RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14126 - 14150 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017100515-formyl-tetrahydrofolate,3TMS,isomer#11JsmolC[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS687.2699Standard polar6009.8555
RI017100505-formyl-tetrahydrofolate,3TMS,isomer#10JsmolC[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)[Si](C)(C)C)N2C=O)[NH]1TMS687.2699Standard polar6081.581
RI017100495-formyl-tetrahydrofolate,3TMS,isomer#9JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1)N2C=OTMS687.2699Standard polar5881.5386
RI017100485-formyl-tetrahydrofolate,3TMS,isomer#8JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CN(C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)[Si](C)(C)C)N2C=OTMS687.2699Standard polar5828.723
RI017100475-formyl-tetrahydrofolate,3TMS,isomer#7JsmolC[Si](C)(C)NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)N2C=O)N1[Si](C)(C)CTMS687.2699Standard polar6216.693
RI017100465-formyl-tetrahydrofolate,3TMS,isomer#6JsmolC[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)[Si](C)(C)C)N2C=O)N1[Si](C)(C)CTMS687.2699Standard polar6146.514
RI017100455-formyl-tetrahydrofolate,3TMS,isomer#5JsmolC[Si](C)(C)NC1=NC(=O)C2=C(N([Si](C)(C)C)CC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)CTMS687.2699Standard polar5855.934
RI017100445-formyl-tetrahydrofolate,3TMS,isomer#4JsmolC[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]3)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS687.2699Standard polar6028.316
RI017100435-formyl-tetrahydrofolate,3TMS,isomer#3JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS687.2699Standard polar5960.663
RI017100425-formyl-tetrahydrofolate,3TMS,isomer#2JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C2)N(C=O)C2=C1[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS687.2699Standard polar5816.3228
RI017100415-formyl-tetrahydrofolate,3TMS,isomer#1JsmolC[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)C)[Si](C)(C)CTMS687.2699Standard polar6140.5835
RI017100405-formyl-tetrahydrofolate,2TMS,isomer#11JsmolC[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N)N3[Si](C)(C)C)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS615.2304Standard polar6631.9854
RI017100395-formyl-tetrahydrofolate,2TMS,isomer#10JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C1TMS615.2304Standard polar6335.871
RI017100385-formyl-tetrahydrofolate,2TMS,isomer#9JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS615.2304Standard polar6549.229
RI017100375-formyl-tetrahydrofolate,2TMS,isomer#8JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C2)N(C=O)C2=C1N([Si](C)(C)C)C(N)=NC2=OTMS615.2304Standard polar6440.953
RI017100365-formyl-tetrahydrofolate,2TMS,isomer#7JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C2)N(C=O)C2=C1[NH]C(N)=NC2=OTMS615.2304Standard polar6277.0854
RI017100355-formyl-tetrahydrofolate,2TMS,isomer#6JsmolC[Si](C)(C)N(CC1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS615.2304Standard polar6215.5874
RI017100345-formyl-tetrahydrofolate,2TMS,isomer#5JsmolC[Si](C)(C)NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)N2C=O)[NH]1TMS615.2304Standard polar6626.086
RI017100335-formyl-tetrahydrofolate,2TMS,isomer#4JsmolC[Si](C)(C)NC1=NC(=O)C2=C(NCC(CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)[Si](C)(C)C)N2C=O)[NH]1TMS615.2304Standard polar6559.457
RI017100325-formyl-tetrahydrofolate,2TMS,isomer#3JsmolC[Si](C)(C)NC1=NC(=O)C2=C([NH]1)N([Si](C)(C)C)CC(CNC1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)N2C=OTMS615.2304Standard polar6309.896
RI017100315-formyl-tetrahydrofolate,2TMS,isomer#2JsmolC[Si](C)(C)NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)N1[Si](C)(C)CTMS615.2304Standard polar6675.0513
RI017100305-formyl-tetrahydrofolate,2TMS,isomer#1JsmolC[Si](C)(C)N(C1=NC(=O)C2=C(NCC(CNC3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)N2C=O)[NH]1)[Si](C)(C)CTMS615.2304Standard polar6560.97
RI017100295-formyl-tetrahydrofolate,1TMS,isomer#5JsmolC[Si](C)(C)N1C(N)=NC(=O)C2=C1NCC(CNC1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1)N2C=OTMS543.1909Standard polar7095.6245
RI017100285-formyl-tetrahydrofolate,1TMS,isomer#4JsmolC[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(C(=O)N=C(N)[NH]3)N2C=O)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS543.1909Standard polar6895.648
RI017100275-formyl-tetrahydrofolate,1TMS,isomer#3JsmolC[Si](C)(C)N(CC1CNC2=C(C(=O)N=C(N)[NH]2)N1C=O)C1=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C1TMS543.1909Standard polar6838.605
Displaying retention index compounds 14126 - 14150 of 1722868 in total