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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20951 - 20975 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703226Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#96JsmolC[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=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=C1TMS853.3133Standard non polar4581.7896
RI01703225Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#88JsmolC[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[Si](C)(C)C)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4629.63
RI01703224Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#84JsmolC[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O[Si](C)(C)C)=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=C1TMS853.3133Standard non polar4593.062
RI01703223Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#83JsmolC[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[Si](C)(C)C)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4627.142
RI01703222Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#82JsmolC[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[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4615.8013
RI01703221Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#67JsmolC[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[Si](C)(C)C)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4613.853
RI01703220Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#66JsmolC[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[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4601.6616
RI01703219Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#62JsmolC[Si](C)(C)OC1=CC(O[Si](C)(C)C)=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=C1TMS853.3133Standard non polar4556.4604
RI01703218Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#21JsmolC[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)CO[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[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)CTMS853.3133Standard non polar4645.943
RI01703217Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#17JsmolC[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[Si](C)(C)C)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4652.2725
RI01703216Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#16JsmolC[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[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4618.4917
RI01703215Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#12JsmolC[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[Si](C)(C)C)[C@H](O)[C@H]3O)C(C3=CC=C(O)C=C3)=[O+]C2=C1TMS853.3133Standard non polar4611.3228
RI01703214Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#6JsmolC[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]1O[Si](C)(C)CTMS853.3133Standard non polar4628.2427
RI01703213Pelargonidin 3-O-[b-D-Xylopyranosyl-(1->2)-a-D-glucopyranoside],4TMS,isomer#5JsmolC[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[Si](C)(C)C)[C@H]1OTMS853.3133Standard non polar4662.098
RI01703212Pelargonidin 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=C1TMS853.3133Standard non polar4652.4736
RI01703211Pelargonidin 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=C1TMS853.3133Standard non polar4624.6064
RI01703210Pelargonidin 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=C12TMS853.3133Standard non polar4615.57
RI01703209Pelargonidin 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]1OTMS781.2738Standard non polar4655.5293
RI01703208Pelargonidin 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=C1TMS781.2738Standard non polar4628.6084
RI01703207Pelargonidin 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=C12TMS781.2738Standard non polar4586.8203
RI01703206Pelargonidin 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=C1TMS781.2738Standard non polar4663.397
RI01703205Pelargonidin 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=C1TMS781.2738Standard non polar4660.4976
RI01703204Pelargonidin 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=C1TMS781.2738Standard non polar4603.233
RI01703203Pelargonidin 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=C1TMS781.2738Standard non polar4605.997
RI01703202Pelargonidin 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)CTMS781.2738Standard non polar4638.288
Displaying retention index compounds 20951 - 20975 of 1722868 in total