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Merck
CN

278602

1-Dodecylpyridinium chloride hydrate

98%

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About This Item

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

1-Dodecylpyridinium chloride hydrate, 98%

InChI key

BDGGUWSWAKGEGH-UHFFFAOYSA-M

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

SMILES string

[Cl-].[H]O[H].CCCCCCCCCCCC[n+]1ccccc1

assay

98%

form

liquid crystal

mp

66-70 °C (lit.)

Quality Level

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.

General description

Dodecylpyridinium chloride is a cationic surfactant.

Legal Information

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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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