Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 12051 - 12075 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00012051Testosterone,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@H](O)[C@@]3(C)CC[C@@H]12TBDMS402.2954Semi standard non polar2917.7356
RI00012052TestosteroneJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized288.2089Standard polar3544.1775
RI00012053Testosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2O[Si](C)(C)CTMS432.288Standard non polar2693.2212
RI00012054Testosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@H](O[Si](C)(C)C(C)(C)C)[C@@]3(C)CC[C@@H]12TBDMS516.3819Standard non polar3170.2192
RI00012055TestosteroneJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized288.2089Standard non polar2567.5908
RI00012056TestosteroneJsmol[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12CUnderivatized288.2089Semi standard non polar2768.4458
RI00012057Testosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2O[Si](C)(C)CTMS432.288Semi standard non polar2694.5388
RI00012058Testosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@H](O[Si](C)(C)C(C)(C)C)[C@@]3(C)CC[C@@H]12TBDMS516.3819Semi standard non polar3233.7773
RI00012059Testosterone,2TMS,isomer#1JsmolC[C@]12CC[C@H]3[C@@H](CCC4=CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC[C@@H]2O[Si](C)(C)CTMS432.288Standard polar2974.6729
RI00012060Testosterone,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)C(=C1)CC[C@H]1[C@@H]3CC[C@H](O[Si](C)(C)C(C)(C)C)[C@@]3(C)CC[C@@H]12TBDMS516.3819Standard polar3231.9224
RI00012061Thiamine,1TMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C)=C2C)C(N)=N1TMS337.1513Semi standard non polar2471.689
RI00012062Thiamine,1TMS,isomer#2JsmolCC1=NC=C(C[N+]2=CSC(CCO)=C2C)C(N[Si](C)(C)C)=N1TMS337.1513Semi standard non polar2549.4272
RI00012063Thiamine,1TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C(C)(C)C)=C2C)C(N)=N1TBDMS379.1982Semi standard non polar2740.737
RI00012064Thiamine,1TBDMS,isomer#2JsmolCC1=NC=C(C[N+]2=CSC(CCO)=C2C)C(N[Si](C)(C)C(C)(C)C)=N1TBDMS379.1982Semi standard non polar2747.3665
RI00012065ThiamineJsmolCC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1NUnderivatized265.1118Standard polar3535.8364
RI00012066Thiamine,2TMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C)=C2C)C(N[Si](C)(C)C)=N1TMS409.1908Standard non polar2467.2117
RI00012067Thiamine,2TMS,isomer#2JsmolCC1=NC=C(C[N+]2=CSC(CCO)=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS409.1908Standard non polar2549.1895
RI00012068Thiamine,3TMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C)=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS481.2303Standard non polar2583.702
RI00012069Thiamine,2TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C(C)(C)C)=C2C)C(N[Si](C)(C)C(C)(C)C)=N1TBDMS493.2847Standard non polar2897.625
RI00012070Thiamine,2TBDMS,isomer#2JsmolCC1=NC=C(C[N+]2=CSC(CCO)=C2C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N1TBDMS493.2847Standard non polar2959.6218
RI00012071Thiamine,3TBDMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C(C)(C)C)=C2C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N1TBDMS607.3712Standard non polar3195.6465
RI00012072ThiamineJsmolCC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1NUnderivatized265.1118Standard non polar2426.2917
RI00012073ThiamineJsmolCC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1NUnderivatized265.1118Semi standard non polar2498.3508
RI00012074Thiamine,2TMS,isomer#1JsmolCC1=NC=C(C[N+]2=CSC(CCO[Si](C)(C)C)=C2C)C(N[Si](C)(C)C)=N1TMS409.1908Semi standard non polar2502.397
RI00012075Thiamine,2TMS,isomer#2JsmolCC1=NC=C(C[N+]2=CSC(CCO)=C2C)C(N([Si](C)(C)C)[Si](C)(C)C)=N1TMS409.1908Semi standard non polar2540.1167
Displaying retention index compounds 12051 - 12075 of 1722868 in total