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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20926 - 20950 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703251Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#3JsmolC[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C=C1TMS853.3133Semi standard non polar4649.606
RI01703250Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#2JsmolC[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Semi standard non polar4640.403
RI01703249Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#1JsmolC[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C=C3)=C(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C=C12TMS853.3133Semi standard non polar4623.911
RI01703248Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#81JsmolC[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1OTMS781.2738Semi standard non polar4734.8438
RI01703247Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#69JsmolC[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)C=C1TMS781.2738Semi standard non polar4736.6963
RI01703246Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#59JsmolC[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C=C3)=C(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)C=C12TMS781.2738Semi standard non polar4707.0215
RI01703245Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#45JsmolC[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS781.2738Semi standard non polar4714.463
RI01703244Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#44JsmolC[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS781.2738Semi standard non polar4697.249
RI01703243Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#40JsmolC[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS781.2738Semi standard non polar4723.4604
RI01703242Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#31JsmolC[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS781.2738Semi standard non polar4685.465
RI01703241Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#28JsmolC[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)CO[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]2OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C=C2)[C@@H]1O[Si](C)(C)CTMS781.2738Semi standard non polar4785.4043
RI01703240Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#4JsmolC[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS781.2738Semi standard non polar4732.8623
RI01703239Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],3TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1CO[C@@H](O[C@H]2[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H]1OTMS781.2738Semi standard non polar4765.7173
RI01703238Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],2TMS,isomer#33JsmolC[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C=C2)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)CTMS709.2342Semi standard non polar4872.661
RI01703237Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],2TMS,isomer#12JsmolC[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS709.2342Semi standard non polar4868.334
RI01703236Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],2TMS,isomer#8JsmolC[Si](C)(C)O[C@@H]1CO[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]2OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C=C2)[C@H](O)[C@H]1O[Si](C)(C)CTMS709.2342Semi standard non polar4912.122
RI01703235Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],2TMS,isomer#7JsmolC[Si](C)(C)O[C@@H]1CO[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]2OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C=C2)[C@H](O[Si](C)(C)C)[C@H]1OTMS709.2342Semi standard non polar4901.755
RI01703234Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1CO[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]2OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C=C2)[C@H](O)[C@H]1OTMS637.1947Semi standard non polar5040.66
RI01703233Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],2TBDMS,isomer#33JsmolCC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C=C2)[C@H](O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)CTBDMS793.3281Standard non polar5084.706
RI01703232Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],2TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TBDMS793.3281Standard non polar5076.0967
RI01703231Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#126JsmolC[Si](C)(C)O[C@H]1[C@H](O)CO[C@@H](O[C@H]2[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS853.3133Standard non polar4638.9243
RI01703230Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#119JsmolC[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2OC[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C=C1TMS853.3133Standard non polar4653.5547
RI01703229Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#118JsmolC[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C=C1TMS853.3133Standard non polar4644.366
RI01703228Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#109JsmolC[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C=C3)=C(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C=C12TMS853.3133Standard non polar4616.8955
RI01703227Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#108JsmolC[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C=C3)=C(O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[C@@H]3OC[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C=C12TMS853.3133Standard non polar4605.8975
Displaying retention index compounds 20926 - 20950 of 1722868 in total