Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 301 - 325 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00000301alpha-Ketoisovaleric acid,2TMS,isomer#1JsmolCC(C)=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS260.1264Standard non polar1230.271
RI00000302alpha-Ketoisovaleric acid,2TBDMS,isomer#1JsmolCC(C)=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS344.2203Standard non polar1664.8069
RI00000303alpha-Ketoisovaleric acidJsmolCC(C)C(=O)C(O)=OUnderivatized116.0473Standard non polar1270.4131
RI00000304alpha-Ketoisovaleric acidJsmolCC(C)C(=O)C(O)=OUnderivatized116.0473Semi standard non polar895.0081
RI00000305alpha-Ketoisovaleric acid,2TMS,isomer#1JsmolCC(C)=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS260.1264Semi standard non polar1228.6582
RI00000306alpha-Ketoisovaleric acid,2TBDMS,isomer#1JsmolCC(C)=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS344.2203Semi standard non polar1654.8745
RI00000307alpha-Ketoisovaleric acid,2TMS,isomer#1JsmolCC(C)=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS260.1264Standard polar1223.4813
RI00000308alpha-Ketoisovaleric acid,2TBDMS,isomer#1JsmolCC(C)=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS344.2203Standard polar1565.0853
RI00000309p-Hydroxyphenylacetic acid,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1=CC=C(O)C=C1TMS224.0869Semi standard non polar1651.5748
RI00000310p-Hydroxyphenylacetic acid,1TMS,isomer#2JsmolC[Si](C)(C)OC1=CC=C(CC(=O)O)C=C1TMS224.0869Semi standard non polar1617.9165
RI00000311p-Hydroxyphenylacetic acid,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CC1=CC=C(O[Si](C)(C)C)C=C1TMS296.1264Semi standard non polar1655.175
RI00000312p-Hydroxyphenylacetic acid,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1=CC=C(O)C=C1TBDMS266.1338Semi standard non polar1892.4467
RI00000313p-Hydroxyphenylacetic acid,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(CC(=O)O)C=C1TBDMS266.1338Semi standard non polar1875.1447
RI00000314p-Hydroxyphenylacetic acid,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1TBDMS380.2203Semi standard non polar2117.3333
RI00000315p-Hydroxyphenylacetic acidJsmolOC(=O)CC1=CC=C(O)C=C1Underivatized152.0473Standard polar3171.0286
RI00000316p-Hydroxyphenylacetic acidJsmolOC(=O)CC1=CC=C(O)C=C1Underivatized152.0473Standard non polar1537.7047
RI00000317p-Hydroxyphenylacetic acidJsmolOC(=O)CC1=CC=C(O)C=C1Underivatized152.0473Semi standard non polar1562.8068
RI00000318Iodotyrosine,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=C(C[C@H](N)C(=O)O)C=C1ITMS379.0101Semi standard non polar2230.6394
RI00000319Iodotyrosine,1TMS,isomer#2JsmolC[Si](C)(C)OC(=O)[C@@H](N)CC1=CC=C(O)C(I)=C1TMS379.0101Semi standard non polar2146.844
RI00000320Iodotyrosine,1TMS,isomer#3JsmolC[Si](C)(C)N[C@@H](CC1=CC=C(O)C(I)=C1)C(=O)OTMS379.0101Semi standard non polar2218.0461
RI00000321Iodotyrosine,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H](N)CC1=CC=C(O[Si](C)(C)C)C(I)=C1TMS451.0496Semi standard non polar2195.4192
RI00000322Iodotyrosine,2TMS,isomer#2JsmolC[Si](C)(C)N[C@@H](CC1=CC=C(O[Si](C)(C)C)C(I)=C1)C(=O)OTMS451.0496Semi standard non polar2252.109
RI00000323Iodotyrosine,2TMS,isomer#3JsmolC[Si](C)(C)N[C@@H](CC1=CC=C(O)C(I)=C1)C(=O)O[Si](C)(C)CTMS451.0496Semi standard non polar2168.6218
RI00000324Iodotyrosine,2TMS,isomer#4JsmolC[Si](C)(C)N([C@@H](CC1=CC=C(O)C(I)=C1)C(=O)O)[Si](C)(C)CTMS451.0496Semi standard non polar2319.4495
RI00000325Iodotyrosine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=C(C[C@H](N)C(=O)O)C=C1ITBDMS421.057Semi standard non polar2482.515
Displaying retention index compounds 301 - 325 of 1722868 in total