- Home
- About Us
- Products
- Services
- Recommendation
- Industries
- Resource
- Order Center
- Contact Us
Benzophenone is an organic compound that belongs to the class of aromatic ketones. It consists of two phenyl groups connected by a carbonyl group. Benzophenone is a pale yellow solid with a distinct odor.
The preparation of benzophenone can be achieved through multiple methods. One of the most common methods is the Friedel-Crafts acylation reaction, which involves the acylation of benzene or substituted benzene with benzoyl chloride in the presence of a Lewis acid catalyst, such as aluminum chloride (AlCl3) or ferric chloride (FeCl3). The reaction proceeds through electrophilic aromatic substitution, resulting in the formation of benzophenone and hydrogen chloride as a byproduct.
Another method for synthesizing benzophenone is the oxidation of diphenylmethanol. This can be accomplished by treating diphenylmethanol with an oxidizing agent, such as chromic acid (H2CrO4) or potassium permanganate (KMnO4), under acidic conditions. The reaction oxidizes the alcohol group to a ketone, leading to the formation of benzophenone.
In addition to these synthetic methods, benzophenone can also be obtained through the photochemical degradation of benzene in the presence of oxygen. This process, known as air oxidation, occurs when benzene is exposed to sunlight or ultraviolet (UV) light, leading to the formation of benzophenone and other byproducts.
Overall, the preparation of benzophenone involves various chemical reactions, including acylation, oxidation, and photochemical degradation. These methods allow for the production of benzophenone on a large scale, making it readily available for its numerous industrial applications.
Product List
Click the product name to view product details.
CAS NO. | Product Name | Inquiry |
---|---|---|
119-61-9 | Benzophenone | Inquiry |
85-29-0 | 2,4'-Dichlorobenzophenone | Inquiry |
7705-08-0 | Ferric Chloride | Inquiry |
Benzophenone is a versatile organic compound that finds wide applications in various industries. Some of the main applications of benzophenone are:
Benzophenone is commonly used as a photoprotective agent in sunscreens and cosmetic products. It acts as a UV absorber, effectively blocking harmful UVB and UVA rays from damaging the skin. Benzophenone derivatives, such as benzophenone-3 (also known as oxybenzone), are particularly effective in providing broad-spectrum UV protection.
Benzophenone is used as a photoinitiator in the field of photopolymerization reactions. When exposed to UV light, it undergoes a photochemical reaction and generates free radicals. These free radicals initiate the polymerization process, facilitating the formation of polymers with desired properties. Benzophenone is commonly employed in the manufacturing of adhesives, coatings, and dental materials.
Benzophenone is used as a fragrance ingredient in perfumes and colognes due to its pleasant odor. It adds a unique aromatic profile to various products, enhancing their appeal to consumers.
Benzophenone derivatives have been investigated for their potential medicinal properties. They have shown promising results in various areas, including anti-inflammatory, antioxidant, and antimicrobial activities. Additionally, benzophenone derivatives have been studied for their potential as anticancer agents.
Benzophenone serves as a starting material in numerous organic synthesis reactions. It can undergo various transformations, including oxidation, reduction, and substitution reactions, to yield a wide range of compounds with different functional groups. As a result, it is widely used in the synthesis of pharmaceuticals, dyes, plastics, and other organic compounds.
Overall, benzophenone is a versatile compound with diverse applications. Its role as a UV absorber in sunscreens, photoinitiator in photopolymerization reactions, fragrance ingredient, and its potential pharmaceutical uses make it an important compound in numerous industries.
Privacy Policy | Cookie Policy | Copyright © 2025 Alfa Chemistry. All rights reserved.
Back to top