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Related Concept Videos

α-Halogenation of Carboxylic Acid Derivatives: Overview01:14

α-Halogenation of Carboxylic Acid Derivatives: Overview

Unlike aldehydes and ketones, carboxylic acids do not readily participate in α halogenation reactions via enols or enolate intermediates. However, α-halogenated acids are obtained through other methods. One of the approaches is the Hell–Volhard–Zelinsky (HVZ) reaction, wherein the carboxylic acid is treated with halogen in the presence of PBr3. It involves the conversion of acid to acid halide, which exists in equilibrium with its enol form. The enol attacks the electrophilic halogen to produce...
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Microbes in Food Production

Microbial fermentation is central to food biotechnology, enhancing flavor, texture, preservation, and stability. Fermentative microorganisms metabolize carbohydrates into organic acids, alcohols, and other metabolites that inhibit spoilage organisms and improve digestibility while contributing distinctive sensory qualities.In baking, amylases naturally present in flour hydrolyze starch into monosaccharides such as glucose, which Saccharomyces cerevisiae ferments anaerobically. Through...
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction01:15

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The method to achieve α-brominated carboxylic acids using a mixture of phosphorus tribromide and bromine is known as the Hell–Volhard–Zelinski reaction. The reaction is catalyzed by phosphorus tribromide, which can be used directly or produced in situ from red phosphorus and bromine. The mechanism comprises PBr3 catalyzed conversion of acid to acid bromide and hydrogen bromide. The acid bromide enolizes to its enol form in the presence of HBr. The nucleophilic enol attacks the bromine molecule...
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.

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Updated: May 12, 2026

Using Tg(Vtg1:mcherry) Zebrafish Embryos to Test the Estrogenic Effects of Endocrine Disrupting Compounds
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[Zearalenone in food].

O Kappenstein1, A Brockmeyer, R Dietrich

  • 1Bundesinstitut für Risikobewertung, Thielallee 88-92, D-14195, Berlin, okappenstein@bfr bund de.

Mycotoxin Research
|April 23, 2013
PubMed
Summary

This research details methods for analyzing Fusarium toxins, specifically deoxynivalenol and zearalenone, and their presence in German food. It provides a comprehensive overview of zearalenone contamination in the food supply.

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Area of Science:

  • Food Science
  • Analytical Chemistry
  • Toxicology

Context:

  • Focuses on Fusarium toxins, deoxynivalenol and zearalenone, significant food contaminants.
  • Addresses the need for robust analytical methods to detect these mycotoxins.
  • Examines the occurrence and levels of these toxins within the German food supply chain.

Purpose:

  • To summarize the contamination of food by zearalenone (ZEA).
  • To outline methods for the analysis of deoxynivalenol and zearalenone.
  • To assess the intake of these toxins by the German consumer.

Summary:

  • This project comprehensively summarizes the contamination of food by zearalenone (ZEA).
  • It details the occurrence of important Fusarium toxins, deoxynivalenol and zearalenone, in food.
  • The research also addresses the intake of these toxins by German consumers.

Impact:

  • Provides crucial data on food safety regarding mycotoxin contamination.
  • Supports regulatory bodies in setting safe limits for zearalenone and deoxynivalenol.
  • Enhances understanding of dietary exposure to Fusarium toxins for the German population.