610-41-3

Usage

Uses

Used in Dye Industry:
3,4-Dinitroaniline is used as a chemical intermediate for the synthesis of various dyes. Its unique chemical structure allows for the creation of a wide range of colors, making it a valuable component in the production of dyes for textiles, plastics, and other materials.
Used in Pesticide Industry:
3,4-Dinitroaniline serves as a key intermediate in the production of certain pesticides. Its properties enable the development of effective compounds that can protect crops from pests and ensure a stable food supply.
Used in Herbicide Industry:
In the herbicide industry, 3,4-dinitroaniline is utilized as a precursor for the synthesis of herbicidal compounds. These compounds are designed to selectively control the growth of unwanted plants, thereby improving crop yields and maintaining healthy agricultural ecosystems.
Used in Research Chemicals:
3,4-Dinitroaniline is also employed as a research chemical, providing scientists with a versatile compound for conducting experiments and developing new chemical processes or products. Its reactivity and structural features make it an essential component in various research applications.

InChI:InChI=1/C6H5N3O4/c7-4-1-2-5(8(10)11)6(3-4)9(12)13/h1-3H,7H2

Upstream product

• 602-03-9 2,3-dinitroaniline 
• 73334-01-7 3,4-dinitroacetanilide 
• 60956-27-6 N-(2,3-dinitrophenyl)acetamide 
• 7664-93-9 sulfuric acid 
• 122-28-1 N-(3-nitrophenyl)acetanilide 

Downstream Products

• 861318-83-4 (3,4-dinitro-phenyl)-picryl-amine 
• 109249-56-1 (3,4-dinitro-phenyl)-amidophosphoric acid diphenyl ester 
• 3698-54-2 2,3,4,6-tetranitroaniline 
• 41252-95-3 1-chloro-4-iodo-2-nitrobenzene 
• 51294-43-0 4-iodo-1,2-dinitro-benzene 
• 116529-42-1 2-bromo-4,5-dinitro-aniline 
• 73334-02-8 N-Nitro-3,4-dinitroaniline 
• 610-40-2 3,4-dinitro-chlorobenzene 
• 528-29-0 1,2-Dinitrobenzene 
• 89-61-2 2,5-dichloronitrobenzene 
• 92398-77-1 trifluoroacetyl-α-L-aspartyl-3,4-dinitroanilide 
• 29906-33-0 4-diazo-2-nitrophenol 
• 30930-62-2 3-nitro-4-chlorobenzenediazonium cation 
• 1132945-23-3 N-(3,4-dinitrophenyl)methanesulfonamide 

Relevant academic research and scientific papers

The Rearragement of Aromatic Nitro Compounds. Part 1. The Reactions of Nitroanilines in Aqueous Sulphuric Acid

A number of substituted 2-nitroanilines rearange in concentrated sulphuric acid at 110 deg C to yield products that appear to be derived from 1,3-migration of the 2-nitro-group.For 2,3-dinitroaniline, the rate of reaction is almost independent of acidity over the range 83-97percent sulphuric acid and the solvent isotope effect k(H2SO4)/k(D2SO4) is 1.3-1.9.Methyl and t-butyl groups, when present as additional substituents in 2,3-dinitroaniline, have only a small effect on the reaction rate but 3-methyl-2-nitroaniline reacts much more slowly than 2,3-dinitroaniline.These results are discussed in terms of a rate-determining migration of the 2-nitro group following protonation at the 2-position.

Synthesis of Polynitro Compounds. Peroxydisulfuric Acid Oxidation of Polynitroarylamines to Polynitro Aromatics.

Peroxydisulfuric acid in sulfuric acid solution, prepared by reaction of hydrogen peroxide with excess oleum or 100percent H2SO4, oxidizes primary polynitroarylamines and their N-acetamido derivatives to polynitro aromatics in good to excellent yields.The new procedure is illustrated by the synthesis of several new polynitro compounds, not preparable by known synthetic methods.Peroxytrifluoromethanesulfonic acid is comparably efficient for such oxidations.The scope and limitations of the new reaction have been examined and compared to other methods of synthesis of polynitro compounds.