Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 76 - 100 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000000762-Ketobutyric acid,2TMS,isomer#1JsmolCC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS246.1107Semi standard non polar1182.5054
RI000000772-Ketobutyric acid,2TBDMS,isomer#1JsmolCC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS330.2046Semi standard non polar1617.2212
RI000000782-Ketobutyric acid,2TMS,isomer#1JsmolCC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS246.1107Standard polar1200.137
RI000000792-Ketobutyric acid,2TBDMS,isomer#1JsmolCC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS330.2046Standard polar1537.5345
RI000000802-Hydroxybutyric acid,1TMS,isomer#1JsmolCC[C@H](O[Si](C)(C)C)C(=O)OTMS176.0869Semi standard non polar1087.2035
RI000000812-Hydroxybutyric acid,1TMS,isomer#2JsmolCC[C@H](O)C(=O)O[Si](C)(C)CTMS176.0869Semi standard non polar983.486
RI000000822-Hydroxybutyric acid,2TMS,isomer#1JsmolCC[C@H](O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS248.1264Semi standard non polar1135.762
RI000000832-Hydroxybutyric acid,1TBDMS,isomer#1JsmolCC[C@H](O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS218.1338Semi standard non polar1313.5461
RI000000842-Hydroxybutyric acid,1TBDMS,isomer#2JsmolCC[C@H](O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS218.1338Semi standard non polar1207.2803
RI000000852-Hydroxybutyric acid,2TBDMS,isomer#1JsmolCC[C@H](O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS332.2203Semi standard non polar1575.4844
RI000000862-Hydroxybutyric acidJsmolCC[C@H](O)C(O)=OUnderivatized104.0473Standard polar1796.2922
RI000000872-Hydroxybutyric acidJsmolCC[C@H](O)C(O)=OUnderivatized104.0473Standard non polar928.5361
RI000000882-Hydroxybutyric acidJsmolCC[C@H](O)C(O)=OUnderivatized104.0473Semi standard non polar990.478
RI000000892-Methoxyestrone,1TMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12TMS372.2121Semi standard non polar2817.397
RI000000902-Methoxyestrone,1TMS,isomer#2JsmolCOC1=CC2=C(C=C1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C)=CC[C@@H]12TMS372.2121Semi standard non polar2755.9983
RI000000912-Methoxyestrone,1TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12TBDMS414.259Semi standard non polar3089.8425
RI000000922-Methoxyestrone,1TBDMS,isomer#2JsmolCOC1=CC2=C(C=C1O)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]12TBDMS414.259Semi standard non polar3023.2258
RI000000932-MethoxyestroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(OC)=C3Underivatized300.1725Standard polar3613.1807
RI000000942-Methoxyestrone,2TMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C)=CC[C@@H]12TMS444.2516Standard non polar2657.1138
RI000000952-Methoxyestrone,2TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]12TBDMS528.3455Standard non polar3055.2786
RI000000962-MethoxyestroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(OC)=C3Underivatized300.1725Standard non polar2578.9956
RI000000972-MethoxyestroneJsmol[H][C@@]12CCC(=O)[C@@]1(C)CC[C@]1([H])C3=C(CC[C@@]21[H])C=C(O)C(OC)=C3Underivatized300.1725Semi standard non polar2787.855
RI000000982-Methoxyestrone,2TMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C)=CC[C@@H]12TMS444.2516Semi standard non polar2734.413
RI000000992-Methoxyestrone,2TBDMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]12TBDMS528.3455Semi standard non polar3197.3948
RI000001002-Methoxyestrone,2TMS,isomer#1JsmolCOC1=CC2=C(C=C1O[Si](C)(C)C)CC[C@@H]1[C@@H]2CC[C@]2(C)C(O[Si](C)(C)C)=CC[C@@H]12TMS444.2516Standard polar3077.2463
Displaying retention index compounds 76 - 100 of 1722868 in total