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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11576 - 11600 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01712601gibberellin 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 non polar3385.3809
RI01712600gibberellin 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 non polar2738.8752
RI01712599gibberellin A34-catabolite,4TBDMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(C)(C(=O)O[Si](C)(C)C(C)(C)C)C1C3C(=O)O[Si](C)(C)C(C)(C)CTBDMS802.4875Standard polar3511.812
RI01712598gibberellin A34-catabolite,4TMS,isomer#1JsmolC=C1CC23CC1CCC2C1=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)CTMS634.2997Standard polar3208.403
RI01712597gibberellin A34-catabolite,4TBDMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(C)(C(=O)O[Si](C)(C)C(C)(C)C)C1C3C(=O)O[Si](C)(C)C(C)(C)CTBDMS802.4875Semi standard non polar3652.1113
RI01712596gibberellin A34-catabolite,4TMS,isomer#1JsmolC=C1CC23CC1CCC2C1=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)CTMS634.2997Semi standard non polar2838.4077
RI01712595gibberellin A34-catabolite,4TBDMS,isomer#1JsmolC=C1CC23CC1CCC2C1=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C(C)(C(=O)O[Si](C)(C)C(C)(C)C)C1C3C(=O)O[Si](C)(C)C(C)(C)CTBDMS802.4875Standard non polar3640.6118
RI01712594gibberellin A34-catabolite,4TMS,isomer#1JsmolC=C1CC23CC1CCC2C1=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)CTMS634.2997Standard non polar2876.1929
RI01712593gibberellin A29-catabolite,4TBDMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C(C)(C)C)CCC2C1=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)CTBDMS802.4875Standard polar3484.2922
RI01712592gibberellin A29-catabolite,4TMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C)CCC2C1=CC(O[Si](C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS634.2997Standard polar3217.0745
RI01712591gibberellin A29-catabolite,4TBDMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C(C)(C)C)CCC2C1=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)CTBDMS802.4875Semi standard non polar3558.3325
RI01712590gibberellin A29-catabolite,4TMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C)CCC2C1=CC(O[Si](C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS634.2997Semi standard non polar2699.997
RI01712589gibberellin A29-catabolite,4TBDMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C(C)(C)C)CCC2C1=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)CTBDMS802.4875Standard non polar3652.569
RI01712588gibberellin A29-catabolite,4TMS,isomer#1JsmolC=C1CC23CC1(O[Si](C)(C)C)CCC2C1=CC(O[Si](C)(C)C)=CC(C)(C(=O)O[Si](C)(C)C)C1C3C(=O)O[Si](C)(C)CTMS634.2997Standard non polar2870.9053
RI01712587gibberellin A12-aldehyde,1TBDMS,isomer#1JsmolC=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C)CCC[C@@](C)(C(=O)[O-])[C@H]1C3=CO[Si](C)(C)C(C)(C)CTBDMS429.283Standard polar3034.1963
RI01712586gibberellin A12-aldehyde,1TMS,isomer#1JsmolC=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C)CCC[C@@](C)(C(=O)[O-])[C@H]1C3=CO[Si](C)(C)CTMS387.2361Standard polar2875.4392
RI01712585gibberellin A12-aldehyde,1TBDMS,isomer#1JsmolC=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C)CCC[C@@](C)(C(=O)[O-])[C@H]1C3=CO[Si](C)(C)C(C)(C)CTBDMS429.283Semi standard non polar2657.1519
RI01712584gibberellin A12-aldehyde,1TMS,isomer#1JsmolC=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C)CCC[C@@](C)(C(=O)[O-])[C@H]1C3=CO[Si](C)(C)CTMS387.2361Semi standard non polar2419.2263
RI01712583gibberellin A12-aldehyde,1TBDMS,isomer#1JsmolC=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C)CCC[C@@](C)(C(=O)[O-])[C@H]1C3=CO[Si](C)(C)C(C)(C)CTBDMS429.283Standard non polar2587.0947
RI01712582gibberellin A12-aldehyde,1TMS,isomer#1JsmolC=C1C[C@]23C[C@H]1CC[C@H]2[C@]1(C)CCC[C@@](C)(C(=O)[O-])[C@H]1C3=CO[Si](C)(C)CTMS387.2361Standard non polar2362.3518
RI01712581furaneol (keto form),1TBDMS,isomer#1JsmolCC1=C([O-])C(O[Si](C)(C)C(C)(C)C)=C(C)O1TBDMS241.1265Standard polar1537.1088
RI01712580furaneol (keto form),1TMS,isomer#1JsmolCC1=C([O-])C(O[Si](C)(C)C)=C(C)O1TMS199.0796Standard polar1342.7988
RI01712579furaneol (keto form),1TBDMS,isomer#1JsmolCC1=C([O-])C(O[Si](C)(C)C(C)(C)C)=C(C)O1TBDMS241.1265Semi standard non polar1483.0841
RI01712578furaneol (keto form),1TMS,isomer#1JsmolCC1=C([O-])C(O[Si](C)(C)C)=C(C)O1TMS199.0796Semi standard non polar1224.4231
RI01712577furaneol (keto form),1TBDMS,isomer#1JsmolCC1=C([O-])C(O[Si](C)(C)C(C)(C)C)=C(C)O1TBDMS241.1265Standard non polar1399.1346
Displaying retention index compounds 11576 - 11600 of 1722868 in total