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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11626 - 11650 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00011626N-Acetylneuraminic acid,4TMS,isomer#17JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](O[Si](C)(C)C)(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)CTMS597.2641Semi standard non polar2508.0364
RI00011627N-Acetylneuraminic acid,4TMS,isomer#18JsmolCC(=O)N([C@@H]1[C@@H](O)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)C)[Si](C)(C)CTMS597.2641Semi standard non polar2527.631
RI00011628N-Acetylneuraminic acid,4TMS,isomer#19JsmolCC(=O)N([C@@H]1[C@@H](O)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)C)[Si](C)(C)CTMS597.2641Semi standard non polar2526.3462
RI00011629N-Acetylneuraminic acid,4TMS,isomer#20JsmolCC(=O)N([C@@H]1[C@@H](O)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)C)[Si](C)(C)CTMS597.2641Semi standard non polar2511.6677
RI00011630N-Acetylneuraminic acid,4TMS,isomer#21JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@@](O)(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 polar2509.8975
RI00011631N-Acetylneuraminic acid,4TMS,isomer#22JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2501.7249
RI00011632N-Acetylneuraminic acid,4TMS,isomer#23JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2482.9746
RI00011633N-Acetylneuraminic acid,4TMS,isomer#24JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2466.9766
RI00011634N-Acetylneuraminic acid,4TMS,isomer#25JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2477.9248
RI00011635N-Acetylneuraminic acid,4TMS,isomer#26JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2471.5315
RI00011636N-Acetylneuraminic acid,4TMS,isomer#27JsmolCC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2439.6035
RI00011637N-Acetylneuraminic acid,4TMS,isomer#28JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2503.6655
RI00011638N-Acetylneuraminic acid,4TMS,isomer#29JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2497.7246
RI00011639N-Acetylneuraminic acid,4TMS,isomer#30JsmolCC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)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)CTMS597.2641Semi standard non polar2481.6587
RI00011640N-Acetylneuraminic acid,4TMS,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[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)CTMS597.2641Semi standard non polar2496.4285
RI00011641N-Acetylneuraminic acid,4TMS,isomer#32JsmolCC(=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](CO)O[Si](C)(C)C)[Si](C)(C)CTMS597.2641Semi standard non polar2486.816
RI00011642N-Acetylneuraminic acid,4TMS,isomer#33JsmolCC(=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)C)[Si](C)(C)CTMS597.2641Semi standard non polar2483.0364
RI00011643N-Acetylneuraminic acid,4TMS,isomer#34JsmolCC(=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)C)[Si](C)(C)CTMS597.2641Semi standard non polar2461.6384
RI00011644N-Acetylneuraminic acid,4TMS,isomer#35JsmolCC(=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)C)[Si](C)(C)CTMS597.2641Semi standard non polar2474.5225
RI00011645N-Acetylneuraminic acid,5TMS,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](CO)O[Si](C)(C)CTMS669.3036Semi standard non polar2504.7522
RI00011646N-Acetylneuraminic acid,5TMS,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[Si](C)(C)C)[C@H](O)CO[Si](C)(C)CTMS669.3036Semi standard non polar2487.8853
RI00011647N-Acetylneuraminic acid,5TMS,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[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)CTMS669.3036Semi standard non polar2510.5127
RI00011648N-Acetylneuraminic acid,5TMS,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](CO[Si](C)(C)C)O[Si](C)(C)CTMS669.3036Semi standard non polar2473.9597
RI00011649N-Acetylneuraminic acid,5TMS,isomer#5JsmolCC(=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)C)[Si](C)(C)CTMS669.3036Semi standard non polar2515.3035
RI00011650N-Acetylneuraminic acid,5TMS,isomer#6JsmolCC(=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)C)[Si](C)(C)CTMS669.3036Semi standard non polar2505.017
Displaying retention index compounds 11626 - 11650 of 1722868 in total