Date published: 2025-9-25

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8-Phenyloctanoic acid (CAS 26547-51-3)

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Application:
8-Phenyloctanoic acid is a long chain fatty acid with a phenyl end group
CAS Number:
26547-51-3
Molecular Weight:
220.31
Molecular Formula:
C14H20O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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8-Phenyloctanoic acid, bearing the CAS number 26547-51-3, is a synthetic organic compound characterized by an eight-carbon chain attached to a phenyl group at the terminal end. This unique structural configuration makes it a subject of interest in various research fields, particularly in organic chemistry and materials science. The phenyl group attached to the relatively long carbon chain impacts the compound′s hydrophobicity and electronic properties, making it useful for studying the interactions between aromatic and aliphatic units in larger molecules. In research, 8-Phenyloctanoic acid is often used to explore the synthesis and properties of complex organic molecules, including the development of new polymers and surfactants where the balance of hydrophilic and hydrophobic properties is crucial. Its molecular structure serves as a model for investigating the behavior of phenyl rings in lipid environments, which can influence the organization and functionality of cell membranes and other biological systems. Additionally, the presence of the phenyl group allows researchers to explore π-π interactions, which are significant in the study of molecular self-assembly processes. These interactions are essential for the development of advanced materials, such as organic semiconductors and nanostructured materials, where controlled assembly and specific functional properties are desired.


8-Phenyloctanoic acid (CAS 26547-51-3) References

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  2. Microbial synthesis of poly(beta-hydroxyalkanoates) bearing phenyl groups from pseudomonas putida: chemical structure and characterization.  |  Abraham, GA., et al. 2001. Biomacromolecules. 2: 562-7. PMID: 11749221
  3. Anaerobic degradation of trans-cinnamate and omega-phenylalkane carboxylic acids by the photosynthetic bacterium Rhodopseudomonas palustris: evidence for a beta-oxidation mechanism.  |  Elder, DJ., et al. 1992. Arch Microbiol. 157: 148-54. PMID: 1550442
  4. Production of 3-hydroxy-n-phenylalkanoic acids by a genetically engineered strain of Pseudomonas putida.  |  Sandoval, A., et al. 2005. Appl Microbiol Biotechnol. 67: 97-105. PMID: 15800732
  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. Poly-3-hydroxyalkanoate synthases from Pseudomonas putida U: substrate specificity and ultrastructural studies.  |  Arias, S., et al. 2008. Microb Biotechnol. 1: 170-6. PMID: 21261834
  7. Structural properties governing drug-plasma protein binding determined by high-performance liquid chromatography method.  |  Kamble, S., et al. 2018. J Pharm Biomed Anal. 149: 16-21. PMID: 29100026
  8. Microbial incubations of 8-phenyloctanoic acid and furan fatty acids in rumen fluid.  |  Wiedmaier-Czerny, N., et al. 2022. J Appl Microbiol. 133: 3669-3677. PMID: 36065520
  9. Aerobic catabolism of phenylacetic acid in Pseudomonas putida U: biochemical characterization of a specific phenylacetic acid transport system and formal demonstration that phenylacetyl-coenzyme A is a catabolic intermediate.  |  Schleissner, C., et al. 1994. J Bacteriol. 176: 7667-76. PMID: 8002592
  10. Identification of aromatic fatty acids in butter fat  |  Schröder, M., Abdurahman, H., Ruoff, T., Lehnert, K., & Vetter, W. 2014. Journal of the American Oil Chemists' Society. 91: 1695-1702.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

8-Phenyloctanoic acid, 250 mg

sc-397602
250 mg
$112.00

8-Phenyloctanoic acid, 1 g

sc-397602A
1 g
$150.00

8-Phenyloctanoic acid, 5 g

sc-397602B
5 g
$592.00