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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 8276 - 8300 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01715901tricoumaroyl spermidine,4TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)NCCCN(CCCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)C=C1TMS871.4263Standard polar6226.9463
RI01715900tricoumaroyl spermidine,4TMS,isomer#5JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCCCN(C(=O)C=CC2=CC=C(O)C=C2)[Si](C)(C)C)CCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1TMS871.4263Semi standard non polar5968.2847
RI01715899tricoumaroyl spermidine,4TMS,isomer#4JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)CCCN(C(=O)C=CC2=CC=C(O)C=C2)[Si](C)(C)C)C=C1TMS871.4263Semi standard non polar5968.3296
RI01715898tricoumaroyl spermidine,4TMS,isomer#3JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCCCN(CCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O)C=C2)[Si](C)(C)C)C=C1TMS871.4263Semi standard non polar5968.3843
RI01715897tricoumaroyl spermidine,4TMS,isomer#2JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)NCCCCN(CCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)C=C1TMS871.4263Semi standard non polar6029.1826
RI01715896tricoumaroyl spermidine,4TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)NCCCN(CCCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)C=C1TMS871.4263Semi standard non polar5981.821
RI01715895tricoumaroyl spermidine,4TMS,isomer#5JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCCCN(C(=O)C=CC2=CC=C(O)C=C2)[Si](C)(C)C)CCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C=C1TMS871.4263Standard non polar4864.0615
RI01715894tricoumaroyl spermidine,4TMS,isomer#4JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)CCCN(C(=O)C=CC2=CC=C(O)C=C2)[Si](C)(C)C)C=C1TMS871.4263Standard non polar4864.0615
RI01715893tricoumaroyl spermidine,4TMS,isomer#3JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)N(CCCCN(CCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O)C=C2)[Si](C)(C)C)C=C1TMS871.4263Standard non polar4865.5063
RI01715892tricoumaroyl spermidine,4TMS,isomer#2JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)NCCCCN(CCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)C=C1TMS871.4263Standard non polar4972.895
RI01715891tricoumaroyl spermidine,4TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C=CC(=O)NCCCN(CCCCN(C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)C(=O)C=CC2=CC=C(O[Si](C)(C)C)C=C2)C=C1TMS871.4263Standard non polar4966.9653
RI01715890trans-zeatin riboside triphosphate,4TMS,isomer#5JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)COTMS876.1895Standard polar5480.358
RI01715889trans-zeatin riboside triphosphate,4TMS,isomer#4JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard polar5501.981
RI01715888trans-zeatin riboside triphosphate,4TMS,isomer#3JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard polar5493.7935
RI01715887trans-zeatin riboside triphosphate,4TMS,isomer#2JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard polar5536.4546
RI01715886trans-zeatin riboside triphosphate,4TMS,isomer#1JsmolCC(=CCNC1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard polar5617.482
RI01715885trans-zeatin riboside triphosphate,4TMS,isomer#5JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)COTMS876.1895Semi standard non polar4006.1138
RI01715884trans-zeatin riboside triphosphate,4TMS,isomer#4JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Semi standard non polar4009.024
RI01715883trans-zeatin riboside triphosphate,4TMS,isomer#3JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Semi standard non polar4008.7883
RI01715882trans-zeatin riboside triphosphate,4TMS,isomer#2JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Semi standard non polar3994.3752
RI01715881trans-zeatin riboside triphosphate,4TMS,isomer#1JsmolCC(=CCNC1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Semi standard non polar4044.9697
RI01715880trans-zeatin riboside triphosphate,4TMS,isomer#5JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)COTMS876.1895Standard non polar3994.6733
RI01715879trans-zeatin riboside triphosphate,4TMS,isomer#4JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard non polar4038.3958
RI01715878trans-zeatin riboside triphosphate,4TMS,isomer#3JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard non polar4031.4897
RI01715877trans-zeatin riboside triphosphate,4TMS,isomer#2JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard non polar3927.654
Displaying retention index compounds 8276 - 8300 of 1722868 in total