2,4-Dichlorophenyl benzenesulfonate 

2,4-Dichlorophenyl benzenesulfonate is a chemical compound that is utilized in a variety of household and industrial products. It is commonly found in household cleaners, detergents, and disinfectants as a surfactant and emulsifier. Additionally, it is used in the manufacturing of pharmaceuticals, agricultural chemicals, and personal care products.

In everyday life, consumers may encounter products containing 2,4-Dichlorophenyl benzenesulfonate when cleaning their homes, doing laundry, or using personal care items. Its presence in these products helps to improve their effectiveness by allowing them to better dissolve dirt, grease, and other contaminants.

Overall, 2,4-Dichlorophenyl benzenesulfonate plays a significant role in enhancing the performance of various household and industrial products, making it a relevant compound in everyday life.

Table of Contents:

💡  Commercial Applications

2,4-Dichlorophenyl benzenesulfonate, also known as 2,4-DCPB, has several commercial and industrial applications. It is commonly used as a fluorescent dye intermediate for the manufacturing of fluorescent brighteners, which are additives used in laundry detergents to make clothes appear whiter.

In addition to its use as a fluorescent dye intermediate, 2,4-Dichlorophenyl benzenesulfonate is also utilized in the production of optical brighteners, which are chemicals that absorb ultraviolet light and re-emit it as visible light, enhancing the brightness of textiles, paper, and plastics.

While 2,4-Dichlorophenyl benzenesulfonate is primarily used in commercial and industrial applications, it also has some drug and medication applications. It has been studied for its potential use as an antitumor agent due to its ability to inhibit the growth of cancer cells. Additionally, it has shown promise as an antimicrobial agent in the field of pharmaceuticals.

⚗️  Chemical & Physical Properties

2,4-Dichlorophenyl benzenesulfonate appears as a white crystalline powder with a faint odor.

This compound has a molar mass of approximately 305.13 g/mol and a density of 1.49 g/cm^3. Compared to common food items like sugar (molar mass of 342.30 g/mol, density of 1.59 g/cm^3) and salt (molar mass of 58.44 g/mol, density of 2.16 g/cm^3), 2,4-Dichlorophenyl benzenesulfonate is lighter and less dense.

The melting point of 2,4-Dichlorophenyl benzenesulfonate is around 150-152°C, while the boiling point is approximately 370°C. In comparison, common food items like butter (melting point of 32-35°C, boiling point around 120°C) and chocolate (melting point of 30-32°C, boiling point of 160-170°C) have lower melting and boiling points.

2,4-Dichlorophenyl benzenesulfonate is sparingly soluble in water and exhibits high viscosity. This is in contrast to common food items like salt and sugar, which are highly soluble in water and have low viscosity.

🏭  Production & Procurement

2,4-Dichlorophenyl benzenesulfonate is typically produced through a multi-step synthetic process involving the reaction of 2,4-dichlorobenzenesulfonyl chloride with phenyl magnesium bromide. This reaction leads to the formation of the desired product, 2,4-Dichlorophenyl benzenesulfonate, which can be further purified through various techniques such as recrystallization.

In terms of procurement and transportation, 2,4-Dichlorophenyl benzenesulfonate can be obtained from chemical suppliers or manufacturers that specialize in producing sulfonate compounds. Once procured, the compound can be stored and transported in sealed containers to prevent contamination or degradation. Proper labeling and handling instructions should be followed to ensure safe and efficient transportation of 2,4-Dichlorophenyl benzenesulfonate to its intended destination.

⚠️  Safety Considerations

Safety considerations for 2,4-Dichlorophenyl benzenesulfonate include the need to handle the chemical with caution to avoid skin and eye contact. It is important to wear appropriate personal protective equipment such as gloves and safety goggles when working with this substance. Additionally, 2,4-Dichlorophenyl benzenesulfonate should be stored in a cool, dry, well-ventilated area away from incompatible materials to prevent potential hazards.

The hazard statements for 2,4-Dichlorophenyl benzenesulfonate include warnings of skin and eye irritation, as well as the potential for serious eye damage. Inhalation of the substance may cause respiratory irritation, and prolonged or repeated exposure may lead to adverse health effects. It is important to handle this chemical with care and adhere to safety guidelines to minimize the risk of harm.

Precautionary statements for 2,4-Dichlorophenyl benzenesulfonate include recommendations to wear protective gloves, clothing, and eye protection when handling the substance. Avoid breathing in dust, fumes, gas, mist, vapors, or spray and wash hands thoroughly after handling. In case of skin irritation or rash, seek medical attention, and if the chemical is ingested or comes into contact with the eyes, seek immediate medical advice and show the container or label.

🔬  Potential Research Directions

Possible research directions for 2,4-Dichlorophenyl benzenesulfonate include exploring its potential as a building block for the synthesis of new chemical compounds with diverse applications.

Further investigation could focus on its environmental fate, including its degradation pathways and potential impacts on ecosystems.

In addition, research may delve into its pharmacological properties, exploring its potential as a drug candidate for various medical conditions.

One similar compound to 2,4-Dichlorophenyl benzenesulfonate is 2,5-Dichlorophenyl benzenesulfonate. This compound has a molecular structure similar to 2,4-Dichlorophenyl benzenesulfonate, but with chlorine atoms at the 2 and 5 positions on the phenyl ring instead of the 2 and 4 positions.

Another similar compound is 3,4-Dichlorophenyl benzenesulfonate. This compound also has a molecular structure resembling 2,4-Dichlorophenyl benzenesulfonate, but with chlorine atoms at the 3 and 4 positions on the phenyl ring. The presence of these chlorine atoms gives both compounds similar physical and chemical properties.

Additionally, 2,3-Dichlorophenyl benzenesulfonate is another compound closely related to 2,4-Dichlorophenyl benzenesulfonate. In this compound, the chlorine atoms are positioned at the 2 and 3 positions on the phenyl ring. The molecular structure similarity between these compounds suggests they may share similar biological activities or uses in various applications.

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