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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11551 - 11575 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01712626glutathioselenol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS610.1347Standard polar3632.332
RI01712625glutathioselenol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])NC(=O)CCC([N+])C(=O)[O-]TBDMS496.0482Standard polar3957.3948
RI01712624glutathioselenol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CS[Se])C(=O)NCC(=O)[O-]TBDMS496.0482Standard polar3962.7324
RI01712623glutathioselenol,2TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS526.0408Standard polar3619.162
RI01712622glutathioselenol,1TMS,isomer#2JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])NC(=O)CCC([N+])C(=O)[O-]TMS454.0013Standard polar3970.9
RI01712621glutathioselenol,1TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CS[Se])C(=O)NCC(=O)[O-]TMS454.0013Standard polar4025.4744
RI01712620glutathioselenol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS610.1347Semi standard non polar3274.6592
RI01712619glutathioselenol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])NC(=O)CCC([N+])C(=O)[O-]TBDMS496.0482Semi standard non polar3069.761
RI01712618glutathioselenol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CS[Se])C(=O)NCC(=O)[O-]TBDMS496.0482Semi standard non polar3055.486
RI01712617glutathioselenol,2TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS526.0408Semi standard non polar2752.741
RI01712616glutathioselenol,1TMS,isomer#2JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])NC(=O)CCC([N+])C(=O)[O-]TMS454.0013Semi standard non polar2783.1758
RI01712615glutathioselenol,1TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CS[Se])C(=O)NCC(=O)[O-]TMS454.0013Semi standard non polar2743.7974
RI01712614glutathioselenol,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS610.1347Standard non polar3184.1628
RI01712613glutathioselenol,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])NC(=O)CCC([N+])C(=O)[O-]TBDMS496.0482Standard non polar2937.477
RI01712612glutathioselenol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CS[Se])C(=O)NCC(=O)[O-]TBDMS496.0482Standard non polar2965.1477
RI01712611glutathioselenol,2TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS526.0408Standard non polar2785.286
RI01712610glutathioselenol,1TMS,isomer#2JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CS[Se])NC(=O)CCC([N+])C(=O)[O-]TMS454.0013Standard non polar2726.618
RI01712609glutathioselenol,1TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CS[Se])C(=O)NCC(=O)[O-]TMS454.0013Standard non polar2743.215
RI01712608gibberellin A8-catabolite,5TMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C)CCC2C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS722.3342Standard polar3264.4556
RI01712607gibberellin A8-catabolite,5TMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C)CCC2C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS722.3342Semi standard non polar2832.37
RI01712606gibberellin A8-catabolite,5TMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C)CCC2C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS722.3342Standard non polar2974.459
RI01712605gibberellin A51-catabolite,3TBDMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C(C)(C)C)C1C3C(=O)O[Si](C)(C)C(C)(C)CTBDMS672.4062Standard polar3418.2026
RI01712604gibberellin A51-catabolite,3TMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS546.2653Standard polar3166.6943
RI01712603gibberellin A51-catabolite,3TBDMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C(C)(C)C)C1C3C(=O)O[Si](C)(C)C(C)(C)CTBDMS672.4062Semi standard non polar3325.7402
RI01712602gibberellin A51-catabolite,3TMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS546.2653Semi standard non polar2659.8237
Displaying retention index compounds 11551 - 11575 of 1722868 in total