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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11101 - 11125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00011101Phenol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1TBDMS208.1283Standard non polar1264.1096
RI00011102Phenol,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1TMS166.0814Semi standard non polar1055.1298
RI00011103Phenol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1TBDMS208.1283Semi standard non polar1308.2908
RI00011104Phenol,1TMS,isomer#1JsmolC[Si](C)(C)OC1=CC=CC=C1TMS166.0814Standard polar1241.9874
RI00011105Phenol,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC1=CC=CC=C1TBDMS208.1283Standard polar1450.5509
RI00011106Nicotinamide ribotide,1TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@@H]1OTMS407.1034Standard non polar2826.0508
RI00011107Nicotinamide ribotide,1TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1[N+]1=CC=CC(C(N)=O)=C1TMS407.1034Standard non polar2829.5085
RI00011108Nicotinamide ribotide,1TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@H](O)[C@@H]1OTMS407.1034Standard non polar2811.1013
RI00011109Nicotinamide ribotide,1TMS,isomer#4JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)=C1TMS407.1034Standard non polar2921.6897
RI00011110Nicotinamide ribotide,2TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@@H]1O[Si](C)(C)CTMS479.1429Standard non polar2869.6118
RI00011111Nicotinamide ribotide,2TMS,isomer#2JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@@H]1OTMS479.1429Standard non polar2854.8906
RI00011112Nicotinamide ribotide,2TMS,isomer#3JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O)=C1TMS479.1429Standard non polar2965.4768
RI00011113Nicotinamide ribotide,2TMS,isomer#4JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1[N+]1=CC=CC(C(N)=O)=C1TMS479.1429Standard non polar2859.5388
RI00011114Nicotinamide ribotide,2TMS,isomer#5JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)=C1TMS479.1429Standard non polar2971.729
RI00011115Nicotinamide ribotide,2TMS,isomer#6JsmolC[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@H](O)[C@@H]1O)O[Si](C)(C)CTMS479.1429Standard non polar2870.5217
RI00011116Nicotinamide ribotide,2TMS,isomer#7JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)=C1TMS479.1429Standard non polar2926.215
RI00011117Nicotinamide ribotide,2TMS,isomer#8JsmolC[Si](C)(C)N(C(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)=C1)[Si](C)(C)CTMS479.1429Standard non polar2993.9688
RI00011118Nicotinamide ribotide,3TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@@H]1O[Si](C)(C)CTMS551.1825Standard non polar2875.2207
RI00011119Nicotinamide ribotide,3TMS,isomer#2JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=C1TMS551.1825Standard non polar2989.291
RI00011120Nicotinamide ribotide,3TMS,isomer#3JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H]([N+]2=CC=CC(C(N)=O)=C2)[C@@H]1OTMS551.1825Standard non polar2899.5566
RI00011121Nicotinamide ribotide,3TMS,isomer#4JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)=C1TMS551.1825Standard non polar2963.8152
RI00011122Nicotinamide ribotide,3TMS,isomer#5JsmolC[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H]([N+]2=CC=CC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C2)[C@@H]1OTMS551.1825Standard non polar3031.4055
RI00011123Nicotinamide ribotide,3TMS,isomer#6JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1[N+]1=CC=CC(C(N)=O)=C1TMS551.1825Standard non polar2903.711
RI00011124Nicotinamide ribotide,3TMS,isomer#7JsmolC[Si](C)(C)NC(=O)C1=CC=C[N+]([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)=C1TMS551.1825Standard non polar2970.9302
RI00011125Nicotinamide ribotide,3TMS,isomer#8JsmolC[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1[N+]1=CC=CC(C(=O)N([Si](C)(C)C)[Si](C)(C)C)=C1TMS551.1825Standard non polar3037.6477
Displaying retention index compounds 11101 - 11125 of 1722868 in total