Displaying retention index compounds 276 - 300 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Nordeoxycholic acid,2TMS,isomer#2JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS522.3561Semi standard non polar3240.6062
Nordeoxycholic acid,2TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12CTMS522.3561Semi standard non polar3350.067
Nordeoxycholic acid,1TMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS450.3165Semi standard non polar3335.8723
Nordeoxycholic acid,1TMS,isomer#2JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12CTMS450.3165Semi standard non polar3383.1619
Nordeoxycholic acid,1TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12CTMS450.3165Semi standard non polar3305.9175
Nordeoxycholic acid,3TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS720.5364Standard non polar3796.2224
Nordeoxycholic acid,2TBDMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS606.45Standard non polar3548.9795
Nordeoxycholic acid,2TBDMS,isomer#2JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS606.45Standard non polar3655.8958
Nordeoxycholic acid,2TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12CTBDMS606.45Standard non polar3653.2747
Nordeoxycholic acid,1TBDMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12CTBDMS492.3635Standard non polar3289.413
Nordeoxycholic acid,1TBDMS,isomer#2JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12CTBDMS492.3635Standard non polar3298.3032
Nordeoxycholic acid,1TBDMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12CTBDMS492.3635Standard non polar3382.0862
Nordeoxycholic acid,3TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS594.3956Standard non polar3092.0159
Nordeoxycholic acid,2TMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS522.3561Standard non polar3025.3079
Nordeoxycholic acid,2TMS,isomer#2JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS522.3561Standard non polar3114.2507
Nordeoxycholic acid,2TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12CTMS522.3561Standard non polar3124.2585
Nordeoxycholic acid,1TMS,isomer#3JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12CTMS450.3165Standard non polar3004.602
Nordeoxycholic acid,1TMS,isomer#2JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12CTMS450.3165Standard non polar3028.661
Nordeoxycholic acid,1TMS,isomer#1JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12CTMS450.3165Standard non polar3105.0322
Indole-3-acetic acid ethyl ester,1TBDMS,isomer#1JsmolCCOC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS317.1811Standard polar2413.374
Indole-3-acetic acid ethyl ester,1TMS,isomer#1JsmolCCOC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS275.1342Standard polar2303.6804
Indole-3-acetic acid ethyl ester,1TBDMS,isomer#1JsmolCCOC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS317.1811Semi standard non polar2148.2441
Indole-3-acetic acid ethyl ester,1TMS,isomer#1JsmolCCOC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS275.1342Semi standard non polar1919.7465
Indole-3-acetic acid ethyl ester,1TBDMS,isomer#1JsmolCCOC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12TBDMS317.1811Standard non polar2087.455
Indole-3-acetic acid ethyl ester,1TMS,isomer#1JsmolCCOC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12TMS275.1342Standard non polar1876.4521
Displaying retention index compounds 276 - 300 of 1722868 in total