Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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(4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1 | 2726.5 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1 | 2708.2 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1 | 2699.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1 | 2701.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1 | 2721.8 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1 | 2706.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #10 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2669.1 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1 | 2700.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1 | 2698.6 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1 | 2680.1 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1 | 2692.1 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #6 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1 | 2687.2 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #7 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1 | 2673.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #8 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1 | 2703.6 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TMS,isomer #9 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1 | 2654.2 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1 | 2715.5 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #10 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2662.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1 | 2722.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1 | 2657.6 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1 | 2712.6 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1 | 2654.5 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #6 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2656.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #7 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1 | 2715.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #8 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1 | 2650.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TMS,isomer #9 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2664.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1 | 2761.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1 | 2664.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2699.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2659.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2638.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,5TMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1 | 2727.3 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TBDMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1 | 2960.4 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TBDMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1 | 2957.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TBDMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1 | 2951.1 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TBDMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 2953.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,1TBDMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 2961.2 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1 | 3160.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #10 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3129.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1 | 3154.2 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3154.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3108.3 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1 | 3168.5 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #6 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3164.4 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #7 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3129.9 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #8 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3172.8 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,2TBDMS,isomer #9 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3107.1 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1 | 3396.3 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #10 | C=C(C)C1CC=C(COC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3327.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3405.8 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3323.4 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3397.1 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3302.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #6 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3321.0 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #7 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3393.8 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #8 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3312.5 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,3TBDMS,isomer #9 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3318.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TBDMS,isomer #1 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1 | 3631.8 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TBDMS,isomer #2 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1 | 3518.5 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TBDMS,isomer #3 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3553.7 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TBDMS,isomer #4 | C=C(C)C1CC=C(COC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3523.3 | Semi standard non polar | 33892256 | (4S,6R)-p-Mentha-1,8-diene-6,7-diol 7-glucoside,4TBDMS,isomer #5 | C=C(C)C1CC=C(COC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1 | 3502.8 | Semi standard non polar | 33892256 |
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