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• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Stilbenes Stilbenes
• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Stilbenes
• Solvents and Organic Chemicals Organic Compounds Aldehyde/Ketone

Comprehensive Guide to 2-(4-Methylphenyl)acetophenone (CAS No. 2430-99-1): Properties, Applications, and Market Insights

2-(4-Methylphenyl)acetophenone (CAS No. 2430-99-1) is an organic compound widely recognized for its versatile applications in pharmaceuticals, fragrances, and specialty chemicals. This aromatic ketone, also known as p-methylacetophenone, has garnered significant attention due to its unique chemical properties and industrial relevance. In this comprehensive guide, we delve into the molecular structure, synthesis methods, applications, and emerging trends surrounding this compound.

The chemical formula of 2-(4-Methylphenyl)acetophenone is C15H14O, with a molecular weight of 210.27 g/mol. Its structure features a methyl group at the para position of the phenyl ring attached to an acetophenone moiety, which contributes to its distinct reactivity and solubility characteristics. Researchers often search for "solubility of 2-(4-Methylphenyl)acetophenone" or "synthesis of p-methylacetophenone," reflecting the compound's importance in organic synthesis.

One of the most prominent applications of CAS 2430-99-1 lies in the fragrance industry, where it serves as a key intermediate for producing floral and woody scent compounds. Recent trends in "sustainable fragrance ingredients" have increased interest in derivatives of this compound. Additionally, its role as a building block in pharmaceutical synthesis makes it valuable for developing new drug candidates, particularly in the field of "anti-inflammatory agents" and "CNS-targeted therapeutics," which are currently hot topics in medicinal chemistry research.

The global market for 2-(4-Methylphenyl)acetophenone has shown steady growth, driven by increasing demand from the cosmetics and pharmaceutical sectors. Industry reports frequently highlight searches for "2-(4-Methylphenyl)acetophenone suppliers" and "high purity p-methylacetophenone," indicating strong commercial interest. Manufacturers are focusing on developing greener production methods to align with the "green chemistry" movement, another trending topic in chemical manufacturing.

From a technical perspective, 2430-99-1 exhibits interesting spectroscopic properties that make it useful in analytical chemistry. Its characteristic UV-Vis absorption and NMR spectra patterns are frequently studied, as evidenced by common search queries like "NMR spectrum of 2-(4-Methylphenyl)acetophenone." The compound's stability under various conditions is another area of research interest, particularly for applications requiring "heat-stable aromatic ketones."

Recent advancements in "catalytic synthesis methods" have improved the production efficiency of 2-(4-Methylphenyl)acetophenone, addressing growing concerns about "cost-effective chemical synthesis." Researchers are also exploring its potential in "advanced material applications," such as in liquid crystal displays and organic semiconductors, which aligns with current interests in "smart materials development."

Quality control remains a critical aspect for CAS 2430-99-1, with many users searching for "analytical methods for p-methylacetophenone purity testing." The compound typically appears as white to light yellow crystals with a characteristic aromatic odor. Its melting point ranges between 50-54°C, and it shows good solubility in common organic solvents, properties that are frequently queried by industrial users and researchers alike.

Environmental and safety considerations for 2-(4-Methylphenyl)acetophenone have become increasingly important, mirroring the broader chemical industry's focus on "sustainable chemical practices." While not classified as hazardous under standard regulations, proper handling procedures are recommended, as indicated by searches for "2-(4-Methylphenyl)acetophenone safety data." The compound's biodegradability and environmental fate are subjects of ongoing research.

Looking ahead, the future of 2430-99-1 appears promising, with potential expansions into new application areas. The growing interest in "bio-based aromatic compounds" and "green synthetic pathways" may drive innovation in its production and utilization. As research continues to uncover novel properties and applications, 2-(4-Methylphenyl)acetophenone is poised to maintain its relevance in various chemical industries.

For researchers and industry professionals seeking detailed technical information, key data points about 2-(4-Methylphenyl)acetophenone include its boiling point (approximately 300°C at 760 mmHg), density (1.03 g/cm3 at 25°C), and refractive index (1.558 at 20°C). These physical properties, along with its chemical behavior, make it a versatile intermediate for numerous synthetic applications, from "fine chemical production" to "specialty material formulation."

• 451-40-1(2-Phenylacetophenone)
• 102225-36-5(Ethanone, 1-(4-ethylphenyl)-2-(4-propylphenyl)-)
• 25423-81-8(Ethanone, 2,2'-(1,3-phenylene)bis[1-phenyl-)
• 2001-28-7(Benzyl p-Toluylketone)
• 64196-54-9(Ethanone, 1,2-bis(3-methylphenyl)-)
• 13892-81-4(1,2-Diphenylethanone)
• 214288-79-6(Ethanone, 2,2'-(1,2-ethanediyldi-3,1-phenylene)bis[1-phenyl-)
• 34403-03-7(2-(3-Methylphenyl)acetophenone)
• 95606-81-8(3'-Methyl-2-phenylacetophenone)
• 51490-06-3(1,2-bis(4-methylphenyl)ethan-1-one)