16081-15-5

Usage

Uses

Used in Analytical Chemistry:
1,4-Benzoquinone-DNPH (Mono) is used as a reagent for the detection and quantification of carbonyl compounds due to its high specificity and sensitivity towards aldehydes and ketones.
Used in Environmental Monitoring:
1,4-Benzoquinone-DNPH (Mono) is utilized for monitoring the presence of carbonyl compounds in the environment, helping to ensure the safety and quality of air, water, and soil.
Used in Industrial Monitoring:
1,4-BENZOQUINONE-DNPH (MONO) is employed in industrial settings to detect and quantify carbonyl compounds, which can be crucial for process control, quality assurance, and worker safety.
It is important to handle 1,4-Benzoquinone-DNPH (Mono) with care, as it is toxic and can cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C12H8N4O5/c17-10-4-1-8(2-5-10)13-14-11-6-3-9(15(18)19)7-12(11)16(20)21/h1-7,14H

Upstream product

• 123-31-9 hydroquinone 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 108-95-2 phenol 
• 106-51-4 p-benzoquinone 

Relevant academic research and scientific papers

Optimization of Synthesis of 2,4-Dinitrophenylhydrazones under Carbon Dioxide Pressure

Catalytic synthesis of 2,4-dinitrophenylhydrazones formed in the aqueous reaction mixture of aliphatic and aromatic carbonyl derivatives with 2,4-dinitrophenylhydrazine in the presence of carbonic acid protons under pressure of the CO2-H2

An efficient tandem oxidative-protection reaction of benzylic alcohols to corresponding arylhydrazones and oximes

A mild and efficient one-pot synthesis of hydrazones and oximes from the reaction of the oxidation product of benzyl alcohols and phenols by 3,6-bis(triphenylphosphonium)cyclohexene dichromate with phenylhydrazine, 2,4-dinitrophenylhydrazine, and hydroxylamine is described. Copyright Taylor & Francis Group, LLC.

Resonance Raman observation of surface carbonyl groups on carbon electrodes following dinitrophenylhydrazine derivatization

Dinitrophenylhydrazine (DNPH) was used to form hydrazone derivatives of carbonyl groups on glassy carbon (GC) and pyrolytic graphite surfaces. The DNPH adducts of benzoquinone and acetone have cross sections of 488 nm, much larger than those of either DNP