69152-89-2

Usage

Uses

Used in Pharmaceutical Industry:
8-Decenoic acid, 10-oxo-, (E)is used as an antimicrobial agent for its ability to inhibit the growth of various bacteria and fungi. Its potential use in the development of new antimicrobial drugs is being explored, particularly for treating infections caused by drug-resistant strains.
Used in Food Preservation Industry:
8-Decenoic acid, 10-oxo-, (E)is used as a natural preservative to extend the shelf life of food products. Its antimicrobial properties help prevent spoilage and contamination by harmful microorganisms, ensuring the safety and quality of the food.
Used in Cosmetics and Personal Care Industry:
8-Decenoic acid, 10-oxo-, (E)is used as an active ingredient in cosmetics and personal care products for its potential anti-inflammatory and immunomodulatory effects. It may help soothe and protect the skin, reducing inflammation and promoting skin health.
Used in Nutraceutical Industry:
8-Decenoic acid, 10-oxo-, (E)is used as a nutraceutical ingredient for its potential health benefits. It can be incorporated into dietary supplements and functional foods to support immune function and overall well-being.
Used in Agricultural Industry:
8-Decenoic acid, 10-oxo-, (E)is used as a biopesticide in agriculture to control pests and diseases affecting crops. Its antimicrobial properties can help protect plants from harmful microorganisms, reducing the need for chemical pesticides.

Upstream product

• 69152-90-5 (Z)-10-hydroxy-8-decenoic acid 
• 90540-32-2 10-hydroperoxy-trans-8-cis-12-octadecadienoic acid 

Downstream Products

• 67803-48-9 trans-Methyl 10-oxodec-8-enoate 

Relevant academic research and scientific papers

Homolytic and Heterolytic Scission of Organic Hydroperoxides by (meso-Tetraphenylporphinato)iron(III) and Its Relation to Olefin Epoxidation

Reaction of 10-hydroperoxyoctadeca-8,12-dienoic acid (10-OOH-18:2) with chloro(meso-tetraphenylporphinato)iron(III) (Fe(3+)-TPP) in CH2Cl2 produces two products identified as 10-oxodec-8-enoic acid (10-oxo-10:1) and 10-oxooctadeca-8,12-dienoic acid (10-oxo-18:2).These compounds are derived from an alkoxyl radical intermediate generated by homolytic cleavage of 10-OOH-18:2.Only a trace of the heterolytic cleavage product 10-hydroxyoctadeca-8,12-dienoic acid (10-OH-18:2) is observed.Inclusion of imidazole alters the product profile so that 10-OH-18:2 is the majorproduct (62percent).Reaction of 10-OOH-18:2 or t-BuOOH (0.05 M) with Fe(3+)-TPP (0.001 M) and cis-stilbene (5 M) produces trans-stilbene oxide as the only oxidation product (55percent based on hydroperoxide).Oxidation in the presence of imidazole (0.3 M) produces approximately equal amounts of cis-stilbene oxide (22percent) and trans-stilbene oxide (23percent).Butylated hydroxytoluene inhibits formation of both epoxides from cis-stilbene whereas p-methoxyanisole selectively inhibits formation of cis-stilbene oxide.The data indicate that two separate oxidizing agents are produced in the reaction of hydroperoxides with Fe(3+)-TPP.In the absence of imidazole, Fe(3+)-TPP cleaves 10-OOH-18:2 and t-BuOOH homolytically to alkoxyl radicals and Fe(4+)=O.TPP.Both species oxidize the hydroperoxide to peroxyl radicals that epoxidize cis-stilbene nonstereospecifically.In the presence of imidazole, Fe(3+)-TPP also cleaves the hydroperoxides heterolytically to alcohol and Fe(4+)=O.TPP.+, which epoxidizes cis-stilbene stereospecifically.The results reconcile apparently conflicting observations in the literature and suggest that the pathway of hydroperoxidecleavage by heme complexes and heme proteins is a sensitive function of the environment of the heme.