Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 626 - 650 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017235514-Allylpyrocatechol sulfate,1TMS,isomer#2JsmolC=CCC1=CC=C(OS(=O)(=O)O[Si](C)(C)C)C(O)=C1TMS302.0644Standard non polar1918.4236
RI017235504-Allylpyrocatechol sulfate,1TMS,isomer#1JsmolC=CCC1=CC=C(OS(=O)(=O)O)C(O[Si](C)(C)C)=C1TMS302.0644Standard non polar1932.2236
RI017235493- Allylphenol sulfate,1TBDMS,isomer#1JsmolC=CCC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS328.1165Standard polar2573.1934
RI017235483- Allylphenol sulfate,1TMS,isomer#1JsmolC=CCC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1TMS286.0695Standard polar2502.1755
RI017235473- Allylphenol sulfate,1TBDMS,isomer#1JsmolC=CCC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS328.1165Semi standard non polar1973.7928
RI017235463- Allylphenol sulfate,1TMS,isomer#1JsmolC=CCC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1TMS286.0695Semi standard non polar1724.6179
RI017235453- Allylphenol sulfate,1TBDMS,isomer#1JsmolC=CCC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS328.1165Standard non polar2005.3888
RI017235443- Allylphenol sulfate,1TMS,isomer#1JsmolC=CCC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1TMS286.0695Standard non polar1757.5582
RI01723543Aminocatechol N-acetate sulfate,3TBDMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS589.2745Standard polar3080.4565
RI01723542Aminocatechol N-acetate sulfate,2TBDMS,isomer#3JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)CTBDMS475.188Standard polar3243.5627
RI01723541Aminocatechol N-acetate sulfate,2TBDMS,isomer#2JsmolCC(=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1O)O[Si](C)(C)C(C)(C)CTBDMS475.188Standard polar3240.7192
RI01723540Aminocatechol N-acetate sulfate,2TBDMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O)=C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS475.188Standard polar3207.6658
RI01723539Aminocatechol N-acetate sulfate,1TBDMS,isomer#3JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1OTBDMS361.1015Standard polar3663.8826
RI01723538Aminocatechol N-acetate sulfate,1TBDMS,isomer#2JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O)=C1O[Si](C)(C)C(C)(C)CTBDMS361.1015Standard polar3632.7905
RI01723537Aminocatechol N-acetate sulfate,1TBDMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O)=C1O)O[Si](C)(C)C(C)(C)CTBDMS361.1015Standard polar3712.735
RI01723536Aminocatechol N-acetate sulfate,3TMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1O[Si](C)(C)C)O[Si](C)(C)CTMS463.1336Standard polar2892.0125
RI01723535Aminocatechol N-acetate sulfate,2TMS,isomer#3JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1O[Si](C)(C)CTMS391.0941Standard polar3183.1057
RI01723534Aminocatechol N-acetate sulfate,2TMS,isomer#2JsmolCC(=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1O)O[Si](C)(C)CTMS391.0941Standard polar3236.6687
RI01723533Aminocatechol N-acetate sulfate,2TMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O)=C1O[Si](C)(C)C)O[Si](C)(C)CTMS391.0941Standard polar3158.0796
RI01723532Aminocatechol N-acetate sulfate,1TMS,isomer#3JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C)=C1OTMS319.0546Standard polar3713.325
RI01723531Aminocatechol N-acetate sulfate,1TMS,isomer#2JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O)=C1O[Si](C)(C)CTMS319.0546Standard polar3633.1877
RI01723530Aminocatechol N-acetate sulfate,1TMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O)=C1O)O[Si](C)(C)CTMS319.0546Standard polar3762.5972
RI01723529Aminocatechol N-acetate sulfate,3TBDMS,isomer#1JsmolCC(=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS589.2745Semi standard non polar2771.038
RI01723528Aminocatechol N-acetate sulfate,2TBDMS,isomer#3JsmolCC(O)=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)CTBDMS475.188Semi standard non polar2582.4126
RI01723527Aminocatechol N-acetate sulfate,2TBDMS,isomer#2JsmolCC(=NC1=CC=CC(OS(=O)(=O)O[Si](C)(C)C(C)(C)C)=C1O)O[Si](C)(C)C(C)(C)CTBDMS475.188Semi standard non polar2537.4321
Displaying retention index compounds 626 - 650 of 1722868 in total