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Displaying retention index compounds 1722176 - 1722200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
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)CTMS601.3151Semi standard non polar2606.199
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)CTMS601.3151Semi standard non polar2621.0376
Tetrahydrobiopterin,5TMS,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)[NH]2)N1[Si](C)(C)CTMS601.3151Semi standard non polar2554.5225
Tetrahydrobiopterin,5TMS,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(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2TMS601.3151Semi standard non polar2580.2498
Tetrahydrobiopterin,5TMS,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)N2[Si](C)(C)CTMS601.3151Semi standard non polar2584.3005
Tetrahydrobiopterin,4TMS,isomer#25JsmolC[C@H](O)[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)CTMS529.2756Semi standard non polar2542.5012
Tetrahydrobiopterin,4TMS,isomer#24JsmolC[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)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2461.0664
Tetrahydrobiopterin,4TMS,isomer#23JsmolC[C@H](O)[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)CTMS529.2756Semi standard non polar2495.6392
Tetrahydrobiopterin,4TMS,isomer#22JsmolC[C@H](O)[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)CTMS529.2756Semi standard non polar2540.0261
Tetrahydrobiopterin,4TMS,isomer#21JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS529.2756Semi standard non polar2489.6335
Tetrahydrobiopterin,4TMS,isomer#20JsmolC[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)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2535.5852
Tetrahydrobiopterin,4TMS,isomer#19JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS529.2756Semi standard non polar2534.459
Tetrahydrobiopterin,4TMS,isomer#18JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)CTMS529.2756Semi standard non polar2564.655
Tetrahydrobiopterin,4TMS,isomer#17JsmolC[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)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2482.1267
Tetrahydrobiopterin,4TMS,isomer#16JsmolC[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)[NH]2TMS529.2756Semi standard non polar2499.7407
Tetrahydrobiopterin,4TMS,isomer#15JsmolC[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)N2[Si](C)(C)CTMS529.2756Semi standard non polar2521.5947
Tetrahydrobiopterin,4TMS,isomer#14JsmolC[C@H](O)[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)CTMS529.2756Semi standard non polar2464.2483
Tetrahydrobiopterin,4TMS,isomer#13JsmolC[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)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2500.7068
Tetrahydrobiopterin,4TMS,isomer#12JsmolC[C@H](O)[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)CTMS529.2756Semi standard non polar2528.1287
Tetrahydrobiopterin,4TMS,isomer#11JsmolC[C@H](O)[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)CTMS529.2756Semi standard non polar2552.5237
Tetrahydrobiopterin,4TMS,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)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2457.2185
Tetrahydrobiopterin,4TMS,isomer#9JsmolC[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)[NH]2TMS529.2756Semi standard non polar2472.9001
Tetrahydrobiopterin,4TMS,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)N2[Si](C)(C)CTMS529.2756Semi standard non polar2513.8235
Tetrahydrobiopterin,4TMS,isomer#7JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS529.2756Semi standard non polar2514.7517
Tetrahydrobiopterin,4TMS,isomer#6JsmolC[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)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2412.803
Displaying retention index compounds 1722176 - 1722200 of 1722868 in total