Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 101 - 125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000001012-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 polar3326.9014
RI000001023-Hydroxybutyric acid,1TMS,isomer#1JsmolC[C@H](CC(=O)O)O[Si](C)(C)CTMS176.0869Semi standard non polar1074.439
RI000001033-Hydroxybutyric acid,1TMS,isomer#2JsmolC[C@@H](O)CC(=O)O[Si](C)(C)CTMS176.0869Semi standard non polar1018.1227
RI000001043-Hydroxybutyric acid,2TMS,isomer#1JsmolC[C@H](CC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS248.1264Semi standard non polar1168.221
RI000001053-Hydroxybutyric acid,1TBDMS,isomer#1JsmolC[C@H](CC(=O)O)O[Si](C)(C)C(C)(C)CTBDMS218.1338Semi standard non polar1313.5819
RI000001063-Hydroxybutyric acid,1TBDMS,isomer#2JsmolC[C@@H](O)CC(=O)O[Si](C)(C)C(C)(C)CTBDMS218.1338Semi standard non polar1235.9379
RI000001073-Hydroxybutyric acid,2TBDMS,isomer#1JsmolC[C@H](CC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS332.2203Semi standard non polar1603.0454
RI000001083-Hydroxybutyric acidJsmolC[C@@H](O)CC(O)=OUnderivatized104.0473Standard polar2109.0015
RI000001093-Hydroxybutyric acidJsmolC[C@@H](O)CC(O)=OUnderivatized104.0473Standard non polar962.0076
RI000001103-Hydroxybutyric acidJsmolC[C@@H](O)CC(O)=OUnderivatized104.0473Semi standard non polar986.0669
RI00000111Deoxyuridine,1TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)C[C@@H]1OTMS300.1141Semi standard non polar2254.5588
RI00000112Deoxyuridine,1TMS,isomer#2JsmolC[Si](C)(C)O[C@H]1C[C@H](N2C=CC(=O)[NH]C2=O)O[C@@H]1COTMS300.1141Semi standard non polar2287.109
RI00000113Deoxyuridine,1TMS,isomer#3JsmolC[Si](C)(C)N1C(=O)C=CN([C@H]2C[C@H](O)[C@@H](CO)O2)C1=OTMS300.1141Semi standard non polar2319.0828
RI00000114Deoxyuridine,2TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)C[C@@H]1O[Si](C)(C)CTMS372.1537Semi standard non polar2260.2354
RI00000115Deoxyuridine,2TMS,isomer#2JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)C[C@@H]1OTMS372.1537Semi standard non polar2329.4456
RI00000116Deoxyuridine,2TMS,isomer#3JsmolC[Si](C)(C)O[C@H]1C[C@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)O[C@@H]1COTMS372.1537Semi standard non polar2334.8098
RI00000117Deoxyuridine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)C[C@@H]1OTBDMS342.1611Semi standard non polar2512.4014
RI00000118Deoxyuridine,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H](N2C=CC(=O)[NH]C2=O)O[C@@H]1COTBDMS342.1611Semi standard non polar2524.4795
RI00000119Deoxyuridine,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C(=O)C=CN([C@H]2C[C@H](O)[C@@H](CO)O2)C1=OTBDMS342.1611Semi standard non polar2545.3242
RI00000120Deoxyuridine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)C[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS456.2476Semi standard non polar2714.509
RI00000121Deoxyuridine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)C[C@@H]1OTBDMS456.2476Semi standard non polar2783.9985
RI00000122Deoxyuridine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@H]1C[C@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)O[C@@H]1COTBDMS456.2476Semi standard non polar2796.3577
RI00000123DeoxyuridineJsmolOC[C@H]1O[C@H](C[C@@H]1O)N1C=CC(=O)NC1=OUnderivatized228.0746Standard polar3237.8398
RI00000124Deoxyuridine,3TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)C[C@@H]1O[Si](C)(C)CTMS444.1932Standard non polar2455.1736
RI00000125Deoxyuridine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)C[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS570.3341Standard non polar3067.8083
Displaying retention index compounds 101 - 125 of 1722868 in total