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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21301 - 21325 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000213013a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#8JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3804.1238
RI000213023a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS652.4554Semi standard non polar3772.6511
RI000213033a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TBDMS,isomer#10JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS652.4554Semi standard non polar3817.116
RI000213043a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3OTBDMS766.5419Semi standard non polar4029.3489
RI000213053a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS766.5419Semi standard non polar3984.7327
RI000213063a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS766.5419Semi standard non polar4032.7893
RI000213073a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#4JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS766.5419Semi standard non polar3988.9707
RI000213083a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#5JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS766.5419Semi standard non polar3985.8186
RI000213093a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#6JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS766.5419Semi standard non polar3943.0962
RI000213103a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#7JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS766.5419Semi standard non polar4001.901
RI000213113a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#8JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS766.5419Semi standard non polar4036.1455
RI000213123a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS766.5419Semi standard non polar4000.043
RI000213133a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TBDMS,isomer#10JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS766.5419Semi standard non polar3976.9521
RI000213143a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3OTBDMS880.6284Semi standard non polar4175.41
RI000213153a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS880.6284Semi standard non polar4206.0527
RI000213163a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS880.6284Semi standard non polar4167.2114
RI000213173a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#4JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS880.6284Semi standard non polar4156.1606
RI000213183a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acid,4TBDMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)C(C)(C)CTBDMS880.6284Semi standard non polar4212.4805
RI000213193a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])[C@@H](O)[C@H](O)CC[C@]12CUnderivatized424.2825Standard polar4247.3994
RI000213203a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])[C@@H](O)[C@H](O)CC[C@]12CUnderivatized424.2825Standard non polar3612.5806
RI000213213a,4b,7a,12a-Tetrahydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@@H](O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])[C@@H](O)[C@H](O)CC[C@]12CUnderivatized424.2825Semi standard non polar3818.2358
RI000213223b,12a-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
RI000213233b,12a-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
RI000213243b,12a-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
RI000213253b,12a-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
Displaying retention index compounds 21301 - 21325 of 1722868 in total