Skip to Content
Merck
All Photos(1)

Key Documents

262226

Sigma-Aldrich

1-Bromo-2,4-dinitrobenzene

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H3(NO2)2
CAS Number:
Molecular Weight:
247.00
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

71-73 °C (lit.)

functional group

bromo
nitro

SMILES string

[O-][N+](=O)c1ccc(Br)c(c1)[N+]([O-])=O

InChI

1S/C6H3BrN2O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H

InChI key

PBOPJYORIDJAFE-UHFFFAOYSA-N

Application

1-Bromo-2,4-dinitrobenzene has been used:
  • in the preparation of 2,4-dinitrophenol via treatment with KO2-crown ether complex in benzene
  • as substrate in protein determination and glutathione S-transferase (GST) assay of chicken and rat prostaglandin D2 synthase (PGDS)

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

K C Chen et al.
Drug and chemical toxicology, 3(3), 305-318 (1980-01-01)
The formation of glutathione (GSH) conjugate in the detoxification of [Ring-UL-14C]-2,4-dinitrobromobenzene (DNBB) was investigated using rat liver cytosolic fraction. The mercapturic acid conjugate in rats was also studied by collection of urine of rats dosed with radioactive DNBB by intraperitoneal
Nucleophilic radical aromatic substituion with superoxide ion.
Frimer A and Rosenthal I.
Tetrahedron Letters, 17(32), 2809-2812 (1976)
The reaction of poly-L-ornithine with 1-halo-2,4-dinitrobenzenes.
R C Parker et al.
The International journal of biochemistry, 13(4), 513-516 (1981-01-01)
A M Thomson et al.
The Biochemical journal, 333 ( Pt 2), 317-325 (1998-07-11)
The Expressed Sequence Tag database has been screened for cDNA clones encoding prostaglandin D2 synthases (PGDSs) by using a BLAST search with the N-terminal amino acid sequence of rat GSH-dependent PGDS, a class Sigma glutathione S-transferase (GST). This resulted in
R L Gupta et al.
Mutation research, 381(1), 41-47 (1997-12-24)
The 1-halogen substituted 2,4-dinitrobenzenes have been found to be mutagenic in Salmonella TA98 with an activity order of 1-fluoro > 1-chloro > 1-bromo > 1-iodo. This specific activity was not lowered in the nitroreductase deficient strain TA98NR and O-acetyltransferase deficient

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service