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Merck

C8147

Hexadecyltrimethylammonium p-toluenesulfonate

Synonym(s):

Cetyltrimethylammonium p-toluenesulfonate

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About This Item

Linear Formula:
CH3(CH2)15N(CH3C6H4SO3)(CH3)3
CAS Number:
138-32-9
Molecular Weight:
455.74
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
24893030
EC Number:
205-324-8
Beilstein/REAXYS Number:
5470332
MDL number:
MFCD00061383

Key Documents

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InChI key

MZMRZONIDDFOGF-UHFFFAOYSA-M

InChI

1S/C19H42N.C7H8O3S/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(2,3)4;1-6-2-4-7(5-3-6)11(8,9)10/h5-19H2,1-4H3;2-5H,1H3,(H,8,9,10)/q+1;/p-1

SMILES string

Cc1ccc(cc1)S([O-])(=O)=O.CCCCCCCCCCCCCCCC[N+](C)(C)C

description

cationic

assay

≥98.0% (HPLC)

form

powder

mol wt

455.74 g/mol

Quality Level

100

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Application

Hexadecyltrimethylammonium p-toluenesulfonate has been used in a study to develop a silica grafted polydentate copper (II) complex. It has also been used in a study to investigate the dispersibility and bundle defoliation of single-walled carbon nanotubes.

General description

Hexadecyltrimethylammonium p-toluenesulfonate is a catatonic surfactant capable of forming wormlike micelles.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - 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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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8498
STBJ7490
STBJ7109
STBJ2580
STBH3046

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Lucia Zakharova et al.
Journal of colloid and interface science, 342(1), 119-127 (2009-11-07)
New amphiphilic pyrimidinic (AP) compounds with two ammonium head groups and different kinds of counterions, inorganic bromide anions (APB) and hydrophobic tosylate anions (APT) were synthesized. Self-organization in these systems has been studied by methods of tensiometry, conductometry, potentiometry and
A Fischer et al.
Journal of colloid and interface science, 248(1), 163-168 (2005-11-18)
The sodium dodecyl benzene sulfonate (SDBS)/cetyltrimethyl-ammonium tosylate (CTAT)/water ternary system has previously been shown to give rise to the formation of vesicles for well-defined compositions requiring an excess of one of the surfactants over the other. Two types of vesicular
Sara B Lioi et al.
Physical chemistry chemical physics : PCCP, 11(41), 9315-9325 (2009-10-16)
Mixtures of oppositely charged surfactants, commonly called catanionic mixtures, are one of the most interesting and promising areas of colloidal chemistry. In this paper we review our previous work and report new results on electrostatic adsorption of organic solutes and
Yongqiang Tan et al.
The journal of physical chemistry. B, 109(30), 14454-14460 (2006-07-21)
The dispersibility and bundle defoliation of single-walled carbon nanotubes (SWNTs) of small diameter (<1 nm) have been evaluated on CoMoCAT samples with narrow distribution of diameters. As previously observed by photoluminescence and Raman spectroscopy, the CoMoCAT sample exhibits a uniquely
N Tepale et al.
Journal of colloid and interface science, 363(2), 595-600 (2011-08-27)
The shear thickening behavior and the transition to shear thinning are examined in dilute cetyltrimethylammonium tosylate (CTAT) micellar solutions as a function of surfactant concentration and ionic strength using electrolytes with different counterion valence. Newtonian behavior at low shear rates
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