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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18151 - 18175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000181511b,3a,12a-Trihydroxy-5b-cholanoic acid,2TBDMS,isomer#6JsmolC[C@H](CCC(=O)O)C1CCC2C3CCC4C[C@H](O)C[C@@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS636.4605Semi standard non polar3869.179
RI000181521b,3a,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)C3C[C@H](O)[C@@]21CTBDMS750.547Semi standard non polar4012.0376
RI000181531b,3a,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H](O)[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar4002.3748
RI000181541b,3a,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4C[C@H](O)C[C@@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3997.7668
RI000181551b,3a,12a-Trihydroxy-5b-cholanoic acid,3TBDMS,isomer#4JsmolC[C@H](CCC(=O)O)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS750.547Semi standard non polar3969.0593
RI000181561b,3a,12a-Trihydroxy-5b-cholanoic acid,4TBDMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)C[C@@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)C3C[C@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS864.6335Semi standard non polar4102.488
RI000181571b,3a,12a-Trihydroxy-5b-cholanoic acidJsmolC[C@H](CCC(O)=O)C1CCC2C3CCC4C[C@H](O)C[C@@H](O)[C@]4(C)C3C[C@H](O)[C@]12CUnderivatized408.2876Standard polar3725.3052
RI000181581b,3a,12a-Trihydroxy-5b-cholanoic acidJsmolC[C@H](CCC(O)=O)C1CCC2C3CCC4C[C@H](O)C[C@@H](O)[C@]4(C)C3C[C@H](O)[C@]12CUnderivatized408.2876Standard non polar3350.5144
RI000181591b,3a,12a-Trihydroxy-5b-cholanoic acidJsmolC[C@H](CCC(O)=O)C1CCC2C3CCC4C[C@H](O)C[C@@H](O)[C@]4(C)C3C[C@H](O)[C@]12CUnderivatized408.2876Semi standard non polar3674.2788
RI0001816012-Ketodeoxycholic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O)[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]3CC(=O)[C@@]21CTMS462.3165Semi standard non polar3384.1245
RI0001816112-Ketodeoxycholic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC(=O)[C@@]21CTMS462.3165Semi standard non polar3345.7295
RI0001816212-Ketodeoxycholic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C)[C@@]21CTMS462.3165Semi standard non polar3294.751
RI0001816312-Ketodeoxycholic acid,2TMS,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]3CC(=O)[C@@]21CTMS534.3561Semi standard non polar3312.2556
RI0001816412-Ketodeoxycholic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O)[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@@]21CTMS534.3561Semi standard non polar3235.1072
RI0001816512-Ketodeoxycholic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C)[C@@]21CTMS534.3561Semi standard non polar3259.5024
RI0001816612-Ketodeoxycholic acid,1TBDMS,isomer#1JsmolC[C@H](CCC(=O)O)[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]3CC(=O)[C@@]21CTBDMS504.3635Semi standard non polar3612.3894
RI0001816712-Ketodeoxycholic acid,1TBDMS,isomer#2JsmolC[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)CC[C@]4(C)[C@H]3CC(=O)[C@@]21CTBDMS504.3635Semi standard non polar3614.2866
RI0001816812-Ketodeoxycholic acid,1TBDMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS504.3635Semi standard non polar3547.493
RI0001816912-Ketodeoxycholic acid,2TBDMS,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]3CC(=O)[C@@]21CTBDMS618.45Semi standard non polar3820.29
RI0001817012-Ketodeoxycholic acid,2TBDMS,isomer#2JsmolC[C@H](CCC(=O)O)[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@@]21CTBDMS618.45Semi standard non polar3678.0393
RI0001817112-Ketodeoxycholic acid,2TBDMS,isomer#3JsmolC[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)CC[C@]4(C)[C@H]3C=C(O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS618.45Semi standard non polar3758.8577
RI0001817212-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)=OUnderivatized390.277Standard polar3587.056
RI0001817312-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 non polar3184.7383
RI0001817412-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 non polar3606.9016
RI0001817512-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)=OUnderivatized390.277Standard non polar3292.6528
Displaying retention index compounds 18151 - 18175 of 1722868 in total