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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18176 - 18200 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001817612-Ketodeoxycholic acidJsmol[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC(=O)[C@]12C)[C@H](C)CCC(O)=OUnderivatized390.277Semi standard non polar3455.2766
RI0001817712-Ketodeoxycholic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C)[C@@]21CTMS606.3956Semi standard non polar3216.8596
RI0001817812-Ketodeoxycholic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS732.5364Semi standard non polar3907.2405
RI0001817912-Ketodeoxycholic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C)[C@@]21CTMS606.3956Standard polar3603.7847
RI0001818012-Ketodeoxycholic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS732.5364Standard polar3860.3154
RI000181812-Phenylbutyric acid,1TMS,isomer#1JsmolCCC(C(=O)O[Si](C)(C)C)C1=CC=CC=C1TMS236.1233Semi standard non polar1375.3176
RI000181822-Phenylbutyric acid,1TBDMS,isomer#1JsmolCCC(C(=O)O[Si](C)(C)C(C)(C)C)C1=CC=CC=C1TBDMS278.1702Semi standard non polar1606.8667
RI000181832-Phenylbutyric acidJsmolCCC(C(O)=O)C1=CC=CC=C1Underivatized164.0837Standard polar2464.267
RI000181842-Phenylbutyric acidJsmolCCC(C(O)=O)C1=CC=CC=C1Underivatized164.0837Standard non polar1373.9556
RI000181852-Phenylbutyric acidJsmolCCC(C(O)=O)C1=CC=CC=C1Underivatized164.0837Semi standard non polar1410.5317
RI000181863a,4b,12a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS480.3271Semi standard non polar3513.5383
RI000181873a,4b,12a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS480.3271Semi standard non polar3551.1729
RI000181883a,4b,12a-Trihydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS480.3271Semi standard non polar3554.613
RI000181893a,4b,12a-Trihydroxy-5b-cholanoic acid,1TMS,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@@]21CTMS480.3271Semi standard non polar3548.125
RI000181903a,4b,12a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS552.3666Semi standard non polar3473.8828
RI000181913a,4b,12a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS552.3666Semi standard non polar3486.0098
RI000181923a,4b,12a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3451.6118
RI000181933a,4b,12a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS552.3666Semi standard non polar3504.4224
RI000181943a,4b,12a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#5JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3440.4363
RI000181953a,4b,12a-Trihydroxy-5b-cholanoic acid,2TMS,isomer#6JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3443.8477
RI000181963a,4b,12a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O)[C@@]21CTMS624.4062Semi standard non polar3443.8003
RI000181973a,4b,12a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS624.4062Semi standard non polar3374.2263
RI000181983a,4b,12a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS624.4062Semi standard non polar3359.6604
RI000181993a,4b,12a-Trihydroxy-5b-cholanoic acid,3TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS624.4062Semi standard non polar3424.4536
RI000182003a,4b,12a-Trihydroxy-5b-cholanoic acid,4TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CCC2C3CCC4[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)CC[C@]4(C)C3C[C@H](O[Si](C)(C)C)[C@@]21CTMS696.4457Semi standard non polar3362.91
Displaying retention index compounds 18176 - 18200 of 1722868 in total