62285-15-8

Basic information

• Product Name: 10-Undecenoic acid, 2,3-dihydroxypropyl ester
• CAS NO: 62285-15-8
• Molecular Formula: C14H26O4
• Mol File: 62285-15-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 10-Undecenoic acid, 2,3-dihydroxypropyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 10-Undecenoic acid, 2,3-dihydroxypropyl ester(62285-15-8)
• EPA Substance Registry System: 10-Undecenoic acid, 2,3-dihydroxypropyl ester(62285-15-8)

Safety Data

• Hazardous Substances Data: 62285-15-8(Hazardous Substances Data)

Usage

Description

10-Undecenoic acid, 2,3-dihydroxypropyl ester is a chemical compound with the molecular formula C15H28O4. It is an ester of 10-undecenoic acid and 2,3-dihydroxypropyl, known for its versatile applications in various industries.

Uses

Used in Plastics Industry:
10-Undecenoic acid, 2,3-dihydroxypropyl ester is used as a stabilizer and lubricant in the production of synthetic plastics, enhancing the manufacturing process and improving the quality of the final product.
Used in Lubricants Industry:
10-Undecenoic acid, 2,3-dihydroxypropyl ester serves as a lubricant in the formulation of various synthetic lubricants, providing smooth operation and reducing friction in mechanical systems.
Used in Pharmaceuticals:
10-Undecenoic acid, 2,3-dihydroxypropyl ester is used as a potential active ingredient in pharmaceutical formulations due to its antifungal and antibacterial properties, making it a candidate for medical treatments and applications.

Upstream product

• 142564-38-3 (2-Dec-9-enyl-[1,3]dioxolan-4-yl)-methanol 
• 112-38-9 10-undecenoic acid 
• 556-52-5 oxiranyl-methanol 
• 143-07-7 lauric acid 
• 931-40-8 4-hydroxymethyl-1,3-dioxolan-2-one 
• 56-81-5 glycerol 

Relevant articles and documents

Photopolymerizable Synthons from Glycerol Derivatives

Photopolymerizable monomers based on monoglycerides were prepared by a convenient two-step procedure. The first one consists of the synthesis of highly pure monoglycerides by an organocatalyzed solvent-free route. This process was carried out by condensation of bio-sourced carboxylic acids (i.e. butyric, decanoic, undecylenic or stearic acids) with glycerol carbonate or glycidol in the presence of a quaternary ammonium salt as a catalyst. The obtained bio-based monoglycerides were modified in the second step by reaction with acryloyl and methacryloyl chloride leading to a series of new diacrylated and dimethacrylated monomers. The structures of the monoglycerides, diacrylated and dimethacrylated monomers were fully characterized by spectroscopic methods. Photopolymerization investigations monitored by infrared spectroscopy were achieved under ultraviolet radiation in the presence of a photoinitiator. The resulting cross-linked materials were analyzed by thermal gravimetric analysis, gel content determination and tests of swelling in water, ethanol and methylene chloride. Data relative to the pendulum hardness of these materials are also included.

Structural Analysis of Partial and Total Esters of Glycerol Undecenoate and Diglycerol Undecenoate

The direct esterification reaction between glycerol and undecylenic acid or between diglycerol and undecylenic acid generates all the possible types of glycerol or diglycerol esters. Purification by silica gel chromatography resulted in the isolation of each of these types of ester in a pure form. The molecular structures of the compounds isolated were characterized and identified by mass spectrometry, 1H NMR, 13C NMR and DEPT-135. We then studied the composition of esters of undecylenic acid formed with glycerol or diglycerol as a function of their reaction conditions, which constitute a highly complex system. We purified undecylenic acid esters from each polyol family to allow the structural identification of each ester of glycerol and each ester of diglycerol with undecylenic acid. We found that the polarity of these non-ionic amphiphilic esters directly affected their affinity for organic and inorganic solvents and that these esters behaved very differently from anionic amphiphilic molecules, such as undecylenic acid.

A Highly Selective Methodology for the Direct Conversion of Acetals to Esters

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