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

Oxidation of Phenols to Quinones01:17

Oxidation of Phenols to Quinones

In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
Oxidations of Aldehydes and Ketones to Carboxylic Acids01:15

Oxidations of Aldehydes and Ketones to Carboxylic Acids

Oxidation of aldehydes and ketones results in the formation of carboxylic acids. Aldehydes, bearing hydrogen next to the carbonyl group, are easily oxidized compared to ketones. This is because an aldehydic proton can easily be abstracted during oxidation.
Aldehydes readily undergo oxidation in strong oxidizing agents such as potassium permanganate and chromic acid. The oxidation can also be carried out using mild oxidizing agents such as silver oxide. In fact, aldehydes can be easily oxidized...
Redox Titration: Other Oxidizing and Reducing Agents01:26

Redox Titration: Other Oxidizing and Reducing Agents

Besides iodine, other oxidizing or reducing agents can serve as titrants in redox titrations. Common oxidizing titrants include KMnO4, cerium(IV), and K2Cr2O7. The choice of oxidizing titrants depends on factors like stability, cost, analyte strength, and reaction rate between the analyte and titrant. KMnO4 is a strong oxidizing titrant that reduces from Mn(VII) to Mn(II) in a highly acidic solution, simultaneously oxidizing the analyte to a higher oxidation state. In this case, KMnO4 acts as a...
Oxidation of Alcohols02:37

Oxidation of Alcohols

In this lesson, the oxidation of alcohols is discussed in depth. The various reagents used for oxidation of primary and secondary alcohols are detailed, and their mechanism of action is provided.
The process of oxidation in a chemical reaction is observed in any of the three forms:
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...
Redox Reactions01:24

Redox Reactions

Oxidation-reduction or redox reactions involve the transfer of electrons from one molecule or atom to another. When an atom gains an electron, another atom must lose an electron, meaning oxidation and reduction must occur together. Since the redox occurs in pairs, the atom that gets oxidized is also called the reducing agent or reductant, and the atom that is reduced is also called the oxidizing agent or oxidant. A straightforward way to remember the definitions of oxidation and reduction is...

You might also read

Related Articles

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

Sort by
Same author

Evaluating case-based learning approaches: Effects on student performance and perceived APPE readiness.

Currents in pharmacy teaching & learning·2026
Same author

Quantitative Host Cell Protein Analysis of Antibody-Based Protein Therapeutics Using the Orbitrap Astral Mass Spectrometer.

Journal of the American Society for Mass Spectrometry·2026
Same author

Response from Webb et al.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists·2025
Same author

Single-Cell Mitochondrial DNA Analysis of Recombinant Chinese Hamster Ovary Cells Reveals Widespread Heteroplasmy.

Biotechnology journal·2025
Same author

Varicella-Zoster Myelitis With Thoracic Demyelination and Lumbosacral Plexopathy in the Setting of Uncontrolled HIV.

Cureus·2025
Same author

The personal cost of nosocomial infections.

Nursing·2025
Same journal

Selected Alkaloids Used in the Cosmetics Industry.

Journal of cosmetic science·2022
Same journal

Dermal Effects of Unsaponifi able Compounds: The Overlooked Perspective of Vegetable Butters and Oils.

Journal of cosmetic science·2022
Same journal

Comparison of Urea-Based Compounding Moisturizers and Similar Commercial Products on Skin Barrier Function: A Randomized Biometric Study.

Journal of cosmetic science·2022
Same journal

Improving Oxidative Stability of Cosmetic Emulsions with Plant Extracts: Current Status and Potential.

Journal of cosmetic science·2022
Same journal

Next-Generation Natural Baby Barrier Cream Formulations: Physicochemical Analysis and Safety Assessment.

Journal of cosmetic science·2022
Same journal

Effectiveness of the Disinfection of Reusable Make-Up Applicators-Initial Experiences.

Journal of cosmetic science·2022
See all related articles

Related Experiment Video

Updated: Jun 23, 2026

Synthesis of Plant Phenol-derived Polymeric Dyes for Direct or Mordant-based Hair Dyeing
09:46

Synthesis of Plant Phenol-derived Polymeric Dyes for Direct or Mordant-based Hair Dyeing

Published on: December 1, 2016

A new oxidant for hair coloring.

Jennifer Marsh1, R Marc Dahlgren, Colin Clarke

  • 1Procter & Gamble, Miami Valley Innovation Center, 11810 East Miami River Road, Cincinnati, OH 45069, USA.

Journal of Cosmetic Science
|May 20, 2009
PubMed
Summary
This summary is machine-generated.

A new hair oxidant using ammonium carbonate, hydrogen peroxide, and glycine at pH 9 matches current performance. This flexible system offers faster lightening or reduced hydrogen peroxide, with glycine preventing damaging radical formation.

More Related Videos

Stimulation of Stem Cell Niches and Tissue Regeneration in Mouse Skin by Switchable Protoporphyrin IX-Dependent Photogeneration of Reactive Oxygen Species In Situ
10:05

Stimulation of Stem Cell Niches and Tissue Regeneration in Mouse Skin by Switchable Protoporphyrin IX-Dependent Photogeneration of Reactive Oxygen Species In Situ

Published on: May 8, 2020

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
06:34

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)

Published on: June 20, 2014

Related Experiment Videos

Last Updated: Jun 23, 2026

Synthesis of Plant Phenol-derived Polymeric Dyes for Direct or Mordant-based Hair Dyeing
09:46

Synthesis of Plant Phenol-derived Polymeric Dyes for Direct or Mordant-based Hair Dyeing

Published on: December 1, 2016

Stimulation of Stem Cell Niches and Tissue Regeneration in Mouse Skin by Switchable Protoporphyrin IX-Dependent Photogeneration of Reactive Oxygen Species In Situ
10:05

Stimulation of Stem Cell Niches and Tissue Regeneration in Mouse Skin by Switchable Protoporphyrin IX-Dependent Photogeneration of Reactive Oxygen Species In Situ

Published on: May 8, 2020

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)
06:34

Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides (CHIPS)

Published on: June 20, 2014

Area of Science:

  • Cosmetic Chemistry
  • Hair Color Science
  • Oxidation Mechanisms

Background:

  • Permanent hair coloring involves melanin lightening and chromophore formation.
  • Conventional oxidants use hydrogen peroxide buffered at pH 10 with ammonium hydroxide.
  • Need for improved oxidant systems with enhanced flexibility and reduced hair damage.

Purpose of the Study:

  • To introduce and evaluate a novel hair oxidant system.
  • To compare its performance against conventional hydrogen peroxide-based oxidants.
  • To elucidate the mechanisms of action and the role of glycine in the new system.

Main Methods:

  • Development of a new oxidant combining ammonium carbonate, hydrogen peroxide, and glycine at pH 9.
  • Assessment of lightening performance based on time, pH, hydrogen peroxide, and carbonate concentrations.
  • Analysis of key oxidizing species and melanin lightening mechanisms.
  • Investigation of glycine's role in controlling radical formation.

Main Results:

  • The new oxidant system demonstrates comparable lightening and color performance to conventional oxidants.
  • Adjustable carbonate and hydrogen peroxide concentrations allow for flexible lightening control.
  • Glycine addition effectively inhibits the formation of detrimental carbonate radicals.
  • The new system achieves excellent lightening with no increase in hair fiber damage.

Conclusions:

  • A novel, flexible hair oxidant system based on ammonium carbonate, hydrogen peroxide, and glycine has been developed.
  • This system offers tunable lightening performance and superior hair protection compared to traditional oxidants.
  • Glycine plays a crucial role in stabilizing the oxidant and preventing oxidative damage to hair fibers.