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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 12401 - 12425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01711776D-fructose 6-phosphate,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS828.4476Semi standard non polar3227.8455
RI01711775D-fructose 6-phosphate,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS828.4476Semi standard non polar3264.7856
RI01711774D-fructose 6-phosphate,5TMS,isomer#2JsmolC[Si](C)(C)OC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS618.2128Semi standard non polar2211.161
RI01711773D-fructose 6-phosphate,5TMS,isomer#1JsmolC[Si](C)(C)OCC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS618.2128Semi standard non polar2204.038
RI01711772D-fructose 6-phosphate,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS828.4476Standard non polar3105.1846
RI01711771D-fructose 6-phosphate,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS828.4476Standard non polar3072.1565
RI01711770D-fructose 6-phosphate,5TMS,isomer#2JsmolC[Si](C)(C)OC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS618.2128Standard non polar2240.4744
RI01711769D-fructose 6-phosphate,5TMS,isomer#1JsmolC[Si](C)(C)OCC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS618.2128Standard non polar2202.71
RI01711768cyclo-dopa 5-O-glucoside,7TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(C=C2O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS861.3827Standard polar3331.5806
RI01711767cyclo-dopa 5-O-glucoside,7TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(C=C2O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS861.3827Semi standard non polar3188.2173
RI01711766cyclo-dopa 5-O-glucoside,7TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(C=C2O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C3)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS861.3827Standard non polar3123.2356
RI01711765cyanidin-3-O-beta-D-glucoside,4TMS,isomer#35JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS736.2587Standard polar4689.5815
RI01711764cyanidin-3-O-beta-D-glucoside,3TMS,isomer#34JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS664.2191Standard polar5074.224
RI01711763cyanidin-3-O-beta-D-glucoside,4TMS,isomer#35JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS736.2587Semi standard non polar3955.6462
RI01711762cyanidin-3-O-beta-D-glucoside,3TMS,isomer#34JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS664.2191Semi standard non polar4045.3442
RI01711761cyanidin-3-O-beta-D-glucoside,4TMS,isomer#35JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS736.2587Standard non polar3903.0583
RI01711760cyanidin-3-O-beta-D-glucoside,3TMS,isomer#34JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS664.2191Standard non polar3968.8794
RI01711759cyanidin 3-(p-coumaroyl)-glucoside,4TMS,isomer#20JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS882.2954Standard polar6126.5264
RI01711758cyanidin 3-(p-coumaroyl)-glucoside,3TMS,isomer#32JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS810.2559Standard polar6616.0713
RI01711757cyanidin 3-(p-coumaroyl)-glucoside,4TMS,isomer#20JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS882.2954Semi standard non polar5328.3647
RI01711756cyanidin 3-(p-coumaroyl)-glucoside,3TMS,isomer#32JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS810.2559Semi standard non polar5429.103
RI01711755cyanidin 3-(p-coumaroyl)-glucoside,4TMS,isomer#20JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS882.2954Standard non polar5074.0312
RI01711754cyanidin 3-(p-coumaroyl)-glucoside,3TMS,isomer#32JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC([O-])=C3C=C2OC2OC(COC(=O)C=CC3=CC=C(O)C=C3)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC=C1OTMS810.2559Standard non polar5178.027
RI01711753codeinone,1TBDMS,isomer#1JsmolCOC1=CC=C2CC3C4C=CC(O[Si](C)(C)C(C)(C)C)=C5OC1=C2C54CC[N+]3CTBDMS411.2224Standard polar3192.4714
RI01711752codeinone,1TMS,isomer#1JsmolCOC1=CC=C2CC3C4C=CC(O[Si](C)(C)C)=C5OC1=C2C54CC[N+]3CTMS369.1755Standard polar3041.2632
Displaying retention index compounds 12401 - 12425 of 1722868 in total