54549-26-7

Basic information

• Product Name: tetradecyl D-glucoside
• Synonyms: tetradecyl D-glucoside;D-Glucopyranoside, tetradecyl
• CAS NO: 54549-26-7
• Molecular Formula: C₂₀H₄₀O₆
• Molecular Weight: 376.528
• EINECS: 259-219-7
• Mol File: 54549-26-7.mol

Chemical Properties

• Boiling Point: 521.5°C at 760 mmHg
• Flash Point: 269.2°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 4.7E-13mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: tetradecyl D-glucoside(CAS DataBase Reference)
• NIST Chemistry Reference: tetradecyl D-glucoside(54549-26-7)
• EPA Substance Registry System: tetradecyl D-glucoside(54549-26-7)

Safety Data

• Hazardous Substances Data: 54549-26-7(Hazardous Substances Data)

Usage

Uses

Used in Personal Care Industry:
Tetradecyl D-glucoside is used as a mild cleansing agent in shampoos, cleansers, and bath products for its ability to effectively remove dirt and oils from the skin and hair without causing irritation. Its suitability for sensitive skin and eco-friendly formulations makes it a preferred choice in this industry.
Used in Household Products Industry:
In household products, tetradecyl D-glucoside is used as a surfactant to enhance the cleaning power of various formulations, such as dishwashing liquids and laundry detergents. Its ability to effectively remove dirt and grease contributes to the overall effectiveness of these products.
Used in Industrial Applications:
Tetradecyl D-glucoside is used as an emulsifier in industrial applications to effectively emulsify oils and improve the stability of formulations. This property makes it valuable in the production of various products, including cosmetics, pharmaceuticals, and food products, where stable emulsions are crucial for performance and quality.

InChI:InChI=1/C20H40O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-25-20-19(24)18(23)17(22)16(15-21)26-20/h16-24H,2-15H2,1H3/t16-,17-,18+,19-,20?/m1/s1

Upstream product

• 2280-44-6 D-Glucose 
• 112-72-1 1-Tetradecanol 

Relevant articles and documents

Method for preparing alkyl glycoside

The invention provides a method for preparing alkyl glycoside. The method comprises the following steps: providing a deep-eutectic solvent as a catalyst, wherein the deep-eutectic solvent consists ofcholine chloride and hydrogen-bond donors, and the structural formula of the choline chloride is shown as the formula (I) in the original specification; performing a reaction on the deep-eutectic solvent, glucose and fatty alcohol, so as to generate the alkyl glycoside, wherein the molar ratio of the choline chloride and the hydrogen-bond donors is 1: 1. Therefore, by utilizing the characteristicsof the deep-eutectic solvent of being uneasy in volatilization and combustion, good in heat stability and solubility, easy in recovery, repeatable in use and the like, the reaction is performed on the deep-eutectic solvent, the glucose and the fatty alcohol to generate the alkyl glycoside, the utilization rate of atoms in a synthesis process is as high as 100%, and the alkyl glycoside is low in toxicity and is biodegradable.

Method for preparing alkyl polyglycoside through concerted catalysis of ionic liquid compounding system

The invention belongs to a preparation method of alkyl polyglycoside, and particularly relates to a method for preparing the alkyl polyglycoside through concerted catalysis of an ionic liquid compounding system. According to the method disclosed by the invention, ionic liquid with catalytic activity is compounded with one or two of sulphuric acid, phosphoric acid, p-toluene sulfonic acid and dodecylbenzene sulfonic acid so that a novel catalysis system is formed, and the alkyl polyglycoside is prepared through the concerted catalysis of the novel catalysis system. The technology of the method disclosed by the invention has the advantages that the reaction efficiency of a unit catalyst is high and the reaction time is short.

Preparation and surface activity of phosphated alkyl oligoglucosides

A family of phosphated alkyl oligoglucoside surfactants was prepared by reacting alkyl oligoglucosides with phosphorus oxychloride. The alkyl oligoglucosides were obtained by an usual method in which the glucose is reacted with a fatty alcohol containing 10-18 carbon atoms. These novel phosphated surfactants have been found to exhibit good surface tension, foaming and wetting power. The critical micelle concentration was found to increase with the length of hydrocarbon chain of the surfactant. The surface excess concentration and the interfacial area per surfactant molecule are reported. These phosphated surfactants also exhibit a good performance to improve the whiteness and wetting of cotton fabrics in a hydrogen oxide bleaching system, and they are also found to be more biodegradable than conventional surfactants. AOCS 2010.