2,4-Dichlorobenzylamine is a chemical compound that has various practical applications in everyday life. It is commonly utilized as an active ingredient in household disinfectants, mouthwashes, and other cleaning products due to its powerful antimicrobial properties. Additionally, it is used in the production of pharmaceuticals and pesticides. Overall, 2,4-Dichlorobenzylamine plays a significant role in maintaining cleanliness and hygiene in daily routines and various industries.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
2,4-Dichlorobenzylamine, commonly known as DCBA, is primarily used in commercial and industrial applications. It is frequently employed as a key ingredient in the manufacturing of various pesticides and fungicides due to its effectiveness in controlling pests and diseases in agricultural settings. Additionally, DCBA is utilized in the production of disinfectants and sanitizers for use in healthcare facilities and household cleaning products.
In the realm of drug and medication applications, 2,4-Dichlorobenzylamine plays a crucial role as an antiseptic and antimicrobial agent. It is commonly found in throat lozenges and mouthwashes to help combat bacterial and fungal infections in the oral cavity. Furthermore, DCBA is utilized in pharmaceutical formulations to treat various skin infections and as a preservative in ophthalmic solutions to prevent microbial contamination.
⚗️ Chemical & Physical Properties
2,4-Dichlorobenzylamine appears as white crystalline solid with a faint odor. It is a derivative of benzylamine and is commonly used in the synthesis of pharmaceuticals and agrochemicals.
The molar mass of 2,4-Dichlorobenzylamine is approximately 175.02 g/mol, with a density of around 1.27 g/cm³. This places it in the range of common food items such as sugar (molar mass of 342.30 g/mol, density of 1.59 g/cm³) and salt (molar mass of 58.44 g/mol, density of 2.17 g/cm³).
The melting point of 2,4-Dichlorobenzylamine is approximately 66-68°C, while the boiling point is around 251-253°C. In comparison, common food items like butter (melting point around 32-35°C) and water (boiling point of 100°C) exhibit lower melting and boiling points.
2,4-Dichlorobenzylamine is sparingly soluble in water and exhibits low viscosity. This is in contrast to common food items like sugar and salt, which are highly soluble in water, and honey, which has high viscosity.
🏭 Production & Procurement
2,4-Dichlorobenzylamine is typically produced through a series of chemical reactions starting with the chlorination of benzylamine to form 4-chlorobenzylamine. This compound is then further chlorinated to produce 2,4-Dichlorobenzylamine. The process involves meticulous control of reaction conditions to ensure a high yield of the desired product.
2,4-Dichlorobenzylamine can be procured from chemical suppliers who specialize in producing and distributing fine chemicals. It is commonly available in both liquid and solid forms, depending on the intended application. Transportation of 2,4-Dichlorobenzylamine is conducted in accordance with strict safety regulations to prevent leaks or spills during transit.
Once procured, 2,4-Dichlorobenzylamine is typically packaged in sealed containers to prevent contamination or degradation. It is important to store the compound in a cool, dry place away from direct sunlight and sources of heat to maintain its stability. Proper labeling and handling procedures should be followed to ensure safe use and storage of 2,4-Dichlorobenzylamine.
⚠️ Safety Considerations
Safety considerations for 2,4-Dichlorobenzylamine should be taken seriously due to its potential hazards. This compound is known to be harmful if swallowed, inhaled, or in contact with skin and eyes. In case of exposure, immediate medical attention should be sought.
It is important to handle 2,4-Dichlorobenzylamine with caution to prevent any accidents or health risks. This chemical should be stored in a well-ventilated area, away from heat, sparks, or open flames. Personal protective equipment such as gloves, goggles, and a lab coat should be worn when handling this compound to minimize exposure.
Hazard statements for 2,4-Dichlorobenzylamine include “Causes skin irritation,” “Causes serious eye irritation,” and “Harmful if swallowed.” These statements indicate the potential dangers associated with this compound and the importance of handling it with care to avoid any negative effects on health.
Precautionary statements for 2,4-Dichlorobenzylamine include “Wash hands thoroughly after handling,” “Wear protective gloves/eye protection/face protection,” and “IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.” These statements provide guidance on how to safely handle this compound and what steps to take in case of accidental exposure. It is essential to follow these precautions to minimize the risks associated with 2,4-Dichlorobenzylamine.
🔬 Potential Research Directions
One potential research direction for 2,4-Dichlorobenzylamine involves investigating its pharmacological properties, particularly its potential use as a therapeutic agent in the treatment of various medical conditions. Studies could focus on its impact on specific biological pathways or cellular targets to elucidate its mechanism of action and potential efficacy in preclinical and clinical settings.
Another avenue for research on 2,4-Dichlorobenzylamine is exploring its potential use as a precursor in the synthesis of novel organic compounds with biological activity. Investigations could aim to identify new derivatives with improved pharmacological profiles or enhanced bioavailability for therapeutic applications. Additionally, studies could focus on developing efficient synthetic methods for the production of these compounds on a larger scale for commercial purposes.
🧪 Related Compounds
One similar compound to 2,4-Dichlorobenzylamine is 2,3-Dichlorobenzylamine. In this compound, the amino group is attached to the benzene ring at the 2 and 3 positions, similar to 2,4-Dichlorobenzylamine. This results in the presence of two chlorine atoms on the benzene ring, providing similar chemical properties.
Another similar compound is 3,4-Dichlorobenzylamine, where the amino group is located at the 3 and 4 positions on the benzene ring. Like 2,4-Dichlorobenzylamine, this compound contains two chlorine atoms on the benzene ring, contributing to its similar chemical properties. The presence of the amino group in a different positional isomer affects the reactivity and properties of the compound.
Additionally, 2,5-Dichlorobenzylamine is a compound with the amino group attached to the benzene ring at the 2 and 5 positions. This compound shares similarities with 2,4-Dichlorobenzylamine in terms of having two chlorine atoms on the benzene ring. The positioning of the amino group on the benzene ring influences the compound’s reactivity and potential applications in various chemical processes.
