RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 12776 - 12800 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01711401avenastenone,1TMS,isomer#2JsmolCC=C(CCC(C)C1CCC2C3=CCC4C=C(O[Si](C)(C)C)CCC4(C)C3CCC21C)C(C)CTMS482.3944Standard non polar3312.3462
RI01711400avenastenone,1TMS,isomer#1JsmolCC=C(CCC(C)C1CCC2C3=CCC4CC(O[Si](C)(C)C)=CCC4(C)C3CCC21C)C(C)CTMS482.3944Standard non polar3281.3672
RI01711399allylsulfenate,1TBDMS,isomer#1JsmolC=CCSO[Si](C)(C)C(C)(C)CTBDMS204.1004Standard polar1251.5742
RI01711398allylsulfenate,1TMS,isomer#1JsmolC=CCSO[Si](C)(C)CTMS162.0535Standard polar1020.3927
RI01711397allylsulfenate,1TBDMS,isomer#1JsmolC=CCSO[Si](C)(C)C(C)(C)CTBDMS204.1004Semi standard non polar1127.011
RI01711396allylsulfenate,1TMS,isomer#1JsmolC=CCSO[Si](C)(C)CTMS162.0535Semi standard non polar896.3525
RI01711395allylsulfenate,1TBDMS,isomer#1JsmolC=CCSO[Si](C)(C)C(C)(C)CTBDMS204.1004Standard non polar1136.6595
RI01711394allylsulfenate,1TMS,isomer#1JsmolC=CCSO[Si](C)(C)CTMS162.0535Standard non polar936.935
RI01711393adenylo-succinate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N2C=NC3=C(N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)N=CN=C32)C1O[Si](C)(C)C(C)(C)CTBDMS801.3044Standard polar4745.308
RI01711392adenylo-succinate,3TMS,isomer#1JsmolC[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N2C=NC3=C(N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)CTMS675.1635Standard polar4784.52
RI01711391adenylo-succinate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N2C=NC3=C(N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)N=CN=C32)C1O[Si](C)(C)C(C)(C)CTBDMS801.3044Semi standard non polar3985.3745
RI01711390adenylo-succinate,3TMS,isomer#1JsmolC[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N2C=NC3=C(N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)CTMS675.1635Semi standard non polar3374.8018
RI01711389adenylo-succinate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N2C=NC3=C(N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)C)N=CN=C32)C1O[Si](C)(C)C(C)(C)CTBDMS801.3044Standard non polar4139.609
RI01711388adenylo-succinate,3TMS,isomer#1JsmolC[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N2C=NC3=C(N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)CTMS675.1635Standard non polar3534.9653
RI01711387acetoacetate,1TBDMS,isomer#2JsmolC=C(CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS215.1109Standard polar1427.1935
RI01711386acetoacetate,1TBDMS,isomer#1JsmolCC(=CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS215.1109Standard polar1436.4623
RI01711385acetoacetate,1TMS,isomer#2JsmolC=C(CC(=O)[O-])O[Si](C)(C)CTMS173.0639Standard polar1261.4904
RI01711384acetoacetate,1TMS,isomer#1JsmolCC(=CC(=O)[O-])O[Si](C)(C)CTMS173.0639Standard polar1275.8633
RI01711383acetoacetate,1TBDMS,isomer#2JsmolC=C(CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS215.1109Semi standard non polar1190.737
RI01711382acetoacetate,1TBDMS,isomer#1JsmolCC(=CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS215.1109Semi standard non polar1274.635
RI01711381acetoacetate,1TMS,isomer#2JsmolC=C(CC(=O)[O-])O[Si](C)(C)CTMS173.0639Semi standard non polar993.6991
RI01711380acetoacetate,1TMS,isomer#1JsmolCC(=CC(=O)[O-])O[Si](C)(C)CTMS173.0639Semi standard non polar1046.751
RI01711379acetoacetate,1TBDMS,isomer#2JsmolC=C(CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS215.1109Standard non polar1177.5818
RI01711378acetoacetate,1TBDMS,isomer#1JsmolCC(=CC(=O)[O-])O[Si](C)(C)C(C)(C)CTBDMS215.1109Standard non polar1172.5223
RI01711377acetoacetate,1TMS,isomer#2JsmolC=C(CC(=O)[O-])O[Si](C)(C)CTMS173.0639Standard non polar982.1444
Displaying retention index compounds 12776 - 12800 of 1722868 in total