113011-13-5

Basic information

• Product Name: N,N-dimethyl-N-(2-phenoxyethyl)-1-decylammonium bromide
• Synonyms: N,N-dimethyl-N-(2-phenoxyethyl)-1-decylammonium bromide
• CAS NO: 113011-13-5
• Molecular Weight: 386.416
• Mol File: 113011-13-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N-dimethyl-N-(2-phenoxyethyl)-1-decylammonium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-N-(2-phenoxyethyl)-1-decylammonium bromide(113011-13-5)
• EPA Substance Registry System: N,N-dimethyl-N-(2-phenoxyethyl)-1-decylammonium bromide(113011-13-5)

Safety Data

• Hazardous Substances Data: 113011-13-5(Hazardous Substances Data)

Upstream product

• 112-29-8 1-bromo dodecane 
• 13468-02-5 dimethyl(2-phenoxyethyl)amine 
• 1120-24-7 N,N-dimethyldecylamine 
• 589-10-6 phenoxyethyl bromide 

Relevant articles and documents

Domiphen impurity synthesis method

The invention discloses a domiphen impurity synthesis method. The method comprises the following steps: S1, dissolving phenol in a solvent A, adding a substance B, carrying out heating, carrying out aheat-preserved reaction, dropwise adding a dimethylaminochloroethane solution, carrying out refluxing, and performing purifying to obtain N,N-dimethyl-2-phenoxyethylamine; and S2, subjecting 1-bromotetradecane and the N,N-dimethyl-2-phenoxyethylamine obtained in the step S1 to refluxing in a solvent C, then carrying out crystallizing, and performing drying to obtain brominated N,N-dimethyl-N-(2-phenoxyethyl)-1-tetradecylamine; or subjecting 1-bromodecane and the N,N-dimethyl-2-phenoxyethylamine obtained in the step S1 to refluxing in ethyl acetate, then carrying out crystallizing, and performing drying to obtain brominated N,N-dimethyl-N-(2-phenoxyethyl)-1-decylamine. The method of the invention has the advantages of short synthesis route, mild reaction conditions, few pollutants, high product purity, high yield, economical performance and environmental protection performance.