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B4136

Sigma-Aldrich

Benzyldimethylhexadecylammonium chloride

cationic detergent

Synonyme(s) :

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

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About This Item

Formule linéaire :
CH3(CH2)15N(Cl)(CH3)2CH2C6H5
Numéro CAS:
122-18-9
Poids moléculaire :
396.09
Numéro Beilstein :
3802341
Numéro CE :
204-526-3
Numéro MDL:
MFCD00011625
Code UNSPSC :
12161900
ID de substance PubChem :
24891752
Nomenclature NACRES :
NA.25

Niveau de qualité

200

Forme

powder

Poids mol.

396.09 g/mol

Pf

55-65 °C (lit.)

Température de stockage

room temp

Chaîne SMILES 

[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

Clé InChI

SXPWTBGAZSPLHA-UHFFFAOYSA-M

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Description générale

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).

Pictogrammes

CorrosionExclamation markEnvironment
GHS05,GHS07,GHS09

Mention d'avertissement

Danger

Mentions de danger

H302,H314,H410

Classification des risques

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

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

143.6 °F - Pensky-Martens closed cup

Point d'éclair (°C)

62 °C - Pensky-Martens closed cup

Équipement de protection individuelle

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

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

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
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
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 Hartinger et al.
Analytical biochemistry, 240(1), 126-133 (1996-08-15)
Integral membrane proteins, particularly those with more than one transmembrane domain, have traditionally been difficult to separate by two-dimensional electrophoretic methods. Here we report the adaptation of a previously published procedure [D. E. Macfarlane (1989) Anal. Biochem. 176, 457-463] for
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