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Merck
CN

B4136

Benzyldimethylhexadecylammonium chloride

cationic detergent

Synonym(s):

16-BAC, Benzylhexadecyldimethylammonium chloride, Cetalkonium chloride, Cetyldimethylbenzylammonium chloride

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About This Item

Linear Formula:
CH3(CH2)15N(Cl)(CH3)2CH2C6H5
CAS Number:
122-18-9
Molecular Weight:
396.09
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
24891752
EC Number:
204-526-3
Beilstein/REAXYS Number:
3802341
MDL number:
MFCD00011625

Key Documents

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Product Name

Benzyldimethylhexadecylammonium chloride, cationic detergent

InChI key

SXPWTBGAZSPLHA-UHFFFAOYSA-M

InChI

1S/C25H46N.ClH/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-20-23-26(2,3)24-25-21-18-17-19-22-25;/h17-19,21-22H,4-16,20,23-24H2,1-3H3;1H/q+1;/p-1

SMILES string

[Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)Cc1ccccc1

form

powder

mol wt

396.09 g/mol

mp

55-65 °C (lit.)

storage temp.

room temp

Quality Level

200

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Application

Benzyldimethylhexadecylammonium chloride has been used in a study to assess the removal of cationic surfactants from aqueous solutions using activated carbon cloth (ACC). It has also been used in a study to investigate the prototropic behavior of the dye, 7-hydroxy-4-methylcoumarin (7H4MC).

General description

Benzyldimethylhexadecylammonium chloride is a cationic surfactant.

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

143.6 °F - Pensky-Martens closed cup

flash_point_c

62 °C - Pensky-Martens closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL3046
BCCF4316
BCBT7848
BCBP5098V
BCBP5098

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Zlata Grenoble et al.
The journal of physical chemistry. B, 117(1), 259-272 (2012-12-29)
The adsorption of the cationic surfactant benzyldimethylhexadecylammonium (BDMHA(+)) chloride has been studied at the hydrophilic silica-water interface by Raman spectroscopy in total internal reflection geometry (TIR Raman). This Raman spectroscopic technique takes advantage of an evanescent electric field that is
Joe J Harrison et al.
Antimicrobial agents and chemotherapy, 52(8), 2870-2881 (2008-06-04)
Biofilms are slimy aggregates of microbes that are likely responsible for many chronic infections as well as for contamination of clinical and industrial environments. Pseudomonas aeruginosa is a prevalent hospital pathogen that is well known for its ability to form
J Sánchez-Martín et al.
Journal of hazardous materials, 174(1-3), 9-16 (2009-09-29)
Natural tannin-based adsorbent has been prepared on the basis of the gelification of Quebracho bark extract. The resulting product, Quebracho Tannin Gel (QTG) was tested as cationic dye adsorbent with Methylene Blue (MB). Kinetics of adsorption process were studied out
Sharmistha Dutta Choudhury et al.
The journal of physical chemistry. B, 113(19), 6736-6744 (2009-04-21)
The prototropic behavior of the dye, 7-hydroxy-4-methylcoumarin (7H4MC), has been studied in cationic benzyldimethylhexadecylammonium chloride (BDHC) and nonionic poly(oxyethylene)(tetramethylbutyl)phenyl ether (TritonX-100, TX-100) reverse micelles using ground-state absorption and steady-state and time-resolved fluorescence measurements. The results have been compared with the
Holly D Coughenour et al.
Proteomics, 4(10), 3141-3155 (2004-09-21)
A proteomic analysis of the synaptic vesicle was undertaken to obtain a better understanding of vesicle regulation. Synaptic vesicles primarily consist of integral membrane proteins that are not well resolved on traditional isoelectric focusing/two-dimensional gel electrophoresis (IEF/2-DE) gels and are
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