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Displaying retention index compounds 21901 - 21925 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
5-Hydroxylysine,2TMS,isomer#8JsmolC[Si](C)(C)N([C@@H](CC[C@@H](O)CN)C(=O)O)[Si](C)(C)CTMS306.1795Semi standard non polar1931.5426
5-Hydroxylysine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H](CN)CC[C@H](N)C(=O)OTBDMS276.1869Semi standard non polar1960.7053
5-Hydroxylysine,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC[C@@H](O)CNTBDMS276.1869Semi standard non polar1896.9518
5-Hydroxylysine,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC[C@H](O)CC[C@H](N)C(=O)OTBDMS276.1869Semi standard non polar2044.7617
5-Hydroxylysine,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N[C@@H](CC[C@@H](O)CN)C(=O)OTBDMS276.1869Semi standard non polar2022.7578
5-Hydroxylysine,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC[C@H](CN)O[Si](C)(C)C(C)(C)CTBDMS390.2734Semi standard non polar2154.8875
5-Hydroxylysine,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC[C@@H](CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS390.2734Semi standard non polar2296.1348
5-Hydroxylysine,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N[C@@H](CC[C@H](CN)O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS390.2734Semi standard non polar2279.2568
5-Hydroxylysine,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N[C@@H](CC[C@@H](O)CN)C(=O)O[Si](C)(C)C(C)(C)CTBDMS390.2734Semi standard non polar2178.2688
5-Hydroxylysine,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)NC[C@H](O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)CTBDMS390.2734Semi standard non polar2225.5679
5-Hydroxylysine,2TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)NC[C@H](O)CC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)OTBDMS390.2734Semi standard non polar2359.388
5-Hydroxylysine,2TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)N(C[C@H](O)CC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)CTBDMS390.2734Semi standard non polar2407.859
5-Hydroxylysine,2TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)N([C@@H](CC[C@@H](O)CN)C(=O)O)[Si](C)(C)C(C)(C)CTBDMS390.2734Semi standard non polar2362.2915
5-HydroxylysineJsmolNC[C@H](O)CC[C@H](N)C(O)=OUnderivatized162.1004Standard polar2370.9365
5-Hydroxylysine,3TMS,isomer#1JsmolC[Si](C)(C)N[C@@H](CC[C@H](CN)O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS378.219Standard non polar1882.5443
5-Hydroxylysine,3TMS,isomer#2JsmolC[Si](C)(C)NC[C@@H](CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS378.219Standard non polar1918.2627
5-Hydroxylysine,3TMS,isomer#3JsmolC[Si](C)(C)NC[C@@H](CC[C@H](N[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS378.219Standard non polar1945.0651
5-Hydroxylysine,3TMS,isomer#4JsmolC[Si](C)(C)O[C@H](CC[C@H](N)C(=O)O)CN([Si](C)(C)C)[Si](C)(C)CTMS378.219Standard non polar1975.4744
5-Hydroxylysine,3TMS,isomer#5JsmolC[Si](C)(C)O[C@@H](CN)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS378.219Standard non polar1932.8322
5-Hydroxylysine,3TMS,isomer#6JsmolC[Si](C)(C)NC[C@H](O)CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS378.219Standard non polar1907.4624
5-Hydroxylysine,3TMS,isomer#7JsmolC[Si](C)(C)OC(=O)[C@H](CC[C@@H](O)CN)N([Si](C)(C)C)[Si](C)(C)CTMS378.219Standard non polar1921.7827
5-Hydroxylysine,3TMS,isomer#8JsmolC[Si](C)(C)OC(=O)[C@@H](N)CC[C@@H](O)CN([Si](C)(C)C)[Si](C)(C)CTMS378.219Standard non polar2002.3954
5-Hydroxylysine,3TMS,isomer#9JsmolC[Si](C)(C)N[C@@H](CC[C@@H](O)CN([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS378.219Standard non polar1981.9996
5-Hydroxylysine,3TMS,isomer#10JsmolC[Si](C)(C)NC[C@H](O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS378.219Standard non polar1934.44
5-Hydroxylysine,4TMS,isomer#1JsmolC[Si](C)(C)NC[C@@H](CC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS450.2585Standard non polar2012.8368
Displaying retention index compounds 21901 - 21925 of 1722868 in total