RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20126 - 20150 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0002012616-Ketoestradiol,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C(O)[C@@]2(C)CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]2C1TBDMS400.2434Semi standard non polar3044.1074
RI0002012716-Ketoestradiol,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=C[C@H]2[C@@H]3CCC4=CC(O)=CC=C4[C@H]3CC[C@]2(C)[C@H]1OTBDMS400.2434Semi standard non polar2996.5437
RI0002012816-Ketoestradiol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC(=O)[C@@H]2O[Si](C)(C)C(C)(C)CTBDMS514.3298Semi standard non polar3432.6675
RI0002012916-Ketoestradiol,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@@H]3C4=CC=C(O)C=C4CC[C@H]3[C@@H]2C1TBDMS514.3298Semi standard non polar3287.0981
RI0002013016-Ketoestradiol,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C[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)CTBDMS514.3298Semi standard non polar3234.5728
RI0002013116-Ketoestradiol,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=C(O)[C@@]2(C)CC[C@@H]3C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4CC[C@H]3[C@@H]2C1TBDMS514.3298Semi standard non polar3320.0073
RI0002013216-Ketoestradiol,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC1=C[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC=C4[C@H]3CC[C@]2(C)[C@H]1OTBDMS514.3298Semi standard non polar3261.5913
RI0002013316-KetoestradiolJsmol[H][C@@]12CC(=O)[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized286.1569Standard polar3624.1257
RI0002013416-Ketoestradiol,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS502.2755Standard non polar2783.1177
RI0002013516-Ketoestradiol,3TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS502.2755Standard non polar2748.5745
RI0002013616-Ketoestradiol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@@H]3C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4CC[C@H]3[C@@H]2C1TBDMS628.4163Standard non polar3465.9905
RI0002013716-Ketoestradiol,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC=C4[C@H]3CC[C@]2(C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS628.4163Standard non polar3366.3186
RI0002013816-KetoestradiolJsmol[H][C@@]12CC(=O)[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized286.1569Standard non polar2807.0151
RI0002013916-KetoestradiolJsmol[H][C@@]12CC(=O)[C@H](O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C=C3Underivatized286.1569Semi standard non polar2864.2222
RI0002014016-Ketoestradiol,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS502.2755Semi standard non polar2905.4187
RI0002014116-Ketoestradiol,3TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS502.2755Semi standard non polar2836.5786
RI0002014216-Ketoestradiol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@@H]3C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4CC[C@H]3[C@@H]2C1TBDMS628.4163Semi standard non polar3616.3499
RI0002014316-Ketoestradiol,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC=C4[C@H]3CC[C@]2(C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS628.4163Semi standard non polar3549.4617
RI0002014416-Ketoestradiol,3TMS,isomer#1JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS502.2755Standard polar2899.0442
RI0002014516-Ketoestradiol,3TMS,isomer#2JsmolC[C@]12CC[C@@H]3C4=CC=C(O[Si](C)(C)C)C=C4CC[C@H]3[C@@H]1C=C(O[Si](C)(C)C)[C@@H]2O[Si](C)(C)CTMS502.2755Standard polar2890.0322
RI0002014616-Ketoestradiol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@@H]3C4=CC=C(O[Si](C)(C)C(C)(C)C)C=C4CC[C@H]3[C@@H]2C1TBDMS628.4163Standard polar3214.0232
RI0002014716-Ketoestradiol,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC=C4[C@H]3CC[C@]2(C)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS628.4163Standard polar3197.7297
RI000201482-Hydroxy-3-methylbutyric acid,1TMS,isomer#1JsmolCC(C)C(O[Si](C)(C)C)C(=O)OTMS190.1025Semi standard non polar1146.3549
RI000201492-Hydroxy-3-methylbutyric acid,1TMS,isomer#2JsmolCC(C)C(O)C(=O)O[Si](C)(C)CTMS190.1025Semi standard non polar1039.2906
RI000201502-Hydroxy-3-methylbutyric acid,2TMS,isomer#1JsmolCC(C)C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS262.142Semi standard non polar1190.6279
Displaying retention index compounds 20126 - 20150 of 1722868 in total