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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21251 - 21275 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000212511,3,7,12-Tetrahydroxycholan-24-oic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)C(O)C[C@@]1([H])[C@@]2([H])C(O)CC2CC(O)CC(O)[C@]12CUnderivatized424.2825Standard non polar3338.8474
RI000212521,3,7,12-Tetrahydroxycholan-24-oic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)C(O)C[C@@]1([H])[C@@]2([H])C(O)CC2CC(O)CC(O)[C@]12CUnderivatized424.2825Semi standard non polar3833.6006
RI00021253Homoveratric acid,1TMS,isomer#1JsmolCOC1=CC=C(CC(=O)O[Si](C)(C)C)C=C1OCTMS268.1131Semi standard non polar1730.9667
RI00021254Homoveratric acid,1TBDMS,isomer#1JsmolCOC1=CC=C(CC(=O)O[Si](C)(C)C(C)(C)C)C=C1OCTBDMS310.16Semi standard non polar1955.5126
RI00021255Homoveratric acidJsmolCOC1=CC=C(CC(O)=O)C=C1OCUnderivatized196.0736Standard polar2934.838
RI00021256Homoveratric acidJsmolCOC1=CC=C(CC(O)=O)C=C1OCUnderivatized196.0736Standard non polar1640.969
RI00021257Homoveratric acidJsmolCOC1=CC=C(CC(O)=O)C=C1OCUnderivatized196.0736Semi standard non polar1716.8523
RI000212583a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTMS496.322Semi standard non polar3503.755
RI000212593a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTMS496.322Semi standard non polar3508.9138
RI000212603a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS496.322Semi standard non polar3431.4072
RI000212613a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS496.322Semi standard non polar3445.8237
RI000212623a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3OTMS496.322Semi standard non polar3481.298
RI000212633a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3446.6777
RI000212643a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3420.9285
RI000212653a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3381.8008
RI000212663a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3365.1814
RI000212673a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3416.8843
RI000212683a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3385.6304
RI000212693a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3414.2004
RI000212703a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3360.215
RI000212713a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3O[Si](C)(C)CTMS568.3615Semi standard non polar3336.8577
RI000212723a,4b,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](C[C@H](O)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS568.3615Semi standard non polar3373.1875
RI000212733a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3387.312
RI000212743a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1C[C@H]3OTMS640.4011Semi standard non polar3347.4333
RI000212753a,4b,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](C[C@H](O[Si](C)(C)C)[C@@]21C)[C@@]1(C)CC[C@@H](O)[C@H](O)[C@H]1C[C@H]3O[Si](C)(C)CTMS640.4011Semi standard non polar3369.127
Displaying retention index compounds 21251 - 21275 of 1722868 in total