Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 1 - 25 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI000000011-Methylhistidine,1TMS,isomer#1JsmolCN1C=NC(C[C@H](N)C(=O)O[Si](C)(C)C)=C1TMS241.1247Semi standard non polar1756.3544
RI000000021-Methylhistidine,1TMS,isomer#2JsmolCN1C=NC(C[C@H](N[Si](C)(C)C)C(=O)O)=C1TMS241.1247Semi standard non polar1822.4111
RI000000031-Methylhistidine,1TBDMS,isomer#1JsmolCN1C=NC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS283.1716Semi standard non polar2006.082
RI000000041-Methylhistidine,1TBDMS,isomer#2JsmolCN1C=NC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=C1TBDMS283.1716Semi standard non polar2057.589
RI000000051-MethylhistidineJsmolCN1C=NC(C[C@H](N)C(O)=O)=C1Underivatized169.0851Standard polar2786.8105
RI000000061-Methylhistidine,2TMS,isomer#1JsmolCN1C=NC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C1TMS313.1642Standard non polar1805.4081
RI000000071-Methylhistidine,2TMS,isomer#2JsmolCN1C=NC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=C1TMS313.1642Standard non polar1927.968
RI000000081-Methylhistidine,3TMS,isomer#1JsmolCN1C=NC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=C1TMS385.2037Standard non polar1962.88
RI000000091-Methylhistidine,2TBDMS,isomer#1JsmolCN1C=NC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS397.2581Standard non polar2257.153
RI000000101-Methylhistidine,2TBDMS,isomer#2JsmolCN1C=NC(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1TBDMS397.2581Standard non polar2352.2932
RI000000111-Methylhistidine,3TBDMS,isomer#1JsmolCN1C=NC(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1TBDMS511.3446Standard non polar2590.718
RI000000121-MethylhistidineJsmolCN1C=NC(C[C@H](N)C(O)=O)=C1Underivatized169.0851Standard non polar1703.9961
RI000000131-MethylhistidineJsmolCN1C=NC(C[C@H](N)C(O)=O)=C1Underivatized169.0851Semi standard non polar1882.5249
RI000000141-Methylhistidine,1TMS,isomer#1JsmolCN1C=NC(C[C@H](N)C(=O)O[Si](C)(C)C)=C1TMS241.1247Standard polar2700.3145
RI000000151-Methylhistidine,1TMS,isomer#2JsmolCN1C=NC(C[C@H](N[Si](C)(C)C)C(=O)O)=C1TMS241.1247Standard polar2717.7344
RI000000161-Methylhistidine,1TBDMS,isomer#1JsmolCN1C=NC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS283.1716Standard polar2783.221
RI000000171-Methylhistidine,1TBDMS,isomer#2JsmolCN1C=NC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=C1TBDMS283.1716Standard polar2753.7178
RI000000181-Methylhistidine,1TMS,isomer#1JsmolCN1C=NC(C[C@H](N)C(=O)O[Si](C)(C)C)=C1TMS241.1247Standard non polar1722.7527
RI000000191-Methylhistidine,1TMS,isomer#2JsmolCN1C=NC(C[C@H](N[Si](C)(C)C)C(=O)O)=C1TMS241.1247Standard non polar1778.9307
RI000000201-Methylhistidine,1TBDMS,isomer#1JsmolCN1C=NC(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS283.1716Standard non polar1955.3805
RI000000211-Methylhistidine,1TBDMS,isomer#2JsmolCN1C=NC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=C1TBDMS283.1716Standard non polar2027.5265
RI000000221-Methylhistidine,2TMS,isomer#1JsmolCN1C=NC(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=C1TMS313.1642Semi standard non polar1829.6735
RI000000231-Methylhistidine,2TMS,isomer#2JsmolCN1C=NC(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=C1TMS313.1642Semi standard non polar1982.1442
RI000000241-Methylhistidine,3TMS,isomer#1JsmolCN1C=NC(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=C1TMS385.2037Semi standard non polar2034.8866
RI000000251-Methylhistidine,2TBDMS,isomer#1JsmolCN1C=NC(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=C1TBDMS397.2581Semi standard non polar2267.6885
Displaying retention index compounds 1 - 25 of 1722868 in total