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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 15001 - 15025 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017091764alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#22JsmolCC(O)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2456.9968
RI017091754alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#21JsmolCC(O)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS545.2705Semi standard non polar2556.8127
RI017091744alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#20JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS545.2705Semi standard non polar2510.975
RI017091734alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#19JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1TMS545.2705Semi standard non polar2462.8745
RI017091724alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#18JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS545.2705Semi standard non polar2470.476
RI017091714alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#17JsmolCC(O)C(O[Si](C)(C)C)C1CNC2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS545.2705Semi standard non polar2526.2075
RI017091704alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#16JsmolCC(O)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2531.8987
RI017091694alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#15JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2451.9097
RI017091684alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#14JsmolCC(O[Si](C)(C)C)C(O)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS545.2705Semi standard non polar2581.3752
RI017091674alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#13JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS545.2705Semi standard non polar2531.4705
RI017091664alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#12JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1TMS545.2705Semi standard non polar2450.5225
RI017091654alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#11JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS545.2705Semi standard non polar2486.9763
RI017091644alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#10JsmolCC(O[Si](C)(C)C)C(O)C1CNC2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS545.2705Semi standard non polar2533.9
RI017091634alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#9JsmolCC(O[Si](C)(C)C)C(O)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2558.7744
RI017091624alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#8JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2441.429
RI017091614alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#7JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N)=NC(=O)C2(O)N1[Si](C)(C)CTMS545.2705Semi standard non polar2501.356
RI017091604alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#6JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CNC2=NC(N[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS545.2705Semi standard non polar2545.7737
RI017091594alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#5JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1TMS545.2705Semi standard non polar2534.5598
RI017091584alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#4JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O)N1TMS545.2705Semi standard non polar2447.892
RI017091574alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#3JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CNC2=NC(N)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS545.2705Semi standard non polar2541.704
RI017091564alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#2JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2446.8213
RI017091554alpha-hydroxy-tetrahydrobiopterin,4TMS,isomer#1JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CNC2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS545.2705Semi standard non polar2490.575
RI017091544alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#16JsmolCC(O)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3557.9126
RI017091534alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#15JsmolCC(O)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3501.7625
RI017091524alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#14JsmolCC(O)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3492.8733
Displaying retention index compounds 15001 - 15025 of 1722868 in total