6068-28-6

Usage

Uses

Used in Surfactant and Detergent Production:
p-Toluenesulfonic acid hexadecyl ester is used as an intermediate in the production of surfactants and detergents due to its ability to enhance the formation of these industrial chemicals.
Used in Cosmetics Industry:
p-Toluenesulfonic acid hexadecyl ester is used as an emulsifier and dispersant in the cosmetics industry, contributing to the stability and texture of various cosmetic products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, p-Toluenesulfonic acid hexadecyl ester is utilized as an emulsifier and dispersant, aiding in the formulation and stabilization of pharmaceutical products.
Used in Agricultural Products:
p-Toluenesulfonic acid hexadecyl ester is employed as an emulsifier and dispersant in agricultural products, helping to improve the performance and effectiveness of these products.
Used as a Catalyst:
p-Toluenesulfonic acid hexadecyl ester is used as a catalyst in various chemical reactions, facilitating the synthesis of different compounds.
Used as a Stabilizer in Polymer and Resin Synthesis:
In the synthesis of polymers and resins, p-Toluenesulfonic acid hexadecyl ester is used as a stabilizer to ensure the quality and consistency of the final products.
Safety Precautions:
It is important to handle p-Toluenesulfonic acid hexadecyl ester with care, as it is corrosive and can cause skin and eye irritation, among other hazards. Proper safety measures should be taken during its use and storage.

InChI:InChI=1/C23H40O3S/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-26-27(24,25)23-19-17-22(2)18-20-23/h17-20H,3-16,21H2,1-2H3

Upstream product

• 36653-82-4 1-Hexadecanol 
• 104-15-4 toluene-4-sulfonic acid 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 106610-41-7 3-n-hexadecyloxyphenol 
• 75768-18-2 1,3-dihexadecyloxybenzene 
• 151237-06-8 1,2-bis(hexadecyloxy)benzene 
• 13037-88-2 p-(hexadecyloxy)phenol 
• 137436-24-9 4,4'-di-n-hexadecyloxybenzene 
• 544-76-3 Hexadecane 
• 2136-71-2 2-(hexadecyloxy)ethanol 
• 96868-38-1 dl-α,β-Di-O-hexadecyl-O-benzylglycerol 
• 103475-80-5 rac-1-O-hexadecyl-3-O-benzylglycerol 
• 36653-82-4 1-Hexadecanol 
• 4721-17-9 hexadecylphosphonic acid 
• 26524-46-9 2-O-hexadecyl-1,3-O-benzylideneglycerol 

Relevant academic research and scientific papers

Preparation method of higher fatty alcohol 2-alkoxy ethanol

The invention provides a preparation method of higher fatty alcohol 2-alkoxy ethanol, and relates to the technical field of organic synthesis, higher fatty alcohol and sulfonyl halide are used as raw materials for cascade reaction, the higher fatty alcohol is completely converted into sulfonate under the action of alkali, and then the sulfonate is subjected to phase transfer reaction under the promotion of a phase transfer catalyst (the used phase transfer catalyst comprises quaternary ammonium salt or crown ether), sulfonate directly performs nucleophilic substitution reaction with ethylene glycol, and the reaction temperature is controlled to complete the reaction within half an hour to obtain the corresponding higher fatty alcohol 2-alkoxy ethanol. The method is low in raw material and reagent cost, simple in process operation, small in pollution, high in product yield and purity, and suitable for large-scale preparation.

NOVEL HYDROXYBUTYRIC ACID ESTER

PROBLEM TO BE SOLVED: To provide a novel 3HB ester that exhibits a cell activation effect in place of 3HB. SOLUTION: The present invention provides a novel hydroxybutyric acid ester represented by the following chemical formula, where n=8 (3HB stearoyl es

HUMAN NORMAL CELL ACTIVATOR

PROBLEM TO BE SOLVED: To provide a human normal cell activator. SOLUTION: The present invention provides a human normal cell activator containing at least one selected from the following 3-hydroxy butyric acid alkyl esters, where R is one selected from li

HYDROXYALKANOIC ACID ESTER AND RESIN COMPOSITION CONTAINING THE SAME

PROBLEM TO BE SOLVED: To provide a novel ester compound from biomass useful as a crystallization promoter for resins; and a resin composition containing the ester compound. SOLUTION: According to the invention, 0.1 to 20 pts.mass of a crystallization prom

Anion-Selective Cholesterol Decorated Macrocyclic Transmembrane Ion Carriers

Anion transporters play a vital role in cellular processes and their dysregulation leads to a range of diseases such as cystic fibrosis, Bartter's syndrome and epilepsy. Synthetic chloride transporters are known to induce apoptosis in cancer cell lines. Herein, we report triamide macrocycles that are easily synthesized and externally functionalized by pendant membrane-permeable groups. Among a variety of chains appended onto the macrocycle scaffold, cholesterol is found to be the best with an EC50 value of 0.44 μM. The macrocycle is highly anion-selective and transports ions via an OH-/X- antiport mechanism. The macrocycle is an interesting scaffold for ion-Transport as it is able to discriminate between various anions and shows a preference for SCN- and Cl-. Such anion-selective transporters are highly attractive model systems to study ion-Transport mechanisms and could potentially be of high therapeutic value.

Structure-Activity Relationships of Glucosamine-Derived Glycerolipids: The Role of the Anomeric Linkage, the Cationic Charge and the Glycero Moiety on the Antitumor Activity

The potent antitumor activity of 1-O-hexadecyl-2-O-methyl-3-O-(2′-amino-2′-deoxy-β-D-glucopyranosyl)-sn-glycerol (1) was previously shown to arise through an apoptosis-independent pathway. Here, a systematic structure-activity study in which the effects o

Solvent-free and selective tosylation of alcohols and phenols with p-toluenesulfonyl chloride by heteropolyacids as highly efficient catalysts

Tosylation of some alcohols and phenols has been directly carried out with p-toluenesulfonyl chloride using heterodoxy acids (H3PW 12O40, H3PMo12O40, A 3PW12O40, and AlPMo12O40) as catalysts in the absence of solvent. We found that heteropoly acids AlPW12O40 and AlPMo 12O40 were effective catalysts for the tosylation of alcohols and phenols. In the case of aliphatic alcohols, secondary alcohols undergo tosylation chemoselectively in the presence of primary hydroxyl groups. This new method consistently has the advantage of excellent yields and short reaction time.

NEW NON-IONIC SURFACTANTS FOR SOLUBILIZING POORLY SOLUBLE MOLECULES

New non-ionic surfactants in the form of polyoxyalkylene glycol hydroxy fatty acid derivatives or monoalkylated polyoxyalkylene glycol hydroxy fatty acid derivatives having a polyoxyalkylene / alkyl polyoxyalkylene chain with a chain-length of 25 - 455 re

ZrCl4 as an efficient catalyst for selective tosylation of alcohols with p-toluenesulfonic acid

Tosylation of alcohols has directly been carried out with p-toluenesulfonic acid in methylene chloride under reflux using ZrCl4 as a catalyst. Primary alcohols were found to be tosylated chemoselectively over secondary alcohols.