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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 26 - 50 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01724151d-Fucitol,2TBDMS,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)[C@H](O)COTBDMS394.2571Standard polar2247.3354
RI01724150d-Fucitol,1TBDMS,isomer#5JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS280.1706Standard polar2627.2585
RI01724149d-Fucitol,1TBDMS,isomer#4JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)CTBDMS280.1706Standard polar2548.0127
RI01724148d-Fucitol,1TBDMS,isomer#3JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COTBDMS280.1706Standard polar2517.1296
RI01724147d-Fucitol,1TBDMS,isomer#2JsmolC[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)COTBDMS280.1706Standard polar2520.5732
RI01724146d-Fucitol,1TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@H](O)COTBDMS280.1706Standard polar2595.0188
RI01724145d-Fucitol,5TMS,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](CO[Si](C)(C)C)O[Si](C)(C)CTMS526.2818Standard polar1667.7637
RI01724144d-Fucitol,4TMS,isomer#5JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS454.2422Standard polar1721.8643
RI01724143d-Fucitol,4TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS454.2422Standard polar1768.4888
RI01724142d-Fucitol,4TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS454.2422Standard polar1704.0388
RI01724141d-Fucitol,4TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS454.2422Standard polar1681.411
RI01724140d-Fucitol,4TMS,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](CO)O[Si](C)(C)CTMS454.2422Standard polar1671.3148
RI01724139d-Fucitol,3TMS,isomer#10JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS382.2027Standard polar1939.221
RI01724138d-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)CTMS382.2027Standard polar1870.9943
RI01724137d-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)CTMS382.2027Standard polar1849.816
RI01724136d-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)CTMS382.2027Standard polar1842.2098
RI01724135d-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)CTMS382.2027Standard polar1949.8815
RI01724134d-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)CTMS382.2027Standard polar1878.8918
RI01724133d-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)CTMS382.2027Standard polar1877.8643
RI01724132d-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)CTMS382.2027Standard polar1881.5865
RI01724131d-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)CTMS382.2027Standard polar1828.8557
RI01724130d-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)COTMS382.2027Standard polar1853.1326
RI01724129d-Fucitol,2TMS,isomer#10JsmolC[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS310.1632Standard polar2157.0132
RI01724128d-Fucitol,2TMS,isomer#9JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS310.1632Standard polar2070.775
RI01724127d-Fucitol,2TMS,isomer#8JsmolC[C@H](O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)CTMS310.1632Standard polar2072.4707
Displaying retention index compounds 26 - 50 of 1722868 in total