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:
Molecular Weight:
263.89
Beilstein:
3915951
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
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description
cationic
Quality Level
grade
purum
Assay
≥98.0% anhydrous basis (AT)
form
solid
mol wt
263.89 g/mol
mp
37 °C
SMILES string
[Cl-].CCCCCCCCCCCC[N+](C)(C)C
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
InChI key
DDXLVDQZPFLQMZ-UHFFFAOYSA-M
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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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
Jonas Carlstedt et al.
Physical chemistry chemical physics : PCCP, 14(27), 9574-9577 (2012-06-14)
Polyelectrolytes with amphiphilic counterions, PEACs, are water insoluble because the amphiphiles self-assemble into highly charged micelles that strongly associate with the equally highly charged polyions. However, in the presence of water soluble cyclodextrins (CDs) that form inclusion complexes with the
Marcos A Villetti et al.
The journal of physical chemistry. B, 115(19), 5868-5876 (2011-04-27)
Interactions between uncharged polymers and cationic surfactants are considered weaker than interactions with the anionic analogues. This work describes the binding occurring between methylcellulose (MC) and the cationic surfactant DTAB in aqueous medium. In the absence of salt, MC-DTAB exhibits
Ye Liu et al.
Lab on a chip, 12(19), 3746-3753 (2012-07-31)
Although biochemical sensing using liquid crystals (LC) has been demonstrated, relatively little attention has been paid towards the fabrication of in situ-formed LC sensing devices. Herein, we demonstrate a highly reproducible method to create uniform LC thin film on treated
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