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Displaying retention index compounds 13451 - 13475 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Pyroglutamic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H]1CCC(=O)N1[Si](C)(C)C(C)(C)CTBDMS357.2155Semi standard non polar1927.9578
Pyroglutamic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H]1CCC(=O)N1[Si](C)(C)CTMS273.1216Standard polar1803.4055
Pyroglutamic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H]1CCC(=O)N1[Si](C)(C)C(C)(C)CTBDMS357.2155Standard polar1985.4645
Tetrahydrocorticosterone,1TMS,isomer#1JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS422.2852Semi standard non polar3123.7078
Tetrahydrocorticosterone,1TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)COTMS422.2852Semi standard non polar3062.4902
Tetrahydrocorticosterone,1TMS,isomer#3JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)COTMS422.2852Semi standard non polar3126.9385
Tetrahydrocorticosterone,1TMS,isomer#4JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS422.2852Semi standard non polar3094.7007
Tetrahydrocorticosterone,1TMS,isomer#5JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS422.2852Semi standard non polar3070.6309
Tetrahydrocorticosterone,2TMS,isomer#1JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS494.3248Semi standard non polar3021.3162
Tetrahydrocorticosterone,2TMS,isomer#2JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS494.3248Semi standard non polar3103.3186
Tetrahydrocorticosterone,2TMS,isomer#3JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS494.3248Semi standard non polar3119.815
Tetrahydrocorticosterone,2TMS,isomer#4JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS494.3248Semi standard non polar3101.76
Tetrahydrocorticosterone,2TMS,isomer#5JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)COTMS494.3248Semi standard non polar3004.3115
Tetrahydrocorticosterone,2TMS,isomer#6JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS494.3248Semi standard non polar3018.212
Tetrahydrocorticosterone,2TMS,isomer#7JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS494.3248Semi standard non polar2983.187
Tetrahydrocorticosterone,2TMS,isomer#8JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS494.3248Semi standard non polar3106.857
Tetrahydrocorticosterone,2TMS,isomer#9JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS494.3248Semi standard non polar3045.1929
Tetrahydrocorticosterone,3TMS,isomer#1JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO[Si](C)(C)CTMS566.3643Semi standard non polar3001.9082
Tetrahydrocorticosterone,3TMS,isomer#2JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3017.4521
Tetrahydrocorticosterone,3TMS,isomer#3JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3034.392
Tetrahydrocorticosterone,3TMS,isomer#4JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CCC2=C(CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3103.0684
Tetrahydrocorticosterone,3TMS,isomer#5JsmolC[C@]12C[C@H](O)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO[Si](C)(C)C)O[Si](C)(C)CTMS566.3643Semi standard non polar3097.9797
Tetrahydrocorticosterone,3TMS,isomer#6JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CCC2=C(CO)O[Si](C)(C)CTMS566.3643Semi standard non polar3000.276
Tetrahydrocorticosterone,3TMS,isomer#7JsmolC[C@]12C[C@H](O[Si](C)(C)C)[C@H]3[C@@H](CC[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]34C)[C@@H]1CC[C@@H]2C(=CO)O[Si](C)(C)CTMS566.3643Semi standard non polar2965.7844
Tetrahydrocorticosterone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12CTBDMS464.3322Semi standard non polar3416.346
Displaying retention index compounds 13451 - 13475 of 1722868 in total