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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20576 - 20600 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703601(-)-jasmonoyl-L-isoleucine,1TBDMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C(C)(C)C)=CCC1CC(=O)NC(C(=O)[O-])C(C)CCTBDMS436.2889Semi standard non polar2661.6438
RI01703600(-)-jasmonoyl-L-isoleucine,1TBDMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C(C)(C)C)CCC1CC(=O)NC(C(=O)[O-])C(C)CCTBDMS436.2889Semi standard non polar2686.2754
RI01703599(-)-jasmonoyl-L-isoleucine,2TMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C)=CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)CTMS466.2814Semi standard non polar2415.022
RI01703598(-)-jasmonoyl-L-isoleucine,2TMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C)CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)CTMS466.2814Semi standard non polar2435.7847
RI01703597(-)-jasmonoyl-L-isoleucine,1TMS,isomer#3JsmolCCC=CCC1C(=O)CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)CTMS394.2419Semi standard non polar2382.593
RI01703596(-)-jasmonoyl-L-isoleucine,1TMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C)=CCC1CC(=O)NC(C(=O)[O-])C(C)CCTMS394.2419Semi standard non polar2420.9924
RI01703595(-)-jasmonoyl-L-isoleucine,1TMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C)CCC1CC(=O)NC(C(=O)[O-])C(C)CCTMS394.2419Semi standard non polar2455.512
RI01703594(-)-jasmonoyl-L-isoleucine,2TBDMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C(C)(C)C)=CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)C(C)(C)CTBDMS550.3753Standard non polar2764.0986
RI01703593(-)-jasmonoyl-L-isoleucine,2TBDMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C(C)(C)C)CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)C(C)(C)CTBDMS550.3753Standard non polar2840.9084
RI01703592(-)-jasmonoyl-L-isoleucine,1TBDMS,isomer#3JsmolCCC=CCC1C(=O)CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)C(C)(C)CTBDMS436.2889Standard non polar2633.014
RI01703591(-)-jasmonoyl-L-isoleucine,1TBDMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C(C)(C)C)=CCC1CC(=O)NC(C(=O)[O-])C(C)CCTBDMS436.2889Standard non polar2594.5674
RI01703590(-)-jasmonoyl-L-isoleucine,1TBDMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C(C)(C)C)CCC1CC(=O)NC(C(=O)[O-])C(C)CCTBDMS436.2889Standard non polar2599.6292
RI01703589(-)-jasmonoyl-L-isoleucine,2TMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C)=CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)CTMS466.2814Standard non polar2482.5735
RI01703588(-)-jasmonoyl-L-isoleucine,2TMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C)CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)CTMS466.2814Standard non polar2476.881
RI01703587(-)-jasmonoyl-L-isoleucine,1TMS,isomer#3JsmolCCC=CCC1C(=O)CCC1CC(=O)N(C(C(=O)[O-])C(C)CC)[Si](C)(C)CTMS394.2419Standard non polar2404.5588
RI01703586(-)-jasmonoyl-L-isoleucine,1TMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C)=CCC1CC(=O)NC(C(=O)[O-])C(C)CCTMS394.2419Standard non polar2467.9111
RI01703585(-)-jasmonoyl-L-isoleucine,1TMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C)CCC1CC(=O)NC(C(=O)[O-])C(C)CCTMS394.2419Standard non polar2421.7256
RI01703584(+)-cis-abscisic aldehyde,2TBDMS,isomer#1JsmolCC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)[C@]1(/C=C/C(C)=C\C=O)O[Si](C)(C)C(C)(C)CTBDMS476.3142Standard polar2528.334
RI01703583(+)-cis-abscisic aldehyde,2TMS,isomer#1JsmolCC1=CC(O[Si](C)(C)C)=CC(C)(C)[C@]1(/C=C/C(C)=C\C=O)O[Si](C)(C)CTMS392.2203Standard polar2332.5515
RI01703582(+)-cis-abscisic aldehyde,2TBDMS,isomer#1JsmolCC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)[C@]1(/C=C/C(C)=C\C=O)O[Si](C)(C)C(C)(C)CTBDMS476.3142Semi standard non polar2682.4373
RI01703581(+)-cis-abscisic aldehyde,2TMS,isomer#1JsmolCC1=CC(O[Si](C)(C)C)=CC(C)(C)[C@]1(/C=C/C(C)=C\C=O)O[Si](C)(C)CTMS392.2203Semi standard non polar2219.8389
RI01703580(+)-cis-abscisic aldehyde,2TBDMS,isomer#1JsmolCC1=CC(O[Si](C)(C)C(C)(C)C)=CC(C)(C)[C@]1(/C=C/C(C)=C\C=O)O[Si](C)(C)C(C)(C)CTBDMS476.3142Standard non polar2509.116
RI01703579(+)-cis-abscisic aldehyde,2TMS,isomer#1JsmolCC1=CC(O[Si](C)(C)C)=CC(C)(C)[C@]1(/C=C/C(C)=C\C=O)O[Si](C)(C)CTMS392.2203Standard non polar2055.6313
RI01703578(+)-7-iso-jasmonate,1TBDMS,isomer#2JsmolCCC=CCC1C(O[Si](C)(C)C(C)(C)C)=CCC1CC(=O)[O-]TBDMS323.2048Standard polar2229.317
RI01703577(+)-7-iso-jasmonate,1TBDMS,isomer#1JsmolCCC=CCC1=C(O[Si](C)(C)C(C)(C)C)CCC1CC(=O)[O-]TBDMS323.2048Standard polar2225.2036
Displaying retention index compounds 20576 - 20600 of 1722868 in total