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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 13976 - 14000 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017102015-beta-pregnan-3,20 dione,1TMS,isomer#3JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard polar3122.0396
RI017102005-beta-pregnan-3,20 dione,1TMS,isomer#2JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard polar3124.1963
RI017101995-beta-pregnan-3,20 dione,1TMS,isomer#1JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Standard polar3108.6338
RI017101985-beta-pregnan-3,20 dione,2TBDMS,isomer#4JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Semi standard non polar3265.9368
RI017101975-beta-pregnan-3,20 dione,2TBDMS,isomer#3JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Semi standard non polar3301.1116
RI017101965-beta-pregnan-3,20 dione,2TBDMS,isomer#2JsmolCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Semi standard non polar3306.894
RI017101955-beta-pregnan-3,20 dione,2TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Semi standard non polar3305.472
RI017101945-beta-pregnan-3,20 dione,1TBDMS,isomer#4JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Semi standard non polar3040.0305
RI017101935-beta-pregnan-3,20 dione,1TBDMS,isomer#3JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Semi standard non polar2994.9478
RI017101925-beta-pregnan-3,20 dione,1TBDMS,isomer#2JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Semi standard non polar3020.941
RI017101915-beta-pregnan-3,20 dione,1TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Semi standard non polar3039.3035
RI017101905-beta-pregnan-3,20 dione,2TMS,isomer#4JsmolC=C(O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Semi standard non polar2776.7393
RI017101895-beta-pregnan-3,20 dione,2TMS,isomer#3JsmolC=C(O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Semi standard non polar2794.2415
RI017101885-beta-pregnan-3,20 dione,2TMS,isomer#2JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Semi standard non polar2831.1882
RI017101875-beta-pregnan-3,20 dione,2TMS,isomer#1JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS460.3193Semi standard non polar2823.8489
RI017101865-beta-pregnan-3,20 dione,1TMS,isomer#4JsmolC=C(O[Si](C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Semi standard non polar2782.873
RI017101855-beta-pregnan-3,20 dione,1TMS,isomer#3JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Semi standard non polar2764.7146
RI017101845-beta-pregnan-3,20 dione,1TMS,isomer#2JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Semi standard non polar2781.6003
RI017101835-beta-pregnan-3,20 dione,1TMS,isomer#1JsmolCC(O[Si](C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTMS388.2798Semi standard non polar2796.221
RI017101825-beta-pregnan-3,20 dione,2TBDMS,isomer#4JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Standard non polar3187.1233
RI017101815-beta-pregnan-3,20 dione,2TBDMS,isomer#3JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Standard non polar3123.7349
RI017101805-beta-pregnan-3,20 dione,2TBDMS,isomer#2JsmolCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Standard non polar3197.329
RI017101795-beta-pregnan-3,20 dione,2TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)=C1CC[C@H]2[C@@H]3CC[C@@H]4CC(O[Si](C)(C)C(C)(C)C)=CC[C@]4(C)[C@H]3CC[C@]12CTBDMS544.4132Standard non polar3131.9136
RI017101785-beta-pregnan-3,20 dione,1TBDMS,isomer#4JsmolC=C(O[Si](C)(C)C(C)(C)C)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Standard non polar2996.6653
RI017101775-beta-pregnan-3,20 dione,1TBDMS,isomer#3JsmolCC(=O)[C@H]1CC[C@H]2[C@@H]3CC[C@@H]4C=C(O[Si](C)(C)C(C)(C)C)CC[C@]4(C)[C@H]3CC[C@]12CTBDMS430.3267Standard non polar2886.4106
Displaying retention index compounds 13976 - 14000 of 1722868 in total