Displaying retention index compounds 176 - 200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
d-Fucitol,2TMS,isomer#6JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS310.1632Standard non polar1537.5852
d-Fucitol,2TMS,isomer#5JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS310.1632Standard non polar1532.0424
d-Fucitol,2TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS310.1632Standard non polar1570.991
d-Fucitol,2TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS310.1632Standard non polar1535.9877
d-Fucitol,2TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS310.1632Standard non polar1519.6017
d-Fucitol,2TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)COTMS310.1632Standard non polar1526.3479
d-Fucitol,1TMS,isomer#5JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS238.1237Standard non polar1443.822
d-Fucitol,1TMS,isomer#4JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS238.1237Standard non polar1415.3164
d-Fucitol,1TMS,isomer#3JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS238.1237Standard non polar1400.9072
d-Fucitol,1TMS,isomer#2JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)COTMS238.1237Standard non polar1409.3599
d-Fucitol,1TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H](O)COTMS238.1237Standard non polar1400.5895
O-Phenolsulfonic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)O[Si](C)(C)C(C)(C)CTBDMS402.1716Standard polar2230.4946
O-Phenolsulfonic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OS(=O)(=O)C1=CC=CC=C1OTBDMS288.0852Standard polar2442.0723
O-Phenolsulfonic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)OTBDMS288.0852Standard polar2354.404
O-Phenolsulfonic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)O[Si](C)(C)CTMS318.0777Standard polar2033.4594
O-Phenolsulfonic acid,1TMS,isomer#2JsmolC[Si](C)(C)OS(=O)(=O)C1=CC=CC=C1OTMS246.0382Standard polar2360.4998
O-Phenolsulfonic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)OTMS246.0382Standard polar2213.6096
O-Phenolsulfonic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)O[Si](C)(C)C(C)(C)CTBDMS402.1716Semi standard non polar2159.824
O-Phenolsulfonic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OS(=O)(=O)C1=CC=CC=C1OTBDMS288.0852Semi standard non polar1905.145
O-Phenolsulfonic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)OTBDMS288.0852Semi standard non polar1954.9492
O-Phenolsulfonic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)O[Si](C)(C)CTMS318.0777Semi standard non polar1686.566
O-Phenolsulfonic acid,1TMS,isomer#2JsmolC[Si](C)(C)OS(=O)(=O)C1=CC=CC=C1OTMS246.0382Semi standard non polar1653.0187
O-Phenolsulfonic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)OTMS246.0382Semi standard non polar1695.4691
O-Phenolsulfonic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1S(=O)(=O)O[Si](C)(C)C(C)(C)CTBDMS402.1716Standard non polar2224.9395
O-Phenolsulfonic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OS(=O)(=O)C1=CC=CC=C1OTBDMS288.0852Standard non polar1822.3195
Displaying retention index compounds 176 - 200 of 1722868 in total