Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 751 - 775 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00000751Tetrahydrobiopterin,4TBDMS,isomer#15JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[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)N2[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3414.5369
RI00000752Tetrahydrobiopterin,4TBDMS,isomer#16JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[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)[Si](C)(C)C(C)(C)C)[NH]2TBDMS697.4634Semi standard non polar3366.4111
RI00000753Tetrahydrobiopterin,4TBDMS,isomer#17JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3290.143
RI00000754Tetrahydrobiopterin,4TBDMS,isomer#18JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3414.4866
RI00000755Tetrahydrobiopterin,4TBDMS,isomer#19JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3363.1414
RI00000756Tetrahydrobiopterin,4TBDMS,isomer#20JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3330.674
RI00000757Tetrahydrobiopterin,4TBDMS,isomer#21JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3358.6907
RI00000758Tetrahydrobiopterin,4TBDMS,isomer#22JsmolC[C@H](O)[C@H](O)[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)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3388.881
RI00000759Tetrahydrobiopterin,4TBDMS,isomer#23JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3339.412
RI00000760Tetrahydrobiopterin,4TBDMS,isomer#24JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3293.067
RI00000761Tetrahydrobiopterin,4TBDMS,isomer#25JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS697.4634Semi standard non polar3365.6685
RI00000762Tetrahydrobiopterin,5TBDMS,isomer#1JsmolC[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[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3564.0645
RI00000763Tetrahydrobiopterin,5TBDMS,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([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2TBDMS811.5499Semi standard non polar3514.263
RI00000764Tetrahydrobiopterin,5TBDMS,isomer#3JsmolC[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(C(=O)N=C(N[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3454.2712
RI00000765Tetrahydrobiopterin,5TBDMS,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(N1)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3562.7512
RI00000766Tetrahydrobiopterin,5TBDMS,isomer#5JsmolC[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[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3516.5151
RI00000767Tetrahydrobiopterin,5TBDMS,isomer#6JsmolC[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([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3469.8389
RI00000768Tetrahydrobiopterin,5TBDMS,isomer#7JsmolC[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(C(=O)N=C(N)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3555.996
RI00000769Tetrahydrobiopterin,5TBDMS,isomer#8JsmolC[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)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3559.7651
RI00000770Tetrahydrobiopterin,5TBDMS,isomer#9JsmolC[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(C(=O)N=C(N[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3529.334
RI00000771Tetrahydrobiopterin,5TBDMS,isomer#10JsmolC[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(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3460.8845
RI00000772Tetrahydrobiopterin,5TBDMS,isomer#11JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3544.7551
RI00000773Tetrahydrobiopterin,5TBDMS,isomer#12JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[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)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3589.5308
RI00000774Tetrahydrobiopterin,5TBDMS,isomer#13JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3544.9297
RI00000775Tetrahydrobiopterin,5TBDMS,isomer#14JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Semi standard non polar3493.9746
Displaying retention index compounds 751 - 775 of 1722868 in total