Understanding 1,2,3,4-Tetramethylbenzene (Prehnitene): Properties, Synthesis, and Supplier Insights
In the competitive landscape of chemical manufacturing and research, a deep understanding of fundamental chemical intermediates is crucial. 1,2,3,4-Tetramethylbenzene, also known as Prehnitene and identified by CAS number 488-23-3, is a key aromatic hydrocarbon that serves as a vital building block in various chemical processes. This article provides a detailed look at its properties, common synthesis pathways, its significant industrial applications, and the importance of reliable procurement from quality suppliers.
Key Properties of 1,2,3,4-Tetramethylbenzene
Prehnitene is a colorless liquid with a molecular formula of C10H14 and a molecular weight of approximately 134.22 g/mol. It exhibits a boiling point of around 203°C and a density of 0.838 g/mL at 25°C. Its chemical structure, a benzene ring substituted with four methyl groups at adjacent positions (1, 2, 3, and 4), dictates its reactivity and utility in synthesis. While it is sparingly soluble in water, it readily dissolves in common organic solvents, facilitating its use in various reaction environments.
Synthesis Routes for Prehnitene
The industrial synthesis of 1,2,3,4-Tetramethylbenzene often involves the methylation of less substituted aromatic compounds. A prominent method is the Friedel-Crafts alkylation of xylene or trimethylbenzenes using methylating agents like methyl chloride or methanol in the presence of a Lewis acid catalyst, such as aluminum chloride. This process requires precise control over reaction parameters to achieve high yields and purity, often necessitating subsequent purification steps like fractional distillation to separate isomers and byproducts.
For chemical manufacturers and R&D professionals seeking to buy 1,2,3,4-tetramethylbenzene, understanding the synthesis process can provide valuable context regarding product quality and potential impurities. Choosing a manufacturer with optimized synthesis protocols and stringent quality control measures is paramount.
Industrial Applications and Significance
The primary industrial significance of 1,2,3,4-Tetramethylbenzene lies in its role as a precursor for pyromellitic dianhydride (PMDA). PMDA is a critical monomer used in the production of high-performance polymers, notably polyimides. These materials are essential for applications demanding exceptional thermal stability, mechanical strength, and electrical insulation, finding widespread use in the electronics, aerospace, and automotive sectors. Consequently, a stable and high-quality supply of Prehnitene is indispensable for manufacturers in these fields.
Beyond polymer precursors, 1,2,3,4-Tetramethylbenzene also serves as an intermediate in the synthesis of various fine chemicals, including pharmaceuticals and specialty organic materials. Its unique structural features make it a versatile building block for complex organic synthesis, enabling the development of new compounds and materials with tailored properties.
NINGBO INNO PHARMCHEM CO.,LTD. is a reliable supplier of 1,2,3,4-tetramethylbenzene, committed to providing high-purity products that meet the rigorous demands of the chemical industry. We understand the critical nature of reliable chemical sourcing and strive to be your trusted partner for all your chemical intermediate needs. We encourage you to contact us for competitive pricing and to explore how our offerings can support your product development and manufacturing goals.
Perspectives & Insights
Bio Analyst 88
“While it is sparingly soluble in water, it readily dissolves in common organic solvents, facilitating its use in various reaction environments.”
Nano Seeker Pro
“Synthesis Routes for PrehniteneThe industrial synthesis of 1,2,3,4-Tetramethylbenzene often involves the methylation of less substituted aromatic compounds.”
Data Reader 7
“A prominent method is the Friedel-Crafts alkylation of xylene or trimethylbenzenes using methylating agents like methyl chloride or methanol in the presence of a Lewis acid catalyst, such as aluminum chloride.”