• 1. Detection of prohibited treatment products on racing tires using headspace solid phase microextraction (SPME) and gas chromatography/mass spectrometry (GC/MS)
  W. D. Kranz,C. J. Carroll,J. V. Goodpaster Anal. Methods 2016 8 177
• 2. A new route to N-aromatic heterocycles from the hydrogenation of diesters in the presence of anilines
  Yiping Shi,Paul C. J. Kamer,David J. Cole-Hamilton,Michelle Harvie,Emma F. Baxter,Kate J. C. Lim,Peter Pogorzelec Chem. Sci. 2017 8 6911
• 3. Muconic acid isomers as platform chemicals and monomers in the biobased economy
  Ibrahim Khalil,Greg Quintens,Tanja Junkers,Michiel Dusselier Green Chem. 2020 22 1517
• 4. Highly selective formation of unsaturated esters or cascade reactions to α,ω-diesters by the methoxycarbonylation of alkynes catalysed by palladium complexes of 1,2-bis(ditertbutylphosphinomethyl)benzene
  A. Alberto Nú?ez Magro,Lynzi-Marie Robb,Peter J. Pogorzelec,Alexandra M. Z. Slawin,Graham R. Eastham,David J. Cole-Hamilton Chem. Sci. 2010 1 723
• 5. Mono-substitution of symmetric diesters: selectivity of Mycobacterium smegmatis acyltransferase variants
  Maja Finnveden,Stefan Semlitsch,Oscar He,Mats Martinelle Catal. Sci. Technol. 2019 9 4920

• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acid methyl esters
• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acid esters Fatty acid methyl esters
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Dimethyl Adipate: A Comprehensive Overview

Dimethyl Adipate (CAS No. 627-93-0) is a versatile organic compound with the molecular formula C8H14O4. It belongs to the class of esters and is widely used in various industrial and commercial applications. Derived from adipic acid, this compound has gained significant attention due to its unique chemical properties and expanding range of uses. In recent years, advancements in synthetic methodologies and its integration into cutting-edge technologies have further solidified its importance in modern chemistry.

The structure of dimethyl adipate consists of a six-carbon chain with two ester groups at each end. This configuration imparts it with excellent solubility in organic solvents and a relatively low melting point, making it ideal for applications that require flexibility and ease of handling. Its ability to form stable complexes with other molecules has also been explored in recent studies, opening new avenues for its use in drug delivery systems and advanced materials science.

One of the most notable applications of dimethyl adipate is as a plasticizer in polyvinyl chloride (PVC) formulations. Its excellent compatibility with PVC resins enhances the flexibility and durability of finished products, ranging from packaging materials to construction components. Recent research has focused on optimizing its performance in high-temperature environments, ensuring its stability under extreme conditions while maintaining its efficacy as a plasticizer.

Beyond plastics, dimethyl adipate has found a niche in the pharmaceutical industry as a solvent for active pharmaceutical ingredients (APIs). Its ability to dissolve a wide range of APIs without causing degradation has made it a preferred choice in drug formulation processes. Additionally, its role as an excipient in tablet manufacturing has been explored, with studies highlighting its potential to improve drug bioavailability by enhancing the dissolution rate of poorly soluble drugs.

In the realm of environmental science, dimethyl adipate has been subjected to rigorous testing to assess its biodegradability and ecological impact. Recent findings suggest that under aerobic conditions, it undergoes rapid microbial degradation, minimizing its persistence in aquatic environments. This characteristic aligns with global efforts to develop eco-friendly chemical compounds, making it an attractive option for sustainable industrial practices.

The synthesis of dimethyl adipate typically involves the esterification of adipic acid with methanol, often catalyzed by acids or enzymes. Innovations in catalytic systems have led to more efficient production methods, reducing energy consumption and waste generation. Enzymatic synthesis, in particular, has emerged as a green chemistry approach, leveraging biocatalysts for higher yields and selectivity.

Looking ahead, the demand for dimethyl adipate is expected to grow as industries continue to seek versatile and reliable chemical solutions. Its integration into emerging technologies such as biodegradable polymers and advanced composites presents exciting opportunities for future research and development. As regulatory frameworks around chemical safety evolve, ensuring the sustainable production and application of dimethyl adipate will remain a critical focus for manufacturers and researchers alike.

• 29823-25-4(Methyl Octadecanoate-d35)
• 14273-92-8(5-Hydroxypentanoic Acid Methyl Ester)
• 1472-87-3(Tridecanedioic acid, 1,13-dimethyl ester)
• 2640-94-0(Decanoic acid,10-hydroxy-, methyl ester)
• 22399-98-0(Docosanedioic acid, dimethyl ester)
• 2442-49-1(Methyl tetracosanoate)
• 20291-40-1(7-Methoxy-7-oxoheptanoic Acid)
• 1931-63-1(Methyl 9-Oxononanoate (90%))
• 1731-94-8(Methyl nonadecanoate)
• 2433-97-8(Methyl Tricosanoate)