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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 12426 - 12450 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00012426Pyruvic acid,1TBDMS,isomer#2JsmolC=C(O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS202.1025Semi standard non polar1219.7184
RI00012427Pyruvic acidJsmolCC(=O)C(O)=OUnderivatized88.016Standard polar1553.1947
RI00012428Pyruvic acid,2TMS,isomer#1JsmolC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS232.0951Standard non polar1108.63
RI00012429Pyruvic acid,2TBDMS,isomer#1JsmolC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS316.189Standard non polar1511.7828
RI00012430Pyruvic acidJsmolCC(=O)C(O)=OUnderivatized88.016Standard non polar1190.3828
RI00012431Pyruvic acidJsmolCC(=O)C(O)=OUnderivatized88.016Semi standard non polar771.3649
RI00012432Pyruvic acid,2TMS,isomer#1JsmolC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS232.0951Semi standard non polar1125.1788
RI00012433Pyruvic acid,2TBDMS,isomer#1JsmolC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS316.189Semi standard non polar1562.366
RI00012434Pyruvic acid,2TMS,isomer#1JsmolC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS232.0951Standard polar1135.6025
RI00012435Pyruvic acid,2TBDMS,isomer#1JsmolC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS316.189Standard polar1467.6665
RI00012436Riboflavin,1TMS,isomer#1JsmolCC1=CC2=C(C=C1C)N(C[C@H](O[Si](C)(C)C)[C@H](O)[C@H](O)CO)C1=NC(=O)[NH]C(=O)C1=N2TMS448.1778Semi standard non polar3392.7776
RI00012437Riboflavin,1TMS,isomer#2JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O[Si](C)(C)C)[C@H](O)CO)C1=NC(=O)[NH]C(=O)C1=N2TMS448.1778Semi standard non polar3382.0342
RI00012438Riboflavin,1TMS,isomer#3JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@@H](CO)O[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS448.1778Semi standard non polar3409.4214
RI00012439Riboflavin,1TMS,isomer#4JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)CO[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS448.1778Semi standard non polar3394.6533
RI00012440Riboflavin,1TMS,isomer#5JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)CO)C1=NC(=O)N([Si](C)(C)C)C(=O)C1=N2TMS448.1778Semi standard non polar3515.4255
RI00012441Riboflavin,2TMS,isomer#1JsmolCC1=CC2=C(C=C1C)N(C[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)CO)C1=NC(=O)[NH]C(=O)C1=N2TMS520.2173Semi standard non polar3254.6116
RI00012442Riboflavin,2TMS,isomer#2JsmolCC1=CC2=C(C=C1C)N(C[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](CO)O[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS520.2173Semi standard non polar3291.0955
RI00012443Riboflavin,2TMS,isomer#3JsmolCC1=CC2=C(C=C1C)N(C[C@H](O[Si](C)(C)C)[C@H](O)[C@H](O)CO[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS520.2173Semi standard non polar3265.1782
RI00012444Riboflavin,2TMS,isomer#4JsmolCC1=CC2=C(C=C1C)N(C[C@H](O[Si](C)(C)C)[C@H](O)[C@H](O)CO)C1=NC(=O)N([Si](C)(C)C)C(=O)C1=N2TMS520.2173Semi standard non polar3377.3096
RI00012445Riboflavin,2TMS,isomer#5JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS520.2173Semi standard non polar3260.072
RI00012446Riboflavin,2TMS,isomer#6JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS520.2173Semi standard non polar3249.459
RI00012447Riboflavin,2TMS,isomer#7JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O[Si](C)(C)C)[C@H](O)CO)C1=NC(=O)N([Si](C)(C)C)C(=O)C1=N2TMS520.2173Semi standard non polar3371.4102
RI00012448Riboflavin,2TMS,isomer#8JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)C1=NC(=O)[NH]C(=O)C1=N2TMS520.2173Semi standard non polar3280.6763
RI00012449Riboflavin,2TMS,isomer#9JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@@H](CO)O[Si](C)(C)C)C1=NC(=O)N([Si](C)(C)C)C(=O)C1=N2TMS520.2173Semi standard non polar3394.6309
RI00012450Riboflavin,2TMS,isomer#10JsmolCC1=CC2=C(C=C1C)N(C[C@H](O)[C@H](O)[C@H](O)CO[Si](C)(C)C)C1=NC(=O)N([Si](C)(C)C)C(=O)C1=N2TMS520.2173Semi standard non polar3387.2234
Displaying retention index compounds 12426 - 12450 of 1722868 in total