2,4-Dinitrophenol, moistened with water, ≥98.0%, 25g

2,4-Dinitrophenol (DNP) is a high-purity aromatic compound, moistened for safe handling, and commonly used in organic synthesis and catalysis. The electron-withdrawing nitro groups make DNP a versatile reagent for forming esters, activating carboxylic acids, and supporting asymmetric catalysis. This compound is also valued for its role in nucleoside chemistry and reduction reactions.

Key Features

• ≥98% purity – Ensures consistent reactivity and product quality
• Moistened formulation – Reduces dust and enhances handling safety
• Activated phenol ring – Facilitates ester formation and nucleophilic substitution
• Versatile synthetic applications – Suitable for both catalytic and preparative reactions
• Stable under proper storage conditions

Specifications

Applications

• Catalytic Reduction – Substrate in hydrogenation and reduction studies
• Carboxylic Acid Activation – Formation of dinitrophenyl esters for coupling reactions
• Acylation Chemistry – Used to synthesize esters in presence of isobutyric anhydride and Lewis acid catalysts
• Organocatalysis – Acts as a cocatalyst in asymmetric aldol reactions involving amino acid-derived catalysts
• Phosphoramidite Coupling – Alternative to tetrazole-based activators in nucleoside chemistry

Ordering Information

2,4-Dinitrophenol (DNP), ≥98%, moistened for enhanced safety, is a highly useful reagent in advanced organic synthesis and catalysis. Its electron-deficient aromatic system and phenolic functionality allow it to participate in a wide array of synthetic transformations, making it indispensable for research laboratories and chemical manufacturers.