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Dodecyl trimethyl ammonium chloride
[CAS# 112-00-5]

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Identification
ClassificationSurfactant >> Cationic surfactant >> Quaternary ammonium salt type
NameDodecyl trimethyl ammonium chloride
SynonymsDodecyltrimethylammonium chloride; N,N,N-Trimethyl-1-dodecanaminium chloride; Trimethyl-1-dodecanaminium chloride; Lauryl trimethyl ammonium chloride; Laurtrimonium chloride
Molecular StructureCAS # 112-00-5, Dodecyl trimethyl ammonium chloride
Molecular FormulaC15H34N.Cl
Molecular Weight263.89
CAS Registry Number112-00-5
EC Number203-927-0
SMILESCCCCCCCCCCCC[N+](C)(C)C.[Cl-]
Properties
Melting point237 °C
Water solubilitySoluble
Safety Data
Hazard Symbolssymbol symbol symbol   GHS05;GHS07;GHS09 Danger  Details
Risk StatementsH302-H314-H315-H318-H319-H335-H400-H410-H411  Details
Safety StatementsP260-P261-P264-P264+P265-P270-P271-P273-P280-P301+P317-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P351+P338-P305+P354+P338-P316-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P363-P391-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Acute hazardous to the aquatic environmentAquatic Acute1H400
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Skin corrosionSkin Corr.1BH314
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Skin corrosionSkin Corr.1CH314
Skin corrosionSkin Corr.1AH314
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.3H301
Transport InformationUN 3077
SDSAvailable
up Discovery and Applications
Dodecyl trimethyl ammonium chloride is a quaternary ammonium compound that has been widely used as a cationic surfactant and biocide. Its chemical structure consists of a quaternary nitrogen atom bonded to a dodecyl (C12) alkyl chain and three methyl groups, with chloride as the counterion. The compound was first developed during the 20th century as part of a broader effort to create surfactants that combined surface-active properties with antimicrobial activity. Quaternary ammonium compounds like dodecyl trimethyl ammonium chloride were found to disrupt microbial cell membranes, causing leakage of cellular contents and rapid cell death. This antimicrobial mechanism made them suitable for applications in sanitation and disinfection.

In industrial and household settings, dodecyl trimethyl ammonium chloride has been applied in disinfectants, sanitizers, and cleaning products. Its ability to reduce surface tension allows it to penetrate and remove soils while simultaneously providing antimicrobial protection. It has been used in formulations for hard surface cleaning, water treatment, and in healthcare environments where control of bacterial and fungal contamination is critical. Its broad-spectrum activity against Gram-positive and Gram-negative bacteria, as well as certain fungi, contributes to its effectiveness in these applications.

The compound also finds use in personal care products, particularly in hair conditioners, shampoos, and other formulations where cationic surfactants improve wet combing, reduce static, and impart softness. The long dodecyl chain adheres to negatively charged surfaces such as hair or skin, while the cationic head reduces friction and improves manageability. In textile and fabric care, it is incorporated into fabric softeners and antistatic treatments, where it binds to fibers, reducing static cling and increasing softness and durability.

Dodecyl trimethyl ammonium chloride has been used as a phase transfer catalyst in organic synthesis due to its amphiphilic structure, allowing efficient transport of reactants between aqueous and organic phases. Its chemical stability under a wide range of pH conditions and temperatures makes it suitable for industrial-scale chemical processes. Additionally, it has applications in emulsions and dispersions, helping to stabilize formulations that include both hydrophobic and hydrophilic components.

Environmental and safety considerations have influenced the use of dodecyl trimethyl ammonium chloride. As with other quaternary ammonium compounds, it can be toxic to aquatic organisms and exhibits persistence in wastewater if not properly treated. Regulatory guidelines specify concentrations and disposal methods to mitigate environmental impact. Occupational exposure is generally controlled through standard safety practices, as the compound can cause skin or eye irritation at higher concentrations.

The development and widespread adoption of dodecyl trimethyl ammonium chloride highlight the balance between chemical functionality and safety in surfactant chemistry. Its discovery as a member of the quaternary ammonium class of compounds enabled a range of industrial, household, and personal care applications, providing effective antimicrobial action, conditioning, and antistatic properties. Over time, it has become a key ingredient in products that require the combination of surface activity, microbial control, and material conditioning, illustrating the versatility and enduring relevance of quaternary ammonium chemistry.

References

2025. Flotation Reagents of Tungsten Ore. Flotation Chemistry of Tungsten Minerals and Its Application.
DOI: 10.1007/978-981-96-5077-4_5

2025. Synthesis and Characterization of Surfactant-Modified Clays for Adsorption Applications. Characterization of Minerals, Metals, and Materials 2025.
DOI: 10.1007/978-3-031-80680-3_46

2024. Fouling-resistant reverse osmosis membranes grafted with 2-aminoethanethiol having a low interaction energy with charged foulants. npj Clean Water, 7(1).
DOI: 10.1038/s41545-024-00326-5
Market Analysis Reports
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