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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
RI01711751codeinone,1TBDMS,isomer#1JsmolCOC1=CC=C2CC3C4C=CC(O[Si](C)(C)C(C)(C)C)=C5OC1=C2C54CC[N+]3CTBDMS411.2224Semi standard non polar2846.6235
RI01711750codeinone,1TMS,isomer#1JsmolCOC1=CC=C2CC3C4C=CC(O[Si](C)(C)C)=C5OC1=C2C54CC[N+]3CTMS369.1755Semi standard non polar2593.3057
RI01711749codeinone,1TBDMS,isomer#1JsmolCOC1=CC=C2CC3C4C=CC(O[Si](C)(C)C(C)(C)C)=C5OC1=C2C54CC[N+]3CTBDMS411.2224Standard non polar2675.7488
RI01711748codeinone,1TMS,isomer#1JsmolCOC1=CC=C2CC3C4C=CC(O[Si](C)(C)C)=C5OC1=C2C54CC[N+]3CTMS369.1755Standard non polar2420.4016
RI01711747cis-zeatin riboside,5TMS,isomer#1JsmolC/C(=C/CN(C1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS711.3519Standard polar3711.1792
RI01711746cis-zeatin riboside,5TMS,isomer#1JsmolC/C(=C/CN(C1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS711.3519Semi standard non polar3075.002
RI01711745cis-zeatin riboside,5TMS,isomer#1JsmolC/C(=C/CN(C1=NC=NC2=C1N=CN2C1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS711.3519Standard non polar3062.0217
RI01711744cinnamoyltyramine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(CCN(C(=O)C=CC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)C=C1TBDMS495.2989Standard polar3186.0215
RI01711743cinnamoyltyramine,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CCN(C(=O)C=CC2=CC=CC=C2)[Si](C)(C)C)C=C1TMS411.205Standard polar3014.8574
RI01711742cinnamoyltyramine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(CCN(C(=O)C=CC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)C=C1TBDMS495.2989Semi standard non polar3229.3047
RI01711741cinnamoyltyramine,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CCN(C(=O)C=CC2=CC=CC=C2)[Si](C)(C)C)C=C1TMS411.205Semi standard non polar2758.6848
RI01711740cinnamoyltyramine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(CCN(C(=O)C=CC2=CC=CC=C2)[Si](C)(C)C(C)(C)C)C=C1TBDMS495.2989Standard non polar3028.3354
RI01711739cinnamoyltyramine,2TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(CCN(C(=O)C=CC2=CC=CC=C2)[Si](C)(C)C)C=C1TMS411.205Standard non polar2628.3936
RI01711738chlorophyllide b,2TBDMS,isomer#1JsmolC=CC1=C(C)/C2=C/C3=N/C(=C4/C5=N/C(=C\C6=C(CC)/C(=C\[O-])C(=N6)/C=C/1[N-]2)C(C)=C5C(O[Si](C)(C)C(C)(C)C)=C4C(=O)OC)C(CCC(=O)O[Si](C)(C)C(C)(C)C)C3CTBDMS832.4062Standard polar7532.4014
RI01711737chlorophyllide b,2TMS,isomer#1JsmolC=CC1=C(C)/C2=C/C3=N/C(=C4/C5=N/C(=C\C6=C(CC)/C(=C\[O-])C(=N6)/C=C/1[N-]2)C(C)=C5C(O[Si](C)(C)C)=C4C(=O)OC)C(CCC(=O)O[Si](C)(C)C)C3CTMS748.3123Standard polar7488.7188
RI01711736chlorophyllide b,2TBDMS,isomer#1JsmolC=CC1=C(C)/C2=C/C3=N/C(=C4/C5=N/C(=C\C6=C(CC)/C(=C\[O-])C(=N6)/C=C/1[N-]2)C(C)=C5C(O[Si](C)(C)C(C)(C)C)=C4C(=O)OC)C(CCC(=O)O[Si](C)(C)C(C)(C)C)C3CTBDMS832.4062Semi standard non polar5340.5386
RI01711735chlorophyllide b,2TMS,isomer#1JsmolC=CC1=C(C)/C2=C/C3=N/C(=C4/C5=N/C(=C\C6=C(CC)/C(=C\[O-])C(=N6)/C=C/1[N-]2)C(C)=C5C(O[Si](C)(C)C)=C4C(=O)OC)C(CCC(=O)O[Si](C)(C)C)C3CTMS748.3123Semi standard non polar5004.526
RI01711734chlorophyllide b,2TBDMS,isomer#1JsmolC=CC1=C(C)/C2=C/C3=N/C(=C4/C5=N/C(=C\C6=C(CC)/C(=C\[O-])C(=N6)/C=C/1[N-]2)C(C)=C5C(O[Si](C)(C)C(C)(C)C)=C4C(=O)OC)C(CCC(=O)O[Si](C)(C)C(C)(C)C)C3CTBDMS832.4062Standard non polar4967.895
RI01711733chlorophyllide b,2TMS,isomer#1JsmolC=CC1=C(C)/C2=C/C3=N/C(=C4/C5=N/C(=C\C6=C(CC)/C(=C\[O-])C(=N6)/C=C/1[N-]2)C(C)=C5C(O[Si](C)(C)C)=C4C(=O)OC)C(CCC(=O)O[Si](C)(C)C)C3CTMS748.3123Standard non polar4585.469
RI01711732CDP-N-methylethanolamine,3TBDMS,isomer#3JsmolC[N+]CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)C(O)C1O[Si](C)(C)C(C)(C)CTBDMS799.3125Standard polar4551.3374
RI01711731CDP-N-methylethanolamine,3TBDMS,isomer#2JsmolC[N+]CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1OTBDMS799.3125Standard polar4554.639
RI01711730CDP-N-methylethanolamine,3TBDMS,isomer#1JsmolC[N+]CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)CTBDMS799.3125Standard polar4575.787
RI01711729CDP-N-methylethanolamine,2TBDMS,isomer#4JsmolC[N+]CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)C(O)C1OTBDMS685.2261Standard polar4886.9277
RI01711728CDP-N-methylethanolamine,2TBDMS,isomer#3JsmolC[N+]CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O)C1O[Si](C)(C)C(C)(C)CTBDMS685.2261Standard polar4900.818
RI01711727CDP-N-methylethanolamine,2TBDMS,isomer#2JsmolC[N+]CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1OTBDMS685.2261Standard polar4905.7397
Displaying retention index compounds 12426 - 12450 of 1722868 in total