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Displaying retention index compounds 22451 - 22475 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
CalciumJsmol[Ca++]Underivatized39.9615Standard non polar273.0861
CalciumJsmol[Ca++]Underivatized39.9615Semi standard non polar64.2528
3-MethylindoleJsmolCC1=CNC2=C1C=CC=C2Underivatized131.0735Standard polar2474.6582
3-Methylindole,1TMS,isomer#1JsmolCC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS203.113Standard non polar1508.4679
3-Methylindole,1TBDMS,isomer#1JsmolCC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS245.16Standard non polar1699.9603
3-MethylindoleJsmolCC1=CNC2=C1C=CC=C2Underivatized131.0735Standard non polar1372.8567
3-MethylindoleJsmolCC1=CNC2=C1C=CC=C2Underivatized131.0735Semi standard non polar1386.6499
3-Methylindole,1TMS,isomer#1JsmolCC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS203.113Semi standard non polar1599.6993
3-Methylindole,1TBDMS,isomer#1JsmolCC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS245.16Semi standard non polar1831.1713
3-Methylindole,1TMS,isomer#1JsmolCC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS203.113Standard polar1695.402
3-Methylindole,1TBDMS,isomer#1JsmolCC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS245.16Standard polar1843.4154
Nutriacholic acid,1TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@@H]3C(=O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTMS462.3165Semi standard non polar3393.0322
Nutriacholic acid,1TMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@@H]3C(=O)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS462.3165Semi standard non polar3436.0884
Nutriacholic acid,1TMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2C3=C(O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTMS462.3165Semi standard non polar3369.6682
Nutriacholic acid,1TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@@H]3C(O[Si](C)(C)C)=C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTMS462.3165Semi standard non polar3317.1826
Nutriacholic acid,2TMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@@H]3C(=O)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS534.3561Semi standard non polar3365.148
Nutriacholic acid,2TMS,isomer#2JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2C3=C(O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTMS534.3561Semi standard non polar3317.643
Nutriacholic acid,2TMS,isomer#3JsmolC[C@@H](CCC(=O)O[Si](C)(C)C)C1CC[C@H]2[C@@H]3C(O[Si](C)(C)C)=C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTMS534.3561Semi standard non polar3231.6587
Nutriacholic acid,2TMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2C3=C(O[Si](C)(C)C)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS534.3561Semi standard non polar3349.2441
Nutriacholic acid,2TMS,isomer#5JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@@H]3C(O[Si](C)(C)C)=C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS534.3561Semi standard non polar3262.1292
Nutriacholic acid,1TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@@H]3C(=O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS504.3635Semi standard non polar3648.975
Nutriacholic acid,1TBDMS,isomer#2JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@@H]3C(=O)C[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS504.3635Semi standard non polar3663.8699
Nutriacholic acid,1TBDMS,isomer#3JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2C3=C(O[Si](C)(C)C(C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS504.3635Semi standard non polar3593.1165
Nutriacholic acid,1TBDMS,isomer#4JsmolC[C@@H](CCC(=O)O)C1CC[C@H]2[C@@H]3C(O[Si](C)(C)C(C)(C)C)=C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS504.3635Semi standard non polar3527.0225
Nutriacholic acid,2TBDMS,isomer#1JsmolC[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C1CC[C@H]2[C@@H]3C(=O)C[C@@H]4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS618.45Semi standard non polar3865.1355
Displaying retention index compounds 22451 - 22475 of 1722868 in total