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 4101 - 4125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00004101Epinephrine,2TBDMS,isomer#6JsmolCN(C[C@H](O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)[Si](C)(C)C(C)(C)CTBDMS411.2625Semi standard non polar2489.7432
RI00004102Epinephrine,3TBDMS,isomer#1JsmolCNC[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1TBDMS525.349Semi standard non polar2520.8315
RI00004103Epinephrine,3TBDMS,isomer#2JsmolCN(C[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)[Si](C)(C)C(C)(C)CTBDMS525.349Semi standard non polar2698.899
RI00004104Epinephrine,3TBDMS,isomer#3JsmolCN(C[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)CTBDMS525.349Semi standard non polar2690.305
RI00004105Epinephrine,3TBDMS,isomer#4JsmolCN(C[C@H](O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)CTBDMS525.349Semi standard non polar2724.7874
RI00004106EpinephrineJsmolCNC[C@H](O)C1=CC(O)=C(O)C=C1Underivatized183.0895Standard polar3056.2068
RI00004107Epinephrine,4TMS,isomer#1JsmolCN(C[C@H](O[Si](C)(C)C)C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)CTMS471.2477Standard non polar1994.581
RI00004108Epinephrine,4TBDMS,isomer#1JsmolCN(C[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)CTBDMS639.4355Standard non polar2767.9702
RI00004109EpinephrineJsmolCNC[C@H](O)C1=CC(O)=C(O)C=C1Underivatized183.0895Standard non polar1820.4512
RI00004110EpinephrineJsmolCNC[C@H](O)C1=CC(O)=C(O)C=C1Underivatized183.0895Semi standard non polar1827.3706
RI00004111Epinephrine,4TMS,isomer#1JsmolCN(C[C@H](O[Si](C)(C)C)C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)CTMS471.2477Semi standard non polar2022.9733
RI00004112Epinephrine,4TBDMS,isomer#1JsmolCN(C[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)CTBDMS639.4355Semi standard non polar2938.8347
RI00004113Epinephrine,4TMS,isomer#1JsmolCN(C[C@H](O[Si](C)(C)C)C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)[Si](C)(C)CTMS471.2477Standard polar1930.8654
RI00004114Epinephrine,4TBDMS,isomer#1JsmolCN(C[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)[Si](C)(C)C(C)(C)CTBDMS639.4355Standard polar2420.0444
RI00004115Pipecolic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CCCCN1TMS201.1185Semi standard non polar1263.1768
RI00004116Pipecolic acid,1TMS,isomer#2JsmolC[Si](C)(C)N1CCCCC1C(=O)OTMS201.1185Semi standard non polar1344.0983
RI00004117Pipecolic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCCN1TBDMS243.1655Semi standard non polar1497.9392
RI00004118Pipecolic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1CCCCC1C(=O)OTBDMS243.1655Semi standard non polar1572.1166
RI00004119Pipecolic acidJsmolOC(=O)C1CCCCN1Underivatized129.079Standard polar1881.1233
RI00004120Pipecolic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CCCCN1[Si](C)(C)CTMS273.158Standard non polar1394.2136
RI00004121Pipecolic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCCN1[Si](C)(C)C(C)(C)CTBDMS357.2519Standard non polar1813.1932
RI00004122Pipecolic acidJsmolOC(=O)C1CCCCN1Underivatized129.079Standard non polar1156.3076
RI00004123Pipecolic acidJsmolOC(=O)C1CCCCN1Underivatized129.079Semi standard non polar1256.0194
RI00004124Pipecolic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CCCCN1[Si](C)(C)CTMS273.158Semi standard non polar1356.8616
RI00004125Pipecolic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCCN1[Si](C)(C)C(C)(C)CTBDMS357.2519Semi standard non polar1842.5009
Displaying retention index compounds 4101 - 4125 of 1722868 in total