Date published: 2026-4-25

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2-Bromooctanoic acid (CAS 2623-82-7)

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Alternate Names:
2-Bromocaprylic acid
CAS Number:
2623-82-7
Purity:
97%
Molecular Weight:
223.11
Molecular Formula:
C8H15BrO2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Bromooctanoic acid is an organic compound categorized as a carboxylic acid and is found in numerous biological systems. This compound has been employed in various applications. While it is insoluble in water, it dissolves in organic solvents. Its applications include serving as a substrate for enzymes in biochemical research, acting as a reagent in organic synthesis, and functioning as a ligand for metal complexes in coordination chemistry. Moreover, it has been utilized as a substrate for polymer synthesis and as a key component in catalysts for organic reactions.


2-Bromooctanoic acid (CAS 2623-82-7) References

  1. Accumulation of polyhydroxyalkanoic acid containing large amounts of unsaturated monomers in Pseudomonas fluorescens BM07 utilizing saccharides and its inhibition by 2-bromooctanoic acid.  |  Lee, HJ., et al. 2001. Appl Environ Microbiol. 67: 4963-74. PMID: 11679314
  2. Extraction of bismuth(III) with 2-bromoalkanoic acid in nondonating solvent from highly acidic aqueous solution.  |  Moriya, Y., et al. 2001. Anal Sci. 17: 297-300. PMID: 11990544
  3. Accumulation of polyhydroxyalkanoate from styrene and phenylacetic acid by Pseudomonas putida CA-3.  |  Ward, PG., et al. 2005. Appl Environ Microbiol. 71: 2046-52. PMID: 15812037
  4. Polyhydroxyalkanoate accumulating diversity of Pseudomonas species utilising aromatic hydrocarbons.  |  Tobin, KM. and O'Connor, KE. 2005. FEMS Microbiol Lett. 253: 111-8. PMID: 16260095
  5. FadD from Pseudomonas putida CA-3 is a true long-chain fatty acyl coenzyme A synthetase that activates phenylalkanoic and alkanoic acids.  |  Hume, AR., et al. 2009. J Bacteriol. 191: 7554-65. PMID: 19820085
  6. Quadruple click: a facile pathway leading to tetrakis(4-(1,2,3-triazolyl)methyl)-ethylenediamine derivatives as a new class of extracting agents for soft metal ions.  |  Watanabe, W., et al. 2012. Chem Asian J. 7: 1679-83. PMID: 22454360
  7. Simultaneous inhibition of rhamnolipid and polyhydroxyalkanoic acid synthesis and biofilm formation in Pseudomonas aeruginosa by 2-bromoalkanoic acids: effect of inhibitor alkyl-chain-length.  |  Gutierrez, M., et al. 2013. PLoS One. 8: e73986. PMID: 24023921
  8. Production and characterization of medium-chain-length polyhydroxyalkanoates by Pseudomonas mosselii TO7.  |  Chen, YJ., et al. 2014. J Biosci Bioeng. 118: 145-52. PMID: 24630613
  9. A remarkable enhancement in Am³⁺/Eu³⁺ selectivity by an ionic liquid based solvent containing bis-1,2,4-triazinyl pyridine derivatives: DFT validation of experimental results.  |  Bhattacharyya, A., et al. 2015. Dalton Trans. 44: 6193-201. PMID: 25736729
  10. Evaluation of inhibitors of fatty acid oxidation in rat myocytes.  |  el-Aleem, SA. and Schulz, H. 1987. Biochem Pharmacol. 36: 4307-12. PMID: 3689454
  11. Involvement of carnitine acyltransferases in peroxisomal fatty acid metabolism by the yeast Pichia guilliermondii.  |  Pagot, Y. and Belin, JM. 1996. Appl Environ Microbiol. 62: 3864-7. PMID: 8837442
  12. Inhibition of sex pheromone production in female lepidopteran moths by 2-halofatty acids.  |  Hernanz, D., et al. 1997. J Lipid Res. 38: 1988-94. PMID: 9374121
  13. Contribution of a chain-shortening pathway to the biosynthesis of the fatty acids of mannosylerythritol lipid (biosurfactant) in the yeast Candida antarctica: Effect of β-oxidation inhibitors on biosurfactant synthesis  |  , et al. (1998. Biotechnology Letters. volume 20,: pages 813–818.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Bromooctanoic acid, 10 g

sc-237950
10 g
$82.00