Date published: 2026-4-30

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Dibromonitromethane (CAS 598-91-4)

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Alternate Names:
Nitrodibromomethane; Dibromo-nitromethane
CAS Number:
598-91-4
Molecular Weight:
218.83
Molecular Formula:
CHBr2NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Dibromonitromethane holds significant prominence in scientific research, particularly within the realms of analytical chemistry and organic synthesis. Its versatile applications encompass serving as a reagent in the synthesis of pharmaceuticals, agrochemicals, and various other organic compounds. Furthermore, it finds utility in the creation of dyes, pigments, and diverse materials. Additionally, Dibromonitromethane contributes to the synthesis of polymers and other compounds of interest. One notable attribute of Dibromonitromethane lies in its potent oxidizing capabilities, allowing it to engage with a wide array of organic compounds. Alcohols, aldehydes, ketones, and numerous other organic compounds can undergo oxidation reactions in the presence of Dibromonitromethane. This reaction results in the formation of a brominated product alongside a nitromethane product, unveiling novel chemical entities with distinct properties.


Dibromonitromethane (CAS 598-91-4) References

  1. Active site generation of a protonically unstable suicide substrate from a stable precursor: glucose oxidase and dibromonitromethane.  |  Porter, DJ., et al. 2000. Biochemistry. 39: 11808-17. PMID: 10995249
  2. Hydrogen abstraction and decomposition of bromopicrin and other trihalogenated disinfection byproducts by GC/MS.  |  Chen, PH., et al. 2002. Environ Sci Technol. 36: 3362-71. PMID: 12188366
  3. Halonitromethane drinking water disinfection byproducts: chemical characterization and mammalian cell cytotoxicity and genotoxicity.  |  Plewa, MJ., et al. 2004. Environ Sci Technol. 38: 62-8. PMID: 14740718
  4. Mutagenicity in Salmonella of halonitromethanes: a recently recognized class of disinfection by-products in drinking water.  |  Kundu, B., et al. 2004. Mutat Res. 562: 39-65. PMID: 15279829
  5. Development of normal human colon cell cultures to identify priority unregulated disinfection by-products with a carcinogenic potential.  |  DeAngelo, AB., et al. 2007. Water Sci Technol. 56: 51-5. PMID: 18075178
  6. One-pot synthesis of benzo[b]thiophenes and benzo[b]selenophenes from o-halo-substituted ethynylbenzenes: convenient approach to mono-, bis-, and tris-chalcogenophene-annulated benzenes.  |  Kashiki, T., et al. 2009. Org Lett. 11: 2473-5. PMID: 19432445
  7. Solvent-minimized extraction for determining halonitromethanes and trihalomethanes in water.  |  Montesinos, I. and Gallego, M. 2012. J Chromatogr A. 1248: 1-8. PMID: 22717036
  8. Kinetics and mechanisms of pH-dependent degradation of halonitromethanes by UV photolysis.  |  Fang, JY., et al. 2013. Water Res. 47: 1257-66. PMID: 23266387
  9. Drinking Water Disinfection Byproducts (DBPs) and Human Health Effects: Multidisciplinary Challenges and Opportunities.  |  Li, XF. and Mitch, WA. 2018. Environ Sci Technol. 52: 1681-1689. PMID: 29283253
  10. Formation, Identification, and Occurrence of New Bromo- and Mixed Halo-Tyrosyl Dipeptides in Chloraminated Water.  |  Huang, G., et al. 2019. Environ Sci Technol. 53: 3672-3680. PMID: 30807126
  11. Trace Analysis of 61 Emerging Br-, Cl-, and I-DBPs: New Methods to Achieve Part-Per-Trillion Quantification in Drinking Water.  |  Cuthbertson, AA., et al. 2020. Anal Chem. 92: 3058-3068. PMID: 31950829
  12. Degradation of aliphatic halogenated contaminants in water by UVA/Cu-TiO2 and UVA/TiO2 photocatalytic processes: Structure-activity relationship and role of reactive species.  |  Yin, R., et al. 2020. Chemosphere. 260: 127644. PMID: 32758766
  13. Targeted and Untargeted Metabolic Profiling to Discover Bioactive Compounds in Seaweeds and Hemp Using Gas and Liquid Chromatography-Mass Spectrometry.  |  Nørskov, NP., et al. 2021. Metabolites. 11: PMID: 33922209
  14. Formation and transformation of halonitromethanes from dimethylamine in the presence of bromide during the UV/chlorine disinfection.  |  Deng, L., et al. 2022. Chemosphere. 291: 132731. PMID: 34743802
  15. Effects of bromide ion on the formation and toxicity alteration of halonitromethanes from nitrate containing humic acid water during UV/chlor(am)ine disinfection.  |  Huang, T., et al. 2022. Water Res. 225: 119175. PMID: 36191529

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dibromonitromethane, 10 mg

sc-471180
10 mg
$374.00