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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 69651 - 69675 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00069651Allysine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCCC=O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS373.2468Standard polar2002.2456
RI00069652Allysine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCC=CO[Si](C)(C)C(C)(C)C)C(=O)OTBDMS373.2468Standard polar2215.965
RI00069653Allysine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N([C@@H](CCCC=O)C(=O)O)[Si](C)(C)C(C)(C)CTBDMS373.2468Standard polar2098.509
RI00069654Allysine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCC=CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS487.3333Standard polar2141.2134
RI00069655Allysine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS487.3333Standard polar2050.7603
RI00069656Allysine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC=CCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS487.3333Standard polar2220.472
RI00069657Allysine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=CCC[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)CTBDMS601.4198Standard polar2177.097
RI00069658Dehydroascorbic acid,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H](CO)[C@H]1OC(=O)C(=O)C1=OTMS246.056Semi standard non polar1709.3506
RI00069659Dehydroascorbic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(=O)C1=OTMS246.056Semi standard non polar1718.8032
RI00069660Dehydroascorbic acid,1TMS,isomer#3JsmolC[Si](C)(C)OC1=C([C@@H](O)CO)OC(=O)C1=OTMS246.056Semi standard non polar1646.3024
RI00069661Dehydroascorbic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)[C@H]1OC(=O)C(=O)C1=OTMS318.0955Semi standard non polar1846.0337
RI00069662Dehydroascorbic acid,2TMS,isomer#2JsmolC[Si](C)(C)OC1=C([C@H](CO)O[Si](C)(C)C)OC(=O)C1=OTMS318.0955Semi standard non polar1786.2332
RI00069663Dehydroascorbic acid,2TMS,isomer#3JsmolC[Si](C)(C)OC[C@H](O)C1=C(O[Si](C)(C)C)C(=O)C(=O)O1TMS318.0955Semi standard non polar1775.9489
RI00069664Dehydroascorbic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H](CO)[C@H]1OC(=O)C(=O)C1=OTBDMS288.1029Semi standard non polar1981.7677
RI00069665Dehydroascorbic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)[C@H]1OC(=O)C(=O)C1=OTBDMS288.1029Semi standard non polar1975.7229
RI00069666Dehydroascorbic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C([C@@H](O)CO)OC(=O)C1=OTBDMS288.1029Semi standard non polar1931.6132
RI00069667Dehydroascorbic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1OC(=O)C(=O)C1=OTBDMS402.1894Semi standard non polar2322.1836
RI00069668Dehydroascorbic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C([C@H](CO)O[Si](C)(C)C(C)(C)C)OC(=O)C1=OTBDMS402.1894Semi standard non polar2314.1123
RI00069669Dehydroascorbic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC[C@H](O)C1=C(O[Si](C)(C)C(C)(C)C)C(=O)C(=O)O1TBDMS402.1894Semi standard non polar2295.0283
RI00069670Dehydroascorbic acidJsmol[H][C@@]1(OC(=O)C(=O)C1=O)[C@@H](O)COUnderivatized174.0164Standard polar2607.4248
RI00069671Dehydroascorbic acid,3TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)C1=C(O[Si](C)(C)C)C(=O)C(=O)O1TMS390.135Standard non polar1861.1653
RI00069672Dehydroascorbic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[C@H](O[Si](C)(C)C(C)(C)C)C1=C(O[Si](C)(C)C(C)(C)C)C(=O)C(=O)O1TBDMS516.2759Standard non polar2536.478
RI00069673Dehydroascorbic acidJsmol[H][C@@]1(OC(=O)C(=O)C1=O)[C@@H](O)COUnderivatized174.0164Standard non polar1635.2988
RI00069674Dehydroascorbic acidJsmol[H][C@@]1(OC(=O)C(=O)C1=O)[C@@H](O)COUnderivatized174.0164Semi standard non polar1661.0505
RI00069675Dehydroascorbic acid,3TMS,isomer#1JsmolC[Si](C)(C)OC[C@H](O[Si](C)(C)C)C1=C(O[Si](C)(C)C)C(=O)C(=O)O1TMS390.135Semi standard non polar1903.786
Displaying retention index compounds 69651 - 69675 of 1722868 in total