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Merck
CN

B5776

Benzyldodecyldimethylammonium bromide

Synonym(s):

Benzyldimethyldodecylammonium bromide

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About This Item

Linear Formula:
CH3(CH2)11N(Br)(CH3)2CH2C6H5
CAS Number:
Molecular Weight:
384.44
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
EC Number:
230-698-4
Beilstein/REAXYS Number:
3579193
MDL number:
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InChI key

KHSLHYAUZSPBIU-UHFFFAOYSA-M

InChI

1S/C21H38N.BrH/c1-4-5-6-7-8-9-10-11-12-16-19-22(2,3)20-21-17-14-13-15-18-21;/h13-15,17-18H,4-12,16,19-20H2,1-3H3;1H/q+1;/p-1

SMILES string

[Br-].CCCCCCCCCCCC[N+](C)(C)Cc1ccccc1

description

cationic

assay

≥96.5% (TLC)

form

powder

mol wt

384.44 g/mol

storage temp.

2-8°C

Quality Level

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Application

Benzyldodecyldimethylammonium bromide has been used in a study to assess the relation between chemical structure and germicidal efficacy in surface-active cations. It has also been used in a study to investigate pore size control during the synthesis of macroporous thermosensitive poly(N-isopropylacrylamide) hydrogels.

General description

Benzyldodecyldimethylammonium bromide is a cationic surfactant that may be used as an adsorbent for certain metals such as Cr(VI).

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Qian Zhao et al.
Langmuir : the ACS journal of surfaces and colloids, 25(5), 3249-3254 (2009-05-14)
Macroporous thermosensitive poly(N-isopropylacrylamide) hydrogels were synthesized in the presence of dodecyl dimethyl benzyl ammonium bromide (DDBAB). Poly(vinyl alcohol) (PVA) was involved to control the pore size of the hydrogels. The morphology of the resulting hydrogels was studied by both an
Biosorption of Cr(VI) from simulated wastewater using a cationic surfactant modified spent mushroom
Jing, et al.
Desalination, 269, 8-8 (2011)
Correlation between Antibacterial Power and Chemical Structure of Higher Alkyl Ammonium Ions.
E I Valko et al.
Journal of bacteriology, 50(4), 481-490 (1945-10-01)
Bozenna Rózycka-Roszak et al.
Chemistry and physics of lipids, 123(2), 209-221 (2003-04-15)
The interaction of N-dodecyl-N,N-dimethyl-N-benzylammonium halides (DBeAX) with two types of phospholipid vesicles (MLV and SUV) was investigated using DSC and 1H NMR. It was suggested that the benzyl group like the micellisation process (J. Colloid Interface Sci. 218 (1999) 529)
Mikrocalorimetric studies on the interaction of N-dodecyl-N,N-dimethyl-N-benzylammonium halides with phosphatidylcholine bilayers: a counterion effect.
Bozenna Rózycka-Roszak et al.
Cellular & molecular biology letters, 7(2), 298-298 (2002-07-05)

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