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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 66401 - 66425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00066401trans-3-Hydroxycotinine glucuronide,2TBDMS,isomer#2JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)CC1C1=CC=CN=C1TBDMS596.2949Semi standard non polar3390.653
RI00066402trans-3-Hydroxycotinine glucuronide,2TBDMS,isomer#3JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS596.2949Semi standard non polar3389.006
RI00066403trans-3-Hydroxycotinine glucuronide,2TBDMS,isomer#4JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)CC1C1=CC=CN=C1TBDMS596.2949Semi standard non polar3394.8328
RI00066404trans-3-Hydroxycotinine glucuronide,2TBDMS,isomer#5JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS596.2949Semi standard non polar3375.653
RI00066405trans-3-Hydroxycotinine glucuronide,2TBDMS,isomer#6JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS596.2949Semi standard non polar3393.048
RI00066406trans-3-Hydroxycotinine glucuronide,3TBDMS,isomer#1JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)CC1C1=CC=CN=C1TBDMS710.3814Semi standard non polar3575.2021
RI00066407trans-3-Hydroxycotinine glucuronide,3TBDMS,isomer#2JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS710.3814Semi standard non polar3597.0576
RI00066408trans-3-Hydroxycotinine glucuronide,3TBDMS,isomer#3JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS710.3814Semi standard non polar3554.8015
RI00066409trans-3-Hydroxycotinine glucuronide,3TBDMS,isomer#4JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS710.3814Semi standard non polar3563.2747
RI00066410trans-3-Hydroxycotinine glucuronide,4TBDMS,isomer#1JsmolCN1C(=O)[C@H](O[C@@H]2O[C@H](C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)CC1C1=CC=CN=C1TBDMS824.4679Semi standard non polar3746.611
RI00066411trans-3-Hydroxycotinine glucuronideJsmol[H][C@@]1(O[C@@H]2CC(N(C)C2=O)C2=CC=CN=C2)O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=OUnderivatized368.122Standard polar4249.395
RI00066412trans-3-Hydroxycotinine glucuronideJsmol[H][C@@]1(O[C@@H]2CC(N(C)C2=O)C2=CC=CN=C2)O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=OUnderivatized368.122Standard non polar2975.9941
RI00066413trans-3-Hydroxycotinine glucuronideJsmol[H][C@@]1(O[C@@H]2CC(N(C)C2=O)C2=CC=CN=C2)O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=OUnderivatized368.122Semi standard non polar3374.6418
RI00066414Acetyl-CoAJsmolCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2NUnderivatized809.1258Standard polar5645.5703
RI00066415Acetyl-CoAJsmolCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2NUnderivatized809.1258Standard non polar4169.079
RI00066416Acetyl-CoAJsmolCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2NUnderivatized809.1258Semi standard non polar6250.714
RI00066417Allantoic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(NC(N)=O)NC(N)=OTMS248.0941Semi standard non polar2010.7809
RI00066418Allantoic acid,1TMS,isomer#2JsmolC[Si](C)(C)NC(=O)NC(NC(N)=O)C(=O)OTMS248.0941Semi standard non polar2111.063
RI00066419Allantoic acid,1TMS,isomer#3JsmolC[Si](C)(C)N(C(N)=O)C(NC(N)=O)C(=O)OTMS248.0941Semi standard non polar2053.764
RI00066420Allantoic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C(NC(N)=O)NC(N)=OTBDMS290.141Semi standard non polar2287.1018
RI00066421Allantoic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(=O)NC(NC(N)=O)C(=O)OTBDMS290.141Semi standard non polar2355.6228
RI00066422Allantoic acid,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(N)=O)C(NC(N)=O)C(=O)OTBDMS290.141Semi standard non polar2302.725
RI00066423Allantoic acidJsmolNC(=O)NC(NC(N)=O)C(O)=OUnderivatized176.0546Standard polar2939.2764
RI00066424Allantoic acid,2TMS,isomer#1JsmolC[Si](C)(C)NC(=O)NC(NC(N)=O)C(=O)O[Si](C)(C)CTMS320.1336Standard non polar1925.2189
RI00066425Allantoic acid,2TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C(NC(N)=O)N(C(N)=O)[Si](C)(C)CTMS320.1336Standard non polar1934.0197
Displaying retention index compounds 66401 - 66425 of 1722868 in total