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Merck
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B4136

Sigma-Aldrich

Benzyldimethylhexadecylammonium chloride

cationic detergent

Sinónimos:

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

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About This Item

Fórmula lineal:
CH3(CH2)15N(Cl)(CH3)2CH2C6H5
Número de CAS:
122-18-9
Peso molecular:
396.09
Beilstein/REAXYS Number:
3802341
EC Number:
204-526-3
MDL number:
MFCD00011625
UNSPSC Code:
12161900
PubChem Substance ID:
24891752
NACRES:
NA.25

Quality Level

200

form

powder

mol wt

396.09 g/mol

mp

55-65 °C (lit.)

storage temp.

room temp

SMILES string

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

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

InChI key

SXPWTBGAZSPLHA-UHFFFAOYSA-M

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General description

Benzyldimethylhexadecylammonium chloride is a cationic surfactant.

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).

signalword

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_germany

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
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
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
D E Macfarlane
Analytical biochemistry, 132(2), 231-235 (1983-07-15)
A discontinuous polyacrylamide gel system operating at pH 4.0-1.5 which resolves proteins bearing base labile groups extracted from intact cells is described. It uses potassium phosphate buffer in the running and stacking gel and glycine as the trailing ion component.
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