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Merck

17104

Dodecyltrimethylammonium chloride

purum, ≥98.0% anhydrous basis (AT)

Synonym(s):

DTAC

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About This Item

Linear Formula:
CH3(CH2)11N(CH3)3Cl
CAS Number:
112-00-5
Molecular Weight:
263.89
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
329751486
EC Number:
203-927-0
Beilstein/REAXYS Number:
3915951
MDL number:
MFCD00041974

Key Documents

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InChI key

DDXLVDQZPFLQMZ-UHFFFAOYSA-M

InChI

1S/C15H34N.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16(2,3)4;/h5-15H2,1-4H3;1H/q+1;/p-1

SMILES string

[Cl-].CCCCCCCCCCCC[N+](C)(C)C

description

cationic

grade

purum

assay

≥98.0% anhydrous basis (AT)

form

solid

mol wt

263.89 g/mol

Quality Level

200

reaction suitability

core: ammonium

mp

37 °C

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General description

Dodecyltrimethylammonium chloride is a quaternary ammonium compound (QAC) commonly used as a cationic surfactant. It is used in antimicrobial sanitizers due to its surface activity and germicidal efficiency.

Application

  • Polyethylene terephthalate depolymerization: Dodecyltrimethylammonium chloride was applied in the enzymatic depolymerization of polyethylene terephthalate, illustrating its utility in enhancing the efficiency of plastic degradation processes (Kawai et al., 2022).

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP3481
BCCN9932
BCCN7691
BCCN6792
BCCN1505

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Sorption of dodecyltrimethylammonium chloride (DTAC) to agricultural soils.
Xiang L Sun
The Science of the Total Environment, 560, 197-203 (2016)
Pathogenicity of dodecyltrimethylammonium chloride-resistant Salmonella enterica.
Kautz MJ
Applied and Environmental Microbiology, 79(7), 2371-2376 (2013)
Marta Baptista et al.
Fertility and sterility, 99(3), 705-712 (2012-12-12)
To determine the mechanisms of spermicidal activity by cationic compounds. In vitro study with human sperm. Academic research institute in collaboration with a university hospital. Normozoospermic men providing samples for routine analysis or assisted reproductive technologies. In vitro incubation of sperm with
I Echavarri Franco et al.
Langmuir : the ACS journal of surfaces and colloids, 28(10), 4815-4828 (2012-02-16)
The binding of cationic surfactants with varying alkyl chain length to a regiorandom conjugated polyanion, poly(3-thiophene acetic acid) (PTAA), is studied in an aqueous buffer by using absorption and emission spectroscopies, photon correlation spectroscopy, isothermal titration calorimetry, and cryogenic transmission
Sriram Sokalingam et al.
PloS one, 7(7), e40410-e40410 (2012-07-14)
Two positively charged basic amino acids, arginine and lysine, are mostly exposed to protein surface, and play important roles in protein stability by forming electrostatic interactions. In particular, the guanidinium group of arginine allows interactions in three possible directions, which
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