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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20126 - 20150 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI0170405117-O-deacetylvindoline,1TBDMS,isomer#2JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O)(C(=O)OC)C1O[Si](C)(C)C(C)(C)C)C32TBDMS528.3014Standard polar4057.3823
RI0170405017-O-deacetylvindoline,1TBDMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C(C)(C)C)(C(=O)OC)C1O)C32TBDMS528.3014Standard polar4145.6206
RI0170404917-O-deacetylvindoline,2TMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C)(C(=O)OC)C1O[Si](C)(C)C)C32TMS558.294Standard polar3852.4453
RI0170404817-O-deacetylvindoline,1TMS,isomer#2JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O)(C(=O)OC)C1O[Si](C)(C)C)C32TMS486.2545Standard polar3919.755
RI0170404717-O-deacetylvindoline,1TMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C)(C(=O)OC)C1O)C32TMS486.2545Standard polar4022.5852
RI0170404617-O-deacetylvindoline,2TBDMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C(C)(C)C)(C(=O)OC)C1O[Si](C)(C)C(C)(C)C)C32TBDMS642.3879Semi standard non polar3548.9487
RI0170404517-O-deacetylvindoline,1TBDMS,isomer#2JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O)(C(=O)OC)C1O[Si](C)(C)C(C)(C)C)C32TBDMS528.3014Semi standard non polar3327.561
RI0170404417-O-deacetylvindoline,1TBDMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C(C)(C)C)(C(=O)OC)C1O)C32TBDMS528.3014Semi standard non polar3355.9192
RI0170404317-O-deacetylvindoline,2TMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C)(C(=O)OC)C1O[Si](C)(C)C)C32TMS558.294Semi standard non polar3144.7085
RI0170404217-O-deacetylvindoline,1TMS,isomer#2JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O)(C(=O)OC)C1O[Si](C)(C)C)C32TMS486.2545Semi standard non polar3128.6113
RI0170404117-O-deacetylvindoline,1TMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C)(C(=O)OC)C1O)C32TMS486.2545Semi standard non polar3137.9443
RI0170404017-O-deacetylvindoline,2TBDMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C(C)(C)C)(C(=O)OC)C1O[Si](C)(C)C(C)(C)C)C32TBDMS642.3879Standard non polar3665.897
RI0170403917-O-deacetylvindoline,1TBDMS,isomer#2JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O)(C(=O)OC)C1O[Si](C)(C)C(C)(C)C)C32TBDMS528.3014Standard non polar3380.37
RI0170403817-O-deacetylvindoline,1TBDMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C(C)(C)C)(C(=O)OC)C1O)C32TBDMS528.3014Standard non polar3433.7974
RI0170403717-O-deacetylvindoline,2TMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C)(C(=O)OC)C1O[Si](C)(C)C)C32TMS558.294Standard non polar3157.6335
RI0170403617-O-deacetylvindoline,1TMS,isomer#2JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O)(C(=O)OC)C1O[Si](C)(C)C)C32TMS486.2545Standard non polar3094.3833
RI0170403517-O-deacetylvindoline,1TMS,isomer#1JsmolCCC12C=CC[N+]3CCC4(C5=CC=C(OC)C=C5N(C)C4C(O[Si](C)(C)C)(C(=O)OC)C1O)C32TMS486.2545Standard non polar3142.7942
RI0170403417-O-acetylnorajmaline,2TBDMS,isomer#1JsmolCCC1C2CC3C4N([Si](C)(C)C(C)(C)C)C5=CC=CC=C5C45CC(C2C5OC(C)=O)N3C1O[Si](C)(C)C(C)(C)CTBDMS582.3673Standard polar3548.2239
RI0170403317-O-acetylnorajmaline,2TMS,isomer#1JsmolCCC1C2CC3C4N([Si](C)(C)C)C5=CC=CC=C5C45CC(C2C5OC(C)=O)N3C1O[Si](C)(C)CTMS498.2734Standard polar3350.2542
RI0170403217-O-acetylnorajmaline,2TBDMS,isomer#1JsmolCCC1C2CC3C4N([Si](C)(C)C(C)(C)C)C5=CC=CC=C5C45CC(C2C5OC(C)=O)N3C1O[Si](C)(C)C(C)(C)CTBDMS582.3673Semi standard non polar3233.0425
RI0170403117-O-acetylnorajmaline,2TMS,isomer#1JsmolCCC1C2CC3C4N([Si](C)(C)C)C5=CC=CC=C5C45CC(C2C5OC(C)=O)N3C1O[Si](C)(C)CTMS498.2734Semi standard non polar2812.2954
RI0170403017-O-acetylnorajmaline,2TBDMS,isomer#1JsmolCCC1C2CC3C4N([Si](C)(C)C(C)(C)C)C5=CC=CC=C5C45CC(C2C5OC(C)=O)N3C1O[Si](C)(C)C(C)(C)CTBDMS582.3673Standard non polar3304.3591
RI0170402917-O-acetylnorajmaline,2TMS,isomer#1JsmolCCC1C2CC3C4N([Si](C)(C)C)C5=CC=CC=C5C45CC(C2C5OC(C)=O)N3C1O[Si](C)(C)CTMS498.2734Standard non polar2818.6804
RI0170402816-oxo-palmitate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=CCCCCCCCCCCCCCC(=O)[O-]TBDMS383.2987Standard polar2584.2969
RI0170402716-oxo-palmitate,1TMS,isomer#1JsmolC[Si](C)(C)OC=CCCCCCCCCCCCCCC(=O)[O-]TMS341.2517Standard polar2496.68
Displaying retention index compounds 20126 - 20150 of 1722868 in total