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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 17826 - 17850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000178263,4-Dihydroxyphenylglycol,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(O)C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1TBDMS398.2309Semi standard non polar2302.6873
RI000178273,4-Dihydroxyphenylglycol,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C(CO)O[Si](C)(C)C(C)(C)C)C=C1OTBDMS398.2309Semi standard non polar2289.9487
RI000178283,4-Dihydroxyphenylglycol,2TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC1=CC(C(CO)O[Si](C)(C)C(C)(C)C)=CC=C1OTBDMS398.2309Semi standard non polar2277.5337
RI000178293,4-Dihydroxyphenylglycol,2TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C(O)CO)C=C1O[Si](C)(C)C(C)(C)CTBDMS398.2309Semi standard non polar2338.4707
RI000178303,4-Dihydroxyphenylglycol,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1TBDMS512.3173Semi standard non polar2506.5354
RI000178313,4-Dihydroxyphenylglycol,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1TBDMS512.3173Semi standard non polar2505.192
RI000178323,4-Dihydroxyphenylglycol,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(O)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1TBDMS512.3173Semi standard non polar2539.8716
RI000178333,4-Dihydroxyphenylglycol,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C(CO)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)CTBDMS512.3173Semi standard non polar2513.2373
RI000178343,4-Dihydroxyphenylglycol,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1TBDMS626.4038Semi standard non polar2732.6174
RI000178353,4-DihydroxyphenylglycolJsmolOCC(O)C1=CC(O)=C(O)C=C1Underivatized170.0579Standard polar3293.2378
RI000178363,4-DihydroxyphenylglycolJsmolOCC(O)C1=CC(O)=C(O)C=C1Underivatized170.0579Standard non polar1795.2604
RI000178373,4-DihydroxyphenylglycolJsmolOCC(O)C1=CC(O)=C(O)C=C1Underivatized170.0579Semi standard non polar1824.8667
RI0001783818-Hydroxycorticosterone,1TMS,isomer#1JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS434.2489Semi standard non polar3405.34
RI0001783918-Hydroxycorticosterone,1TMS,isomer#2JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO)CC[C@@H]12TMS434.2489Semi standard non polar3347.9827
RI0001784018-Hydroxycorticosterone,1TMS,isomer#3JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=O)CO)CC[C@@H]12TMS434.2489Semi standard non polar3371.8508
RI0001784118-Hydroxycorticosterone,1TMS,isomer#4JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS434.2489Semi standard non polar3361.8235
RI0001784218-Hydroxycorticosterone,1TMS,isomer#5JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=CO)O[Si](C)(C)C)CC[C@@H]12TMS434.2489Semi standard non polar3355.454
RI0001784318-Hydroxycorticosterone,1TMS,isomer#6JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=O)CO)CC[C@@H]12TMS434.2489Semi standard non polar3308.4868
RI0001784418-Hydroxycorticosterone,2TMS,isomer#1JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3348.6577
RI0001784518-Hydroxycorticosterone,2TMS,isomer#2JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3335.9465
RI0001784618-Hydroxycorticosterone,2TMS,isomer#3JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)C(=C(CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3369.3835
RI0001784718-Hydroxycorticosterone,2TMS,isomer#4JsmolC[C@]12CC=C(O[Si](C)(C)C)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=O)CO[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3302.2412
RI0001784818-Hydroxycorticosterone,2TMS,isomer#5JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO)[C@@H](C(=CO[Si](C)(C)C)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3391.1035
RI0001784918-Hydroxycorticosterone,2TMS,isomer#6JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O[Si](C)(C)C)C[C@]2(CO[Si](C)(C)C)[C@@H](C(=O)CO)CC[C@@H]12TMS506.2884Semi standard non polar3278.9993
RI0001785018-Hydroxycorticosterone,2TMS,isomer#7JsmolC[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@]2(CO[Si](C)(C)C)C(=C(CO)O[Si](C)(C)C)CC[C@@H]12TMS506.2884Semi standard non polar3334.7024
Displaying retention index compounds 17826 - 17850 of 1722868 in total