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Benzyltrimethylammonium chloride
[CAS# 56-93-9]

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Complete supplier list of Benzyltrimethylammonium chloride
Identification
Classification Chemical reagent >> Organic reagent >> Amine salt (ammonium salt)
Name Benzyltrimethylammonium chloride
Synonyms BTM; N,N,N-Trimethylbenzenemethanaminium chloride; TMBAC
Molecular Structure CAS # 56-93-9, Benzyltrimethylammonium chloride, BTM, N,N,N-Trimethylbenzenemethanaminium chloride, TMBAC
Molecular Formula C10H16N.Cl
Molecular Weight 185.70
CAS Registry Number 56-93-9
EC Number 200-300-3
SMILES C[N+](C)(C)CC1=CC=CC=C1.[Cl-]
Properties
Density 0.99 g/mL (Expl.)
Melting point 230-235 ºC (dec.) (Expl.)
Refraction index 1.444 (Expl.)Water solubility|800 g/L
Safety Data
Hazard Symbols symbol symbol symbol symbol   GHS05;GHS07;GHS08;GHS09 Danger    Details
Hazard Statements H301+H311-H301-H311-H315-H319-H332-H341-H400-H412    Details
Precautionary Statements P203-P261-P262-P264-P264+P265-P270-P271-P273-P280-P301+P316-P302+P352-P304+P340-P305+P351+P338-P316-P317-P318-P321-P330-P332+P317-P337+P317-P361+P364-P362+P364-P391-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.4H332
Germ cell mutagenicityMuta.2H341
Acute toxicityAcute Tox.3H311
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Acute hazardous to the aquatic environmentAquatic Acute1H400
Acute toxicityAcute Tox.4H302
Skin corrosionSkin Corr.1BH314
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Skin corrosionSkin Corr.1H314
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H336
SDS Available
up Discovory and Applicatios
Benzyltrimethylammonium chloride is a quaternary ammonium salt with the molecular formula C9H12ClN. It is formed by the reaction of benzyl chloride with trimethylamine. The compound is typically a white or colorless crystalline solid that is soluble in water and a variety of organic solvents. As a quaternary ammonium compound, it has a positively charged nitrogen atom surrounded by three methyl groups and a benzyl group, with chloride serving as the counterion.

Benzyltrimethylammonium chloride is widely utilized in the chemical industry, particularly as a phase transfer catalyst. In this role, it facilitates the transfer of ionic species between immiscible phases, such as water and organic solvents. The compound helps accelerate reactions involving ionic reactants in one phase with non-ionic reactants in another. This ability to promote the transfer of ions across different phases makes benzyltrimethylammonium chloride valuable in a variety of organic syntheses, especially in processes where traditional methods may not be effective or efficient.

One key application of benzyltrimethylammonium chloride is in the synthesis of organic compounds. It is commonly used in nucleophilic substitution reactions, where it can enhance the reactivity of nucleophiles and electrophiles in a non-aqueous environment. This feature makes it particularly useful in processes like alkylation, acylation, and the preparation of esters. In these reactions, the compound helps solvate the ionic intermediates, thereby improving reaction rates and yields.

In addition to its use in organic synthesis, benzyltrimethylammonium chloride also finds application in the preparation of ionic liquids. Ionic liquids are salts that are in a liquid state at relatively low temperatures, and they have gained attention in recent years for their unique properties, such as low volatility, high ionic conductivity, and good solvating ability. Benzyltrimethylammonium chloride can be used as a precursor or an additive in the formation of ionic liquids, which are employed in a wide range of processes, including electrochemical applications and green chemistry initiatives.

The compound is also involved in the production of surfactants. Due to the presence of both a hydrophilic ammonium group and a hydrophobic benzyl group, benzyltrimethylammonium chloride can act as a surfactant, helping to reduce surface tension and stabilize emulsions. This property is beneficial in various cleaning applications, including in the formulation of disinfectants, detergents, and fabric softeners.

Benzyltrimethylammonium chloride has also been explored for its potential in antimicrobial applications. Like other quaternary ammonium compounds, it is thought to possess some degree of antimicrobial activity. It is believed to work by disrupting the structure of microbial cell membranes, leading to cell death. However, while it has been studied for such applications, it is primarily recognized for its utility as a chemical reagent and catalyst in industrial processes.

In terms of safety, benzyltrimethylammonium chloride should be handled with care. As with other quaternary ammonium compounds, it may cause irritation to the skin, eyes, and respiratory system upon exposure. It is important to follow proper safety protocols, including wearing appropriate personal protective equipment such as gloves, goggles, and ensuring adequate ventilation when working with this substance.

In conclusion, benzyltrimethylammonium chloride is a versatile chemical compound widely used in organic synthesis, phase transfer catalysis, the preparation of ionic liquids, and as a surfactant. Its ability to facilitate the transfer of ionic species between immiscible phases makes it particularly valuable in a variety of chemical processes. Additionally, its potential antimicrobial properties add to its range of applications in industrial and cleaning products. However, as with all chemicals, it should be handled with appropriate safety precautions.

References

2024 Supramolecular deep eutectic solvents in extraction processes: a review Environmental Chemistry Letters
DOI: 10.1007/s10311-024-01795-3

2024 Esterification of lignin-derived phenolic compound eugenol to eugenol benzoate using acidic deep eutectic solvent as a catalyst Chemical Papers
DOI: 10.1007/s11696-024-03762-2

2024 Rapid degradation of thermosetting ester epoxies and monomer recovery methods Colloid and Polymer Science
DOI: 10.1007/s00396-024-05287-2
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