCCCCCCCCCCCCC(O)=OUnderivatized256.2402Standard non polar1929.4259
RI00010923Palmitic acidJsmolCCCCCCCCCCCCCCCC(O)=OUnderivatized256.2402Semi standard non polar1976.9105
RI00010924NADPHJsmolNC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1OUnderivatized745.0911Standard polar5599.7915
RI00010925NADPHJsmolNC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1OUnderivatized745.0911Standard non polar3976.005
Displaying retention index compounds 10901 - 10925 of 1722868 in total