2′-Hydroxyacetophenone, also known as salicylaldoxime, is a compound that is commonly used in industries such as pharmaceuticals, cosmetics, and food production. It is mainly utilized as a chelating agent, which means it has the ability to bind and remove metal ions from solutions.
In everyday life, 2′-Hydroxyacetophenone plays a crucial role in various applications such as medical treatments, hair care products, and food preservation. For example, it is used in pharmaceuticals to treat metal poisoning, in cosmetics to enhance the stability and shelf life of products, and in food production to prevent oxidation of ingredients.
Overall, 2′-Hydroxyacetophenone serves as a key ingredient in numerous products and processes that we encounter on a day-to-day basis, highlighting its significance in our everyday lives.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
2′-Hydroxyacetophenone, also known as ortho-hydroxyacetophenone, is a chemical compound with various commercial and industrial applications. It is commonly used as an intermediate in the synthesis of pharmaceuticals, perfumes, and fragrances. Additionally, it serves as a key ingredient in the production of UV stabilizers for plastics and polymers.
In the realm of drug and medication applications, 2′-Hydroxyacetophenone has garnered significant attention for its potential therapeutic properties. Research suggests that this compound exhibits antioxidant and anti-inflammatory properties, making it a promising candidate for the development of pharmaceutical drugs. Additionally, 2′-Hydroxyacetophenone has shown potential as an antiviral agent, with studies highlighting its efficacy against certain viral strains.
⚗️ Chemical & Physical Properties
2′-Hydroxyacetophenone is a white crystalline solid with a slight aromatic odor. It is commonly used as a flavoring agent in the food industry due to its pleasant scent and taste.
The molar mass of 2′-Hydroxyacetophenone is approximately 136.15 g/mol, with a density of around 1.166 g/cm³. This places it in a similar range to common food items such as sugars and salts in terms of molar mass and density.
2′-Hydroxyacetophenone has a melting point of about 115-117°C and a boiling point of around 290-292°C. These values are higher than those of many common food items, such as sugar and salt, which have lower melting and boiling points.
2′-Hydroxyacetophenone is slightly soluble in water, with a low viscosity. This makes it different from many common food items, which are often more soluble and have a higher viscosity in water.
🏭 Production & Procurement
In the production of 2′-Hydroxyacetophenone, one common method involves the catalytic hydrogenation of 2′-nitroacetophenone in the presence of a suitable catalyst, such as palladium on carbon or Raney nickel. This process results in the reduction of the nitro group to the amine, followed by oxidation of the amine to yield the desired product.
2′-Hydroxyacetophenone can be procured through various commercial suppliers or chemical manufacturers. The compound is typically available in solid form and can be packaged in drums, bags, or other appropriate containers for transportation. Proper safety precautions must be taken when handling and transporting 2′-Hydroxyacetophenone due to its potential flammability and irritant properties.
Transportation of 2′-Hydroxyacetophenone is usually carried out using standard shipping methods, such as ground transport or air freight. The compound should be handled and stored in accordance with regulations set forth by the appropriate governing bodies to ensure safety and compliance with hazardous material guidelines. It is essential to work with reputable suppliers and carriers to guarantee the secure and lawful transport of 2′-Hydroxyacetophenone.
⚠️ Safety Considerations
Safety considerations for 2′-Hydroxyacetophenone must be taken into account due to its potential hazards. This compound may cause skin irritation and serious eye damage upon contact. It is also harmful if swallowed, inhaled, or absorbed through the skin. Proper protective equipment, such as gloves, goggles, and a lab coat, should be worn when handling 2′-Hydroxyacetophenone to minimize the risk of exposure.
The hazard statements for 2′-Hydroxyacetophenone include: “Causes skin irritation,” “Causes serious eye damage,” “Harmful if swallowed,” “Harmful if inhaled,” and “Harmful if absorbed through skin.” These statements highlight the potential dangers associated with this compound and emphasize the importance of taking necessary precautions when working with it to prevent adverse health effects.
Precautionary statements for 2′-Hydroxyacetophenone recommend various safety measures to minimize the risks associated with this compound. These include wearing protective gloves, eye protection, and clothing to prevent skin contact. It is also advised to avoid breathing in vapors, mist, or gas generated from the substance. In case of ingestion, seek medical advice immediately and show the container or label of the product to the healthcare provider for proper treatment.
🔬 Potential Research Directions
One potential research direction for 2′-Hydroxyacetophenone is its use as a building block in organic synthesis. By investigating its reactivity with various functional groups, researchers can explore new pathways for the creation of complex molecules.
Additionally, the biological activity of 2′-Hydroxyacetophenone can be further studied to explore potential medicinal applications. Investigating its interactions with different biological targets can shed light on its potential as a drug candidate for various conditions.
Furthermore, the environmental impact of 2′-Hydroxyacetophenone and its derivatives can be another avenue of research. Assessing its degradation pathways and potential toxicity can aid in the development of strategies for its safe disposal and minimize its impact on the environment.
🧪 Related Compounds
One similar compound to 2′-Hydroxyacetophenone is 2′-Methoxyacetophenone. This compound has a similar molecular structure to 2′-Hydroxyacetophenone, with a methoxy group (-OCH3) in place of the hydroxyl group (-OH). The presence of the methoxy group gives 2′-Methoxyacetophenone different chemical properties compared to 2′-Hydroxyacetophenone, making it useful in various applications.
Another similar compound to 2′-Hydroxyacetophenone is 2′-Aminoacetophenone. This compound contains an amino group (-NH2) in place of the hydroxyl group (-OH) found in 2′-Hydroxyacetophenone. The presence of the amino group makes 2′-Aminoacetophenone useful in different chemical reactions and applications compared to 2′-Hydroxyacetophenone. The substitution of functional groups can have a significant impact on the chemical properties and reactivity of a compound.
A third similar compound to 2′-Hydroxyacetophenone is 2′-Chloroacetophenone. This compound contains a chlorine atom (-Cl) in place of the hydroxyl group (-OH) found in 2′-Hydroxyacetophenone. The presence of the chlorine atom changes the chemical properties and reactivity of 2′-Chloroacetophenone compared to 2′-Hydroxyacetophenone. Each substitution of a functional group in a compound can lead to different potential applications and uses in various industries.
