Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene01:14

Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene

Electrophilic addition of halogens to alkenes proceeds via a cyclic halonium ion to form a 1,2-dihalide or a vicinal dihalide.
Radical Autoxidation01:20

Radical Autoxidation

The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
Masking and Demasking Agents01:19

Masking and Demasking Agents

EDTA titrations may necessitate masking and demasking agents to temporarily protect a particular metal ion in a mixture from the EDTA reaction. These agents facilitate the sequential analysis of the metal ions by forming stable complexes with some—but not all—metal ions during certain steps.
There are many masking agents, such as cyanide, fluoride, triethanolamine, thiourea, and 2,3-bis(sulfanyl)propan-1-ol (formerly 2,3-dimercapto-1-propanol), with the masking agent chosen based on the metal...
Autoxidation of Ethers to Peroxides and Hydroperoxides02:23

Autoxidation of Ethers to Peroxides and Hydroperoxides

Ethers represent a class of chemical compounds that become more dangerous with prolonged storage because they tend to form explosive peroxides when standing in the air. Autoxidation is the spontaneous oxidation of a compound in air. In the presence of oxygen, ethers slowly oxidize to form hydroperoxides and dialkyl peroxides.
Cross-reactivity00:42

Cross-reactivity

Overview
EDTA: Auxiliary Complexing Reagents01:26

EDTA: Auxiliary Complexing Reagents

EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Are We Reading Patch Test Reactions in a Uniform Way? An International Contact Dermatitis Research Group Study.

Dermatitis : contact, atopic, occupational, drug·2025
Same author

Photopatch testing: Clinical characteristics, test results, and final diagnoses from the North American Contact Dermatitis Group, 2009-2020.

Contact dermatitis·2024
Same author

Nonmedical Adhesive Allergens: Retrospective Analysis of Cross-Sectional Data From the North American Contact Dermatitis® Group, 2001-2018.

Dermatitis : contact, atopic, occupational, drug·2024
Same author

Patch Testing With Nickel, Cobalt, and Chromium in Patients With Suspected Allergic Contact Dermatitis.

Dermatitis : contact, atopic, occupational, drug·2023
Same author

The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications.

Journal of cutaneous medicine and surgery·2023
Same author

A case-control pharmacovigilance study of TNF-alpha inhibitors and interleukin inhibitors on tuberculosis, Candida, lymphoma and suicidality using the FAERS database (2014-2020).

Journal of the American Academy of Dermatology·2023

Related Experiment Video

Updated: Jul 12, 2026

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry
07:02

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry

Published on: August 25, 2016

Cross-reactions between xanthates and rubber additives.

Denis Sasseville1, Mowza Al-Sowaidi, Linda Moreau

  • 1McGill University Health Centre, Royal Victoria Hospital, Montréal, Quebec, Canada.

Dermatitis : Contact, Atopic, Occupational, Drug
|August 30, 2007
PubMed
Summary

Xanthates can cause allergic reactions and cross-react with common rubber additives like carbamates and thiurams. Lowering xanthate patch-test concentrations may help identify true sensitivities.

More Related Videos

Three-dimensional Biomimetic Technology: Novel Biorubber Creates Defined Micro- and Macro-scale Architectures in Collagen Hydrogels
12:07

Three-dimensional Biomimetic Technology: Novel Biorubber Creates Defined Micro- and Macro-scale Architectures in Collagen Hydrogels

Published on: February 12, 2016

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
11:17

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction

Published on: January 19, 2016

Related Experiment Videos

Last Updated: Jul 12, 2026

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry
07:02

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry

Published on: August 25, 2016

Three-dimensional Biomimetic Technology: Novel Biorubber Creates Defined Micro- and Macro-scale Architectures in Collagen Hydrogels
12:07

Three-dimensional Biomimetic Technology: Novel Biorubber Creates Defined Micro- and Macro-scale Architectures in Collagen Hydrogels

Published on: February 12, 2016

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
11:17

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction

Published on: January 19, 2016

Area of Science:

  • Dermatology
  • Occupational Health
  • Toxicology

Background:

  • Allergic contact dermatitis from xanthates in mining has been previously reported.
  • Cross-reactions with carbamates were observed, likely due to a shared chemical structure.

Purpose of the Study:

  • To determine the frequency of cross-reactions between xanthates and various rubber additives.
  • To investigate the relationship between xanthate sensitivity and sensitivity to other common allergens.

Main Methods:

  • 1,220 patients underwent patch testing with xanthates (sodium isopropyl xanthate, potassium amyl xanthate) and standard series.
  • Concentrations of xanthates used were initially 10% and later reduced to 5%.

Main Results:

  • 25 patients showed positive reactions to xanthates and/or rubber additives.
  • 12 patients reacted to xanthates and either carba mix or thiuram mix.
  • 50% of patients sensitized to carbamates, thiurams, or mercaptobenzothiazole cross-reacted with xanthates.

Conclusions:

  • Xanthates can induce allergic contact dermatitis and exhibit cross-reactivity with common rubber additives.
  • Xanthates are irritants; reduced patch-test concentrations (5% or less) are recommended.