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Assay
94%
form
solid
mp
151-153 °C (lit.)
SMILES string
Nc1c(Br)cc(cc1[N+]([O-])=O)[N+]([O-])=O
InChI
1S/C6H4BrN3O4/c7-4-1-3(9(11)12)2-5(6(4)8)10(13)14/h1-2H,8H2
InChI key
KWMDHCLJYMVBNS-UHFFFAOYSA-N
General description
2-Bromo-4,6-dinitroaniline is an important metabolite of the azo dye Disperse Blue 79. It can be easily recognized by all rat monoclonal antibodies.
Application
2-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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Environmental science & technology, 50(23), 12669-12677 (2016-12-10)
Characterization of toxicological profiles by use of traditional targeted strategies might underestimate the risk of environmental mixtures. Unbiased identification of prioritized compounds provides a promising strategy for meeting regulatory needs. In this study, untargeted screening of brominated compounds in house
Mutagenesis, 24(5), 433-438 (2009-07-08)
We have developed the bioluminescent Salmonella reverse mutation assay as a tool for detecting mutagenicity applicable for high-throughput screening of new chemicals. In this study, we report the inter-laboratory evaluation of the assay using 10 model chemicals in five independent
Journal of toxicology and environmental health, 17(1), 37-50 (1986-01-01)
The disposition of [14C]-2-bromo-4,6-dinitroaniline (BDNA) was studied in male F344 rats following oral or intravenous (iv) administration. The gastrointestinal absorption of BDNA was nearly complete and was not affected by dose in the range (10-100 mumol/kg body weight) studied. Following
Analytical and bioanalytical chemistry, 391(5), 1821-1835 (2008-05-28)
The development and characterization of one rat monoclonal antibody (mAb) for 2,4-dinitroaniline and of two rat mAbs for 2,6-dinitroaniline are described. With the immunization of rats with 2,4,6-trinitrophenyl-glycylglycine-keyhole limpet hemocyanine (KLH) conjugate one mAb (PK 5H6) has been developed and
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