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| | 2,4,6-Trimethylphenol-d11 Basic information |
| | 2,4,6-Trimethylphenol-d11 Chemical Properties |
| Boiling point | 215.824±9.00 °C(Press: 760.00 Torr)(predicted) | | density | 0.996±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | solubility | Chloroform (Slightly), DMSO (Slightly) | | pka | 10.974±0.23(predicted) | | form | Solid | | color | White to Off-White |
| | 2,4,6-Trimethylphenol-d11 Usage And Synthesis |
| Uses | 2,4,6-Trimethylphenol-d11 is the deuterium labeled 2,4,6-Trimethylphenol[1]. 2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter (3DOM*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution[2][3]. | | References | [1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110
[2] Rosado-Lausell SL, et al. Roles of singlet oxygen and triplet excited state of dissolved organic matter formed by different organic matters in bacteriophage MS2 inactivation. Water Res. 2013;47(14):4869-4879. DOI:10.1016/j.watres.2013.05.018
[3] Paul G.Tratnyek, et al. Photo-oxidation of 2,4,6-trimethylphenol in aqueous laboratory solutions and natural waters: kinetics of reaction with singlet oxygen. Journal of Photochemistry and Photobiology A: Chemistry. Volume 84, Issue 2, 6 December 1994, Pages 153-160.
[4] Libby RD, et al. Defining the involvement of HOCl or Cl2 as enzyme-generated intermediates in chloroperoxidase-catalyzed reactions. J Biol Chem. 1992;267(3):1769-1775. PMID:1309797 |
| | 2,4,6-Trimethylphenol-d11 Preparation Products And Raw materials |
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