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Tempo Free Radical ||CAS No : 2564-83-2||Manufacturer || India

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  • Tempo Free Radical ||CAS No : 2564-83-2||Manufacturer || India


    Tempo-Free Radical is a stable free radical widely used in organic chemistry for various oxidation reactions and other applications. This guide aims to provide detailed information about TEMPO, including its chemical properties, uses, mechanisms, handling precautions, and more.

    What is TEMPO?


    TEMPO is a persistent free radical that is an efficient catalyst and reagent in organic synthesis. Its stability and unique properties make it valuable for numerous chemical transformations, particularly in the field of oxidation.

    Chemical Properties
    • Chemical Formula: C9H18NO
    • Molecular Weight: 156.25 g/mol
    • Appearance: Orange-red crystalline solid
    • Melting Point: 36-38°C
    • Solubility: Soluble in organic solvents such as dichloromethane, ethanol, and acetonitrile; sparingly soluble in water.
    • Case No: 2564-83-2

    Manufacturer


    TEMPO is produced by various chemical companies specializing in fine chemicals and laboratory reagents. These manufacturers ensure high purity and quality standards to meet the requirements of research and industrial applications.

    Lifechempharma Best Products:-
    Uses of TEMPO


    TEMPO is primarily used in:
    • Oxidation Reactions: TEMPO is an excellent catalyst for the selective oxidation of alcohols to aldehydes or ketones, and the oxidation of primary alcohols to carboxylic acids.
    • Polymer Chemistry: It is used in the controlled radical polymerization (CRP) process and in the modification of polymers.
    • Biochemistry: TEMPO derivatives are utilized as spin labels in electron spin resonance (ESR) spectroscopy to study protein structures and dynamics.
    • Organic Synthesis: TEMPO is used in various organic transformations, including C-H activation and amination reactions.

    How TEMPO Works


    TEMPO operates through a free radical mechanism, making it a versatile reagent in oxidative processes. The typical steps in a TEMPO-mediated oxidation reaction include:
    1. Activation: TEMPO abstracts a hydrogen atom from the substrate (e.g., an alcohol), generating a radical intermediate.
    2. Oxidation: The radical intermediate undergoes further oxidation, often in the presence of a co-oxidant (e.g., bleach or sodium hypochlorite), leading to the formation of the desired product (e.g., an aldehyde or ketone).
    3. Catalytic Cycle: TEMPO is regenerated at the end of the reaction cycle, allowing it to be used catalytically in small amounts.

    Handling and Storage


    Proper handling and storage of TEMPO are crucial to maintaining its stability and effectiveness:
    • Storage: Store TEMPO in a cool, dry place, ideally below 25 °C, in a tightly sealed container away from light and moisture.
    • Handling: When handling TEMPO, wear appropriate personal protective equipment (PPE), such as gloves and safety goggles. Work in a well-ventilated area or under a fume hood to avoid inhalation and contact.

    Precautions


    When using TEMPO, consider the following safety precautions:
    • Health Hazards: TEMPO can cause skin and eye irritation. Avoid direct contact and inhalation of dust or vapours.
    • Chemical Stability: Ensure TEMPO is stored properly to prevent degradation and loss of activity.
    • Environmental Safety: Dispose of TEMPO and its byproducts according to local regulations and guidelines for hazardous waste.

    Side Effects and Toxicity
    • Acute Exposure: May cause irritation to the skin, eyes, and respiratory system. In case of contact, rinse thoroughly with water and seek medical attention if necessary.
    • Chronic Exposure: Prolonged exposure may lead to sensitization and allergic reactions in some individuals.

    Applications in Research and Industry
    • Pharmaceuticals: TEMPO is used to synthesise pharmaceutical intermediates and active ingredients.
    • Material Science: It is employed in the functionalization of materials and in the preparation of advanced polymers.
    • Biochemistry: TEMPO derivatives serve as spin labels for structural and dynamic studies of biomolecules.
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