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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 19576 - 19600 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000195762'-Deoxysepiapterin,2TBDMS,isomer#6JsmolCCC(=O)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS449.2642Standard polar4280.0034
RI000195772'-Deoxysepiapterin,2TBDMS,isomer#7JsmolCCC(=O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS449.2642Standard polar3837.6035
RI000195782'-Deoxysepiapterin,3TBDMS,isomer#1JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS563.3507Standard polar4203.808
RI000195792'-Deoxysepiapterin,3TBDMS,isomer#2JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS563.3507Standard polar4290.363
RI000195802'-Deoxysepiapterin,3TBDMS,isomer#3JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS563.3507Standard polar4209.749
RI000195812'-Deoxysepiapterin,3TBDMS,isomer#4JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS563.3507Standard polar3818.0298
RI000195822'-Deoxysepiapterin,3TBDMS,isomer#5JsmolCCC(=O)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS563.3507Standard polar3996.8596
RI000195832'-Deoxysepiapterin,3TBDMS,isomer#6JsmolCCC(=O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS563.3507Standard polar3898.7063
RI000195842'-Deoxysepiapterin,3TBDMS,isomer#7JsmolCCC(=O)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS563.3507Standard polar4008.209
RI000195852'-Deoxysepiapterin,4TBDMS,isomer#1JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS677.4372Standard polar3953.2817
RI000195862'-Deoxysepiapterin,4TBDMS,isomer#2JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS677.4372Standard polar3863.9287
RI000195872'-Deoxysepiapterin,4TBDMS,isomer#3JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS677.4372Standard polar3929.7148
RI000195882'-Deoxysepiapterin,4TBDMS,isomer#4JsmolCCC(=O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS677.4372Standard polar3643.504
RI000195892'-Deoxysepiapterin,5TBDMS,isomer#1JsmolCC=C(O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS791.5237Standard polar3667.236
RI000195903a,7b,12b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS480.3271Semi standard non polar3395.4204
RI000195913a,7b,12b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#2JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O[Si](C)(C)C)[C@@]21CTMS480.3271Semi standard non polar3422.1797
RI000195923a,7b,12b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#3JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS480.3271Semi standard non polar3367.0347
RI000195933a,7b,12b-Trihydroxy-5b-cholanoic acid,1TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS480.3271Semi standard non polar3442.5322
RI000195943a,7b,12b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS552.3666Semi standard non polar3314.0388
RI000195953a,7b,12b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#2JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS552.3666Semi standard non polar3385.428
RI000195963a,7b,12b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#3JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3379.4204
RI000195973a,7b,12b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#4JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3C[C@@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3337.051
RI000195983a,7b,12b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#5JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O[Si](C)(C)C)[C@@]21CTMS552.3666Semi standard non polar3372.2803
RI000195993a,7b,12b-Trihydroxy-5b-cholanoic acid,2TMS,isomer#6JsmolC[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS552.3666Semi standard non polar3336.18
RI000196003a,7b,12b-Trihydroxy-5b-cholanoic acid,3TMS,isomer#1JsmolC[C@H](CCC(=O)O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3[C@@H](O[Si](C)(C)C)C[C@@H]4C[C@H](O[Si](C)(C)C)CC[C@]4(C)[C@H]3C[C@@H](O)[C@@]21CTMS624.4062Semi standard non polar3321.5957
Displaying retention index compounds 19576 - 19600 of 1722868 in total