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 11076 - 11100 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00011076Mevalonic acid,2TMS,isomer#2JsmolC[C@@](CCO)(CC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS292.1526Semi standard non polar1467.8323
RI00011077Mevalonic acid,2TMS,isomer#3JsmolC[C@@](O)(CCO[Si](C)(C)C)CC(=O)O[Si](C)(C)CTMS292.1526Semi standard non polar1474.8536
RI00011078Mevalonic acid,3TMS,isomer#1JsmolC[C@@](CCO[Si](C)(C)C)(CC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS364.1921Semi standard non polar1555.973
RI00011079Mevalonic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@](C)(CCO)CC(=O)OTBDMS262.16Semi standard non polar1662.6163
RI00011080Mevalonic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC[C@@](C)(O)CC(=O)OTBDMS262.16Semi standard non polar1660.1926
RI00011081Mevalonic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C[C@](C)(O)CCOTBDMS262.16Semi standard non polar1612.9822
RI00011082Mevalonic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC[C@](C)(CC(=O)O)O[Si](C)(C)C(C)(C)CTBDMS376.2465Semi standard non polar1977.2839
RI00011083Mevalonic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C[C@@](C)(CCO)O[Si](C)(C)C(C)(C)CTBDMS376.2465Semi standard non polar1912.7096
RI00011084Mevalonic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC[C@@](C)(O)CC(=O)O[Si](C)(C)C(C)(C)CTBDMS376.2465Semi standard non polar1911.7986
RI00011085Mevalonic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC[C@](C)(CC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS490.333Semi standard non polar2208.2297
RI00011086Mevalonic acid,1TMS,isomer#1JsmolC[C@@](CCO)(CC(=O)O)O[Si](C)(C)CTMS220.1131Standard polar1918.2738
RI00011087Mevalonic acid,1TMS,isomer#2JsmolC[C@@](O)(CCO[Si](C)(C)C)CC(=O)OTMS220.1131Standard polar1919.8748
RI00011088Mevalonic acid,1TMS,isomer#3JsmolC[C@@](O)(CCO)CC(=O)O[Si](C)(C)CTMS220.1131Standard polar1909.1748
RI00011089Mevalonic acid,2TMS,isomer#1JsmolC[C@@](CCO[Si](C)(C)C)(CC(=O)O)O[Si](C)(C)CTMS292.1526Standard polar1667.7048
RI00011090Mevalonic acid,2TMS,isomer#2JsmolC[C@@](CCO)(CC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS292.1526Standard polar1658.7579
RI00011091Mevalonic acid,2TMS,isomer#3JsmolC[C@@](O)(CCO[Si](C)(C)C)CC(=O)O[Si](C)(C)CTMS292.1526Standard polar1672.0521
RI00011092Mevalonic acid,3TMS,isomer#1JsmolC[C@@](CCO[Si](C)(C)C)(CC(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS364.1921Standard polar1497.3191
RI00011093Mevalonic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@](C)(CCO)CC(=O)OTBDMS262.16Standard polar1958.2498
RI00011094Mevalonic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC[C@@](C)(O)CC(=O)OTBDMS262.16Standard polar2021.4332
RI00011095Mevalonic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C[C@](C)(O)CCOTBDMS262.16Standard polar1985.8176
RI00011096Mevalonic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC[C@](C)(CC(=O)O)O[Si](C)(C)C(C)(C)CTBDMS376.2465Standard polar1903.3523
RI00011097Mevalonic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C[C@@](C)(CCO)O[Si](C)(C)C(C)(C)CTBDMS376.2465Standard polar1883.6699
RI00011098Mevalonic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC[C@@](C)(O)CC(=O)O[Si](C)(C)C(C)(C)CTBDMS376.2465Standard polar1916.1252
RI00011099Mevalonic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC[C@](C)(CC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS490.333Standard polar1917.2023
RI00011100Phenol,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1TMS166.0814Standard non polar1038.142
Displaying retention index compounds 11076 - 11100 of 1722868 in total