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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19801 - 19825 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000198013a,6b,7a,12a-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](O)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS496.322Semi standard non polar3481.1973
RI000198023a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS496.322Semi standard non polar3498.5728
RI000198033a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS496.322Semi standard non polar3411.7537
RI000198043a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS496.322Semi standard non polar3416.3167
RI000198053a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,1TMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS496.322Semi standard non polar3501.7183
RI000198063a,6b,7a,12a-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](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS568.3615Semi standard non polar3356.3003
RI000198073a,6b,7a,12a-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](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS568.3615Semi standard non polar3356.5732
RI000198083a,6b,7a,12a-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](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS568.3615Semi standard non polar3423.0608
RI000198093a,6b,7a,12a-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](O)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS568.3615Semi standard non polar3429.763
RI000198103a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS568.3615Semi standard non polar3395.607
RI000198113a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS568.3615Semi standard non polar3350.1492
RI000198123a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#7JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS568.3615Semi standard non polar3416.5295
RI000198133a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#8JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS568.3615Semi standard non polar3315.1226
RI000198143a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS568.3615Semi standard non polar3359.4102
RI000198153a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,2TMS,isomer#10JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS568.3615Semi standard non polar3358.4783
RI000198163a,6b,7a,12a-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](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS640.4011Semi standard non polar3292.4775
RI000198173a,6b,7a,12a-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](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS640.4011Semi standard non polar3327.9382
RI000198183a,6b,7a,12a-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](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS640.4011Semi standard non polar3357.6035
RI000198193a,6b,7a,12a-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](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS640.4011Semi standard non polar3318.596
RI000198203a,6b,7a,12a-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](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS640.4011Semi standard non polar3320.3381
RI000198213a,6b,7a,12a-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](O)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS640.4011Semi standard non polar3375.3433
RI000198223a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#7JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS640.4011Semi standard non polar3341.0134
RI000198233a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#8JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS640.4011Semi standard non polar3378.0374
RI000198243a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#9JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O[Si](C)(C)C)[C@@]21CTMS640.4011Semi standard non polar3339.8428
RI000198253a,6b,7a,12a-Tetrahydroxy-5b-cholanoic acid,3TMS,isomer#10JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@H](O)[C@@]21CTMS640.4011Semi standard non polar3327.5493
Displaying retention index compounds 19801 - 19825 of 1722868 in total