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 18076 - 18100 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000180763-Amino-2-piperidone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1CCCNC1=O)[Si](C)(C)C(C)(C)CTBDMS342.2523Semi standard non polar1955.6313
RI000180773-Amino-2-piperidone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1CCCN([Si](C)(C)C(C)(C)C)C1=OTBDMS342.2523Semi standard non polar1876.2784
RI000180783-Amino-2-piperidone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1CCCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1=OTBDMS456.3387Semi standard non polar2218.063
RI000180793-Amino-2-piperidone,1TMS,isomer#1JsmolC[Si](C)(C)NC1CCCNC1=OTMS186.1188Standard polar2328.8801
RI000180803-Amino-2-piperidone,1TMS,isomer#2JsmolC[Si](C)(C)N1CCCC(N)C1=OTMS186.1188Standard polar2224.521
RI000180813-Amino-2-piperidone,2TMS,isomer#1JsmolC[Si](C)(C)N(C1CCCNC1=O)[Si](C)(C)CTMS258.1584Standard polar2146.4546
RI000180823-Amino-2-piperidone,2TMS,isomer#2JsmolC[Si](C)(C)NC1CCCN([Si](C)(C)C)C1=OTMS258.1584Standard polar1983.192
RI000180833-Amino-2-piperidone,3TMS,isomer#1JsmolC[Si](C)(C)N1CCCC(N([Si](C)(C)C)[Si](C)(C)C)C1=OTMS330.1979Standard polar1777.7205
RI000180843-Amino-2-piperidone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1CCCNC1=OTBDMS228.1658Standard polar2489.7424
RI000180853-Amino-2-piperidone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1CCCC(N)C1=OTBDMS228.1658Standard polar2438.3066
RI000180863-Amino-2-piperidone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C1CCCNC1=O)[Si](C)(C)C(C)(C)CTBDMS342.2523Standard polar2201.8462
RI000180873-Amino-2-piperidone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC1CCCN([Si](C)(C)C(C)(C)C)C1=OTBDMS342.2523Standard polar2130.8477
RI000180883-Amino-2-piperidone,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1CCCC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1=OTBDMS456.3387Standard polar2109.4468
RI000180893alpha,16alpha-Dihydroxyandrostenone,1TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@H](O)CC[C@@]43C)[C@@H]1C[C@@H](O[Si](C)(C)C)C2=OTMS376.2434Semi standard non polar2802.305
RI000180903alpha,16alpha-Dihydroxyandrostenone,1TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1C[C@@H](O)C2=OTMS376.2434Semi standard non polar2769.5457
RI000180913alpha,16alpha-Dihydroxyandrostenone,1TMS,isomer#3JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@H](O)CC[C@@]43C)[C@@H]1CC(O)=C2O[Si](C)(C)CTMS376.2434Semi standard non polar2759.1052
RI000180923alpha,16alpha-Dihydroxyandrostenone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1C[C@@H](O[Si](C)(C)C)C2=OTMS448.2829Semi standard non polar2828.383
RI000180933alpha,16alpha-Dihydroxyandrostenone,2TMS,isomer#2JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@H](O)CC[C@@]43C)[C@@H]1CC(O[Si](C)(C)C)=C2O[Si](C)(C)CTMS448.2829Semi standard non polar2833.7637
RI000180943alpha,16alpha-Dihydroxyandrostenone,2TMS,isomer#3JsmolC[C@]12CC[C@H]3[C@@H](CC=C4C[C@H](O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC(O)=C2O[Si](C)(C)CTMS448.2829Semi standard non polar2765.2012
RI000180953alpha,16alpha-Dihydroxyandrostenone,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1C[C@H]2[C@@H]3CC=C4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]2(C)C1=OTBDMS418.2903Semi standard non polar3073.1123
RI000180963alpha,16alpha-Dihydroxyandrostenone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4C[C@@H](O)C(=O)[C@@]4(C)CC[C@@H]32)C1TBDMS418.2903Semi standard non polar3042.5715
RI000180973alpha,16alpha-Dihydroxyandrostenone,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C(O)C[C@H]2[C@@H]3CC=C4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS418.2903Semi standard non polar3042.9072
RI000180983alpha,16alpha-Dihydroxyandrostenone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4C[C@@H](O[Si](C)(C)C(C)(C)C)C(=O)[C@@]4(C)CC[C@@H]32)C1TBDMS532.3768Semi standard non polar3359.602
RI000180993alpha,16alpha-Dihydroxyandrostenone,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)[C@@]2(C)CC[C@H]3[C@@H](CC=C4C[C@H](O)CC[C@@]43C)[C@@H]2C1TBDMS532.3768Semi standard non polar3384.4893
RI000181003alpha,16alpha-Dihydroxyandrostenone,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC1=C(O)C[C@H]2[C@@H]3CC=C4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS532.3768Semi standard non polar3308.7676
Displaying retention index compounds 18076 - 18100 of 1722868 in total