Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 101 - 125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01724076d-Fucitol,3TMS,isomer#9JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS382.2027Semi standard non polar1667.7281
RI01724075d-Fucitol,3TMS,isomer#8JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS382.2027Semi standard non polar1658.0648
RI01724074d-Fucitol,3TMS,isomer#7JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)CTMS382.2027Semi standard non polar1646.6279
RI01724073d-Fucitol,3TMS,isomer#6JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS382.2027Semi standard non polar1687.3958
RI01724072d-Fucitol,3TMS,isomer#5JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS382.2027Semi standard non polar1682.0166
RI01724071d-Fucitol,3TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)CTMS382.2027Semi standard non polar1666.9478
RI01724070d-Fucitol,3TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS382.2027Semi standard non polar1691.948
RI01724069d-Fucitol,3TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS382.2027Semi standard non polar1683.1095
RI01724068d-Fucitol,3TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS382.2027Semi standard non polar1663.9854
RI01724067d-Fucitol,2TMS,isomer#10JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS310.1632Semi standard non polar1593.238
RI01724066d-Fucitol,2TMS,isomer#9JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS310.1632Semi standard non polar1585.7865
RI01724065d-Fucitol,2TMS,isomer#8JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)CTMS310.1632Semi standard non polar1562.5059
RI01724064d-Fucitol,2TMS,isomer#7JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS310.1632Semi standard non polar1602.9573
RI01724063d-Fucitol,2TMS,isomer#6JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS310.1632Semi standard non polar1588.8219
RI01724062d-Fucitol,2TMS,isomer#5JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS310.1632Semi standard non polar1558.9282
RI01724061d-Fucitol,2TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS310.1632Semi standard non polar1633.4265
RI01724060d-Fucitol,2TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS310.1632Semi standard non polar1609.3889
RI01724059d-Fucitol,2TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS310.1632Semi standard non polar1586.0815
RI01724058d-Fucitol,2TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)COTMS310.1632Semi standard non polar1585.7131
RI01724057d-Fucitol,1TMS,isomer#5JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS238.1237Semi standard non polar1555.3002
RI01724056d-Fucitol,1TMS,isomer#4JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)CTMS238.1237Semi standard non polar1508.1887
RI01724055d-Fucitol,1TMS,isomer#3JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)COTMS238.1237Semi standard non polar1503.1978
RI01724054d-Fucitol,1TMS,isomer#2JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)COTMS238.1237Semi standard non polar1500.446
RI01724053d-Fucitol,1TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@H](O)COTMS238.1237Semi standard non polar1537.1702
RI01724052d-Fucitol,5TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS736.5165Standard non polar2695.8335
Displaying retention index compounds 101 - 125 of 1722868 in total