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Chemical structure of 2,6-Dinitroaniline | 606-22-4
CAS: 606-22-4
SKU: S1475
2,6-Dinitroaniline | SKU: S1475
Chemical structure of 2,6-Dinitroaniline | 606-22-4
Request Quote — S1475

Specifications

AppearanceCrystalline solid / powder
Melting PointApprox. 134 – 140 °C
pH of Liquid, Typical (10% soln)substance is practically insoluble in water, therefore a stable aqueous pH cannot be measured
Specific Gravity Approx~1.60 – 1.63 g/cm³ (20 °C)
OdorAromatic amine-type odor
ColorYellow to orange or brownish crystalline solid
Linear Formula(O₂N)₂-C₆H₃-NH₂
IUPAC Name2,6-dinitroaniline
Formula Weight183.12 g/mol
percent purity≥ 98 %
Physical FormSolid – crystalline powder/crystals
Chemical Name or Material2,6-Dinitroaniline
UN Number1596
Content / Assay Percent Range≥ 98.0 %

Applications

No Application Found

Product Description

69070

2,6-Dinitroaniline is a high-purity aromatic nitro compound supplied by Sarchem Labs for laboratory and industrial applications. With consistent quality and controlled manufacturing standards, it is widely used as an intermediate in chemical synthesis, dye production, agrochemical research, and specialty formulations. Each batch is tested to ensure reliable performance, accurate composition, and compliance with industry requirements for research and production use.

Synonym: benzenamine, 2,6-dinitro, 2,6-dinitrobenzenamine, aniline, 2,6-dinitro, unii-8w27g0qbd7, ccris 3108, pubchem22911, wln: wnr bz cnw, acmc-209ml1, 2,6-dinitroaniline, 2,6-dinitro-phenyl-amine

Safety Information

No Safety Information Found

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FAQs: 2,6-Dinitroaniline

2,6-dinitroaniline is an aromatic compound containing nitro groups on the benzene ring. It’s used as an intermediate in dyes, pigments, and agricultural chemicals due to its chemical stability and reactivity.

The 2,6-dinitroaniline formula is C₆H₅N₃O₄. It features a benzene ring with two nitro groups at the 2 and 6 positions and an amine group, influencing its chemical behavior and applications.

2,6-dinitroaniline is typically produced by nitrating aniline under controlled conditions. The reaction introduces nitro groups in specific positions, followed by purification processes to obtain a high-purity product for industrial use.

In pigment production, 2,6-dinitroaniline acts as a precursor for azo dyes. Its structure allows easy coupling reactions, producing vibrant and stable colors for textiles, plastics, and coatings industries.

Yes, 2,6-dinitroaniline should be handled with care due to potential toxicity. Appropriate personal protective equipment and controlled storage conditions are essential to ensure safety during manufacturing and laboratory processes.