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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18451 - 18475 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000184512-Methylbutyrylglycine,2TBDMS,isomer#1JsmolCCC(C)C(=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS387.2625Standard polar1904.6437
RI000184523a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3568.698
RI000184533a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[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@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3563.165
RI000184543a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS496.322Semi standard non polar3526.681
RI000184553a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3611.585
RI000184563a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3538.8284
RI000184573a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3502.9155
RI000184583a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3486.5186
RI000184593a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3542.5024
RI000184603a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#4JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3465.2617
RI000184613a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,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@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3483.0073
RI000184623a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#6JsmolC[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@@]21C)[C@@]1(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3515.9578
RI000184633a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,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@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3483.0347
RI000184643a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,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(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3448.2205
RI000184653a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,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(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3474.5073
RI000184663a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,2TMS,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(CO[Si](C)(C)C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3500.0393
RI000184673a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3456.8474
RI000184683a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3461.3757
RI000184693a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(CO)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3436.2837
RI000184703a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#4JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3455.753
RI000184713a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#5JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3413.7534
RI000184723a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#6JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@H]3[C@H](C[C@H](O)[C@@]21C)[C@@]1(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3414.621
RI000184733a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,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@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3451.8042
RI000184743a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,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@@]21C)[C@@]1(CO[Si](C)(C)C)CC[C@@H](O)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3443.3997
RI000184753a,7a,12a,19-Tetrahydroxy-5b-cholanoic acid,3TMS,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@@]21C)[C@@]1(CO)CC[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3435.5122
Displaying retention index compounds 18451 - 18475 of 1722868 in total