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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 5176 - 5200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00005176Cytidine monophosphate,3TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C=C1TBDMS665.3113Standard polar4043.48
RI00005177Cytidine monophosphate,3TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@H](O)[C@@H]1OTBDMS665.3113Standard polar4114.313
RI00005178Cytidine monophosphate,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N)=NC2=O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS779.3978Standard polar4077.1333
RI00005179Cytidine monophosphate,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=C1TBDMS779.3978Standard polar3994.3032
RI00005180Cytidine monophosphate,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS779.3978Standard polar4004.4053
RI00005181Cytidine monophosphate,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C1TBDMS779.3978Standard polar3856.2422
RI00005182Cytidine monophosphate,4TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]1OTBDMS779.3978Standard polar3852.2793
RI00005183Cytidine monophosphate,4TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C1TBDMS779.3978Standard polar3891.3188
RI00005184Cytidine monophosphate,4TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC1=OTBDMS779.3978Standard polar3872.684
RI00005185Cytidine monophosphate,4TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)CTBDMS779.3978Standard polar3792.3516
RI00005186Cytidine monophosphate,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)N([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C=C1TBDMS893.4842Standard polar3791.9792
RI00005187Cytidine monophosphate,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS893.4842Standard polar3750.3184
RI00005188Cytidine monophosphate,5TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)[C@@H]1OTBDMS893.4842Standard polar3646.7832
RI00005189Cytidine monophosphate,5TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC1=OTBDMS893.4842Standard polar3681.1013
RI00005190Choline,1TMS,isomer#1JsmolC[N+](C)(C)CCO[Si](C)(C)CTMS176.1465Semi standard non polar957.7267
RI00005191Choline,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC[N+](C)(C)CTBDMS218.1935Semi standard non polar1157.3417
RI00005192CholineJsmolC[N+](C)(C)CCOUnderivatized104.107Standard polar1419.5618
RI00005193CholineJsmolC[N+](C)(C)CCOUnderivatized104.107Standard non polar723.1231
RI00005194CholineJsmolC[N+](C)(C)CCOUnderivatized104.107Semi standard non polar819.9929
RI00005195D-Xylose,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1COC(O)[C@H](O)[C@H]1OTMS222.0924Semi standard non polar1506.1984
RI00005196D-Xylose,1TMS,isomer#2JsmolC[Si](C)(C)OC1OC[C@@H](O)[C@H](O)[C@H]1OTMS222.0924Semi standard non polar1495.1107
RI00005197D-Xylose,1TMS,isomer#3JsmolC[Si](C)(C)O[C@H]1C(O)OC[C@@H](O)[C@@H]1OTMS222.0924Semi standard non polar1507.291
RI00005198D-Xylose,1TMS,isomer#4JsmolC[Si](C)(C)O[C@H]1[C@H](O)COC(O)[C@@H]1OTMS222.0924Semi standard non polar1509.1788
RI00005199D-Xylose,2TMS,isomer#1JsmolC[Si](C)(C)OC1OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1OTMS294.1319Semi standard non polar1539.2114
RI00005200D-Xylose,2TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1COC(O)[C@H](O[Si](C)(C)C)[C@H]1OTMS294.1319Semi standard non polar1524.2902
Displaying retention index compounds 5176 - 5200 of 1722868 in total