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 9976 - 10000 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00009976InosineJsmolOC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C(O)N=CN=C12Underivatized268.0808Semi standard non polar2504.527
RI00009977Indoleacetic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1=C[NH]C2=CC=CC=C12TMS247.1029Semi standard non polar1928.6272
RI00009978Indoleacetic acid,1TMS,isomer#2JsmolC[Si](C)(C)N1C=C(CC(=O)O)C2=CC=CC=C21TMS247.1029Semi standard non polar2016.4098
RI00009979Indoleacetic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1=C[NH]C2=CC=CC=C12TBDMS289.1498Semi standard non polar2189.091
RI00009980Indoleacetic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(=O)O)C2=CC=CC=C21TBDMS289.1498Semi standard non polar2270.7058
RI00009981Indoleacetic acidJsmolOC(=O)CC1=CNC2=C1C=CC=C2Underivatized175.0633Standard polar3255.8147
RI00009982Indoleacetic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS319.1424Standard non polar1933.4069
RI00009983Indoleacetic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS403.2363Standard non polar2359.275
RI00009984Indoleacetic acidJsmolOC(=O)CC1=CNC2=C1C=CC=C2Underivatized175.0633Standard non polar1714.1764
RI00009985Indoleacetic acidJsmolOC(=O)CC1=CNC2=C1C=CC=C2Underivatized175.0633Semi standard non polar1908.764
RI00009986Indoleacetic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS319.1424Semi standard non polar1966.0428
RI00009987Indoleacetic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS403.2363Semi standard non polar2415.3052
RI00009988Indoleacetic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS319.1424Standard polar2138.915
RI00009989Indoleacetic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS403.2363Standard polar2374.4395
RI00009990L-Acetylcarnitine,1TMS,isomer#1JsmolCC(=O)O[C@H](CC(=O)O[Si](C)(C)C)C[N+](C)(C)CTMS276.1626Semi standard non polar1423.9633
RI00009991L-Acetylcarnitine,1TBDMS,isomer#1JsmolCC(=O)O[C@H](CC(=O)O[Si](C)(C)C(C)(C)C)C[N+](C)(C)CTBDMS318.2095Semi standard non polar1660.2375
RI00009992L-AcetylcarnitineJsmolCC(=O)O[C@H](CC(O)=O)C[N+](C)(C)CUnderivatized204.123Standard polar2322.8694
RI00009993L-AcetylcarnitineJsmolCC(=O)O[C@H](CC(O)=O)C[N+](C)(C)CUnderivatized204.123Standard non polar1232.0162
RI00009994L-AcetylcarnitineJsmolCC(=O)O[C@H](CC(O)=O)C[N+](C)(C)CUnderivatized204.123Semi standard non polar1468.5836
RI00009995Methylmalonic acid,1TMS,isomer#1JsmolCC(C(=O)O)C(=O)O[Si](C)(C)CTMS190.0661Semi standard non polar1148.0852
RI00009996Methylmalonic acid,2TMS,isomer#1JsmolCC(C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS262.1057Semi standard non polar1233.1223
RI00009997Methylmalonic acid,1TBDMS,isomer#1JsmolCC(C(=O)O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS232.1131Semi standard non polar1396.3704
RI00009998Methylmalonic acid,2TBDMS,isomer#1JsmolCC(C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS346.1996Semi standard non polar1660.4006
RI00009999Methylmalonic acidJsmolCC(C(O)=O)C(O)=OUnderivatized118.0266Standard polar1770.8378
RI00010000Methylmalonic acidJsmolCC(C(O)=O)C(O)=OUnderivatized118.0266Standard non polar967.4996
Displaying retention index compounds 9976 - 10000 of 1722868 in total