Displaying retention index compounds 1526 - 1550 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Ascorbic acid,3TMS,isomer#2JsmolC[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(O[Si](C)(C)C)=C1O[Si](C)(C)CTMS392.1507Semi standard non polar1899.1772
Ascorbic acid,3TMS,isomer#3JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H]1OC(=O)C(O[Si](C)(C)C)=C1OTMS392.1507Semi standard non polar1841.2637
Ascorbic acid,3TMS,isomer#4JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H]1OC(=O)C(O)=C1O[Si](C)(C)CTMS392.1507Semi standard non polar1900.3777
Ascorbic acid,4TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H]1OC(=O)C(O[Si](C)(C)C)=C1O[Si](C)(C)CTMS464.1902Semi standard non polar1998.375
Ascorbic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O)[C@@H]([C@@H](O)CO)OC1=OTBDMS290.1186Semi standard non polar1967.8154
Ascorbic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C(O)C(=O)O[C@@H]1[C@@H](O)COTBDMS290.1186Semi standard non polar1985.9357
Ascorbic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@@H](CO)[C@H]1OC(=O)C(O)=C1OTBDMS290.1186Semi standard non polar1982.4359
Ascorbic acid,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(O)=C1OTBDMS290.1186Semi standard non polar1976.5728
Ascorbic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@H]([C@@H](O)CO)OC1=OTBDMS404.205Semi standard non polar2299.6006
Ascorbic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C(O)[C@@H]([C@H](CO)O[Si](C)(C)C(C)(C)C)OC1=OTBDMS404.205Semi standard non polar2273.625
Ascorbic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(O[Si](C)(C)C(C)(C)C)=C1OTBDMS404.205Semi standard non polar2271.3113
Ascorbic acid,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=C(O)C(=O)O[C@@H]1[C@H](CO)O[Si](C)(C)C(C)(C)CTBDMS404.205Semi standard non polar2309.0552
Ascorbic acid,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(O)=C1O[Si](C)(C)C(C)(C)CTBDMS404.205Semi standard non polar2297.3572
Ascorbic acid,2TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1OC(=O)C(O)=C1OTBDMS404.205Semi standard non polar2253.9473
Ascorbic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@H]([C@H](CO)O[Si](C)(C)C(C)(C)C)OC1=OTBDMS518.2915Semi standard non polar2620.357
Ascorbic acid,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)CTBDMS518.2915Semi standard non polar2615.4841
Ascorbic acid,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1OC(=O)C(O[Si](C)(C)C(C)(C)C)=C1OTBDMS518.2915Semi standard non polar2540.3252
Ascorbic acid,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1OC(=O)C(O)=C1O[Si](C)(C)C(C)(C)CTBDMS518.2915Semi standard non polar2575.137
Ascorbic acid,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1OC(=O)C(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)CTBDMS632.378Semi standard non polar2867.1672
Ascorbic acidJsmol[H][C@@]1(OC(=O)C(O)=C1O)[C@@H](O)COUnderivatized176.0321Standard polar3155.3127
Ascorbic acidJsmol[H][C@@]1(OC(=O)C(O)=C1O)[C@@H](O)COUnderivatized176.0321Standard non polar1812.7074
Ascorbic acidJsmol[H][C@@]1(OC(=O)C(O)=C1O)[C@@H](O)COUnderivatized176.0321Semi standard non polar1558.2362
Adenosine monophosphate,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N)N=CN=C32)[C@@H]1OTMS419.1026Semi standard non polar3077.793
Adenosine monophosphate,1TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N)N=CN=C21TMS419.1026Semi standard non polar3063.6353
Adenosine monophosphate,1TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C(N)N=CN=C32)[C@H](O)[C@@H]1OTMS419.1026Semi standard non polar3168.5747
Displaying retention index compounds 1526 - 1550 of 1722868 in total