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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 15051 - 15075 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017091264alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#13JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3305.6638
RI017091254alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#12JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS713.4583Standard non polar3246.46
RI017091244alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#11JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3341.142
RI017091234alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#10JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CNC2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3335.1501
RI017091224alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#9JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CNC2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard non polar3219.6343
RI017091214alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#8JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard non polar3261.1975
RI017091204alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#7JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3303.2727
RI017091194alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#6JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3322.8352
RI017091184alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#5JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS713.4583Standard non polar3226.6697
RI017091174alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#4JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS713.4583Standard non polar3224.3723
RI017091164alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#3JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3306.0537
RI017091154alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#2JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard non polar3218.477
RI017091144alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard non polar3215.559
RI017091134alpha-hydroxy-tetrahydrobiopterin,7TMS,isomer#1JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS761.3891Standard non polar2694.613
RI017091124alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#6JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard non polar2697.7803
RI017091114alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#5JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard non polar2685.7698
RI017091104alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#4JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS689.3496Standard non polar2625.2224
RI017091094alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#3JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard non polar2625.9363
RI017091084alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#2JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard non polar2616.6265
RI017091074alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#1JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS689.3496Standard non polar2594.411
RI017091064alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#16JsmolCC(O)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard non polar2694.211
RI017091054alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#15JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS617.31Standard non polar2622.6155
RI017091044alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#14JsmolCC(O)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard non polar2621.956
RI017091034alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#13JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard non polar2597.8938
RI017091024alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#12JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS617.31Standard non polar2580.9377
Displaying retention index compounds 15051 - 15075 of 1722868 in total