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Displaying retention index compounds 7401 - 7425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Guanine,2TMS,isomer#4JsmolC[Si](C)(C)N1C=NC2=C1C(=O)N=C(N)N2[Si](C)(C)CTMS295.1285Standard polar2809.0298
Guanine,3TMS,isomer#1JsmolC[Si](C)(C)N(C1=NC(=O)C2=C(N=CN2[Si](C)(C)C)[NH]1)[Si](C)(C)CTMS367.168Standard polar2519.7974
Guanine,3TMS,isomer#2JsmolC[Si](C)(C)N(C1=NC(=O)C2=C(N=C[NH]2)N1[Si](C)(C)C)[Si](C)(C)CTMS367.168Standard polar2570.2922
Guanine,3TMS,isomer#3JsmolC[Si](C)(C)NC1=NC(=O)C2=C(N=CN2[Si](C)(C)C)N1[Si](C)(C)CTMS367.168Standard polar2592.3582
Guanine,4TMS,isomer#1JsmolC[Si](C)(C)N(C1=NC(=O)C2=C(N=CN2[Si](C)(C)C)N1[Si](C)(C)C)[Si](C)(C)CTMS439.2075Standard polar2331.6638
Guanine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N=C[NH]2)[NH]1TBDMS265.1359Standard polar3275.908
Guanine,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C(N)=NC(=O)C2=C1N=C[NH]2TBDMS265.1359Standard polar3127.5178
Guanine,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C=NC2=C1C(=O)N=C(N)[NH]2TBDMS265.1359Standard polar3081.3186
Guanine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N=C[NH]2)[NH]1)[Si](C)(C)C(C)(C)CTBDMS379.2224Standard polar2963.8962
Guanine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N=CN2[Si](C)(C)C(C)(C)C)[NH]1TBDMS379.2224Standard polar2903.6062
Guanine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N=C[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS379.2224Standard polar2869.578
Guanine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N1C=NC2=C1C(=O)N=C(N)N2[Si](C)(C)C(C)(C)CTBDMS379.2224Standard polar2861.3909
Guanine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N=CN2[Si](C)(C)C(C)(C)C)[NH]1)[Si](C)(C)C(C)(C)CTBDMS493.3088Standard polar2701.042
Guanine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N=C[NH]2)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS493.3088Standard polar2706.5215
Guanine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC(=O)C2=C(N=CN2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS493.3088Standard polar2746.5452
Guanine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1=NC(=O)C2=C(N=CN2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS607.3953Standard polar2673.1455
Guanosine,1TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O)[C@@H]1OTMS355.1312Semi standard non polar2775.093
Guanosine,1TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@@H]1OTMS355.1312Semi standard non polar2791.9856
Guanosine,1TMS,isomer#3JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=C(N)[NH]C2=OTMS355.1312Semi standard non polar2783.8938
Guanosine,1TMS,isomer#4JsmolC[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C(=O)[NH]1TMS355.1312Semi standard non polar2817.5698
Guanosine,1TMS,isomer#5JsmolC[Si](C)(C)N1C(N)=NC2=C(N=CN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C1=OTMS355.1312Semi standard non polar2845.888
Guanosine,2TMS,isomer#1JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O[Si](C)(C)C)[C@@H]1OTMS427.1707Semi standard non polar2713.5276
Guanosine,2TMS,isomer#2JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)[NH]C3=O)[C@H](O)[C@@H]1O[Si](C)(C)CTMS427.1707Semi standard non polar2714.7117
Guanosine,2TMS,isomer#3JsmolC[Si](C)(C)NC1=NC2=C(N=CN2[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H]2O)C(=O)[NH]1TMS427.1707Semi standard non polar2715.962
Guanosine,2TMS,isomer#4JsmolC[Si](C)(C)OC[C@H]1O[C@@H](N2C=NC3=C2N=C(N)N([Si](C)(C)C)C3=O)[C@H](O)[C@@H]1OTMS427.1707Semi standard non polar2792.7659
Displaying retention index compounds 7401 - 7425 of 1722868 in total