14156-10-6

Basic information

• Product Name: Peroxydecanoic acid
• Synonyms: Peroxydecanoic acid
• CAS NO: 14156-10-6
• Molecular Formula: C₁₀H₂₀O₃
• Molecular Weight: 0
• Mol File: 14156-10-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 272.6°Cat760mmHg
• Flash Point: 96.4°C
• Appearance: /
• Density: 0.967g/cm³
• Vapor Pressure: 0.000779mmHg at 25°C
• Refractive Index: 1.443
• CAS DataBase Reference: Peroxydecanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: Peroxydecanoic acid(14156-10-6)
• EPA Substance Registry System: Peroxydecanoic acid(14156-10-6)

Safety Data

• Hazardous Substances Data: 14156-10-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H20O3/c1-2-3-4-5-6-7-8-9-10(11)13-12/h12H,2-9H2,1H3

Upstream product

• 334-48-5 1-decanoic acid 
• 112-13-0 n-decanoyl chloride 
• 86960-46-5 4-n-decanoyloxybenzoic acid 

Downstream Products

• 111-84-2 nonane 
• 112-05-0 nonanoic acid 
• 334-48-5 1-decanoic acid 
• 143-08-8 nonyl alcohol 
• 593-45-3 octadecane 
• 42231-48-1 decanoic acid nonyl ester 

Relevant articles and documents

A Mechanistic Study on the Reaction of Non-Heme Diiron(III)-Peroxido Complexes with Benzoyl Chloride

Dinuclear iron peroxido complexes are important intermediates for selective oxidation reactions. A detailed kinetic study of the reaction of benzoyl chloride (BzCl) with a dinuclear iron non-heme cis end-on peroxido complex with the ligand EtHPTB (N,N,N′,

Effect of solvents on the rate of epoxidation of α-pinene and Δ3-carene with peroxydecanoic acid

Reaction of epoxidation of α-pinene and Δ3-carene with peroxydecanoic acid in various organic solvents was studied. Effective activation energies of oxidation of α-pinene and Δ3- carene with peroxydecanoic acid in various media are evaluated. It is shown that reaction medium significantly affects the rate of the process. Correlation dependences connecting the rate of epoxidation with main parameters of solvents are found.

Effect of Organic Solvents on the Rate of Oxidation of Sulfoxides with Peroxy Acids

Abstract: The reaction of sulfoxides with peroxy acids in various organic media was studied. The reaction mechanism involves the rapid formation of a sulfoxide-–peroxy acid intermediate which decomposes in the second stage to form carboxylic acid and the corresponding sulfone. The second stage is the rate-limiting step. The reaction medium significantly affects the rate of oxidation. The calculated activation parameters of the oxidation process indicate a compensation effect in the investigated reaction. Correlations between the main physicochemical parameters of solvents and the effective rate constants (k) of dimethyl sulfoxide oxidation with peroxy acids were found. Depending on the reaction conditions, the main factors affecting the k values are specific and nonspecific solvation of the reactants and structural factors.