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 1721576 - 1721600 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00001293Dihydrobiopterin,2TMS,isomer#7JsmolC[C@H](O)[C@H](O[Si](C)(C)C)C1=NC2=C([NH]C(N)=NC2=O)N([Si](C)(C)C)C1TMS383.1809Semi standard non polar2236.678
RI00001292Dihydrobiopterin,2TMS,isomer#6JsmolC[C@H](O)[C@H](O[Si](C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C)C(N)=NC2=OTMS383.1809Semi standard non polar2315.7498
RI00001291Dihydrobiopterin,2TMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C)C1=NC2=C(NC1)[NH]C(N[Si](C)(C)C)=NC2=OTMS383.1809Semi standard non polar2337.7537
RI00001290Dihydrobiopterin,2TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@H](O)C1=NC2=C([NH]C(N)=NC2=O)N([Si](C)(C)C)C1TMS383.1809Semi standard non polar2253.621
RI00001289Dihydrobiopterin,2TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@H](O)C1=NC2=C(NC1)N([Si](C)(C)C)C(N)=NC2=OTMS383.1809Semi standard non polar2316.5835
RI00001288Dihydrobiopterin,2TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@H](O)C1=NC2=C(NC1)[NH]C(N[Si](C)(C)C)=NC2=OTMS383.1809Semi standard non polar2348.6375
RI00001287Dihydrobiopterin,2TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C1=NC2=C(NC1)[NH]C(N)=NC2=OTMS383.1809Semi standard non polar2330.2654
RI00001286Dihydrobiopterin,1TMS,isomer#5JsmolC[C@H](O)[C@H](O)C1=NC2=C(NC1)N([Si](C)(C)C)C(N)=NC2=OTMS311.1414Semi standard non polar2381.1333
RI00001285Dihydrobiopterin,1TMS,isomer#4JsmolC[C@H](O)[C@H](O)C1=NC2=C([NH]C(N)=NC2=O)N([Si](C)(C)C)C1TMS311.1414Semi standard non polar2307.2705
RI00001284Dihydrobiopterin,1TMS,isomer#3JsmolC[C@H](O)[C@H](O)C1=NC2=C(NC1)[NH]C(N[Si](C)(C)C)=NC2=OTMS311.1414Semi standard non polar2453.6082
RI00001283Dihydrobiopterin,1TMS,isomer#2JsmolC[C@H](O)[C@H](O[Si](C)(C)C)C1=NC2=C(NC1)[NH]C(N)=NC2=OTMS311.1414Semi standard non polar2373.3103
RI00001282Dihydrobiopterin,1TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O)C1=NC2=C(NC1)[NH]C(N)=NC2=OTMS311.1414Semi standard non polar2388.314
RI00001281Aldosterone,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12C=OTBDMS816.5396Standard polar3924.411
RI00001280Aldosterone,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12C=OTBDMS816.5396Standard polar3884.6243
RI00001279Aldosterone,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]2(C=O)[C@@H](C(=CO)O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS702.4531Standard polar4060.2656
RI00001278Aldosterone,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]2(C=O)C(=C(CO)O[Si](C)(C)C(C)(C)C)CC[C@@H]12TBDMS702.4531Standard polar4036.4585
RI00001277Aldosterone,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12C=OTBDMS702.4531Standard polar4059.837
RI00001276Aldosterone,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O)C[C@]12C=OTBDMS702.4531Standard polar4028.6235
RI00001275Aldosterone,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12C=OTBDMS702.4531Standard polar3982.4534
RI00001274Aldosterone,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12C=OTBDMS702.4531Standard polar3996.5994
RI00001273Aldosterone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@]12C=OTBDMS702.4531Standard polar3978.6282
RI00001272Aldosterone,4TMS,isomer#2JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(C=O)[C@@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS648.3518Standard polar3719.561
RI00001271Aldosterone,4TMS,isomer#1JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(C=O)C(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS648.3518Standard polar3662.7542
RI00001270Aldosterone,3TMS,isomer#7JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(C=O)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS576.3123Standard polar3839.4907
RI00001269Aldosterone,3TMS,isomer#6JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(C=O)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS576.3123Standard polar3809.2542
Displaying retention index compounds 1721576 - 1721600 of 1722868 in total