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Displaying retention index compounds 3576 - 3600 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
beta-Alanine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS431.3071Semi standard non polar2065.5325
beta-Alanine,2TMS,isomer#1JsmolC[Si](C)(C)NCCC(=O)O[Si](C)(C)CTMS233.1267Standard polar1331.6678
beta-Alanine,2TMS,isomer#2JsmolC[Si](C)(C)N(CCC(=O)O)[Si](C)(C)CTMS233.1267Standard polar1576.1492
beta-Alanine,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCN([Si](C)(C)C)[Si](C)(C)CTMS305.1663Standard polar1367.9668
beta-Alanine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NCCC(=O)O[Si](C)(C)C(C)(C)CTBDMS317.2206Standard polar1611.8962
beta-Alanine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CCC(=O)O)[Si](C)(C)C(C)(C)CTBDMS317.2206Standard polar1734.9436
beta-Alanine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS431.3071Standard polar1763.9453
Cyclic AMP,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H]2OP(=O)(O)OC[C@H]2O[C@H]1N1C=NC2=C(N)N=CN=C21TMS401.092Semi standard non polar2963.188
Cyclic AMP,1TMS,isomer#2JsmolC[Si](C)(C)OP1(=O)OC[C@H]2O[C@@H](N3C=NC4=C(N)N=CN=C43)[C@H](O)[C@@H]2O1TMS401.092Semi standard non polar2965.4758
Cyclic AMP,1TMS,isomer#3JsmolC[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O)O[C@H]2[C@H]1OTMS401.092Semi standard non polar3027.01
Cyclic AMP,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H]2OP(=O)(O)OC[C@H]2O[C@H]1N1C=NC2=C(N)N=CN=C21TBDMS443.139Semi standard non polar3186.6978
Cyclic AMP,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OP1(=O)OC[C@H]2O[C@@H](N3C=NC4=C(N)N=CN=C43)[C@H](O)[C@@H]2O1TBDMS443.139Semi standard non polar3169.4023
Cyclic AMP,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O)O[C@H]2[C@H]1OTBDMS443.139Semi standard non polar3204.1528
Cyclic AMPJsmol[H][C@@]12COP(O)(=O)O[C@@]1([H])[C@@H](O)[C@@H](O2)N1C=NC2=C1N=CN=C2NUnderivatized329.0525Standard polar3561.4336
Cyclic AMP,2TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H]2OP(=O)(O[Si](C)(C)C)OC[C@H]2O[C@H]1N1C=NC2=C(N)N=CN=C21TMS473.1316Standard non polar2813.1702
Cyclic AMP,2TMS,isomer#2JsmolC[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O)O[C@H]2[C@H]1O[Si](C)(C)CTMS473.1316Standard non polar2862.0146
Cyclic AMP,2TMS,isomer#3JsmolC[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O[Si](C)(C)C)O[C@H]2[C@H]1OTMS473.1316Standard non polar2867.4827
Cyclic AMP,2TMS,isomer#4JsmolC[Si](C)(C)N(C1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O)O[C@H]2[C@H]1O)[Si](C)(C)CTMS473.1316Standard non polar2936.3198
Cyclic AMP,3TMS,isomer#1JsmolC[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O[Si](C)(C)C)O[C@H]2[C@H]1O[Si](C)(C)CTMS545.1711Standard non polar2901.928
Cyclic AMP,3TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@@H]2OP(=O)(O)OC[C@H]2O[C@H]1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21TMS545.1711Standard non polar2955.1736
Cyclic AMP,3TMS,isomer#3JsmolC[Si](C)(C)OP1(=O)OC[C@H]2O[C@@H](N3C=NC4=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C43)[C@H](O)[C@@H]2O1TMS545.1711Standard non polar2959.265
Cyclic AMP,4TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H]2OP(=O)(O[Si](C)(C)C)OC[C@H]2O[C@H]1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21TMS617.2106Standard non polar2968.4238
Cyclic AMP,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H]2OP(=O)(O[Si](C)(C)C(C)(C)C)OC[C@H]2O[C@H]1N1C=NC2=C(N)N=CN=C21TBDMS557.2255Standard non polar3207.0186
Cyclic AMP,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O)O[C@H]2[C@H]1O[Si](C)(C)C(C)(C)CTBDMS557.2255Standard non polar3278.956
Cyclic AMP,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]2COP(=O)(O[Si](C)(C)C(C)(C)C)O[C@H]2[C@H]1OTBDMS557.2255Standard non polar3242.0637
Displaying retention index compounds 3576 - 3600 of 1722868 in total