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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 3651 - 3675 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01720526Ala-Phe-Ala,4TBDMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS763.4991Semi standard non polar3152.5576
RI01720525Ala-Phe-Ala,5TMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS667.3508Semi standard non polar2661.2134
RI01720524Ala-Phe-Ala,4TMS,isomer#4JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS595.3113Semi standard non polar2641.015
RI01720523Ala-Phe-Ala,4TMS,isomer#3JsmolCC(N=C(O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS595.3113Semi standard non polar2612.4456
RI01720522Ala-Phe-Ala,4TMS,isomer#2JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS595.3113Semi standard non polar2620.7244
RI01720521Ala-Phe-Ala,4TMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS595.3113Semi standard non polar2454.084
RI01720520Ala-Phe-Ala,5TBDMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS877.5856Standard non polar3281.93
RI01720519Ala-Phe-Ala,4TBDMS,isomer#4JsmolCC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=CC=C1)N=C(O)C(C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS763.4991Standard non polar3219.6267
RI01720518Ala-Phe-Ala,4TBDMS,isomer#3JsmolCC(N=C(O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS763.4991Standard non polar3214.5469
RI01720517Ala-Phe-Ala,4TBDMS,isomer#2JsmolCC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS763.4991Standard non polar3094.307
RI01720516Ala-Phe-Ala,4TBDMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS763.4991Standard non polar3005.6252
RI01720515Ala-Phe-Ala,5TMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS667.3508Standard non polar2533.7607
RI01720514Ala-Phe-Ala,4TMS,isomer#4JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS595.3113Standard non polar2560.503
RI01720513Ala-Phe-Ala,4TMS,isomer#3JsmolCC(N=C(O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS595.3113Standard non polar2568.733
RI01720512Ala-Phe-Ala,4TMS,isomer#2JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS595.3113Standard non polar2499.1711
RI01720511Ala-Phe-Ala,4TMS,isomer#1JsmolCC(N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(C)N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS595.3113Standard non polar2393.8064
RI017205107,11-Dioxolanost-8-en-3-yl acetate,2TBDMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)C(C)(C)CTBDMS726.5439Standard polar3880.5771
RI017205097,11-Dioxolanost-8-en-3-yl acetate,1TBDMS,isomer#2JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)CC3=OTBDMS612.4574Standard polar3777.1638
RI017205087,11-Dioxolanost-8-en-3-yl acetate,1TBDMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(=O)CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)C(C)(C)CTBDMS612.4574Standard polar3779.551
RI017205077,11-Dioxolanost-8-en-3-yl acetate,2TMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)CTMS642.45Standard polar3709.13
RI017205067,11-Dioxolanost-8-en-3-yl acetate,1TMS,isomer#2JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)CC3=OTMS570.4104Standard polar3668.4536
RI017205057,11-Dioxolanost-8-en-3-yl acetate,1TMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(=O)CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)CTMS570.4104Standard polar3668.5925
RI017205047,11-Dioxolanost-8-en-3-yl acetate,2TBDMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)C(C)(C)CTBDMS726.5439Semi standard non polar3778.7524
RI017205037,11-Dioxolanost-8-en-3-yl acetate,1TBDMS,isomer#2JsmolCC(=O)OC1CCC2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)CC3=OTBDMS612.4574Semi standard non polar3821.9458
RI017205027,11-Dioxolanost-8-en-3-yl acetate,1TBDMS,isomer#1JsmolCC(=O)OC1CCC2(C)C3=C(C(=O)CC2C1(C)C)C1(C)CCC(C(C)CCCC(C)C)C1(C)C=C3O[Si](C)(C)C(C)(C)CTBDMS612.4574Semi standard non polar3761.7139
Displaying retention index compounds 3651 - 3675 of 1722868 in total