67691-10-5

Basic information

• Product Name: 2-(2-{2-[2-(2-{2-[2-(2-{2-[2-(4-Dodecyl-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol
• CAS NO: 67691-10-5
• Molecular Weight: 702.967
• Mol File: 67691-10-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2-{2-[2-(2-{2-[2-(2-{2-[2-(4-Dodecyl-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-{2-[2-(2-{2-[2-(2-{2-[2-(4-Dodecyl-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol(67691-10-5)
• EPA Substance Registry System: 2-(2-{2-[2-(2-{2-[2-(2-{2-[2-(4-Dodecyl-phenoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol(67691-10-5)

Safety Data

• Hazardous Substances Data: 67691-10-5(Hazardous Substances Data)

Usage

Molecular Composition

Consists of multiple ethylene glycol units, a dodecylphenol moiety, and an alcohol group.

Elements Present

Composed of carbon (C), hydrogen (H), and oxygen (O) atoms.

Chemical Class

Belongs to the class of alcohols.

Industrial Applications

Commonly used in the production of surfactants, emulsifiers, and lubricants.

Solubility

Exhibits high solubility in non-polar solvents and surfaces.

Suitability

Ideal for use in cleaning and coating products due to its solubility and structure.

Detergent Properties

Known to possess detergent-like properties.

Household and Personal Care Products

Often found in various household and personal care products, such as cleaners and shampoos.

Upstream product

• 75-21-8 oxirane 
• 104-43-8 4-dodecylphenol 

Relevant articles and documents

Synthesis, characterization, and functional evaluation of branched dodecyl phenol polyoxyethylene ethers: A novel class of surfactants with excellent wetting properties

A series of branched dodecyl phenol polyoxyethylene ethers (b-DPEOn) were successfully synthesized via alkylation and ethylene oxide addition reactions. The alkylation reaction was conducted by using a branched internal olefin as the raw material. Furthermore, the conversion rate of the branched dodecene was measured to be 98.1% and the selectivity towards branched dodecyl phenol (b-DP) was 95.9%. Moreover, b-DPEOn (b-DPEO7, b-DPEO10, b-DPEO12) were obtained via the reaction of ethylene oxide with b-DP. Notably, b-DPEO10 can efficiently reduce the surface tension of water below 31.55 mN m-1 at the critical micelle concentration (cmc) and the cmc value in water was approximately 1.3 × 10-2 g L-1 at 25 °C. The preferable wetting ability of b-DPEO10 was superior to that of commercialized dodecyl phenol polyoxyethylene ether (c-DPEOn), so it will be promoted and used in the textile and pesticide industries.