Related Experiment Video
Updated: Jan 18, 2026

Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile
Published on: October 30, 2018
Extraction and determination of esteric compounds in wound disinfectants
Mir Ali Farajzadeh1,2, Zahra Hallaji1, Sakha Pezhhanfar1
1Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz Tabriz Iran mafarajzadeh@yahoo.com mafarajzadeh@tabrizu.ac.ir +98 41 33340191 +98 41 33393084.
None:
This study focuses on developing an analytical method to efficiently extract and concentrate several adipate and phthalate plasticizers that can migrate from plastic packaging into various wound disinfectants. The study employed an approach that combined dispersive micro solid phase extraction with dispersive liquid-liquid microextraction using ZIF-4 as an adsorbent. The adsorbent was thoroughly characterized to understand its properties. The microextraction step concentrated the target compounds for analysis using gas chromatography. After plasticizer adsorption onto ZIF-4, the analytes were desorbed using acetonitrile. The method demonstrated good performance by high extraction recoveries (61-95%) and enrichment factors (305-475), low detection (0.16-0.28 μg L-1) and quantification (0.54-0.93 μg L-1) limits, and good precision (relative standard deviation less than 7% for intra- and inter-day precisions).
More Related Videos
09:49Use of a Battery of Chemical and Ecotoxicological Methods for the Assessment of the Efficacy of Wastewater Treatment Processes to Remove Estrogenic Potency
Published on: September 11, 2016
13:05Enzymatic Synthesis of Epoxidized Metabolites of Docosahexaenoic, Eicosapentaenoic, and Arachidonic Acids
Published on: June 28, 2019
Related Concept Videos
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
β-Dicarbonyl Compounds via Crossed Claisen Condensations