Displaying retention index compounds 1476 - 1500 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Dihydrobiopterin,3TBDMS,isomer#7JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS581.3613Standard polar4023.1218
Dihydrobiopterin,3TBDMS,isomer#8JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Standard polar4249.7163
Dihydrobiopterin,3TBDMS,isomer#9JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Standard polar4351.1973
Dihydrobiopterin,3TBDMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS581.3613Standard polar4298.8467
Dihydrobiopterin,3TBDMS,isomer#11JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS581.3613Standard polar3901.5864
Dihydrobiopterin,3TBDMS,isomer#12JsmolC[C@H](O)[C@H](O)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Standard polar4258.3223
Dihydrobiopterin,3TBDMS,isomer#13JsmolC[C@H](O)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Standard polar4208.6577
Dihydrobiopterin,3TBDMS,isomer#14JsmolC[C@H](O)[C@H](O)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS581.3613Standard polar4280.4683
Dihydrobiopterin,4TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar4077.1714
Dihydrobiopterin,4TBDMS,isomer#2JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar4155.743
Dihydrobiopterin,4TBDMS,isomer#3JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS695.4477Standard polar4111.124
Dihydrobiopterin,4TBDMS,isomer#4JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS695.4477Standard polar3826.9924
Dihydrobiopterin,4TBDMS,isomer#5JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar4071.7214
Dihydrobiopterin,4TBDMS,isomer#6JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar4017.1162
Dihydrobiopterin,4TBDMS,isomer#7JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS695.4477Standard polar4078.0818
Dihydrobiopterin,4TBDMS,isomer#8JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar3960.847
Dihydrobiopterin,4TBDMS,isomer#9JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar3893.5173
Dihydrobiopterin,4TBDMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS695.4477Standard polar3972.3252
Dihydrobiopterin,4TBDMS,isomer#11JsmolC[C@H](O)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar3938.0654
Dihydrobiopterin,5TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3864.8245
Dihydrobiopterin,5TBDMS,isomer#2JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3803.5679
Dihydrobiopterin,5TBDMS,isomer#3JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS809.5342Standard polar3865.0076
Dihydrobiopterin,5TBDMS,isomer#4JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3825.9355
Dihydrobiopterin,5TBDMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3697.6987
Butyric acid,1TMS,isomer#1JsmolCCCC(=O)O[Si](C)(C)CTMS160.092Semi standard non polar880.4771
Displaying retention index compounds 1476 - 1500 of 1722868 in total