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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 21826 - 21850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01702351Kapporphin,4TMS,isomer#9JsmolC[Si](C)(C)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)NC(CO[Si](C)(C)C)C(=O)NC(CC1=CC=CC=C1)C(=O)N(CC(=O)NCC(=O)O)[Si](C)(C)CTMS817.3754Standard non polar4090.4802
RI01702350Kapporphin,4TMS,isomer#8JsmolC[Si](C)(C)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)NC(CO[Si](C)(C)C)C(=O)N(C(CC1=CC=CC=C1)C(=O)NCC(=O)NCC(=O)O)[Si](C)(C)CTMS817.3754Standard non polar4065.9102
RI01702349Kapporphin,4TMS,isomer#7JsmolC[Si](C)(C)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)N(C(CO[Si](C)(C)C)C(=O)NC(CC1=CC=CC=C1)C(=O)NCC(=O)NCC(=O)O)[Si](C)(C)CTMS817.3754Standard non polar4089.8728
RI01702348Kapporphin,4TMS,isomer#6JsmolC[Si](C)(C)OCC(NC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NC(CC1=CC=CC=C1)C(=O)NCC(=O)NCC(=O)OTMS817.3754Standard non polar4149.4263
RI01702347Kapporphin,4TMS,isomer#5JsmolC[Si](C)(C)OCC(NC(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)NC(CC1=CC=CC=C1)C(=O)NCC(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)CTMS817.3754Standard non polar4038.9768
RI01702346Kapporphin,4TMS,isomer#4JsmolC[Si](C)(C)OCC(NC(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)NC(CC1=CC=CC=C1)C(=O)N(CC(=O)NCC(=O)O[Si](C)(C)C)[Si](C)(C)CTMS817.3754Standard non polar4015.9893
RI01702345Kapporphin,4TMS,isomer#3JsmolC[Si](C)(C)OCC(NC(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)N(C(CC1=CC=CC=C1)C(=O)NCC(=O)NCC(=O)O[Si](C)(C)C)[Si](C)(C)CTMS817.3754Standard non polar3990.0833
RI01702344Kapporphin,4TMS,isomer#2JsmolC[Si](C)(C)OCC(C(=O)NC(CC1=CC=CC=C1)C(=O)NCC(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)CTMS817.3754Standard non polar4001.3064
RI01702343Kapporphin,4TMS,isomer#1JsmolC[Si](C)(C)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)NC(CO[Si](C)(C)C)C(=O)NC(CC1=CC=CC=C1)C(=O)NCC(=O)NCC(=O)O[Si](C)(C)CTMS817.3754Standard non polar4050.1167
RI017023427-Epi-12-hydroxyjasmonic acid,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC/C=C\C[C@@H]1C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]1CC(=O)O[Si](C)(C)C(C)(C)CTBDMS568.3799Standard polar2537.3542
RI017023417-Epi-12-hydroxyjasmonic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC/C=C\CC1=C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1CC(=O)O[Si](C)(C)C(C)(C)CTBDMS568.3799Standard polar2538.192
RI017023407-Epi-12-hydroxyjasmonic acid,3TMS,isomer#2JsmolC[Si](C)(C)OCC/C=C\C[C@@H]1C(O[Si](C)(C)C)=CC[C@@H]1CC(=O)O[Si](C)(C)CTMS442.2391Standard polar2262.1296
RI017023397-Epi-12-hydroxyjasmonic acid,3TMS,isomer#1JsmolC[Si](C)(C)OCC/C=C\CC1=C(O[Si](C)(C)C)CC[C@@H]1CC(=O)O[Si](C)(C)CTMS442.2391Standard polar2213.9197
RI017023387-Epi-12-hydroxyjasmonic acid,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC/C=C\C[C@@H]1C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]1CC(=O)O[Si](C)(C)C(C)(C)CTBDMS568.3799Semi standard non polar2797.648
RI017023377-Epi-12-hydroxyjasmonic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC/C=C\CC1=C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1CC(=O)O[Si](C)(C)C(C)(C)CTBDMS568.3799Semi standard non polar2832.8005
RI017023367-Epi-12-hydroxyjasmonic acid,3TMS,isomer#2JsmolC[Si](C)(C)OCC/C=C\C[C@@H]1C(O[Si](C)(C)C)=CC[C@@H]1CC(=O)O[Si](C)(C)CTMS442.2391Semi standard non polar2104.1248
RI017023357-Epi-12-hydroxyjasmonic acid,3TMS,isomer#1JsmolC[Si](C)(C)OCC/C=C\CC1=C(O[Si](C)(C)C)CC[C@@H]1CC(=O)O[Si](C)(C)CTMS442.2391Semi standard non polar2116.731
RI017023347-Epi-12-hydroxyjasmonic acid,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC/C=C\C[C@@H]1C(O[Si](C)(C)C(C)(C)C)=CC[C@@H]1CC(=O)O[Si](C)(C)C(C)(C)CTBDMS568.3799Standard non polar2590.8318
RI017023337-Epi-12-hydroxyjasmonic acid,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC/C=C\CC1=C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1CC(=O)O[Si](C)(C)C(C)(C)CTBDMS568.3799Standard non polar2738.967
RI017023327-Epi-12-hydroxyjasmonic acid,3TMS,isomer#2JsmolC[Si](C)(C)OCC/C=C\C[C@@H]1C(O[Si](C)(C)C)=CC[C@@H]1CC(=O)O[Si](C)(C)CTMS442.2391Standard non polar2190.429
RI017023317-Epi-12-hydroxyjasmonic acid,3TMS,isomer#1JsmolC[Si](C)(C)OCC/C=C\CC1=C(O[Si](C)(C)C)CC[C@@H]1CC(=O)O[Si](C)(C)CTMS442.2391Standard non polar2191.5776
RI017023306-Hydroxykaempferol 3,6,7-triglucoside,1TMS,isomer#14JsmolC[Si](C)(C)OC1C(CO)OC(OC2=CC3=C(C(O)=C2OC2OC(CO)C(O)C(O)C2O)C(=O)C(OC2OC(CO)C(O)C(O)C2O)=C(C2=CC=C(O)C=C2)O3)C(O)C1OTMS860.2406Standard polar12833.011
RI017023296-Hydroxykaempferol 3,6,7-triglucoside,1TMS,isomer#13JsmolC[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC3=C(C(O)=C2OC2OC(CO)C(O)C(O)C2O)C(=O)C(OC2OC(CO)C(O)C(O)C2O)=C(C2=CC=C(O)C=C2)O3)C1OTMS860.2406Standard polar12804.464
RI017023286-Hydroxykaempferol 3,6,7-triglucoside,1TMS,isomer#2JsmolC[Si](C)(C)OC1=C(OC2OC(CO)C(O)C(O)C2O)C(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OC(CO)C(O)C(O)C1O)=C(C1=CC=C(O)C=C1)O2TMS860.2406Standard polar13030.133
RI017023276-Hydroxykaempferol 3,6,7-triglucoside,1TMS,isomer#1JsmolC[Si](C)(C)OCC1OC(OC2=CC3=C(C(O)=C2OC2OC(CO)C(O)C(O)C2O)C(=O)C(OC2OC(CO)C(O)C(O)C2O)=C(C2=CC=C(O)C=C2)O3)C(O)C(O)C1OTMS860.2406Standard polar13017.508
Displaying retention index compounds 21826 - 21850 of 1722868 in total