Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 151 - 175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01724026d-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 non polar1658.6564
RI01724025d-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 non polar1628.265
RI01724024d-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 non polar1621.8496
RI01724023d-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 non polar1625.7485
RI01724022d-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 non polar1623.724
RI01724021d-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 non polar1804.9908
RI01724020d-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 non polar1730.9845
RI01724019d-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 non polar1728.4728
RI01724018d-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 non polar1724.0807
RI01724017d-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 non polar1725.2607
RI01724016d-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 non polar1722.2594
RI01724015d-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 non polar1654.2037
RI01724014d-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 non polar1647.9373
RI01724013d-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 non polar1650.2491
RI01724012d-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 non polar1636.1184
RI01724011d-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 non polar1653.5366
RI01724010d-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 non polar1649.7375
RI01724009d-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 non polar1631.9117
RI01724008d-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 non polar1648.8776
RI01724007d-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 non polar1630.2028
RI01724006d-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 non polar1630.006
RI01724005d-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 non polar1566.1173
RI01724004d-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 non polar1564.0083
RI01724003d-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 non polar1537.5558
RI01724002d-Fucitol,2TMS,isomer#7JsmolC[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@H](O)CO[Si](C)(C)CTMS310.1632Standard non polar1566.8953
Displaying retention index compounds 151 - 175 of 1722868 in total