4-Methoxy-2-methylaniline, a chemical compound commonly known as Anisidine, holds significant relevance to everyday life due to its wide utilization in various industries. This compound is primarily employed in the production of dyes, pharmaceuticals, and pesticides, making it a crucial ingredient in the manufacturing of a myriad of consumer products. Furthermore, 4-Methoxy-2-methylaniline plays a vital role in the development of advanced materials such as conductive polymers and photochromic substances, thereby influencing numerous aspects of modern living ranging from fashion to technology. Its versatility and importance in multiple sectors underscore its prominence in everyday life.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
4-Methoxy-2-methylaniline, also known as Anisidine, has several commercial and industrial applications. It is commonly used as a dye intermediate in the production of various synthetic dyes. Additionally, it is used as a chemical intermediate in the manufacturing of pharmaceuticals, agrochemicals, and other specialty chemicals.
In the pharmaceutical industry, 4-Methoxy-2-methylaniline is employed in the synthesis of some drugs and medications. It is utilized in the production of certain anti-inflammatory drugs and as an intermediate in the manufacturing of some antibiotics. Due to its chemical properties, it is also used in the creation of pharmaceuticals for specific medical conditions.
Furthermore, 4-Methoxy-2-methylaniline finds applications in the field of agrochemicals. It is utilized in the synthesis of pesticides and herbicides to protect crops from pests and diseases. Its chemical structure allows it to be a key component in the formulation of effective agricultural products used to enhance crop yields and quality.
⚗️ Chemical & Physical Properties
4-Methoxy-2-methylaniline, a compound also known as p-Anisidine, appears as a colorless to light yellow liquid with a faint amine odor. This chemical is commonly used in the production of dyes, pharmaceuticals, and agricultural chemicals due to its unique properties.
The molar mass of 4-Methoxy-2-methylaniline is approximately 153.2 g/mol, and its density is around 1.07 g/cm³. In comparison to common food items, this compound has a lower molar mass than glucose (180.2 g/mol) and a similar density to vegetable oil (0.92 g/cm³).
With a melting point of approximately 7.5°C and a boiling point of around 243-245°C, 4-Methoxy-2-methylaniline exhibits relatively low melting and boiling points compared to common food items such as sugar (melting point around 186°C) and water (boiling point at 100°C).
4-Methoxy-2-methylaniline is sparingly soluble in water and has a low viscosity, making it easier to dissolve in organic solvents. This contrasts with common food items like salt (highly soluble in water) and honey (high viscosity), highlighting the differences in solubility and viscosity between this compound and everyday food products.
🏭 Production & Procurement
4-Methoxy-2-methylaniline, a chemical compound commonly used in various industrial processes, is produced through a series of chemical reactions involving aniline and methanol. The synthesis typically involves the reaction of aniline with methanol in the presence of an acidic catalyst to yield the desired product.
In terms of procurement, 4-Methoxy-2-methylaniline can be obtained from chemical suppliers specializing in industrial chemicals. These suppliers often carry a range of chemical compounds for various applications and can provide 4-Methoxy-2-methylaniline in bulk quantities suitable for industrial use. The compound can be transported in sealed containers to ensure its stability during transit.
Transportation of 4-Methoxy-2-methylaniline is typically done via specialized chemical transport companies that adhere to strict safety regulations to prevent leaks or spills. The compound is often transported in sealed containers or drums to minimize any potential risks during transit. Proper labeling and documentation are also essential for the safe transport of 4-Methoxy-2-methylaniline to ensure compliance with regulatory standards.
⚠️ Safety Considerations
Safety considerations for 4-Methoxy-2-methylaniline must be taken seriously due to its potential hazards. This compound is considered harmful if swallowed, inhaled, or absorbed through the skin. It can cause skin and eye irritation, as well as respiratory irritation if inhaled. In case of exposure, immediate medical attention is necessary. Proper personal protective equipment, such as gloves and goggles, should be worn when handling this chemical to minimize the risk of accidents.
The hazard statements for 4-Methoxy-2-methylaniline include “Harmful if swallowed,” “Causes skin irritation,” and “May cause respiratory irritation.” These statements highlight the potential dangers associated with this compound and emphasize the need for caution when handling it. It is important to follow all safety protocols and guidelines to prevent any adverse effects on health or the environment.
Precautionary statements for 4-Methoxy-2-methylaniline include “Wear protective gloves/protective clothing/eye protection/face protection,” “IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell,” and “IF ON SKIN: Wash with plenty of soap and water.” These statements outline specific precautions that should be taken when working with this chemical to reduce the risk of exposure and minimize potential harm. It is crucial to follow these recommendations closely to ensure safe handling and usage of 4-Methoxy-2-methylaniline.
🔬 Potential Research Directions
One potential research direction for 4-Methoxy-2-methylaniline is the investigation of its pharmacological properties, particularly its potential in drug discovery and development. Studies could focus on its interactions with biological targets, as well as its potential therapeutic applications in various diseases.
Another area of interest could be the study of the synthesis and characterization of novel derivatives of 4-Methoxy-2-methylaniline. Researchers may explore different substitution patterns and modifications to elucidate the structure-activity relationships and potentially develop compounds with improved properties.
Furthermore, research could be conducted on the environmental fate and toxicity of 4-Methoxy-2-methylaniline. This could involve studies on its degradation pathways, environmental impact, and potential health risks associated with exposure. Understanding these aspects could help in the development of strategies for environmental remediation and risk assessment.
Lastly, studies could be undertaken to explore the use of 4-Methoxy-2-methylaniline as a building block in organic synthesis. Its reactivity and versatility in chemical transformations could be investigated to develop new methodologies for the synthesis of complex molecules and materials. This research could have implications in various fields, including pharmaceuticals, materials science, and agrochemicals.
🧪 Related Compounds
One similar compound to 4-Methoxy-2-methylaniline based upon molecular structure is 4-Ethoxy-2-methylaniline. In this compound, the methoxy group is replaced by an ethoxy group while the methyl group remains unchanged. This substitution results in a compound with similar chemical properties but with a slightly different molecular structure.
Another similar compound to 4-Methoxy-2-methylaniline is 4-Methoxy-2-ethylaniline. In this compound, the methyl group is replaced by an ethyl group while the methoxy group remains unchanged. This substitution leads to a compound with comparable chemical characteristics but with a variation in its molecular structure.
A third similar compound to 4-Methoxy-2-methylaniline is 4-Chloro-2-methylaniline. In this compound, the methoxy group is substituted with a chlorine atom while the methyl group remains the same. This alteration results in a compound with analogous chemical properties but with a different molecular structure.