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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21126 - 21150 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0002112624,25-Dihydroxyvitamin D,2TMS,isomer#2JsmolC=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C)C(C)(C)O[Si](C)(C)CTMS560.4081Semi standard non polar3502.9973
RI0002112724,25-Dihydroxyvitamin D,2TMS,isomer#3JsmolC=C1CC[C@@H](O[Si](C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)CTMS560.4081Semi standard non polar3466.168
RI0002112824,25-Dihydroxyvitamin D,3TMS,isomer#1JsmolC=C1CC[C@@H](O[Si](C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C)C(C)(C)O[Si](C)(C)CTMS632.4476Semi standard non polar3461.808
RI0002112924,25-Dihydroxyvitamin D,1TBDMS,isomer#1JsmolC=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)OTBDMS530.4155Semi standard non polar3710.0088
RI0002113024,25-Dihydroxyvitamin D,1TBDMS,isomer#2JsmolC=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)C(C)(C)CTBDMS530.4155Semi standard non polar3730.6448
RI0002113124,25-Dihydroxyvitamin D,1TBDMS,isomer#3JsmolC=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)OTBDMS530.4155Semi standard non polar3638.7722
RI0002113224,25-Dihydroxyvitamin D,2TBDMS,isomer#1JsmolC=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)OTBDMS644.502Semi standard non polar3879.4692
RI0002113324,25-Dihydroxyvitamin D,2TBDMS,isomer#2JsmolC=C1CC[C@@H](O)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)O[Si](C)(C)C(C)(C)CTBDMS644.502Semi standard non polar3977.9524
RI0002113424,25-Dihydroxyvitamin D,2TBDMS,isomer#3JsmolC=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O)C(C)(C)O[Si](C)(C)C(C)(C)CTBDMS644.502Semi standard non polar3914.515
RI0002113524,25-Dihydroxyvitamin D,3TBDMS,isomer#1JsmolC=C1CC[C@@H](O[Si](C)(C)C(C)(C)C)C/C1=C/C=C1\CCC[C@@]2(C)[C@H]1CC[C@@H]2[C@H](C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)O[Si](C)(C)C(C)(C)CTBDMS758.5885Semi standard non polar4179.481
RI0002113624,25-Dihydroxyvitamin DJsmolC[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=CUnderivatized416.329Standard polar3678.3806
RI0002113724,25-Dihydroxyvitamin DJsmolC[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=CUnderivatized416.329Standard non polar3406.193
RI0002113824,25-Dihydroxyvitamin DJsmolC[C@H](CCC(O)C(C)(C)O)[C@H]1CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@H](O)CCC1=CUnderivatized416.329Semi standard non polar3558.8318
RI0002113916,17-Epiestriol,1TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@H]2OTMS360.2121Semi standard non polar2789.2388
RI0002114016,17-Epiestriol,1TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@H](O)[C@H]2O[Si](C)(C)CTMS360.2121Semi standard non polar2794.0862
RI0002114116,17-Epiestriol,1TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O)[C@H]2OTMS360.2121Semi standard non polar2771.8933
RI0002114216,17-Epiestriol,2TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@H]2OTMS432.2516Semi standard non polar2842.8718
RI0002114316,17-Epiestriol,2TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)CTMS432.2516Semi standard non polar2782.1436
RI0002114416,17-Epiestriol,2TMS,isomer#3JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O)[C@H]2O[Si](C)(C)CTMS432.2516Semi standard non polar2842.8809
RI0002114516,17-Epiestriol,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)CTMS504.2911Semi standard non polar2907.424
RI0002114616,17-Epiestriol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@]2(C)[C@@H]1OTBDMS402.259Semi standard non polar3065.0571
RI0002114716,17-Epiestriol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@]12CTBDMS402.259Semi standard non polar3081.2944
RI0002114816,17-Epiestriol,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@H](O)[C@@H](O)C[C@@H]12TBDMS402.259Semi standard non polar3084.2534
RI0002114916,17-Epiestriol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@]2(C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@H]12TBDMS516.3455Semi standard non polar3374.4844
RI0002115016,17-Epiestriol,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@]2(C)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS516.3455Semi standard non polar3303.1072
Displaying retention index compounds 21126 - 21150 of 1722868 in total