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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 7526 - 7550 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01716651gamma-Aminobutyric acid-betaxanthin,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCC/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)C1TBDMS752.4467Standard non polar3073.2056
RI01716650gamma-Aminobutyric acid-betaxanthin,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCC/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)C1TMS584.2589Standard non polar2499.6514
RI01716649Valine-betaxanthin,4TBDMS,isomer#1JsmolCC(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)CTBDMS766.4624Standard polar3368.8037
RI01716648Valine-betaxanthin,4TMS,isomer#1JsmolCC(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)CTMS598.2746Standard polar3147.8926
RI01716647Valine-betaxanthin,4TBDMS,isomer#1JsmolCC(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)CTBDMS766.4624Semi standard non polar3421.571
RI01716646Valine-betaxanthin,4TMS,isomer#1JsmolCC(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)CTMS598.2746Semi standard non polar2595.02
RI01716645Valine-betaxanthin,4TBDMS,isomer#1JsmolCC(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)CTBDMS766.4624Standard non polar2996.0303
RI01716644Valine-betaxanthin,4TMS,isomer#1JsmolCC(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)CTMS598.2746Standard non polar2427.1096
RI01716643Thujan-3-ol,3TBDMS,isomer#1JsmolCC(=N[C@H](CSC(=NCCCC[S@](C)=O)S[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS682.318Standard polar3675.1177
RI01716642Thujan-3-ol,3TMS,isomer#1JsmolCC(=N[C@H](CSC(=NCCCC[S@](C)=O)S[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS556.1771Standard polar3623.6572
RI01716641Thujan-3-ol,3TBDMS,isomer#1JsmolCC(=N[C@H](CSC(=NCCCC[S@](C)=O)S[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS682.318Semi standard non polar3385.9001
RI01716640Thujan-3-ol,3TMS,isomer#1JsmolCC(=N[C@H](CSC(=NCCCC[S@](C)=O)S[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS556.1771Semi standard non polar2800.1973
RI01716639Thujan-3-ol,3TBDMS,isomer#1JsmolCC(=N[C@H](CSC(=NCCCC[S@](C)=O)S[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS682.318Standard non polar3888.297
RI01716638Thujan-3-ol,3TMS,isomer#1JsmolCC(=N[C@H](CSC(=NCCCC[S@](C)=O)S[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS556.1771Standard non polar3263.6296
RI01716637Sitostanol-beta,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[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)CTBDMS868.5125Standard polar3492.4944
RI01716636Sitostanol-beta,5TMS,isomer#1JsmolC[Si](C)(C)OC[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)CTMS658.2777Standard polar3209.6045
RI01716635Sitostanol-beta,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[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)CTBDMS868.5125Semi standard non polar3706.735
RI01716634Sitostanol-beta,5TMS,isomer#1JsmolC[Si](C)(C)OC[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)CTMS658.2777Semi standard non polar2706.225
RI01716633Sitostanol-beta,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC[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)CTBDMS868.5125Standard non polar3229.4763
RI01716632Sitostanol-beta,5TMS,isomer#1JsmolC[Si](C)(C)OC[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)CTMS658.2777Standard non polar2540.027
RI01716631Sinensal-alpha,5TMS,isomer#1JsmolCOC1=CC=C([C@H]2CC(=O)C3=C(O[C@@H]4O[C@@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C1TMS808.3346Standard polar4076.6223
RI01716630Sinensal-alpha,5TMS,isomer#1JsmolCOC1=CC=C([C@H]2CC(=O)C3=C(O[C@@H]4O[C@@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C1TMS808.3346Semi standard non polar3700.5918
RI01716629Sinensal-alpha,5TMS,isomer#1JsmolCOC1=CC=C([C@H]2CC(=O)C3=C(O[C@@H]4O[C@@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C1TMS808.3346Standard non polar3665.8083
RI01716628Quercetin 3-O-sophoroside,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H]1CC(=CC=[N+]2CCC[C@H]2C(=O)O[Si](C)(C)C(C)(C)C)C=C(C(=O)[O-])N1[Si](C)(C)C(C)(C)CTBDMS650.3603Standard polar3555.7812
RI01716627Quercetin 3-O-sophoroside,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H]1CC(=CC=[N+]2CCC[C@H]2C(=O)O[Si](C)(C)C)C=C(C(=O)[O-])N1[Si](C)(C)CTMS524.2194Standard polar3436.7488
Displaying retention index compounds 7526 - 7550 of 1722868 in total