Displaying retention index compounds 376 - 400 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Glycohyodeoxycholic acid,3TMS,isomer#2JsmolCC(CCC(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CC(O[Si](C)(C)C)C4CC(O)CCC4(C)C3CCC12CTMS665.4327Standard non polar3781.085
Glycohyodeoxycholic acid,3TMS,isomer#1JsmolCC(CCC(=O)NCC(=O)O[Si](C)(C)C)C1CCC2C3CC(O[Si](C)(C)C)C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS665.4327Standard non polar3737.5325
Glycohyodeoxycholic acid,2TMS,isomer#6JsmolCC(CCC(=O)N(CC(=O)O)[Si](C)(C)C)C1CCC2C3CC(O)C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS593.3932Standard non polar3822.941
Glycohyodeoxycholic acid,2TMS,isomer#5JsmolCC(CCC(=O)N(CC(=O)O)[Si](C)(C)C)C1CCC2C3CC(O[Si](C)(C)C)C4CC(O)CCC4(C)C3CCC12CTMS593.3932Standard non polar3706.0647
Glycohyodeoxycholic acid,2TMS,isomer#4JsmolCC(CCC(=O)NCC(=O)O)C1CCC2C3CC(O[Si](C)(C)C)C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS593.3932Standard non polar3665.72
Glycohyodeoxycholic acid,2TMS,isomer#3JsmolCC(CCC(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)C1CCC2C3CC(O)C4CC(O)CCC4(C)C3CCC12CTMS593.3932Standard non polar3852.7605
Glycohyodeoxycholic acid,2TMS,isomer#2JsmolCC(CCC(=O)NCC(=O)O[Si](C)(C)C)C1CCC2C3CC(O)C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS593.3932Standard non polar3794.2717
Glycohyodeoxycholic acid,2TMS,isomer#1JsmolCC(CCC(=O)NCC(=O)O[Si](C)(C)C)C1CCC2C3CC(O[Si](C)(C)C)C4CC(O)CCC4(C)C3CCC12CTMS593.3932Standard non polar3688.3694
Glycohyodeoxycholic acid,1TMS,isomer#4JsmolCC(CCC(=O)N(CC(=O)O)[Si](C)(C)C)C1CCC2C3CC(O)C4CC(O)CCC4(C)C3CCC12CTMS521.3537Standard non polar3790.984
Glycohyodeoxycholic acid,1TMS,isomer#3JsmolCC(CCC(=O)NCC(=O)O)C1CCC2C3CC(O)C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS521.3537Standard non polar3683.5144
Glycohyodeoxycholic acid,1TMS,isomer#2JsmolCC(CCC(=O)NCC(=O)O)C1CCC2C3CC(O[Si](C)(C)C)C4CC(O)CCC4(C)C3CCC12CTMS521.3537Standard non polar3578.8003
Glycohyodeoxycholic acid,1TMS,isomer#1JsmolCC(CCC(=O)NCC(=O)O[Si](C)(C)C)C1CCC2C3CC(O)C4CC(O)CCC4(C)C3CCC12CTMS521.3537Standard non polar3721.943
3-Methyloxindole,1TBDMS,isomer#1JsmolCC1C(=O)N([Si](C)(C)C(C)(C)C)C2=CC=CC=C21TBDMS261.1549Standard polar1979.5948
3-Methyloxindole,1TMS,isomer#1JsmolCC1C(=O)N([Si](C)(C)C)C2=CC=CC=C21TMS219.1079Standard polar1838.0845
3-Methyloxindole,1TBDMS,isomer#1JsmolCC1C(=O)N([Si](C)(C)C(C)(C)C)C2=CC=CC=C21TBDMS261.1549Semi standard non polar1739.9712
3-Methyloxindole,1TMS,isomer#1JsmolCC1C(=O)N([Si](C)(C)C)C2=CC=CC=C21TMS219.1079Semi standard non polar1498.921
3-Methyloxindole,1TBDMS,isomer#1JsmolCC1C(=O)N([Si](C)(C)C(C)(C)C)C2=CC=CC=C21TBDMS261.1549Standard non polar1790.4146
3-Methyloxindole,1TMS,isomer#1JsmolCC1C(=O)N([Si](C)(C)C)C2=CC=CC=C21TMS219.1079Standard non polar1552.8595
3-Amino-5-hydroxybenzoic acid,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(O[Si](C)(C)C(C)(C)C)=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1TBDMS609.3885Standard polar2367.7869
3-Amino-5-hydroxybenzoic acid,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C1=CC(O)=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1TBDMS495.302Standard polar2381.4214
3-Amino-5-hydroxybenzoic acid,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC(C(=O)O)=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1TBDMS495.302Standard polar2342.1746
3-Amino-5-hydroxybenzoic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS495.302Standard polar2347.8508
3-Amino-5-hydroxybenzoic acid,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C1=CC(O)=CC(C(=O)O)=C1)[Si](C)(C)C(C)(C)CTBDMS381.2155Standard polar2396.2053
3-Amino-5-hydroxybenzoic acid,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=CC(O)=CC(C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS381.2155Standard polar2356.2563
3-Amino-5-hydroxybenzoic acid,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C(=O)O)=C1TBDMS381.2155Standard polar2296.8687
Displaying retention index compounds 376 - 400 of 1722868 in total