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Acetaminophen Dimer: sc-479405
Acetaminophen Dimer (CAS 98966-14-4)
CAS Number:
98966-14-4
Molecular Weight:
300.31
Molecular Formula:
C16H16N2O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Acetaminophen Dimer, a dihydroxybiphenyl compound, has garnered attention in recent scientific research for its potential applications. This amphiphilic molecule possesses two hydrophobic and two hydrophilic groups, making it a valuable tool to explore interactions between various molecules. Scientists have employed Acetaminophen Dimer in various biochemical and physiological experiments, including to study of the impact of different environmental factors on biological systems.
References:
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- Removal of acetaminophen using enzyme-mediated oxidative coupling processes: I. Reaction rates and pathways. | Lu, J., et al. 2009. Environ Sci Technol. 43: 7062-7. PMID: 19806742
- Electrochemical simulation of oxidation processes involving nucleic acids monitored with electrospray ionization-mass spectrometry. | Pitterl, F., et al. 2010. Anal Bioanal Chem. 397: 1203-15. PMID: 20393841
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- The influence of the textural properties of activated carbons on acetaminophen adsorption at different temperatures. | Galhetas, M., et al. 2015. Phys Chem Chem Phys. 17: 12340-9. PMID: 25898008
- Photosensitized degradation of acetaminophen in natural organic matter solutions: The role of triplet states and oxygen. | Li, Y., et al. 2017. Water Res. 109: 266-273. PMID: 27914257
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- Formation of Larger Molecular Weight Disinfection Byproducts from Acetaminophen in Chlorine Disinfection. | Li, W., et al. 2022. Environ Sci Technol. 56: 16929-16939. PMID: 36409822
- Identification of acetaminophen polymerization products catalyzed by horseradish peroxidase. | Potter, DW., et al. 1985. J Biol Chem. 260: 12174-80. PMID: 4044591
- Removal of acetaminophen and carbamazepine in single and binary systems with immobilized laccase from Trametes hirsuta | Mohamed Hachi, Abdelmalek Chergui, Ahmed Reda Yeddou, Ammar Selatnia & Hubert Cabana. 2017. Taylor & Francis. 51-62.
- Use of delta -manganese dioxide for the removal of acetaminophen from aquatic environment: Kinetic – thermodynamic analysis and transformation products identification | Tryfon Kekes a, Maria-Christina Nika b, Fotios Tsopelas c, Nikolaos S. Thomaidis b, Constantina Tzia. 2020. Journal of Environmental, Elsevier. Volume 8, Issue 6.
- Enhanced photoelectrocatalytic degradation of acetaminophen using a bifacial electrode of praseodymium-polyethylene glycol-PbO2//Ti//TiO2-nanotubes | Bin Zhao a b, Hongbin Yu a b, Yanpeng Liu a b, Ying Lu a b, Wei Fan a b, Weichao Qin a b, Mingxin Huo a b. 2021. Elsevier Chemical Engineering Journal. 410.
- Tunable oxidative release of N-acetyl-p-benzoquinone-imine and acetamide from electrochemically derived sub-monolayer acetaminophen modified glassy carbon electrode | Hamid Salehzadeh. 2021. Journal of Electroanalytical Chemistry, Elsevier. Volume 880.