19855-52-8

Basic information

• Product Name: allyl oleate
• Synonyms: allyl oleate;(Z)-9-Octadecenoic acid 2-propenyl ester;Oleic acid allyl ester;9-Octadecenoic acid, (Z)-, 2-propenyl ester;Ai3-32461;Einecs 243-375-8
• CAS NO: 19855-52-8
• Molecular Formula: C₂₁H₃₈O₂
• Molecular Weight: 322.52522
• EINECS: 243-375-8
• Mol File: 19855-52-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 404.3°Cat760mmHg
• Flash Point: 96.2°C
• Appearance: /
• Density: 0.877g/cm³
• Vapor Pressure: 9.55E-07mmHg at 25°C
• Refractive Index: 1.461
• CAS DataBase Reference: allyl oleate(CAS DataBase Reference)
• NIST Chemistry Reference: allyl oleate(19855-52-8)
• EPA Substance Registry System: allyl oleate(19855-52-8)

Safety Data

• Hazardous Substances Data: 19855-52-8(Hazardous Substances Data)

Usage

General Description

Allyl oleate is a chemical compound that belongs to the group of esters and is derived from oleic acid and allyl alcohol. It is commonly used as a flavoring agent and fragrance in food and cosmetic products due to its pleasant, fruity odor. Allyl oleate also has potential applications in industrial processes, including the production of resins, plasticizers, and synthetic lubricants. Additionally, it has been studied for its potential as a renewable and biodegradable fuel additive due to its high energy content and low emissions. However, further research is needed to fully understand its environmental and toxicological properties. Overall, allyl oleate is a versatile chemical with a wide range of industrial and commercial applications.

InChI:InChI=1/C21H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21(22)23-20-4-2/h4,11-12H,2-3,5-10,13-20H2,1H3/b12-11-

Upstream product

• 112-80-1 cis-Octadecenoic acid 
• 107-05-1 3-chloroprop-1-ene 
• 143-18-0 potassium oleate 
• 106-95-6 allyl bromide 
• 107-18-6 allyl alcohol 

Downstream Products

• 112-80-1 cis-Octadecenoic acid 

Relevant articles and documents

Fatty acid monomer, preparation method and thermoplastic macromolecule synthesized through application

The invention discloses a fatty acid monomer, a preparation method and a thermoplastic macromolecule synthesized through application. Tetramethyl guanidine and other catalysts are mainly utilized to catalyze a monomer containing halogen elements (Cl, Br and I) or halogen element and fatty acid, and the fatty acid monomer and thermoplastic macromolecule are obtained through efficient reaction. The application range can be thus widened by functionally improving the obtained fatty acid monomer and thermoplastic macromolecule. The reaction process is mild in condition, the catalytic efficiency of the catalysts is very high, few side reactions is produced, products are easy to separate and purify, and the fatty acid monomer and the thermoplastic macromolecule have a very high industrial application prospect.

A green approach toward oleic- and undecylenic acid-derived polyurethanes

Naturally occurring oleic and undecylenic acids were used as raw materials for the synthesis of novel polyurethanes (PUs). The application of environmentally friendly thiol-ene additions to 10-undecenoate and oleate derivatives was studied with the goal of obtaining renewable diols. The resulting monomers were then polymerized with 4,4′-methylenebis (phenylisocyanate), in N,N-dimethylformamide solution using tin (II) 2-ethylhexanoate as catalyst, to produce the corresponding thermoplastic PUs (TPUs). Also, ultrasound irradiation has been tested to improve the synthesis of PU. Under these conditions, TPUs were obtained in high yields (80-99%) with weight-average molecular weights in the 36-83 kDa range. The chemical structures of PUs were assessed by FTIR and NMR spectroscopy. The thermal and mechanical properties of the synthesized TPUs have been studied and they showed a clear dependence on the structure of the parent diol. MTT test was carried out to asses the potential cytotoxicity of the prepared PUs, indicating no cytotoxic response.