2-Amino-4,6-dichlorophenol, also known as ADCP, is a chemical compound that has various applications in everyday life. It is commonly used in the production of personal care products such as shampoos, soaps, and cosmetics, due to its antibacterial properties. In addition, ADCP is utilized in the manufacturing of agricultural chemicals and pharmaceuticals. Its relevance lies in its ability to enhance the effectiveness of these products, contributing to maintaining cleanliness, hygiene, and health in daily routines.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
2-Amino-4,6-dichlorophenol is a chemical compound that finds commercial and industrial applications in various fields. It is commonly used as a precursor in the synthesis of dyes, pigments, and pharmaceuticals due to its unique chemical properties. Additionally, it is utilized in the manufacturing of pesticides and fungicides for agricultural purposes.
In the realm of drug and medication applications, 2-Amino-4,6-dichlorophenol plays a crucial role in the production of pharmaceutical drugs. It is often incorporated as an intermediate in the synthesis of certain medications, such as antifungal agents and antibacterial drugs. Furthermore, it is utilized in the formulation of topical creams and lotions for various dermatological treatments.
Overall, 2-Amino-4,6-dichlorophenol serves as a versatile compound with diverse commercial and industrial applications. Its use in the pharmaceutical, agricultural, and chemical industries highlights its significance as a building block for various products and formulations.
⚗️ Chemical & Physical Properties
2-Amino-4,6-dichlorophenol appears as a white crystalline powder with no distinct odor. It is commonly used in the synthesis of pharmaceuticals and dyes due to its unique chemical properties.
The molar mass of 2-Amino-4,6-dichlorophenol is approximately 186.00 g/mol, with a density of about 1.49 g/cm3. This molar mass is higher than common food items such as sugar (180.16 g/mol) and salt (58.44 g/mol), while the density is similar to that of common food ingredients.
The melting point of 2-Amino-4,6-dichlorophenol is around 120-122 degrees Celsius, while the boiling point is approximately 295-300 degrees Celsius. These values are notably higher than those of common food items such as sugar (melting point: 160-186 degrees Celsius) and salt (boiling point: 801 degrees Celsius).
2-Amino-4,6-dichlorophenol is sparingly soluble in water, forming a slightly viscous solution. This solubility and viscosity are lower than that of common food items like sugar and salt, which dissolve readily in water and do not exhibit significant viscosity.
🏭 Production & Procurement
2-Amino-4,6-dichlorophenol is typically produced through a multistep synthetic process involving the chlorination of 2,4-dichlorophenol followed by amination of the resulting compound. This chemical synthesis method allows for the preparation of high purity 2-Amino-4,6-dichlorophenol for various applications in the pharmaceutical, agricultural, and chemical industries.
Once produced, 2-Amino-4,6-dichlorophenol can be procured from chemical suppliers specializing in fine chemicals and specialty intermediates. The compound is commonly packaged in drums, bags, or custom containers depending on the quantity needed by the end user. Transportation of 2-Amino-4,6-dichlorophenol is typically done via ground shipping, air freight, or ocean freight in compliance with international regulations governing the handling and transport of hazardous materials.
It is essential to ensure proper handling procedures are followed when procuring and transporting 2-Amino-4,6-dichlorophenol due to its toxic and potentially hazardous properties. Proper storage conditions, labeling, and handling practices should be observed to prevent accidental exposure and ensure product integrity during transit and storage. Suppliers and end users alike must adhere to safety guidelines and regulations set forth by regulatory authorities to maintain a safe and secure supply chain for 2-Amino-4,6-dichlorophenol.
⚠️ Safety Considerations
Safety considerations for 2-Amino-4,6-dichlorophenol must be carefully observed to prevent harm to individuals handling or being exposed to this chemical compound. It is crucial to wear appropriate personal protective equipment, such as gloves, goggles, and a lab coat, when working with 2-Amino-4,6-dichlorophenol to minimize skin contact and inhalation of fumes. The use of a fume hood is also recommended to ensure adequate ventilation and reduce the risk of exposure to hazardous vapors.
Additionally, it is important to store 2-Amino-4,6-dichlorophenol in a cool, dry place away from direct sunlight and incompatible substances to prevent chemical reactions and potential hazards. Proper labeling of containers containing this compound is essential for easy identification and to ensure that it is not mistaken for another substance. In case of accidental exposure or ingestion, immediate medical attention should be sought, and the appropriate emergency procedures followed to minimize the risk of serious health effects.
The hazard statements for 2-Amino-4,6-dichlorophenol include phrases such as “May be harmful if swallowed or inhaled,” “Causes skin and eye irritation,” and “May cause respiratory irritation.” These statements indicate the potential risks associated with exposure to 2-Amino-4,6-dichlorophenol and emphasize the importance of taking necessary precautions to prevent harm. It is crucial to handle this compound with care, wear appropriate personal protective equipment, and follow safe handling procedures to minimize the risks of adverse health effects.
Precautionary statements for 2-Amino-4,6-dichlorophenol include directives such as “Avoid breathing dust/fume/gas/mist/vapors/spray,” “Wear protective gloves/protective clothing/eye protection/face protection,” and “If in eyes, rinse cautiously with water for several minutes.” These statements provide specific recommendations on how to safely handle 2-Amino-4,6-dichlorophenol to reduce the risk of exposure and potential harm. By following these precautions, individuals can minimize the risks associated with working with this chemical compound and ensure their safety and well-being.
🔬 Potential Research Directions
Research on 2-Amino-4,6-dichlorophenol holds promising potential in the field of organic chemistry. Studies may focus on its synthesis, properties, and reactivity, contributing to a better understanding of its chemical behavior and potential applications.
Exploration of the biological activities of 2-Amino-4,6-dichlorophenol can lead to the discovery of its pharmacological properties. Research in this area may include investigating its antimicrobial, antifungal, or antiviral potential, providing insights into its possible medical applications.
Further investigations on the environmental impact of 2-Amino-4,6-dichlorophenol can shed light on its toxicological properties and degradation pathways. Studies may elucidate its persistence in the environment, potential for bioaccumulation, and effects on ecosystems, informing strategies for its management and remediation.
🧪 Related Compounds
One similar compound to 2-Amino-4,6-dichlorophenol is 2-Amino-4,6-dibromophenol. This compound shares the same molecular structure as 2-Amino-4,6-dichlorophenol, with the only difference being the substitution of chlorine atoms with bromine atoms. This leads to similar chemical properties and potential applications in various fields such as pharmaceuticals or organic synthesis.
Another compound that is structurally similar to 2-Amino-4,6-dichlorophenol is 2-Amino-6-methyl-4-chlorophenol. In this compound, the chlorine atom is positioned at a different carbon atom than in 2-Amino-4,6-dichlorophenol, but the overall molecular structure remains comparable. This similarity in structure may result in similar reactivity and potential uses in chemical processes.
Additionally, a compound with resemblance to 2-Amino-4,6-dichlorophenol is 2-Amino-4,6-difluorophenol. The difference in this compound lies in the substitution of chlorine atoms with fluorine atoms. Despite this variation, the overall molecular structure is akin to that of 2-Amino-4,6-dichlorophenol, potentially leading to comparable properties and applications in various chemical contexts.
