RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 9726 - 9750 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01714451solasodine 3-O-beta-D-glucopyranoside,2TMS,isomer#3JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO[Si](C)(C)C)C(O)C(O)C6O[Si](C)(C)C)CCC5(C)C4CCC3(C)C1C2CTMS718.4529Standard non polar4603.0156
RI01714450solasodine 3-O-beta-D-glucopyranoside,2TMS,isomer#2JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C6O)CCC5(C)C4CCC3(C)C1C2CTMS718.4529Standard non polar4632.0786
RI01714449solasodine 3-O-beta-D-glucopyranoside,2TMS,isomer#1JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C6O)CCC5(C)C4CCC3(C)C1C2CTMS718.4529Standard non polar4604.321
RI01714448solasodine 3-O-beta-D-glucopyranoside,1TMS,isomer#4JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO)C(O)C(O)C6O[Si](C)(C)C)CCC5(C)C4CCC3(C)C1C2CTMS646.4134Standard non polar4523.741
RI01714447solasodine 3-O-beta-D-glucopyranoside,1TMS,isomer#3JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO)C(O)C(O[Si](C)(C)C)C6O)CCC5(C)C4CCC3(C)C1C2CTMS646.4134Standard non polar4541.2935
RI01714446solasodine 3-O-beta-D-glucopyranoside,1TMS,isomer#2JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO)C(O[Si](C)(C)C)C(O)C6O)CCC5(C)C4CCC3(C)C1C2CTMS646.4134Standard non polar4521.105
RI01714445solasodine 3-O-beta-D-glucopyranoside,1TMS,isomer#1JsmolCC1CCC2([N+]C1)OC1CC3C4CC=C5CC(OC6OC(CO[Si](C)(C)C)C(O)C(O)C6O)CCC5(C)C4CCC3(C)C1C2CTMS646.4134Standard non polar4560.896
RI01714444sinapoyltyramine,3TBDMS,isomer#1JsmolCOC1=CC(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)=CC(OC)=C1O[Si](C)(C)C(C)(C)CTBDMS685.4014Standard polar3694.6716
RI01714443sinapoyltyramine,3TMS,isomer#1JsmolCOC1=CC(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)=CC(OC)=C1O[Si](C)(C)CTMS559.2606Standard polar3490.7185
RI01714442sinapoyltyramine,3TBDMS,isomer#1JsmolCOC1=CC(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)=CC(OC)=C1O[Si](C)(C)C(C)(C)CTBDMS685.4014Semi standard non polar4041.1853
RI01714441sinapoyltyramine,3TMS,isomer#1JsmolCOC1=CC(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)=CC(OC)=C1O[Si](C)(C)CTMS559.2606Semi standard non polar3327.3884
RI01714440sinapoyltyramine,3TBDMS,isomer#1JsmolCOC1=CC(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2)[Si](C)(C)C(C)(C)C)=CC(OC)=C1O[Si](C)(C)C(C)(C)CTBDMS685.4014Standard non polar3520.03
RI01714439sinapoyltyramine,3TMS,isomer#1JsmolCOC1=CC(C=CC(=O)N(CCC2=CC=C(O[Si](C)(C)C)C=C2)[Si](C)(C)C)=CC(OC)=C1O[Si](C)(C)CTMS559.2606Standard non polar3002.1191
RI01714438secologanin,5TMS,isomer#1JsmolC=C[C@H]1[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)OC=C(C(=O)OC)[C@H]1C=CO[Si](C)(C)CTMS748.3346Standard polar3437.0945
RI01714437secologanin,5TMS,isomer#1JsmolC=C[C@H]1[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)OC=C(C(=O)OC)[C@H]1C=CO[Si](C)(C)CTMS748.3346Semi standard non polar2750.2002
RI01714436secologanin,5TMS,isomer#1JsmolC=C[C@H]1[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)OC=C(C(=O)OC)[C@H]1C=CO[Si](C)(C)CTMS748.3346Standard non polar2910.0757
RI01714435secologanate,6TMS,isomer#1JsmolC=CC1C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC=C(C(=O)O[Si](C)(C)C)C1C=CO[Si](C)(C)CTMS806.3585Standard polar3387.2168
RI01714434secologanate,6TMS,isomer#1JsmolC=CC1C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC=C(C(=O)O[Si](C)(C)C)C1C=CO[Si](C)(C)CTMS806.3585Semi standard non polar2805.0422
RI01714433secologanate,6TMS,isomer#1JsmolC=CC1C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC=C(C(=O)O[Si](C)(C)C)C1C=CO[Si](C)(C)CTMS806.3585Standard non polar3076.3828
RI01714432salutaridinol,2TBDMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C(C)(C)C)=C42)C3=CC1O[Si](C)(C)C(C)(C)CTBDMS557.3357Standard polar3550.9155
RI01714431salutaridinol,1TBDMS,isomer#2JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O)=C42)C3=CC1O[Si](C)(C)C(C)(C)CTBDMS443.2492Standard polar3568.1055
RI01714430salutaridinol,1TBDMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C(C)(C)C)=C42)C3=CC1OTBDMS443.2492Standard polar3606.9836
RI01714429salutaridinol,2TMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C)=C42)C3=CC1O[Si](C)(C)CTMS473.2418Standard polar3308.9822
RI01714428salutaridinol,1TMS,isomer#2JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O)=C42)C3=CC1O[Si](C)(C)CTMS401.2022Standard polar3409.358
RI01714427salutaridinol,1TMS,isomer#1JsmolCOC1=CC23CCN(C)C(CC4=CC=C(OC)C(O[Si](C)(C)C)=C42)C3=CC1OTMS401.2022Standard polar3445.3608
Displaying retention index compounds 9726 - 9750 of 1722868 in total