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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11951 - 11975 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00011951N-Acetylneuraminic acid,3TBDMS,isomer#4JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3723.4365
RI00011952N-Acetylneuraminic acid,3TBDMS,isomer#5JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3703.5334
RI00011953N-Acetylneuraminic acid,3TBDMS,isomer#6JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COTBDMS651.3654Standard polar3671.977
RI00011954N-Acetylneuraminic acid,3TBDMS,isomer#7JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3637.2136
RI00011955N-Acetylneuraminic acid,3TBDMS,isomer#8JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3687.9626
RI00011956N-Acetylneuraminic acid,3TBDMS,isomer#9JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3650.8276
RI00011957N-Acetylneuraminic acid,3TBDMS,isomer#10JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3663.2012
RI00011958N-Acetylneuraminic acid,3TBDMS,isomer#11JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3685.4404
RI00011959N-Acetylneuraminic acid,3TBDMS,isomer#12JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3658.0283
RI00011960N-Acetylneuraminic acid,3TBDMS,isomer#13JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3703.6292
RI00011961N-Acetylneuraminic acid,3TBDMS,isomer#14JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3644.913
RI00011962N-Acetylneuraminic acid,3TBDMS,isomer#15JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3693.5745
RI00011963N-Acetylneuraminic acid,3TBDMS,isomer#16JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COTBDMS651.3654Standard polar3576.1438
RI00011964N-Acetylneuraminic acid,3TBDMS,isomer#17JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3551.5532
RI00011965N-Acetylneuraminic acid,3TBDMS,isomer#18JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3601.95
RI00011966N-Acetylneuraminic acid,3TBDMS,isomer#19JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3584.8398
RI00011967N-Acetylneuraminic acid,3TBDMS,isomer#20JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3633.0916
RI00011968N-Acetylneuraminic acid,3TBDMS,isomer#21JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3655.1233
RI00011969N-Acetylneuraminic acid,3TBDMS,isomer#22JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3647.6904
RI00011970N-Acetylneuraminic acid,3TBDMS,isomer#23JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3671.8665
RI00011971N-Acetylneuraminic acid,3TBDMS,isomer#24JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3632.0583
RI00011972N-Acetylneuraminic acid,3TBDMS,isomer#25JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@](O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3682.3416
RI00011973N-Acetylneuraminic acid,3TBDMS,isomer#26JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3581.764
RI00011974N-Acetylneuraminic acid,3TBDMS,isomer#27JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3602.8596
RI00011975N-Acetylneuraminic acid,3TBDMS,isomer#28JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS651.3654Standard polar3572.1384
Displaying retention index compounds 11951 - 11975 of 1722868 in total