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Assay
98%
form
liquid crystal
mp
66-70 °C (lit.)
SMILES string
[Cl-].[H]O[H].CCCCCCCCCCCC[n+]1ccccc1
InChI
1S/C17H30N.ClH.H2O/c1-2-3-4-5-6-7-8-9-10-12-15-18-16-13-11-14-17-18;;/h11,13-14,16-17H,2-10,12,15H2,1H3;1H;1H2/q+1;;/p-1
InChI key
BDGGUWSWAKGEGH-UHFFFAOYSA-M
Related Categories
General description
Dodecylpyridinium chloride is a cationic surfactant.
Application
Micellization characteristics of dodecylpyridinium chloride have been studied. Properties such as molar conductivity, surface tension and surface adsorption parameters has been reported. A non-ionic-cationic mixed system composed of Triton X-100™ and dodecylpyridinium chloride respectively was studied for its clouding behavior.
Legal Information
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis and properties of cationic surfactants with tuned hydrophylicity
Journal of Colloid and Interface Science, 340(2), 269-276 (2009)
Clouding behavior of nonionic?cationic and nonionic?anionic mixed surfactant systems in presence of carboxylic acids and their sodium salts
Coll. Polymer Sci., 285(6), 631- 640 null
Chemosphere, 242, 125109-125109 (2019-11-02)
Organoclays have been applied as efficient adsorbents for pharmaceutical pollutants from aqueous solution. In this work, dodecylpyridinium chloride (C12pyCl) and hexadecylpyridinium chloride (C16pyCl) cationic surfactants were used for the preparation of organobentonites destined for diclofenac sodium (DFNa) adsorption, an anionic
Co- and Counterion Effect on the Micellization Characteristics of Dodecylpyridinium Chloride,
Journal of Dispersion Science and Technology, 29(4) null
Journal of colloid and interface science, 505, 445-453 (2017-06-20)
The interaction of α-cyclodextrin (α-CD) with ten ionic surfactants (S) in water was systematically examined using isothermal titration calorimetry. The S comprised cationic and anionic head groups while the hydrocarbon alkyl chain length varied from eight to fourteen carbon atoms.
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