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Usage

Uses

Used in Organic Chemistry:
2,4-Dihydroxybenzaldehyde 2,4-dinitrophenyl hydrazone is used as a reagent for the qualitative analysis of carbonyl compounds, such as aldehydes and ketones. It facilitates the identification of these compounds by forming bright yellow crystalline precipitates upon reaction.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4-Dihydroxybenzaldehyde 2,4-dinitrophenyl hydrazone is utilized as a building block in the synthesis of various organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 2,4-Dihydroxybenzaldehyde 2,4-dinitrophenyl hydrazone serves as a key intermediate in the synthesis of different agrochemical products, playing a role in the creation of pesticides and other agricultural chemicals.
Used in Cancer Research:
2,4-Dihydroxybenzaldehyde 2,4-dinitrophenyl hydrazone has been investigated for its potential as an anti-cancer agent, with studies exploring its effects on cancer cells and its possible integration into cancer treatment strategies.
Used in Material Science:
2,4-Dihydroxybenzaldehyde 2,4-dinitrophenyl hydrazone is also being studied for its application in the development of new materials for electronics and optics, where its unique properties may contribute to advancements in these fields.

Upstream product

• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 95-01-2 2,4-Dihydroxybenzaldehyde 

Relevant academic research and scientific papers

8(E)-4-[{2-(2,4-dinitrophenyl)hydrazono}benzene-1,3-diol] as a solvatochromic Schiff base and chromogenic signaling of water content by its deprotonated form in acetonitrile

A simple, cost effective Schiff base (E)-4-[{2-(2,4-dinitrophenyl) hydrazono}benzene-1,3-diol] (DBH) is synthesized and characterized by various physico-chemical and spectroscopic tools along with single crystal X-ray crystallography. This is the first report which describes its solvatochromism in solution and the signaling behavior of deprotonated DBH for the determination of water content in acetonitrile through UV-visible absorption spectra. Addition of acetate ions in acetonitrile solution of DBH results in the formation of deprotonated DBH. The effect of water content on the formation of deprotonated DBH is utilized in signaling. The deprotonated DBH exhibits a pronounced chromogenic signaling behavior that can be detected by the naked eye in response to the changes in water content in acetonitrile. Prominent color changes are observed up to 2% water content in acetonitrile and limit of detection (LOD) of the deprotonated DBH for determination of the water content in acetonitrile is calculated as 0.012%.

2,4-Dinitrophenylhydrazones of 2,4-dihydroxybenzaldehyde, 2,4-dihydroxyacetophenone and 2,4-dihydroxybenzophenone

In 2,4-dihydroxybenzaldehyde 2,4-dinitrophenylhydrazone N,N-dimethylformamide solvate (or 4-[(2,4-dinitrophenyl)-hydrazonomethyl]benzene-1,3-diol N,N-dimethylformamide solvate}, C13H10N4O6·C 3H7