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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11601 - 11625 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00011601N-Acetylneuraminic acid,3TMS,isomer#27JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS525.2246Semi standard non polar2491.3516
RI00011602N-Acetylneuraminic acid,3TMS,isomer#28JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)CTMS525.2246Semi standard non polar2443.528
RI00011603N-Acetylneuraminic acid,3TMS,isomer#29JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS525.2246Semi standard non polar2450.3706
RI00011604N-Acetylneuraminic acid,3TMS,isomer#30JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)CTMS525.2246Semi standard non polar2438.8652
RI00011605N-Acetylneuraminic acid,3TMS,isomer#31JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)CTMS525.2246Semi standard non polar2436.0586
RI00011606N-Acetylneuraminic acid,3TMS,isomer#32JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS525.2246Semi standard non polar2442.6033
RI00011607N-Acetylneuraminic acid,3TMS,isomer#33JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)CTMS525.2246Semi standard non polar2478.983
RI00011608N-Acetylneuraminic acid,3TMS,isomer#34JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)CTMS525.2246Semi standard non polar2476.261
RI00011609N-Acetylneuraminic acid,3TMS,isomer#35JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)CTMS525.2246Semi standard non polar2451.782
RI00011610N-Acetylneuraminic acid,4TMS,isomer#1JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)COTMS597.2641Semi standard non polar2462.0054
RI00011611N-Acetylneuraminic acid,4TMS,isomer#2JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)CTMS597.2641Semi standard non polar2476.0605
RI00011612N-Acetylneuraminic acid,4TMS,isomer#3JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)CTMS597.2641Semi standard non polar2435.649
RI00011613N-Acetylneuraminic acid,4TMS,isomer#4JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)CTMS597.2641Semi standard non polar2467.9563
RI00011614N-Acetylneuraminic acid,4TMS,isomer#5JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)CTMS597.2641Semi standard non polar2529.6729
RI00011615N-Acetylneuraminic acid,4TMS,isomer#6JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS597.2641Semi standard non polar2520.7783
RI00011616N-Acetylneuraminic acid,4TMS,isomer#7JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)CTMS597.2641Semi standard non polar2502.0186
RI00011617N-Acetylneuraminic acid,4TMS,isomer#8JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS597.2641Semi standard non polar2495.269
RI00011618N-Acetylneuraminic acid,4TMS,isomer#9JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)CTMS597.2641Semi standard non polar2517.33
RI00011619N-Acetylneuraminic acid,4TMS,isomer#10JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)CTMS597.2641Semi standard non polar2500.8264
RI00011620N-Acetylneuraminic acid,4TMS,isomer#11JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)CTMS597.2641Semi standard non polar2495.049
RI00011621N-Acetylneuraminic acid,4TMS,isomer#12JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS597.2641Semi standard non polar2492.2947
RI00011622N-Acetylneuraminic acid,4TMS,isomer#13JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)CTMS597.2641Semi standard non polar2468.2903
RI00011623N-Acetylneuraminic acid,4TMS,isomer#14JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS597.2641Semi standard non polar2472.9617
RI00011624N-Acetylneuraminic acid,4TMS,isomer#15JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)CTMS597.2641Semi standard non polar2484.3657
RI00011625N-Acetylneuraminic acid,4TMS,isomer#16JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)CTMS597.2641Semi standard non polar2478.1067
Displaying retention index compounds 11601 - 11625 of 1722868 in total