Displaying retention index compounds 551 - 575 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Tetrahydrobiopterin,5TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)CTMS601.3151Standard non polar2773.0
Tetrahydrobiopterin,5TMS,isomer#5JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2628.0662
Tetrahydrobiopterin,5TMS,isomer#6JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS601.3151Standard non polar2726.9106
Tetrahydrobiopterin,5TMS,isomer#7JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2646.45
Tetrahydrobiopterin,5TMS,isomer#8JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)CTMS601.3151Standard non polar2936.8203
Tetrahydrobiopterin,5TMS,isomer#9JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2706.0618
Tetrahydrobiopterin,5TMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS601.3151Standard non polar2815.741
Tetrahydrobiopterin,5TMS,isomer#11JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2783.5393
Tetrahydrobiopterin,5TMS,isomer#12JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)CTMS601.3151Standard non polar2883.3557
Tetrahydrobiopterin,5TMS,isomer#13JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2675.3953
Tetrahydrobiopterin,5TMS,isomer#14JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS601.3151Standard non polar2784.9963
Tetrahydrobiopterin,5TMS,isomer#15JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2725.2375
Tetrahydrobiopterin,5TMS,isomer#16JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS601.3151Standard non polar2863.3535
Tetrahydrobiopterin,6TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)CTMS673.3547Standard non polar2921.5906
Tetrahydrobiopterin,6TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS673.3547Standard non polar2689.6035
Tetrahydrobiopterin,6TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS673.3547Standard non polar2792.1238
Tetrahydrobiopterin,6TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS673.3547Standard non polar2745.0022
Tetrahydrobiopterin,6TMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS673.3547Standard non polar2857.9988
Tetrahydrobiopterin,6TMS,isomer#6JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS673.3547Standard non polar2826.4014
Tetrahydrobiopterin,7TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS745.3942Standard non polar2833.112
Tetrahydrobiopterin,3TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C(C)(C)C)[NH]2TBDMS583.3769Standard non polar3283.4062
Tetrahydrobiopterin,3TBDMS,isomer#2JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N=C(N)[NH]2TBDMS583.3769Standard non polar3259.7576
Tetrahydrobiopterin,3TBDMS,isomer#3JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N)N2[Si](C)(C)C(C)(C)CTBDMS583.3769Standard non polar3168.981
Tetrahydrobiopterin,3TBDMS,isomer#4JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS583.3769Standard non polar3257.6362
Tetrahydrobiopterin,3TBDMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N=C(N[Si](C)(C)C(C)(C)C)[NH]2TBDMS583.3769Standard non polar3350.462
Displaying retention index compounds 551 - 575 of 1722868 in total