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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 12551 - 12575 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01711626CDP-N-dimethylethanolamine,3TBDMS,isomer#2JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1OTBDMS814.336Standard non polar4039.7024
RI01711625CDP-N-dimethylethanolamine,3TBDMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)CTBDMS814.336Standard non polar3908.616
RI01711624CDP-N-dimethylethanolamine,2TBDMS,isomer#4JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)C(O)C1OTBDMS700.2495Standard non polar3908.5388
RI01711623CDP-N-dimethylethanolamine,2TBDMS,isomer#3JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O)C1O[Si](C)(C)C(C)(C)CTBDMS700.2495Standard non polar3782.7842
RI01711622CDP-N-dimethylethanolamine,2TBDMS,isomer#2JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1OTBDMS700.2495Standard non polar3801.5857
RI01711621CDP-N-dimethylethanolamine,2TBDMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)CTBDMS700.2495Standard non polar3676.5107
RI01711620CDP-N-dimethylethanolamine,1TBDMS,isomer#3JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C(C)(C)C)=NC2=O)C(O)C1OTBDMS586.1631Standard non polar3623.7107
RI01711619CDP-N-dimethylethanolamine,1TBDMS,isomer#2JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N)=NC2=O)C(O)C1O[Si](C)(C)C(C)(C)CTBDMS586.1631Standard non polar3516.9487
RI01711618CDP-N-dimethylethanolamine,1TBDMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N)=NC2=O)C(O[Si](C)(C)C(C)(C)C)C1OTBDMS586.1631Standard non polar3523.282
RI01711617CDP-N-dimethylethanolamine,4TMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)CTMS760.2347Standard non polar3496.7957
RI01711616CDP-N-dimethylethanolamine,3TMS,isomer#3JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)C(O)C1O[Si](C)(C)CTMS688.1952Standard non polar3536.5232
RI01711615CDP-N-dimethylethanolamine,3TMS,isomer#2JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)C(O[Si](C)(C)C)C1OTMS688.1952Standard non polar3554.548
RI01711614CDP-N-dimethylethanolamine,3TMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C)=NC2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)CTMS688.1952Standard non polar3412.3555
RI01711613CDP-N-dimethylethanolamine,2TMS,isomer#4JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)C(O)C1OTMS616.1556Standard non polar3580.5244
RI01711612CDP-N-dimethylethanolamine,2TMS,isomer#3JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C)=NC2=O)C(O)C1O[Si](C)(C)CTMS616.1556Standard non polar3402.5813
RI01711611CDP-N-dimethylethanolamine,2TMS,isomer#2JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C)=NC2=O)C(O[Si](C)(C)C)C1OTMS616.1556Standard non polar3415.7756
RI01711610CDP-N-dimethylethanolamine,2TMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N)=NC2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)CTMS616.1556Standard non polar3310.163
RI01711609CDP-N-dimethylethanolamine,1TMS,isomer#3JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N[Si](C)(C)C)=NC2=O)C(O)C1OTMS544.1161Standard non polar3417.011
RI01711608CDP-N-dimethylethanolamine,1TMS,isomer#2JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N)=NC2=O)C(O)C1O[Si](C)(C)CTMS544.1161Standard non polar3300.4404
RI01711607CDP-N-dimethylethanolamine,1TMS,isomer#1JsmolC[N+](C)CCOP(=O)([O-])OP(=O)([O-])OCC1OC(N2C=CC(N)=NC2=O)C(O[Si](C)(C)C)C1OTMS544.1161Standard non polar3305.582
RI01711606cathasterone,3TBDMS,isomer#2JsmolCC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3C=C(O[Si](C)(C)C(C)(C)C)C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12CTBDMS774.6198Standard polar3795.9507
RI01711605cathasterone,3TBDMS,isomer#1JsmolCC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3CC(O[Si](C)(C)C(C)(C)C)=C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12CTBDMS774.6198Standard polar3845.4897
RI01711604cathasterone,3TMS,isomer#2JsmolCC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3C=C(O[Si](C)(C)C)C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS648.4789Standard polar3595.0447
RI01711603cathasterone,3TMS,isomer#1JsmolCC(C)C(C)CC(O[Si](C)(C)C)C(C)C1CCC2C3CC(O[Si](C)(C)C)=C4CC(O[Si](C)(C)C)CCC4(C)C3CCC12CTMS648.4789Standard polar3636.374
RI01711602cathasterone,3TBDMS,isomer#2JsmolCC(C)C(C)CC(O[Si](C)(C)C(C)(C)C)C(C)C1CCC2C3C=C(O[Si](C)(C)C(C)(C)C)C4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12CTBDMS774.6198Semi standard non polar4114.3276
Displaying retention index compounds 12551 - 12575 of 1722868 in total