Discover Isobarbituric Acid (CAS 496-76-4): Properties, Applications, and Chemical Insights

Uncover the versatile chemical nature and research applications of 2,4,5-Trihydroxypyrimidine.

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Key Advantages

Biochemical Functionality

Leverage the unique biochemical functionality of 2,4,5-Trihydroxypyrimidine, which acts as a glycosylase, to investigate DNA repair mechanisms and damage pathways.

Research Precision

Utilize Isobarbituric acid (CAS 496-76-4) for precise research into oxidative DNA damage, enabling accurate biomarker identification and quantification.

Chemical Versatility

Benefit from the chemical versatility of this pyrimidine derivative, which reacts with nucleophilic groups at neutral pH, offering broad utility in synthetic chemistry.

Key Applications

DNA Damage Research

Isobarbituric acid (CAS 496-76-4) is instrumental in studying oxidative DNA damage, serving as a critical biomarker in various biological contexts.

Biochemical Assays

Employ 2,4,5-Trihydroxypyrimidine in biochemical assays that require precise cleavage of specific DNA bonds or interaction with nucleophilic groups.

Chemical Synthesis

Utilize this pyrimidine derivative as a building block or reagent in the synthesis of more complex organic molecules and pharmaceutical intermediates.

Analytical Standards

Source Isobarbituric acid as a reliable analytical standard for laboratory use, ensuring accuracy in analytical chemistry procedures.