2-Bromo-4,6-dinitroaniline

2-Bromo-4,6-dinitroaniline
  • CAS No.:1817-73-8
Other grades of this product :
2-Bromo-4,6-dinitroaniline Basic information
Product Name:2-Bromo-4,6-dinitroaniline
Synonyms:6-BROMO-2,4-DINITROANILINE;1-Amino-6-bromo-2,4-dinitrobenzene;Benzenamine, 2-bromo-4,6-dinitro-;2-BROMO-4,6-DINITRONANILINE;2,4-dinitro-6-bromanilin;2,4-dinitro-6-bromoanilin(czech);2,4-DINITRO-6-BROMO ANILINE;2-bromo-4,6-dinitroaminobenzene
CAS:1817-73-8
MF:C6H4BrN3O4
MW:262.02
EINECS:217-329-2
Product Categories:Building Blocks;C6;Intermediates of Dyes and Pigments;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Amines;C2 to C6;Nitrogen Compounds
Mol File:1817-73-8.mol
2-Bromo-4,6-dinitroaniline Chemical Properties
Melting point 151-153 °C (lit.)
Boiling point 400.8±40.0 °C(Predicted)
density 2.1534 (rough estimate)
refractive index 1.6200 (estimate)
storage temp. 2-8°C(protect from light)
solubility Chloroform (Slightly), Methanol (Slightly, Sonicated)
pkapK1: -6.94(+1) (25°C)
form Solid
color Pale Yellow to Light Yellow
CAS DataBase Reference1817-73-8(CAS DataBase Reference)
EPA Substance Registry System2-Bromo-4,6-dinitroaniline (1817-73-8)
Safety Information
Hazard Codes Xi,F
Risk Statements 36/37/38-11
Safety Statements 37/39-26-16
RIDADR 1325
WGK Germany 2
RTECS BW9303000
TSCA Yes
HazardClass 4.1
PackingGroup III
Hazardous Substances Data1817-73-8(Hazardous Substances Data)
MSDS Information
ProviderLanguage
2-Bromo-4,6-dinitroaminobenzene English
ACROS English
SigmaAldrich English
ALFA English
2-Bromo-4,6-dinitroaniline Usage And Synthesis
Chemical PropertiesYELLOW TO ORANGE POWDER
Uses2-Bromo-4,6-dinitroaniline was used as a model chemical in the inter-laboratory evaluation of the bioluminescent Salmonella reverse mutation assay for detecting mutagenicity.
General DescriptionBright yellow powder.
Air & Water Reactions2-Bromo-4,6-dinitroaniline may be sensitive to exposure to air . Insoluble in water.
Reactivity ProfileA halogenated and nitrated amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
Fire HazardFlash point data for 2-Bromo-4,6-dinitroaniline are not available, but 2-Bromo-4,6-dinitroaniline is probably combustible.

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