Date published: 2025-10-15

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Domiphen bromide (CAS 538-71-6)

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Alternate Names:
(Dodecyldimethyl-2-phenoxyethyl)ammonium bromide
Application:
Domiphen bromide is a quaternary ammonium with cationic surfactant properties
CAS Number:
538-71-6
Molecular Weight:
414.46
Molecular Formula:
CH3(CH2)11N(CH3)2(CH2CH2OC6H5)Br
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Domiphen bromide, an organic quaternary ammonium compound, has gained significant attention in scientific research due to its potent antimicrobial properties and surfactant capabilities. Its mechanism of action primarily involves disrupting the integrity of bacterial cell membranes, leading to cell lysis and death. Domiphen bromide achieves this by interacting with the negatively charged phospholipid components of bacterial cell membranes, causing membrane destabilization and permeabilization. This disrupts essential cellular processes such as nutrient uptake, ion transport, and energy production, ultimately resulting in bacterial death. In research settings, Domiphen bromide has been widely utilized as a disinfectant and preservative in microbiological studies, particularly for the inhibition of bacterial growth in laboratory cultures and experimental setups. Additionally, its surfactant properties make it useful for solubilizing hydrophobic compounds and enhancing the stability of emulsions in various biochemical assays. Moreover, Domiphen bromide has shown potential applications in the development of antimicrobial coatings for medical devices and surfaces to prevent bacterial colonization and biofilm formation. Overall, the versatile antimicrobial and surfactant properties of Domiphen bromide make it a valuable tool in research for studying microbial biology, antimicrobial resistance, and biomedical applications.


Domiphen bromide (CAS 538-71-6) References

  1. Development of a novel adenovirus purification process utilizing selective precipitation of cellular DNA.  |  Goerke, AR., et al. 2005. Biotechnol Bioeng. 91: 12-21. PMID: 15889400
  2. A reversed phase HPLC assay for the simultaneous quantitation of non-ionic and ionic surfactants in bioprocess intermediates.  |  Chen, LH., et al. 2006. J Pharm Biomed Anal. 40: 964-70. PMID: 16242286
  3. Inhibition of HERG potassium channels by domiphen bromide and didecyl dimethylammonium bromide.  |  Long, Y., et al. 2014. Eur J Pharmacol. 737: 202-9. PMID: 24846011
  4. Stressed degradation studies of domiphen bromide by LC-ESI-MS/MS identify a novel promising antimicrobial agent.  |  Fumagalli, L., et al. 2018. J Pharm Biomed Anal. 159: 224-228. PMID: 29990889
  5. Data on thermal and hydrolytic stability of both domiphen bromide and para-bromodomiphen bromide.  |  Fumagalli, L., et al. 2018. Data Brief. 20: 1363-1366. PMID: 30246118
  6. Combination of Miconazole and Domiphen Bromide Is Fungicidal against Biofilms of Resistant Candida spp.  |  Tits, J., et al. 2020. Antimicrob Agents Chemother. 64: PMID: 32690639
  7. Combining Miconazole and Domiphen Bromide Results in Excess of Reactive Oxygen Species and Killing of Biofilm Cells.  |  Tits, J., et al. 2020. Front Cell Dev Biol. 8: 617214. PMID: 33553152
  8. Proarrhythmic effects induced by benzethonium chloride and domiphen bromide in vitro and in vivo.  |  Long, Y., et al. 2021. Toxicol Appl Pharmacol. 431: 115731. PMID: 34592322
  9. Characterization of Domiphen Bromide as a New Fast-Acting Antiplasmodial Agent Inhibiting the Apicoplastidic Methyl Erythritol Phosphate Pathway.  |  Biosca, A., et al. 2022. Pharmaceutics. 14: PMID: 35890216
  10. Combining with domiphen bromide restores colistin efficacy against colistin-resistant Gram-negative bacteria in vitro and in vivo.  |  Chen, H., et al. 2024. Int J Antimicrob Agents. 63: 107066. PMID: 38135012

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Domiphen bromide, 25 g

sc-234842
25 g
$39.00