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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 18876 - 18900 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0001887617a-Hydroxypregnenolone,2TMS,isomer#3JsmolC=C(O[Si](C)(C)C)[C@@]1(O)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTMS476.3142Semi standard non polar2854.981
RI0001887717a-Hydroxypregnenolone,1TBDMS,isomer#1JsmolCC(=O)[C@@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS446.3216Semi standard non polar3183.6978
RI0001887817a-Hydroxypregnenolone,1TBDMS,isomer#2JsmolCC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS446.3216Semi standard non polar3170.4824
RI0001887917a-Hydroxypregnenolone,1TBDMS,isomer#3JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O)CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS446.3216Semi standard non polar3115.0708
RI0001888017a-Hydroxypregnenolone,2TBDMS,isomer#1JsmolCC(=O)[C@@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS560.4081Semi standard non polar3457.9395
RI0001888117a-Hydroxypregnenolone,2TBDMS,isomer#2JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS560.4081Semi standard non polar3503.6533
RI0001888217a-Hydroxypregnenolone,2TBDMS,isomer#3JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS560.4081Semi standard non polar3385.021
RI0001888317a-HydroxypregnenoloneJsmol[H][C@@]12CC[C@](O)(C(C)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12CUnderivatized332.2351Standard polar2657.7366
RI0001888417a-HydroxypregnenoloneJsmol[H][C@@]12CC[C@](O)(C(C)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12CUnderivatized332.2351Standard non polar2730.6206
RI0001888517a-Hydroxypregnenolone,3TMS,isomer#1JsmolC=C(O[Si](C)(C)C)[C@@]1(O[Si](C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTMS548.3537Standard non polar2903.9827
RI0001888617a-Hydroxypregnenolone,3TBDMS,isomer#1JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS674.4946Standard non polar3605.8247
RI0001888717a-HydroxypregnenoloneJsmol[H][C@@]12CC[C@](O)(C(C)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12CUnderivatized332.2351Semi standard non polar2873.4329
RI0001888817a-Hydroxypregnenolone,3TMS,isomer#1JsmolC=C(O[Si](C)(C)C)[C@@]1(O[Si](C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTMS548.3537Semi standard non polar2964.5356
RI0001888917a-Hydroxypregnenolone,3TBDMS,isomer#1JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS674.4946Semi standard non polar3724.6775
RI0001889017a-Hydroxypregnenolone,3TMS,isomer#1JsmolC=C(O[Si](C)(C)C)[C@@]1(O[Si](C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTMS548.3537Standard polar3228.3308
RI0001889117a-Hydroxypregnenolone,3TBDMS,isomer#1JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CC[C@H]2[C@@H]3CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS674.4946Standard polar3481.9216
RI000188923a,6a,7b-Trihydroxy-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](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@@H](O)[C@@H]3OTMS480.3271Semi standard non polar3405.8645
RI000188933a,6a,7b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@@H](O)[C@@H]3O[Si](C)(C)CTMS480.3271Semi standard non polar3355.7654
RI000188943a,6a,7b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@@H](O[Si](C)(C)C)[C@@H]3OTMS480.3271Semi standard non polar3361.7646
RI000188953a,6a,7b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1[C@@H](O)[C@@H]3OTMS480.3271Semi standard non polar3431.537
RI000188963a,6a,7b-Trihydroxy-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](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1[C@@H](O)[C@@H]3OTMS552.3666Semi standard non polar3381.337
RI000188973a,6a,7b-Trihydroxy-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](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@@H](O[Si](C)(C)C)[C@@H]3OTMS552.3666Semi standard non polar3310.436
RI000188983a,6a,7b-Trihydroxy-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](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@@H](O)[C@@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3307.992
RI000188993a,6a,7b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O[Si](C)(C)C)C[C@H]1[C@@H](O)[C@@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3309.3237
RI000189003a,6a,7b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@@]21C)[C@@]1(C)CC[C@@H](O)C[C@H]1[C@@H](O[Si](C)(C)C)[C@@H]3O[Si](C)(C)CTMS552.3666Semi standard non polar3282.6968
Displaying retention index compounds 18876 - 18900 of 1722868 in total