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4-Nitrophenyl bromoacetate (CAS 19199-82-7)

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Alternate Names:
p-Nitrophenyl bromoacetate; Bromoacetic acid, p-nitrophenyl ester
Application:
4-Nitrophenyl bromoacetate is a haloacetamide
CAS Number:
19199-82-7
Purity:
≥97%
Molecular Weight:
260.04
Molecular Formula:
C8H6BrNO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Nitrophenyl bromoacetate, known as 4-NPBA, is a widely used chemical compound in scientific research. It presents as a yellow crystalline solid, exhibiting solubility in water and ethanol. With its versatility as a reagent, 4-Nitrophenyl bromoacetate serves various purposes in laboratory applications, including synthesis, analysis, and biological research. In scientific research, 4-Nitrophenyl bromoacetate finds application across multiple domains. It is employed as a reagent for synthesizing diverse organic compounds, ranging from amines and esters to amides. Furthermore, it plays a vital role in protein and peptide analysis, facilitating the determination of molecular weight. Additionally, 4-Nitrophenyl bromoacetate contributes to the study of enzyme kinetics and enzyme inhibition. Regarding the mechanism of action, 4-Nitrophenyl bromoacetate acts as a competitive inhibitor of enzymes. By binding to the enzyme′s active site, it prevents the enzyme from interacting with its substrate. As a result, the enzyme is unable to catalyze the intended reaction, leading to inhibition of its activity.


4-Nitrophenyl bromoacetate (CAS 19199-82-7) References

  1. Reactive 5'-substituted 2',5'-dideoxyuridine derivatives as potential inhibitors of nucleotide biosynthesis.  |  Elliott, RD., et al. 1987. J Med Chem. 30: 927-30. PMID: 3572980
  2. 5'-bromoacetamido-5'-deoxyadenosine. A novel reagent for labeling adenine nucleotide sites in proteins.  |  Samant, BR. and Sweet, F. 1983. J Biol Chem. 258: 12779-82. PMID: 6605345
  3. Synthesis of potential inhibitors of hypoxanthine-guaine phosphoribosyltransferase for testing as antiprotozoal agents. 2. 1-Substituted hypoxanthines.  |  Piper, JR., et al. 1980. J Med Chem. 23: 1136-9. PMID: 7420359
  4. Immunospecific reduction of antioligonucleotide antibody-forming cells with a tetrakis-oligonucleotide conjugate (LJP 394), a therapeutic candidate for the treatment of lupus nephritis.  |  Jones, DS., et al. 1995. J Med Chem. 38: 2138-44. PMID: 7783145

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Nitrophenyl bromoacetate, 10 g

sc-267702
10 g
$153.00