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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 20351 - 20375 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01703826(R)-cysteate,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N[C@@H](CS(=O)(=O)O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS397.1774Standard non polar2335.7827
RI01703825(R)-cysteate,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N[C@@H](CS(=O)(=O)O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS397.1774Standard non polar2309.4717
RI01703824(R)-cysteate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CS(=O)(=O)O[Si](C)(C)C(C)(C)CTBDMS397.1774Standard non polar2311.8308
RI01703823(R)-cysteate,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@H](CS(=O)(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS457.1626Standard non polar2174.6697
RI01703822(R)-cysteate,3TMS,isomer#3JsmolC[Si](C)(C)OS(=O)(=O)C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS385.1231Standard non polar2014.9337
RI01703821(R)-cysteate,3TMS,isomer#2JsmolC[Si](C)(C)OC(=O)[C@H](CS(=O)(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS385.1231Standard non polar2024.8732
RI01703820(R)-cysteate,3TMS,isomer#1JsmolC[Si](C)(C)N[C@@H](CS(=O)(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS385.1231Standard non polar1923.7593
RI01703819(R)-cysteate,2TMS,isomer#4JsmolC[Si](C)(C)N([C@@H](CS(=O)(=O)O)C(=O)O)[Si](C)(C)CTMS313.0835Standard non polar1886.6483
RI01703818(R)-cysteate,2TMS,isomer#3JsmolC[Si](C)(C)N[C@@H](CS(=O)(=O)O[Si](C)(C)C)C(=O)OTMS313.0835Standard non polar1747.9227
RI01703817(R)-cysteate,2TMS,isomer#2JsmolC[Si](C)(C)N[C@@H](CS(=O)(=O)O)C(=O)O[Si](C)(C)CTMS313.0835Standard non polar1760.1681
RI01703816(R)-cysteate,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@@H](N)CS(=O)(=O)O[Si](C)(C)CTMS313.0835Standard non polar1723.7416
RI01703815(E)-indol-3-ylacetaldoxime,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C=C(CC=NO)C2=CC=CC=C21TBDMS288.1658Standard polar2661.6426
RI01703814(E)-indol-3-ylacetaldoxime,1TMS,isomer#1JsmolC[Si](C)(C)N1C=C(CC=NO)C2=CC=CC=C21TMS246.1188Standard polar2577.5623
RI01703813(E)-indol-3-ylacetaldoxime,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C=C(CC=NO)C2=CC=CC=C21TBDMS288.1658Semi standard non polar2209.1687
RI01703812(E)-indol-3-ylacetaldoxime,1TMS,isomer#1JsmolC[Si](C)(C)N1C=C(CC=NO)C2=CC=CC=C21TMS246.1188Semi standard non polar1998.1337
RI01703811(E)-indol-3-ylacetaldoxime,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C=C(CC=NO)C2=CC=CC=C21TBDMS288.1658Standard non polar2140.2861
RI01703810(E)-indol-3-ylacetaldoxime,1TMS,isomer#1JsmolC[Si](C)(C)N1C=C(CC=NO)C2=CC=CC=C21TMS246.1188Standard non polar1929.4863
RI01703809(9Z)-12-oxo-dodec-9-enoate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=CC=CCCCCCCCC(=O)[O-]TBDMS325.2204Standard polar2305.869
RI01703808(9Z)-12-oxo-dodec-9-enoate,1TMS,isomer#1JsmolC[Si](C)(C)OC=CC=CCCCCCCCC(=O)[O-]TMS283.1735Standard polar2198.0898
RI01703807(9Z)-12-oxo-dodec-9-enoate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=CC=CCCCCCCCC(=O)[O-]TBDMS325.2204Semi standard non polar2187.4292
RI01703806(9Z)-12-oxo-dodec-9-enoate,1TMS,isomer#1JsmolC[Si](C)(C)OC=CC=CCCCCCCCC(=O)[O-]TMS283.1735Semi standard non polar1963.2648
RI01703805(9Z)-12-oxo-dodec-9-enoate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC=CC=CCCCCCCCC(=O)[O-]TBDMS325.2204Standard non polar2028.3156
RI01703804(9Z)-12-oxo-dodec-9-enoate,1TMS,isomer#1JsmolC[Si](C)(C)OC=CC=CCCCCCCCC(=O)[O-]TMS283.1735Standard non polar1825.1583
RI01703803(5alpha)-campestan-3-one,1TBDMS,isomer#2JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4C=C(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CCC12CTBDMS514.457Standard polar3530.6538
RI01703802(5alpha)-campestan-3-one,1TBDMS,isomer#1JsmolCC(C)C(C)CCC(C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)=CCC4(C)C3CCC12CTBDMS514.457Standard polar3536.2295
Displaying retention index compounds 20351 - 20375 of 1722868 in total