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

Chemical Name: 4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl

Molecular Formula: C₉H₁₈NO₂

CAS Number: 2226-96-2

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.

HTempo Structure

Technical Specifications

Discover the technical specifications of our 4-Hydroxy-TEMPO (TEMPOL / H-TEMPO) products.

Chemical Identity

Chemical Name4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl
SynonymsH-TEMPO, TEMPOL, 4-Hydroxy-TEMPO, 4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy
CAS Number2226-96-2
EC Number218-760-9
Molecular FormulaC₉H₁₈NO₂
Molecular Weight172.24 g/mol
HTempo Structure

VUP Specifications (Standard Grade)

PropertySpecification
AppearanceOrange or reddish-orange crystalline solid/powder
Purity≥98.0 % wt

Note: Specifications that are provided above are typical values and should not be considered as guaranteed analysis.

Key Features & Benefits

Discover the unique advantages of VUP's 4-Hydroxy-TEMPO (TEMPOL / H-TEMPO) for your applications.

Functionalized Stable Radical

Combines unique properties of TEMPO nitroxyl radical with a hydroxyl group, allowing for further chemical modification and enhanced solubility.

Key Inhibitor Intermediate

Serves as direct precursor for VUP's VUPIN range of liquid polymerization inhibitors, demonstrating significant industrial relevance.

Versatile Research Tool

Widely used as water-soluble antioxidant, catalyst in oxidation reactions, and spin label probe in EPR spectroscopy applications.

Building Block Potential

Hydroxyl group provides reactive site for synthesizing other functionalized TEMPO derivatives or incorporating nitroxyl moiety into larger molecules.

Pilot Scale Production

Manufactured at VUP's dedicated pilot plant facility ensuring availability for larger scale R&D, inhibitor production, and industrial applications.

High Purity Quality

VUP's production capabilities deliver high purity suitable for demanding applications including research and specialty chemical synthesis.

Applications

Discover the applications of our 4-Hydroxy-TEMPO (TEMPOL / H-TEMPO) products.

Polymerization Inhibitor Synthesis

Key raw material for producing formulated liquid polymerization inhibitors like the VUPIN range used in petrochemicals and monomer stabilization applications.

Catalysis & Oxidation

Used as catalyst or co-catalyst in selective oxidation reactions, offering different solubility and reactivity profiles compared to standard TEMPO.

EPR Spectroscopy

Utilized as a spin label probe to study molecular structure, dynamics, and environments in biophysical and chemical research applications.

Antioxidant Research

Employed as a water-soluble antioxidant standard or protective agent in biochemical and cell-based studies investigating oxidative stress mechanisms.

Product Information & Technical Documents

Essential information and documentation for 4-Hydroxy-TEMPO (TEMPOL / H-TEMPO)

Product Identification

Key product details and identifiers

Chemical Name4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl
SynonymsH-TEMPO, TEMPOL, 4-Hydroxy-TEMPO, 4-Hydroxy-2,2,6,6-tetramethylpiperidinooxy
CAS Number2226-96-2
EC Number218-760-9

Technical Documents

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Technical Data Sheet (TDS)

Complete technical specifications, physical properties, and application information for 4-Hydroxy-TEMPO (TEMPOL / H-TEMPO)

Safety Data Sheet (SDS)

Safety information, handling procedures, and regulatory details for 4-Hydroxy-TEMPO (TEMPOL / H-TEMPO)

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Frequently Asked Questions

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