27899-21-4

Usage

Uses

Used in Organic Synthesis:
2,4-Diethylglutaric acid is utilized as a key intermediate in organic synthesis, playing a crucial role in the formation of complex organic molecules. Its unique structure allows for the creation of a wide range of compounds, making it a valuable component in chemical research and development.
Used in Pharmaceutical Preparation:
As a building block for the preparation of pharmaceuticals, 2,4-diethylglutaric acid contributes to the development of new drugs and medicines. Its properties enable the synthesis of bioactive molecules with potential therapeutic applications, enhancing the scope of available treatments.
Used in Fragrance Manufacturing:
2,4-Diethylglutaric acid is employed as an intermediate in the manufacturing of fragrances, where its chemical properties contribute to the creation of various scent profiles. Its use in this industry highlights its versatility and the breadth of its applications.
Used in Dye Production:
In the dye industry, 2,4-diethylglutaric acid serves as an important intermediate, facilitating the production of a diverse array of dyes. Its role in this process underscores its significance in the creation of colorants for various applications, including textiles, plastics, and printing inks.
Used in Chemical Product Manufacturing:
Beyond its applications in organic synthesis, pharmaceuticals, fragrances, and dyes, 2,4-diethylglutaric acid is also utilized as an intermediate in the manufacturing of other chemical products. Its presence in this sector further emphasizes its multifaceted role in the chemical industry.

InChI:InChI=1/C9H16O4/c1-3-6(8(10)11)5-7(4-2)9(12)13/h6-7H,3-5H2,1-2H3,(H,10,11)(H,12,13)

Upstream product

• 903502-60-3 tetramethyl heptane-3,3,5,5-tetracarboxylate 
• 28781-92-2 Propane-1,1,3,3-tetracarboxylic acid tetramethyl ester 
• 75-03-6 ethyl iodide 
• 57987-55-0 2,4-diethyl-1,5-pentanediol 

Downstream Products

• 57987-55-0 2,4-diethyl-1,5-pentanediol 
• 100951-20-0 (+/-)-erythro-2,4-diethyl-N-(4-chloro-phenyl)-glutaramic acid 

Relevant academic research and scientific papers

Unprecedented formation of stable ketene-N,O-acetals and their rearrangement under basic conditions

Treatment of 2,4-disubstituted glutaryl dichlorides with benzimidic acid ethyl ester hydrochloride in the presence of triethylamine did not give the expected bis(acylbenzimidates), but delivered O-acyl-N-ethoxybenzylidene-ketene-N,O-acetals in good to exc

Synthesis of Dicarboxylic Acids from Aqueous Solutions of Diols with Hydrogen Evolution Catalyzed by an Iridium Complex

A catalytic system for the synthesis of dicarboxylic acids from aqueous solutions of diols accompanied by the evolution of hydrogen was developed. An iridium complex bearing a functional bipyridonate ligand with N,N-dimethylamino substituents exhibited a high catalytic performance for this type of dehydrogenative reaction. For example, adipic acid was synthesized from an aqueous solution of 1,6-hexanediol in 97 % yield accompanied by the evolution of four equivalents of hydrogen by the present catalytic system. It should be noted that the simultaneous production of industrially important dicarboxylic acids and hydrogen, which is useful as an energy carrier, was achieved. In addition, the selective dehydrogenative oxidation of vicinal diols to give α-hydroxycarboxylic acids was also accomplished.

DIBASIC ACID DIESTER

The present invention provides dibasic acid diesters, which are suitable for use in lubricating base oils, etc. and excellent in hydrolysis resistance, etc., represented by general formula (I): (wherein R2 and R3, which may be the same or different, each represent lower alkyl; and R1 and R4, which may be the same or different, each represent alkyl having 7 or more carbon atoms).

OILY INGREDIENT FOR COSMETIC PREPARATION AND COSMETIC PREPARATION

The present invention provides oils for cosmetics comprising a dibasic acid diester represented by general formula (I) (wherein R1, R2, R3 and R4, which are the same or different, each represent lower alkyl) and excellent in solubility of a long-wave ultraviolet light absorber or the like, and so forth.