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Displaying retention index compounds 20176 - 20200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
2-Methyl-3-ketovaleric acid,2TBDMS,isomer#1JsmolCCC(O[Si](C)(C)C(C)(C)C)=C(C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS358.2359Standard polar1657.6937
2-Methyl-3-ketovaleric acid,2TBDMS,isomer#2JsmolCC=C(O[Si](C)(C)C(C)(C)C)C(C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS358.2359Standard polar1669.4128
(5R)-5-Hydroxyhexanoic acid,1TMS,isomer#1JsmolC[C@H](CCCC(=O)O)O[Si](C)(C)CTMS204.1182Semi standard non polar1284.7192
(5R)-5-Hydroxyhexanoic acid,1TMS,isomer#2JsmolC[C@@H](O)CCCC(=O)O[Si](C)(C)CTMS204.1182Semi standard non polar1260.2983
(5R)-5-Hydroxyhexanoic acid,2TMS,isomer#1JsmolC[C@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS276.1577Semi standard non polar1361.2708
(5R)-5-Hydroxyhexanoic acid,1TBDMS,isomer#1JsmolC[C@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)CTBDMS246.1651Semi standard non polar1532.3217
(5R)-5-Hydroxyhexanoic acid,1TBDMS,isomer#2JsmolC[C@@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)CTBDMS246.1651Semi standard non polar1479.5007
(5R)-5-Hydroxyhexanoic acid,2TBDMS,isomer#1JsmolC[C@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS360.2516Semi standard non polar1812.8855
(5R)-5-Hydroxyhexanoic acidJsmolC[C@@H](O)CCCC(O)=OUnderivatized132.0786Standard polar2439.0923
(5R)-5-Hydroxyhexanoic acidJsmolC[C@@H](O)CCCC(O)=OUnderivatized132.0786Standard non polar1149.6758
(5R)-5-Hydroxyhexanoic acidJsmolC[C@@H](O)CCCC(O)=OUnderivatized132.0786Semi standard non polar1185.055
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acid,1TMS,isomer#1JsmolC[C@@H](O[Si](C)(C)C)[C@@H](C)C(=O)OTMS190.1025Semi standard non polar1128.6089
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acid,1TMS,isomer#2JsmolC[C@@H](O)[C@@H](C)C(=O)O[Si](C)(C)CTMS190.1025Semi standard non polar1061.2828
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acid,2TMS,isomer#1JsmolC[C@@H](O[Si](C)(C)C)[C@@H](C)C(=O)O[Si](C)(C)CTMS262.142Semi standard non polar1206.7295
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acid,1TBDMS,isomer#1JsmolC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C)C(=O)OTBDMS232.1495Semi standard non polar1367.0887
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acid,1TBDMS,isomer#2JsmolC[C@@H](O)[C@@H](C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS232.1495Semi standard non polar1283.6986
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acid,2TBDMS,isomer#1JsmolC[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS346.2359Semi standard non polar1646.0823
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acidJsmolC[C@@H](O)[C@@H](C)C(O)=OUnderivatized118.063Standard polar2083.5176
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acidJsmolC[C@@H](O)[C@@H](C)C(O)=OUnderivatized118.063Standard non polar1019.9437
3-Hydroxy-2-methyl-[S-(R,R)]-butanoic acidJsmolC[C@@H](O)[C@@H](C)C(O)=OUnderivatized118.063Semi standard non polar1040.2854
3a,12b-Dihydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS464.3322Semi standard non polar3290.7327
3a,12b-Dihydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O[Si](C)(C)C)[C@@]21CTMS464.3322Semi standard non polar3366.5308
3a,12b-Dihydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS464.3322Semi standard non polar3376.256
3a,12b-Dihydroxy-5b-cholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS536.3717Semi standard non polar3307.6038
3a,12b-Dihydroxy-5b-cholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O[Si](C)(C)C)[C@@]21CTMS536.3717Semi standard non polar3285.4995
Displaying retention index compounds 20176 - 20200 of 1722868 in total