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1-Dodecylpyridinium chloride hydrate

98%

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About This Item

Empirical Formula (Hill Notation):
C17H30ClN · xH2O
CAS Number:
207234-02-4
Molecular Weight:
283.88 (anhydrous basis)
EC Number:
203-232-2
MDL number:
MFCD00150002
UNSPSC Code:
12352103
PubChem Substance ID:
24856822
NACRES:
NA.23

Quality Level

100

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Clouding behavior of nonionic?cationic and nonionic?anionic mixed surfactant systems in presence of carboxylic acids and their sodium salts
Jan M, et al.
Coll. Polymer Sci., 285(6), 631-640 null
Co- and Counterion Effect on the Micellization Characteristics of Dodecylpyridinium Chloride,
Bhat MA, et al.
Journal of Dispersion Science and Technology, 29(4) null
Synthesis and properties of cationic surfactants with tuned hydrophylicity
Quagliotto P, et al.
Journal of Colloid and Interface Science, 340(2), 269-276 (2009)
D B França et al.
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
Daniel Ondo et al.
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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