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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 22051 - 22075 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000220515-Hydroxylysine,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC[C@@H](CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS732.5328Standard polar2528.1216
RI000220525-Hydroxylysine,5TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)O[C@H](CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS732.5328Standard polar2573.6562
RI000220535-Hydroxylysine,5TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CC[C@@H](O)CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS732.5328Standard polar2571.3943
RI000220545-Hydroxylysine,6TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CC[C@H](CN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS846.6193Standard polar2605.704
RI00022055cis-4-Hydroxycyclohexylacetic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC1CCC(CC(=O)O)CC1TMS230.1338Semi standard non polar1536.7598
RI00022056cis-4-Hydroxycyclohexylacetic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC(=O)CC1CCC(O)CC1TMS230.1338Semi standard non polar1515.9822
RI00022057cis-4-Hydroxycyclohexylacetic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1CCC(O[Si](C)(C)C)CC1TMS302.1733Semi standard non polar1576.8533
RI00022058cis-4-Hydroxycyclohexylacetic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1CCC(CC(=O)O)CC1TBDMS272.1808Semi standard non polar1804.3218
RI00022059cis-4-Hydroxycyclohexylacetic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1CCC(O)CC1TBDMS272.1808Semi standard non polar1773.1721
RI00022060cis-4-Hydroxycyclohexylacetic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1CCC(O[Si](C)(C)C(C)(C)C)CC1TBDMS386.2672Semi standard non polar2044.8478
RI00022061cis-4-Hydroxycyclohexylacetic acidJsmolOC1CCC(CC(O)=O)CC1Underivatized158.0943Standard polar2771.8313
RI00022062cis-4-Hydroxycyclohexylacetic acidJsmolOC1CCC(CC(O)=O)CC1Underivatized158.0943Standard non polar1397.6875
RI00022063cis-4-Hydroxycyclohexylacetic acidJsmolOC1CCC(CC(O)=O)CC1Underivatized158.0943Semi standard non polar1442.4308
RI00022064L-alpha-Aminobutyric acid,1TMS,isomer#1JsmolCC[C@H](N)C(=O)O[Si](C)(C)CTMS175.1029Semi standard non polar1033.6877
RI00022065L-alpha-Aminobutyric acid,1TMS,isomer#2JsmolCC[C@H](N[Si](C)(C)C)C(=O)OTMS175.1029Semi standard non polar1141.2067
RI00022066L-alpha-Aminobutyric acid,1TBDMS,isomer#1JsmolCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)CTBDMS217.1498Semi standard non polar1253.8102
RI00022067L-alpha-Aminobutyric acid,1TBDMS,isomer#2JsmolCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)OTBDMS217.1498Semi standard non polar1379.1766
RI00022068L-alpha-Aminobutyric acidJsmolCC[C@H](N)C(O)=OUnderivatized103.0633Standard polar1783.7278
RI00022069L-alpha-Aminobutyric acid,2TMS,isomer#1JsmolCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS247.1424Standard non polar1198.3335
RI00022070L-alpha-Aminobutyric acid,2TMS,isomer#2JsmolCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS247.1424Standard non polar1241.7228
RI00022071L-alpha-Aminobutyric acid,3TMS,isomer#1JsmolCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS319.1819Standard non polar1319.2034
RI00022072L-alpha-Aminobutyric acid,2TBDMS,isomer#1JsmolCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS331.2363Standard non polar1617.8201
RI00022073L-alpha-Aminobutyric acid,2TBDMS,isomer#2JsmolCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS331.2363Standard non polar1681.9508
RI00022074L-alpha-Aminobutyric acid,3TBDMS,isomer#1JsmolCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS445.3228Standard non polar1965.0415
RI00022075L-alpha-Aminobutyric acidJsmolCC[C@H](N)C(O)=OUnderivatized103.0633Standard non polar971.0805
Displaying retention index compounds 22051 - 22075 of 1722868 in total