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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18201 - 18225 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000182013a,4b,12a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3758.2456
RI000182023a,4b,12a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3758.898
RI000182033a,4b,12a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS522.3741Semi standard non polar3755.7827
RI000182043a,4b,12a-Trihydroxy-5b-cholanoic acid,1TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS522.3741Semi standard non polar3768.1235
RI000182053a,4b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3893.9285
RI000182063a,4b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3906.1394
RI000182073a,4b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3930.5693
RI000182083a,4b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS636.4605Semi standard non polar3912.374
RI000182093a,4b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#5JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3853.1177
RI000182103a,4b,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3857.3833
RI000182113a,4b,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS750.547Semi standard non polar4054.8164
RI000182123a,4b,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3992.8584
RI000182133a,4b,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3984.9824
RI000182143a,4b,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar4013.566
RI000182153a,4b,12a-Trihydroxy-5b-cholanoic acid,4TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS864.6335Semi standard non polar4134.4263
RI000182163a,4b,12a-Trihydroxy-5b-cholanoic acidJsmolC[C@@H](CCC(O)=O)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@]12CUnderivatized408.2876Standard polar3467.3232
RI000182173a,4b,12a-Trihydroxy-5b-cholanoic acidJsmolC[C@@H](CCC(O)=O)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@]12CUnderivatized408.2876Standard non polar3370.2144
RI000182183a,4b,12a-Trihydroxy-5b-cholanoic acidJsmolC[C@@H](CCC(O)=O)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@]12CUnderivatized408.2876Semi standard non polar3623.4072
RI000182193a,7b,12a-Trihydroxyoxocholanyl-Glycine,1TMS,isomer#1JsmolC[C@H](CCC(=O)NCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS537.3486Semi standard non polar3873.8289
RI000182203a,7b,12a-Trihydroxyoxocholanyl-Glycine,1TMS,isomer#2JsmolC[C@H](CCC(=O)NCC(=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)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS537.3486Semi standard non polar3978.4602
RI000182213a,7b,12a-Trihydroxyoxocholanyl-Glycine,1TMS,isomer#3JsmolC[C@H](CCC(=O)NCC(=O)O)[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@@]21CTMS537.3486Semi standard non polar3941.972
RI000182223a,7b,12a-Trihydroxyoxocholanyl-Glycine,1TMS,isomer#4JsmolC[C@H](CCC(=O)NCC(=O)O[Si](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)[C@@]21CTMS537.3486Semi standard non polar3966.3672
RI000182233a,7b,12a-Trihydroxyoxocholanyl-Glycine,1TMS,isomer#5JsmolC[C@H](CCC(=O)N(CC(=O)O)[Si](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)[C@@]21CTMS537.3486Semi standard non polar3976.7078
RI000182243a,7b,12a-Trihydroxyoxocholanyl-Glycine,2TMS,isomer#1JsmolC[C@H](CCC(=O)NCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS609.3881Semi standard non polar3834.7493
RI000182253a,7b,12a-Trihydroxyoxocholanyl-Glycine,2TMS,isomer#2JsmolC[C@H](CCC(=O)NCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS609.3881Semi standard non polar3845.242
Displaying retention index compounds 18201 - 18225 of 1722868 in total