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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19726 - 19750 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000197263b,7b,12a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3578.9705
RI000197273b,7b,12a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3656.766
RI000197283b,7b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,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](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3752.9692
RI000197293b,7b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,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](O)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3849.5317
RI000197303b,7b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,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](O)C[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3838.8474
RI000197313b,7b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3767.2058
RI000197323b,7b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3798.5913
RI000197333b,7b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3761.4182
RI000197343b,7b,12a-Trihydroxy-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](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTBDMS750.547Semi standard non polar3941.7725
RI000197353b,7b,12a-Trihydroxy-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](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3958.451
RI000197363b,7b,12a-Trihydroxy-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](O)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3986.646
RI000197373b,7b,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3967.247
RI000197383b,7b,12a-Trihydroxy-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](O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS864.6335Semi standard non polar4162.0063
RI000197393b,7b,12a-Trihydroxy-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[C@@H](O)CC[C@]12CUnderivatized408.2876Standard polar4216.655
RI000197403b,7b,12a-Trihydroxy-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[C@@H](O)CC[C@]12CUnderivatized408.2876Standard non polar3464.1238
RI000197413b,7b,12a-Trihydroxy-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[C@@H](O)CC[C@]12CUnderivatized408.2876Semi standard non polar3681.9438
RI000197422-Ethylhydracrylic acid,1TMS,isomer#1JsmolCCC(CO[Si](C)(C)C)C(=O)OTMS190.1025Semi standard non polar1159.9355
RI000197432-Ethylhydracrylic acid,1TMS,isomer#2JsmolCCC(CO)C(=O)O[Si](C)(C)CTMS190.1025Semi standard non polar1105.239
RI000197442-Ethylhydracrylic acid,2TMS,isomer#1JsmolCCC(CO[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS262.142Semi standard non polar1221.8944
RI000197452-Ethylhydracrylic acid,1TBDMS,isomer#1JsmolCCC(CO[Si](C)(C)C(C)(C)C)C(=O)OTBDMS232.1495Semi standard non polar1381.3615
RI000197462-Ethylhydracrylic acid,1TBDMS,isomer#2JsmolCCC(CO)C(=O)O[Si](C)(C)C(C)(C)CTBDMS232.1495Semi standard non polar1336.5305
RI000197472-Ethylhydracrylic acid,2TBDMS,isomer#1JsmolCCC(CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS346.2359Semi standard non polar1649.6846
RI000197482-Ethylhydracrylic acidJsmolCCC(CO)C(O)=OUnderivatized118.063Standard polar2224.8296
RI000197492-Ethylhydracrylic acidJsmolCCC(CO)C(O)=OUnderivatized118.063Standard non polar1029.32
RI000197502-Ethylhydracrylic acidJsmolCCC(CO)C(O)=OUnderivatized118.063Semi standard non polar1088.1606
Displaying retention index compounds 19726 - 19750 of 1722868 in total