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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17401 - 17425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00017401Tyramine,2TMS,isomer#2JsmolC[Si](C)(C)N(CCC1=CC=C(O)C=C1)[Si](C)(C)CTMS281.1631Standard polar1970.98
RI00017402Tyramine,3TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CCN([Si](C)(C)C)[Si](C)(C)C)C=C1TMS353.2026Standard polar1759.9832
RI00017403Tyramine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NCCC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1TBDMS365.257Standard polar2045.9125
RI00017404Tyramine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CCC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)CTBDMS365.257Standard polar2132.091
RI00017405Tyramine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1TBDMS479.3435Standard polar2121.308
RI000174061beta-Hydroxycholic acid,1TMS,isomer#1JsmolC[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)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS496.322Semi standard non polar3498.547
RI000174071beta-Hydroxycholic acid,1TMS,isomer#2JsmolC[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)[C@H](O)C[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS496.322Semi standard non polar3554.3638
RI000174081beta-Hydroxycholic 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(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS496.322Semi standard non polar3510.0164
RI000174091beta-Hydroxycholic acid,1TMS,isomer#4JsmolC[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(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3OTMS496.322Semi standard non polar3553.8345
RI000174101beta-Hydroxycholic acid,1TMS,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(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3OTMS496.322Semi standard non polar3534.1777
RI000174111beta-Hydroxycholic 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)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3432.5793
RI000174121beta-Hydroxycholic acid,2TMS,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(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3464.523
RI000174131beta-Hydroxycholic acid,2TMS,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(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3431.7798
RI000174141beta-Hydroxycholic acid,2TMS,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(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3403.967
RI000174151beta-Hydroxycholic acid,2TMS,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(C)[C@H](O)C[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3483.9053
RI000174161beta-Hydroxycholic 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(C)[C@H](O)C[C@@H](O[Si](C)(C)C)C[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3475.7998
RI000174171beta-Hydroxycholic acid,2TMS,isomer#7JsmolC[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)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS568.3615Semi standard non polar3425.7305
RI000174181beta-Hydroxycholic acid,2TMS,isomer#8JsmolC[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(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS568.3615Semi standard non polar3436.3848
RI000174191beta-Hydroxycholic acid,2TMS,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(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3OTMS568.3615Semi standard non polar3443.373
RI000174201beta-Hydroxycholic acid,2TMS,isomer#10JsmolC[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(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3OTMS568.3615Semi standard non polar3493.7632
RI000174211beta-Hydroxycholic 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(C)[C@@H](C[C@H](O)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3407.0842
RI000174221beta-Hydroxycholic 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)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3382.33
RI000174231beta-Hydroxycholic 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)[C@@]21C)[C@]1(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3368.2937
RI000174241beta-Hydroxycholic acid,3TMS,isomer#4JsmolC[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(C)[C@@H](C[C@H](O[Si](C)(C)C)C[C@H]1O)C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3419.625
RI000174251beta-Hydroxycholic acid,3TMS,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(C)[C@@H](C[C@H](O)C[C@H]1O[Si](C)(C)C)C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3407.457
Displaying retention index compounds 17401 - 17425 of 1722868 in total