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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 8051 - 8075 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01716126Cyanidin 3-O-arabinoside,3TMS,isomer#50JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1OTMS665.2264Semi standard non polar4022.3022
RI01716125Cyanidin 3-O-arabinoside,5TMS,isomer#50JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1OTMS809.3055Standard non polar4009.8386
RI01716124Cyanidin 3-O-arabinoside,4TMS,isomer#66JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1OTMS737.2659Standard non polar4062.7346
RI01716123Cyanidin 3-O-arabinoside,4TMS,isomer#54JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1OTMS737.2659Standard non polar4041.8015
RI01716122Cyanidin 3-O-arabinoside,3TMS,isomer#50JsmolC[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)=CC=C1OTMS665.2264Standard non polar4080.1292
RI01716121Cyanidin 3-O-(6''-dioxalyl-glucoside),3TMS,isomer#1JsmolCCCCCCCC/C=C\CCCCCCCCCCCCCC(=O)N([C@@H](CO[Si](C)(C)C)C(CCCCCCCCCCCCCC)O[Si](C)(C)C)[Si](C)(C)CTMS851.7402Standard polar4505.734
RI01716120Cyanidin 3-O-(6''-dioxalyl-glucoside),3TMS,isomer#1JsmolCCCCCCCC/C=C\CCCCCCCCCCCCCC(=O)N([C@@H](CO[Si](C)(C)C)C(CCCCCCCCCCCCCC)O[Si](C)(C)C)[Si](C)(C)CTMS851.7402Semi standard non polar4756.1685
RI01716119Cyanidin 3-O-(6''-dioxalyl-glucoside),3TMS,isomer#1JsmolCCCCCCCC/C=C\CCCCCCCCCCCCCC(=O)N([C@@H](CO[Si](C)(C)C)C(CCCCCCCCCCCCCC)O[Si](C)(C)C)[Si](C)(C)CTMS851.7402Standard non polar4468.9595
RI01716118Asparagine-betaxanthin,5TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)N=C(O)C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O[Si](C)(C)C(C)(C)CTBDMS895.5234Standard polar4057.5776
RI01716117Asparagine-betaxanthin,5TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS895.5234Standard polar4015.9287
RI01716116Asparagine-betaxanthin,5TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O)C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS895.5234Standard polar4008.1484
RI01716115Asparagine-betaxanthin,5TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS895.5234Standard polar4076.9778
RI01716114Asparagine-betaxanthin,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=N)C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O[Si](C)(C)C(C)(C)CTBDMS895.5234Standard polar3939.8074
RI01716113Asparagine-betaxanthin,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS895.5234Standard polar4227.694
RI01716112Asparagine-betaxanthin,6TMS,isomer#1JsmolC[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS757.3282Standard polar3527.9504
RI01716111Asparagine-betaxanthin,5TMS,isomer#6JsmolC[Si](C)(C)N=C(O)C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C1)C(=O)O[Si](C)(C)CTMS685.2886Standard polar3933.8591
RI01716110Asparagine-betaxanthin,5TMS,isomer#5JsmolC[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS685.2886Standard polar3889.3955
RI01716109Asparagine-betaxanthin,5TMS,isomer#4JsmolC[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O)C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS685.2886Standard polar3893.2532
RI01716108Asparagine-betaxanthin,5TMS,isomer#3JsmolC[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C1)C(=O)O)O[Si](C)(C)CTMS685.2886Standard polar3966.119
RI01716107Asparagine-betaxanthin,5TMS,isomer#2JsmolC[Si](C)(C)OC(=N)C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[C@H](C(=O)O[Si](C)(C)C)C1)C(=O)O[Si](C)(C)CTMS685.2886Standard polar3834.8733
RI01716106Asparagine-betaxanthin,5TMS,isomer#1JsmolC[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C)N[C@H](C(=O)O[Si](C)(C)C)C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS685.2886Standard polar4186.9414
RI01716105Asparagine-betaxanthin,5TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)N=C(O)C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O[Si](C)(C)C(C)(C)CTBDMS895.5234Semi standard non polar3907.0183
RI01716104Asparagine-betaxanthin,5TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS895.5234Semi standard non polar3966.0535
RI01716103Asparagine-betaxanthin,5TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O)C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS895.5234Semi standard non polar3938.9993
RI01716102Asparagine-betaxanthin,5TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N=C(C[C@H](/N=C/C=C1/C=C(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[C@H](C(=O)O[Si](C)(C)C(C)(C)C)C1)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS895.5234Semi standard non polar3924.0068
Displaying retention index compounds 8051 - 8075 of 1722868 in total