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Displaying retention index compounds 20026 - 20050 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
2-Hydroxyadenine,2TMS,isomer#4JsmolC[Si](C)(C)NC1=NC(O)=NC2=C1N([Si](C)(C)C)C=N2TMS295.1285Standard non polar2061.1304
2-Hydroxyadenine,3TMS,isomer#1JsmolC[Si](C)(C)OC1=NC(N([Si](C)(C)C)[Si](C)(C)C)=C2[NH]C=NC2=N1TMS367.168Standard non polar2137.1152
2-Hydroxyadenine,3TMS,isomer#2JsmolC[Si](C)(C)NC1=NC(O[Si](C)(C)C)=NC2=C1N([Si](C)(C)C)C=N2TMS367.168Standard non polar2006.2377
2-Hydroxyadenine,3TMS,isomer#3JsmolC[Si](C)(C)N(C1=NC(O)=NC2=C1N([Si](C)(C)C)C=N2)[Si](C)(C)CTMS367.168Standard non polar2196.0764
2-Hydroxyadenine,4TMS,isomer#1JsmolC[Si](C)(C)OC1=NC(N([Si](C)(C)C)[Si](C)(C)C)=C2C(=N1)N=CN2[Si](C)(C)CTMS439.2075Standard non polar2127.876
2-Hydroxyadenine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=NC(O[Si](C)(C)C(C)(C)C)=NC2=C1[NH]C=N2TBDMS379.2224Standard non polar2439.3298
2-Hydroxyadenine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=NC(N)=C2C(=N1)N=CN2[Si](C)(C)C(C)(C)CTBDMS379.2224Standard non polar2377.2876
2-Hydroxyadenine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C1=NC(O)=NC2=C1[NH]C=N2)[Si](C)(C)C(C)(C)CTBDMS379.2224Standard non polar2568.3643
2-Hydroxyadenine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC1=NC(O)=NC2=C1N([Si](C)(C)C(C)(C)C)C=N2TBDMS379.2224Standard non polar2458.6697
2-Hydroxyadenine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2[NH]C=NC2=N1TBDMS493.3088Standard non polar2755.0977
2-Hydroxyadenine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC(O[Si](C)(C)C(C)(C)C)=NC2=C1N([Si](C)(C)C(C)(C)C)C=N2TBDMS493.3088Standard non polar2629.1975
2-Hydroxyadenine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C1=NC(O)=NC2=C1N([Si](C)(C)C(C)(C)C)C=N2)[Si](C)(C)C(C)(C)CTBDMS493.3088Standard non polar2783.7073
2-Hydroxyadenine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C2C(=N1)N=CN2[Si](C)(C)C(C)(C)CTBDMS607.3953Standard non polar2925.5854
2-HydroxyadenineJsmolNC1=NC(O)=NC2=C1NC=N2Underivatized151.0494Standard non polar2091.217
2-HydroxyadenineJsmolNC1=NC(O)=NC2=C1NC=N2Underivatized151.0494Semi standard non polar1918.531
2-Hydroxyadenine,2TMS,isomer#1JsmolC[Si](C)(C)NC1=NC(O[Si](C)(C)C)=NC2=C1[NH]C=N2TMS295.1285Semi standard non polar2053.7388
2-Hydroxyadenine,2TMS,isomer#2JsmolC[Si](C)(C)OC1=NC(N)=C2C(=N1)N=CN2[Si](C)(C)CTMS295.1285Semi standard non polar2096.9785
2-Hydroxyadenine,2TMS,isomer#3JsmolC[Si](C)(C)N(C1=NC(O)=NC2=C1[NH]C=N2)[Si](C)(C)CTMS295.1285Semi standard non polar2119.4258
2-Hydroxyadenine,2TMS,isomer#4JsmolC[Si](C)(C)NC1=NC(O)=NC2=C1N([Si](C)(C)C)C=N2TMS295.1285Semi standard non polar2183.128
2-Hydroxyadenine,3TMS,isomer#1JsmolC[Si](C)(C)OC1=NC(N([Si](C)(C)C)[Si](C)(C)C)=C2[NH]C=NC2=N1TMS367.168Semi standard non polar2029.2043
2-Hydroxyadenine,3TMS,isomer#2JsmolC[Si](C)(C)NC1=NC(O[Si](C)(C)C)=NC2=C1N([Si](C)(C)C)C=N2TMS367.168Semi standard non polar2111.1558
2-Hydroxyadenine,3TMS,isomer#3JsmolC[Si](C)(C)N(C1=NC(O)=NC2=C1N([Si](C)(C)C)C=N2)[Si](C)(C)CTMS367.168Semi standard non polar2128.332
2-Hydroxyadenine,4TMS,isomer#1JsmolC[Si](C)(C)OC1=NC(N([Si](C)(C)C)[Si](C)(C)C)=C2C(=N1)N=CN2[Si](C)(C)CTMS439.2075Semi standard non polar2106.8188
2-Hydroxyadenine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=NC(O[Si](C)(C)C(C)(C)C)=NC2=C1[NH]C=N2TBDMS379.2224Semi standard non polar2482.0732
2-Hydroxyadenine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=NC(N)=C2C(=N1)N=CN2[Si](C)(C)C(C)(C)CTBDMS379.2224Semi standard non polar2497.1104
Displaying retention index compounds 20026 - 20050 of 1722868 in total