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Displaying retention index compounds 10901 - 10925 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
L-histidinol-phosphate,5TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(OC[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)CTMS581.2542Standard non polar2458.9043
L-histidinol-phosphate,4TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)CTMS509.2146Standard non polar2423.4946
L-histidinol-phosphate,4TMS,isomer#2JsmolC[Si](C)(C)N[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1TMS509.2146Standard non polar2354.0496
L-histidinol-phosphate,4TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(OC[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)CTMS509.2146Standard non polar2386.1243
L-histidinol-phosphate,3TMS,isomer#5JsmolC[Si](C)(C)N([C@H](COP(=O)(O)O)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)CTMS437.1751Standard non polar2441.5344
L-histidinol-phosphate,3TMS,isomer#4JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1TMS437.1751Standard non polar2294.6501
L-histidinol-phosphate,3TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)CTMS437.1751Standard non polar2340.1726
L-histidinol-phosphate,3TMS,isomer#2JsmolC[Si](C)(C)OP(=O)(OC[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)O[Si](C)(C)CTMS437.1751Standard non polar2281.4695
L-histidinol-phosphate,3TMS,isomer#1JsmolC[Si](C)(C)N[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=C[NH]C=N1TMS437.1751Standard non polar2317.308
L-histidinol-phosphate,2TMS,isomer#5JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O)CC1=CN([Si](C)(C)C)C=N1TMS365.1356Standard non polar2286.0618
L-histidinol-phosphate,2TMS,isomer#4JsmolC[Si](C)(C)N([C@H](COP(=O)(O)O)CC1=C[NH]C=N1)[Si](C)(C)CTMS365.1356Standard non polar2323.4917
L-histidinol-phosphate,2TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@@H](N)CC1=CN([Si](C)(C)C)C=N1TMS365.1356Standard non polar2237.0464
L-histidinol-phosphate,2TMS,isomer#2JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O[Si](C)(C)C)CC1=C[NH]C=N1TMS365.1356Standard non polar2265.461
L-histidinol-phosphate,2TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(OC[C@@H](N)CC1=C[NH]C=N1)O[Si](C)(C)CTMS365.1356Standard non polar2181.2395
L-histidinol-phosphate,1TMS,isomer#3JsmolC[Si](C)(C)N1C=NC(C[C@H](N)COP(=O)(O)O)=C1TMS293.0961Standard non polar2166.059
L-histidinol-phosphate,1TMS,isomer#2JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O)CC1=C[NH]C=N1TMS293.0961Standard non polar2179.6372
L-histidinol-phosphate,1TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(O)OC[C@@H](N)CC1=C[NH]C=N1TMS293.0961Standard non polar2097.5894
L-glyceraldehyde 3-phosphate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS396.1564Standard polar2021.8871
L-glyceraldehyde 3-phosphate,2TMS,isomer#1JsmolC[Si](C)(C)OC=C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS312.0625Standard polar1852.5852
L-glyceraldehyde 3-phosphate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS396.1564Semi standard non polar2005.0988
L-glyceraldehyde 3-phosphate,2TMS,isomer#1JsmolC[Si](C)(C)OC=C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS312.0625Semi standard non polar1591.8872
L-glyceraldehyde 3-phosphate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=C(COP(=O)([O-])[O-])O[Si](C)(C)C(C)(C)CTBDMS396.1564Standard non polar1975.3246
L-glyceraldehyde 3-phosphate,2TMS,isomer#1JsmolC[Si](C)(C)OC=C(COP(=O)([O-])[O-])O[Si](C)(C)CTMS312.0625Standard non polar1557.1696
L-arginino-succinate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CCCC([N+])C(=O)[O-])C(=[N+])N(C(CC(=O)[O-])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS512.2492Standard polar3427.3494
L-arginino-succinate,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C(=[N+])NCCCC([N+])C(=O)[O-])C(CC(=O)[O-])C(=O)[O-]TBDMS398.1627Standard polar3595.8477
Displaying retention index compounds 10901 - 10925 of 1722868 in total