173725-25-2

Basic information

• Product Name: TETRADECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE
• Synonyms: TETRADECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE;Tetradecyl2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-b-D-glucopyranoside;TETRADECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-SS-D-GLUCOPYRANOSIDE;Tetradecyl 2-acetaMido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside
• CAS NO: 173725-25-2
• Molecular Formula: C28H49NO9
• Molecular Weight: 543.693
• EINECS: 1533716-785-6
• Mol File: 173725-25-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: TETRADECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: TETRADECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE(173725-25-2)
• EPA Substance Registry System: TETRADECYL 2-ACETAMIDO-2-DEOXY-3,4,6-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSIDE(173725-25-2)

Safety Data

• Hazardous Substances Data: 173725-25-2(Hazardous Substances Data)

Usage

General Description

Tetradecyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-beta-D-glucopyranoside is a chemical compound that is derived from glucose and has a long hydrophobic chain attached to it, making it amphiphilic in nature. It is often used as a surfactant in various pharmaceutical and cosmetic products due to its ability to lower surface tension and increase the solubility of other substances. The acetyl groups on the sugar molecule provide stability and solubility in organic solvents, making it useful in the formulation of emulsions and creams. This chemical compound also has potential applications in drug delivery systems and as an ingredient in skincare products.

Upstream product

• 2873-29-2 D-glucal triacetate 
• 108-24-7 acetic anhydride 
• 112-72-1 1-Tetradecanol 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 

Downstream Products

• 152914-69-7 n-tetradecyl 2-acetamido-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

Novel stereocontrolled amidoglycosylation of alcohols with acetylated glycals and sulfamate ester

A regio- and stereo-controlled, one-pot amidoglycosylation of alcohols has been achieved using O-acetylated glycals, trichloroethoxysulfonamide, and iodosobenzene in the presence of a rhodium(ii) catalyst. The reaction would proceed via stereoselective intermolecular aziridination of the glycal. This journal is the Partner Organisations 2014.

Synthesis and surface-active properties of some alkyl 2-amino-2-deoxy-β-D-glucopyranosides

Several alkyl 2-acetamido-2-deoxy-β-D-glucopyranosides were synthesized using either the oxazoline or the N-allyloxycarbonyl procedure.The latter procedure gave better yields with fatty alcohols and cholesterol.The derivatives thus prepared were partly of fully deprotected and their surface-active properties assessed.Keywords: 2-Amino-2-deoxy-D-glucose; Amphiphiles; Surfactant; 14C-labelled