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Dodecyltrimethylammonium Chloride (CAS 112-00-5)

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Alternate Names:
DTAC
Application:
Dodecyltrimethylammonium Chloride is a useful quaternary ammonium salt
CAS Number:
112-00-5
Purity:
≥99%
Molecular Weight:
263.89
Molecular Formula:
C15H34ClN
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Dodecyltrimethylammonium chloride (DTAC) is a quaternary ammonium compound extensively studied for its surfactant properties and various research applications. Its mechanism of action primarily involves disrupting the structure and function of biological membranes. DTAC′s hydrophobic tail interacts with lipid bilayers, while its positively charged headgroup interacts with negatively charged components on cell membranes, leading to membrane destabilization. This disrupts membrane integrity and permeability, causing leakage of cellular contents and ultimately cell death. In research, DTAC has been widely employed as a surfactant in molecular biology techniques such as DNA extraction, purification, and manipulation. Its ability to solubilize and denature proteins makes it valuable in protein extraction and membrane protein solubilization. Additionally, DTAC is utilized in various analytical methods, including spectrophotometry and chromatography, for its ability to enhance solubility and facilitate separation of analytes. Furthermore, DTAC′s surfactant properties have found applications in nanoparticle synthesis, drug delivery systems, and colloidal stabilization. Overall, DTAC′s mechanism of action in disrupting biological membranes and its versatile applications in research make it a valuable tool in various scientific disciplines, ranging from molecular biology to nanotechnology.


Dodecyltrimethylammonium Chloride (CAS 112-00-5) References

  1. Micellar behavior of aqueous solutions of dodecyldimethylethylammonium bromide, dodecyltrimethylammonium chloride and tetradecyltrimethylammonium chloride in the presence of alpha-, beta-, HPbeta- and gamma-cyclodextrins.  |  Mehta, SK., et al. 2008. J Colloid Interface Sci. 321: 442-51. PMID: 18342875
  2. Temperature and salt-induced micellization of dodecyltrimethylammonium chloride in aqueous solution: a thermodynamic study.  |  Sarac, B. and Bester-Rogac, M. 2009. J Colloid Interface Sci. 338: 216-21. PMID: 19596125
  3. Pathogenicity of dodecyltrimethylammonium chloride-resistant Salmonella enterica.  |  Kautz, MJ., et al. 2013. Appl Environ Microbiol. 79: 2371-6. PMID: 23377943
  4. Salicylate isomer-specific effect on the micellization of dodecyltrimethylammonium chloride: large effects from small changes.  |  Šarac, B., et al. 2013. Langmuir. 29: 4460-9. PMID: 23477611
  5. Molecular Dynamics Simulations of Adsorption of Poly(acrylic acid) and Poly(methacrylic acid) on Dodecyltrimethylammonium Chloride Micelle in Water: Effect of Charge Density.  |  Sulatha, MS. and Natarajan, U. 2015. J Phys Chem B. 119: 12526-39. PMID: 26355463
  6. Sorption of dodecyltrimethylammonium chloride (DTAC) to agricultural soils.  |  Xiang, L., et al. 2016. Sci Total Environ. 560-561: 197-203. PMID: 27101455
  7. Foam Separation of Dyes Using Anionic, Cationic, and Amphoteric Surfactants.  |  Goto, Y., et al. 2020. J Oleo Sci. 69: 549-555. PMID: 32522916
  8. Anti-biofilm activity of dodecyltrimethylammonium chloride microcapsules against Salmonella enterica serovar Enteritidis and Staphylococcus aureus.  |  Khelissa, S., et al. 2021. Biofouling. 37: 49-60. PMID: 33522301
  9. Photoionization of 3-Methylindole Embedded in Sodium Dodecyl Sulfate and Dodecyltrimethylammonium Chloride Micelles: Migration of Electrons Generated in Micelle Cores and Their Solvation in Outside Water.  |  Goryo, S. and Iwata, K. 2023. J Phys Chem Lett. 14: 1479-1484. PMID: 36744965

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dodecyltrimethylammonium Chloride, 100 mg

sc-211373
100 mg
$260.00