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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20201 - 20225 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000202013a,12b-Dihydroxy-5b-cholanoic acid,2TMS,isomer#3JsmolC[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@@H](O[Si](C)(C)C)[C@@]21CTMS536.3717Semi standard non polar3308.271
RI000202023a,12b-Dihydroxy-5b-cholanoic 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@@H](O[Si](C)(C)C)[C@@]21CTMS608.4112Semi standard non polar3270.3984
RI000202033a,12b-Dihydroxy-5b-cholanoic acid,1TBDMS,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)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTBDMS506.3791Semi standard non polar3553.3845
RI000202043a,12b-Dihydroxy-5b-cholanoic acid,1TBDMS,isomer#2JsmolC[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@@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS506.3791Semi standard non polar3585.1748
RI000202053a,12b-Dihydroxy-5b-cholanoic acid,1TBDMS,isomer#3JsmolC[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@@H](O)[C@@]21CTBDMS506.3791Semi standard non polar3592.5366
RI000202063a,12b-Dihydroxy-5b-cholanoic 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]3C[C@@H](O)[C@@]21CTBDMS620.4656Semi standard non polar3785.22
RI000202073a,12b-Dihydroxy-5b-cholanoic acid,2TBDMS,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]3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS620.4656Semi standard non polar3775.7417
RI000202083a,12b-Dihydroxy-5b-cholanoic acid,2TBDMS,isomer#3JsmolC[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@@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS620.4656Semi standard non polar3758.63
RI000202093a,12b-Dihydroxy-5b-cholanoic 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@@H](O[Si](C)(C)C(C)(C)C)[C@@]21CTBDMS734.5521Semi standard non polar3984.1072
RI000202103a,12b-Dihydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@H](O)C[C@@]1([H])[C@@]2([H])CC[C@]2([H])C[C@H](O)CC[C@]12CUnderivatized392.2927Standard polar3905.3838
RI000202113a,12b-Dihydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@H](O)C[C@@]1([H])[C@@]2([H])CC[C@]2([H])C[C@H](O)CC[C@]12CUnderivatized392.2927Standard non polar3315.4275
RI000202123a,12b-Dihydroxy-5b-cholanoic acidJsmol[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)[C@H](O)C[C@@]1([H])[C@@]2([H])CC[C@]2([H])C[C@H](O)CC[C@]12CUnderivatized392.2927Semi standard non polar3477.9966
RI000202133beta,17alpha-Dihydroxy-5alpha-androstane,1TMS,isomer#1JsmolC[C@]12CC[C@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC[C@H]2O[Si](C)(C)CTMS364.2798Semi standard non polar2563.9248
RI000202143beta,17alpha-Dihydroxy-5alpha-androstane,1TMS,isomer#2JsmolC[C@]12CC[C@H](O[Si](C)(C)C)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC[C@H]2OTMS364.2798Semi standard non polar2552.9375
RI000202153beta,17alpha-Dihydroxy-5alpha-androstane,2TMS,isomer#1JsmolC[C@]12CC[C@H](O[Si](C)(C)C)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC[C@H]2O[Si](C)(C)CTMS436.3193Semi standard non polar2573.2834
RI000202163beta,17alpha-Dihydroxy-5alpha-androstane,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@@]21CTBDMS406.3267Semi standard non polar2857.0637
RI000202173beta,17alpha-Dihydroxy-5alpha-androstane,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@@H]3[C@@H]2CC[C@@]2(C)[C@H]3CC[C@H]2O)C1TBDMS406.3267Semi standard non polar2820.685
RI000202183beta,17alpha-Dihydroxy-5alpha-androstane,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@@H]3[C@@H]2CC[C@@]2(C)[C@H]3CC[C@H]2O[Si](C)(C)C(C)(C)C)C1TBDMS520.4132Semi standard non polar3133.5986
RI000202193beta,17alpha-Dihydroxy-5alpha-androstaneJsmol[H][C@@]12CC[C@@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized292.2402Standard polar2433.331
RI000202203beta,17alpha-Dihydroxy-5alpha-androstaneJsmol[H][C@@]12CC[C@@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized292.2402Standard non polar2438.0845
RI000202213beta,17alpha-Dihydroxy-5alpha-androstaneJsmol[H][C@@]12CC[C@@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@@H](O)CC[C@]12CUnderivatized292.2402Semi standard non polar2611.2896
RI000202223-Hydroxydodecanedioic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(CCCCCCCCC(=O)O)CC(=O)OTMS318.1863Semi standard non polar2137.605
RI000202233-Hydroxydodecanedioic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC(=O)CCCCCCCCC(O)CC(=O)OTMS318.1863Semi standard non polar2164.0269
RI000202243-Hydroxydodecanedioic acid,1TMS,isomer#3JsmolC[Si](C)(C)OC(=O)CC(O)CCCCCCCCC(=O)OTMS318.1863Semi standard non polar2156.398
RI000202253-Hydroxydodecanedioic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCCCCCCCC(CC(=O)O)O[Si](C)(C)CTMS390.2258Semi standard non polar2201.334
Displaying retention index compounds 20201 - 20225 of 1722868 in total