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2,6-Dinitroaniline

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2,6-Dinitroaniline Basic information

Product Name:
2,6-Dinitroaniline
Synonyms:
  • 1-Amino-2,6-dinitrobenzene
  • 2,6-Dinitrobenzenamine
  • 2,6-Dinitroanilin
  • 2,6-DINITROANILINE
  • 2,6-Dinitroaniline,98%
  • 2,6-Dinitroaniline/2,6-DNA
  • N-Cyanoethyl-Ortho-Chloroaniline
  • 202,6-DINITROANILINE
CAS:
606-22-4
MF:
C6H5N3O4
MW:
183.12
EINECS:
210-108-1
Product Categories:
  • Amines
  • C2 to C6
  • Intermediates of Dyes and Pigments
  • Amines and Anilines
  • Anilines, Aromatic Amines and Nitro Compounds
  • Nitrogen Compounds
Mol File:
606-22-4.mol
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2,6-Dinitroaniline Chemical Properties

Melting point:
134 °C (dec.) (lit.)
Boiling point:
316.77°C (rough estimate)
Density 
1.6188 (rough estimate)
refractive index 
1.6910 (estimate)
storage temp. 
Store below +30°C.
form 
Crystalline Powder or Crystals
pka
pK1:-5.23(+1) (25°C)
color 
White to off-white
Water Solubility 
practically insoluble
Merck 
14,3271
BRN 
2214886
InChIKey
QFUSCYRJMXLNRB-UHFFFAOYSA-N
CAS DataBase Reference
606-22-4(CAS DataBase Reference)
NIST Chemistry Reference
Benzenamine, 2,6-dinitro-(606-22-4)
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Safety Information

Hazard Codes 
T,T+
Risk Statements 
23/24/25-33-44-26/27/28
Safety Statements 
28-37-45-36/37-28A
RIDADR 
UN 1596 6.1/PG 2
WGK Germany 
2
RTECS 
BX9200000
HazardClass 
6.1
PackingGroup 
II
HS Code 
29214210

MSDS

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2,6-Dinitroaniline Usage And Synthesis

Chemical Properties

orange-brown crystalline powder

Uses

2,6-Dinitroaniline is used for organic synthesis intermediates, dyes intermediates, used in the preparation of 2,6-dinitroiodobenzene. It act as a precursor for various new 1,2,3-trisubstituted halobenzene derivatives.

Production Methods

Chlorobenzene-4-sulfonic acid is dinitrated to give 4- chloro-3,5-dinitrobenzenesulfonic acid [88-91-5], which is desulfonated by heating the diluted sulfuric acid solution from the nitration mix to give 2- chloro-1,3- dinitrobenzene [606-21-3]; the latter is aminated to 2,6-Dinitroaniline.

General Description

2,6-Dinitroaniline is a dinitroaniline. It serves as precursor to various new 1,2,3-trisubstituted halobenzene derivatives.

Purification Methods

Purify the nitroaniline by chromatography on alumina, then crystallise it from *benzene or EtOH. The N-acetyl derivative has m 197o (from EtOH). [Beilstein 12 IV 1729.]

2,6-Dinitroaniline Preparation Products And Raw materials

Raw materials

Preparation Products

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