RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Displaying retention index compounds 12401 - 12425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Protoporphyrin IX,2TBDMS,isomer#3JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C(C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C(C)(C)C)C(CCC(=O)O)=C4C)[NH]3TBDMS790.431Semi standard non polar5664.1284
Protoporphyrin IX,2TBDMS,isomer#4JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5[NH]C(=CC1=N2)C(C)=C5CCC(=O)O)C(CCC(=O)O[Si](C)(C)C(C)(C)C)=C4C)N3[Si](C)(C)C(C)(C)CTBDMS790.431Semi standard non polar5666.853
Protoporphyrin IX,2TBDMS,isomer#5JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O)=C(C)C(=CC1=N2)N5[Si](C)(C)C(C)(C)C)C(CCC(=O)O[Si](C)(C)C(C)(C)C)=C4C)[NH]3TBDMS790.431Semi standard non polar5660.8315
Protoporphyrin IX,2TBDMS,isomer#6JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O)=C(C)C(=CC1=N2)N5[Si](C)(C)C(C)(C)C)C(CCC(=O)O)=C4C)N3[Si](C)(C)C(C)(C)CTBDMS790.431Semi standard non polar5687.198
Protoporphyrin IXJsmolCC1=C(CCC(O)=O)/C2=C/C3=N/C(=C\C4=C(C)C(C=C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C=C)=C4C)/C(C)=C3CCC(O)=OUnderivatized562.258Standard polar6245.915
Protoporphyrin IX,3TMS,isomer#1JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5[NH]C(=CC1=N2)C(C)=C5CCC(=O)O[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS778.3766Standard non polar4475.476
Protoporphyrin IX,3TMS,isomer#2JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)[NH]3TMS778.3766Standard non polar4460.95
Protoporphyrin IX,3TMS,isomer#3JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O)=C4C)N3[Si](C)(C)CTMS778.3766Standard non polar4484.5093
Protoporphyrin IX,3TMS,isomer#4JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS778.3766Standard non polar4480.369
Protoporphyrin IX,4TMS,isomer#1JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS850.4161Standard non polar4462.6196
Protoporphyrin IXJsmolCC1=C(CCC(O)=O)/C2=C/C3=N/C(=C\C4=C(C)C(C=C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C=C)=C4C)/C(C)=C3CCC(O)=OUnderivatized562.258Standard non polar3858.4224
Protoporphyrin IXJsmolCC1=C(CCC(O)=O)/C2=C/C3=N/C(=C\C4=C(C)C(C=C)=C(N4)/C=C4\N=C(\C=C\1/N\2)C(C=C)=C4C)/C(C)=C3CCC(O)=OUnderivatized562.258Semi standard non polar5813.2754
Protoporphyrin IX,3TMS,isomer#1JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5[NH]C(=CC1=N2)C(C)=C5CCC(=O)O[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS778.3766Semi standard non polar5237.876
Protoporphyrin IX,3TMS,isomer#2JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)[NH]3TMS778.3766Semi standard non polar5213.469
Protoporphyrin IX,3TMS,isomer#3JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O)=C4C)N3[Si](C)(C)CTMS778.3766Semi standard non polar5282.546
Protoporphyrin IX,3TMS,isomer#4JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS778.3766Semi standard non polar5277.191
Protoporphyrin IX,4TMS,isomer#1JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS850.4161Semi standard non polar5182.635
Protoporphyrin IX,3TMS,isomer#1JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5[NH]C(=CC1=N2)C(C)=C5CCC(=O)O[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS778.3766Standard polar6148.087
Protoporphyrin IX,3TMS,isomer#2JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)[NH]3TMS778.3766Standard polar6237.896
Protoporphyrin IX,3TMS,isomer#3JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O)=C4C)N3[Si](C)(C)CTMS778.3766Standard polar6111.8076
Protoporphyrin IX,3TMS,isomer#4JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS778.3766Standard polar6123.1855
Protoporphyrin IX,4TMS,isomer#1JsmolC=CC1=C(C)C2=CC3=C(C=C)C(C)=C(C=C4N=C(C=C5C(CCC(=O)O[Si](C)(C)C)=C(C)C(=CC1=N2)N5[Si](C)(C)C)C(CCC(=O)O[Si](C)(C)C)=C4C)N3[Si](C)(C)CTMS850.4161Standard polar5851.9287
Pyruvic acid,1TMS,isomer#1JsmolCC(=O)C(=O)O[Si](C)(C)CTMS160.0556Semi standard non polar908.7652
Pyruvic acid,1TMS,isomer#2JsmolC=C(O[Si](C)(C)C)C(=O)OTMS160.0556Semi standard non polar974.2478
Pyruvic acid,1TBDMS,isomer#1JsmolCC(=O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS202.1025Semi standard non polar1145.2899
Displaying retention index compounds 12401 - 12425 of 1722868 in total