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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 1721351 - 1721375 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00001518Ascorbic acid,1TMS,isomer#4JsmolC[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(O)=C1OTMS248.0716Semi standard non polar1710.899
RI00001517Ascorbic acid,1TMS,isomer#3JsmolC[Si](C)(C)O[C@@H](CO)[C@H]1OC(=O)C(O)=C1OTMS248.0716Semi standard non polar1711.3145
RI00001516Ascorbic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC1=C(O)C(=O)O[C@@H]1[C@@H](O)COTMS248.0716Semi standard non polar1709.5911
RI00001515Ascorbic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC1=C(O)[C@@H]([C@@H](O)CO)OC1=OTMS248.0716Semi standard non polar1685.6381
RI00001514BetaineJsmolC[N+](C)(C)CC(O)=OUnderivatized118.0863Semi standard non polar952.6458
RI00001513BetaineJsmolC[N+](C)(C)CC(O)=OUnderivatized118.0863Standard non polar846.7283
RI00001512BetaineJsmolC[N+](C)(C)CC(O)=OUnderivatized118.0863Standard polar1860.8778
RI00001511Betaine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C[N+](C)(C)CTBDMS232.1727Semi standard non polar1250.735
RI00001510Betaine,1TMS,isomer#1JsmolC[N+](C)(C)CC(=O)O[Si](C)(C)CTMS190.1258Semi standard non polar1043.7235
RI00001509Acetic acidJsmolCC(O)=OUnderivatized60.0211Semi standard non polar608.9136
RI00001508Acetic acidJsmolCC(O)=OUnderivatized60.0211Standard non polar594.6506
RI00001507Acetic acidJsmolCC(O)=OUnderivatized60.0211Standard polar1428.1372
RI00001506Acetic acid,1TBDMS,isomer#1JsmolCC(=O)O[Si](C)(C)C(C)(C)CTBDMS174.1076Semi standard non polar915.898
RI00001505Acetic acid,1TMS,isomer#1JsmolCC(=O)O[Si](C)(C)CTMS132.0607Semi standard non polar687.647
RI00001504Butyric acidJsmolCCCC(O)=OUnderivatized88.0524Semi standard non polar799.933
RI00001503Butyric acidJsmolCCCC(O)=OUnderivatized88.0524Standard non polar776.2217
RI00001502Butyric acidJsmolCCCC(O)=OUnderivatized88.0524Standard polar1578.3232
RI00001501Butyric acid,1TBDMS,isomer#1JsmolCCCC(=O)O[Si](C)(C)C(C)(C)CTBDMS202.1389Semi standard non polar1084.2543
RI00001500Butyric acid,1TMS,isomer#1JsmolCCCC(=O)O[Si](C)(C)CTMS160.092Semi standard non polar880.4771
RI00001499Dihydrobiopterin,5TBDMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3697.6987
RI00001498Dihydrobiopterin,5TBDMS,isomer#4JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3825.9355
RI00001497Dihydrobiopterin,5TBDMS,isomer#3JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS809.5342Standard polar3865.0076
RI00001496Dihydrobiopterin,5TBDMS,isomer#2JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3803.5679
RI00001495Dihydrobiopterin,5TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS809.5342Standard polar3864.8245
RI00001494Dihydrobiopterin,4TBDMS,isomer#11JsmolC[C@H](O)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Standard polar3938.0654
Displaying retention index compounds 1721351 - 1721375 of 1722868 in total