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Free Radicals

Specialty stable radicals — primarily TEMPO (2,2,6,6-Tetramethylpiperidin-1-oxyl) and its key derivatives — designed for controlled oxidation, polymerisation moderation, and mechanistic research. With over five decades of chemical R&D expertise, VUP offers pilot-plant and laboratory-scale radicals for precise control in organic synthesis, living polymerisation (NMP), and redox catalysis.

TEMPO Structure

Our Free Radicals Portfolio

Discover our range of high-quality Free Radicals products for your specific application needs.

TEMPO Structure
Product
CAS: 2564-83-2

TEMPO (2,2,6,6-Tetramethylpiperidin-1-oxyl)

A highly versatile and stable nitroxyl radical, renowned for its utility as a catalyst in selective organic oxidations and as a mediator in controlled radical polymerization (NMP). VUP produces high-purity TEMPO at pilot scale.

Key Properties

Highly Selective Oxidation
Stable Radical Source
Controlled Polymerization
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2226-96-2 Structure
Product
CAS: 2226-96-2

4-Hydroxy-TEMPO (TEMPOL / H-TEMPO)

A key functionalized derivative of TEMPO featuring both a stable nitroxyl radical and reactive hydroxyl group. Serves as a versatile antioxidant, catalyst, spin label, and crucial intermediate for synthesizing specialty chemicals.

Key Properties

Functionalized Stable Radical
Key Inhibitor Intermediate
Versatile Research Tool
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TEMPONE Structure
Product
CAS: 2896-70-0

4-Oxo-TEMPO (TEMPone)

A ketone-functionalized stable nitroxyl radical based on TEMPO, offering alternative reactivity in selective oxidation catalysis and serving as a versatile intermediate for synthesizing complex nitroxide derivatives.

Key Properties

Functionalized TEMPO Radical
Alternative Oxidant Properties
Versatile Intermediate
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Acetamido TEMPO Structure
Product
CAS: 14691-89-5

4-Acetamido-TEMPO

A functionalized derivative of the stable nitroxyl radical TEMPO featuring an acetamido group. Primarily used as a spin label probe for Electron Paramagnetic Resonance (EPR) spectroscopy in biochemical and materials science research.

Key Properties

Functionalized Spin Label
Research Grade Purity
Membrane Probe Capability
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14691-88-4 Structure
Product
CAS: 14691-88-4

4-Amino-TEMPO

Amino-functionalized TEMPO radical featuring stable nitroxyl functionality combined with reactive amino group. Ideal for spin labeling, bioconjugation, and advanced materials research. VUP Lab Researched quality.

Key Properties

Persistent Radical Stability
Dual Functionality
High Purity
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2370-18-5 Structure
Product
CAS: 2370-18-5

Galvinoxyl Free Radical

A highly stable phenoxyl radical structurally distinct from TEMPO derivatives. Used as analytical standard for radical scavenging studies and antioxidant research. Deep blue color provides visual indication of radical concentration.

Key Properties

Phenoxyl Radical Structure
Visual Color Indicator
Exceptional Stability
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Applications

Industry Applications for Free Radicals

Our Free Radicals serve diverse applications across industry sectors.

Catalytic Oxidation

Selective alcohol-to-aldehyde and amine-to-imine transformations under mild conditions for fine chemical and pharmaceutical synthesis.

Controlled Radical Polymerisation (NMP)

Nitroxide-mediated polymerisation for precise molecular weight control and synthesis of well-defined polymer architectures.

Redox Catalysis

Employed in electrochemical and chemical redox cycles for organic synthesis and catalytic transformations.

Spin Labeling & EPR Research

Stable radicals for mechanistic and structural analysis in ESR/EPR spectroscopy and biophysical studies.

Antioxidant & Stability Studies

Used in oxidative stability modelling of polymers and organic materials for research and development applications.

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