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Sodium 3-Hydroxy-2-naphthoate (CAS 14206-62-3)

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Alternate Names:
3-Hydroxy-2-naphthoic Acid Sodium Salt
CAS Number:
14206-62-3
Molecular Weight:
210.16
Molecular Formula:
C11H7NaO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Sodium 3-Hydroxy-2-naphthoate (NaHNA) is a member of the naphthoate family of compounds. Sodium 3-Hydroxy-2-naphthoate is a versatile compound with various applications. In scientific research, Sodium 3-hydroxy-2-naphthoate finds diverse applications. It serves as a valuable reagent in organic synthesis, a biochemical probe, and a tool for examining the structure and function of proteins. Researchers have utilized Sodium 3-hydroxy-2-naphthoate to study the intricate details of enzymes involved in fatty acid metabolism, as well as to investigate membrane proteins responsible for signal transduction. Furthermore, it has been instrumental in unraveling the structure and function of proteins involved in gene expression regulation. The mechanism of action of Sodium 3-hydroxy-2-naphthoate involves its role as an inhibitor. It inhibits the activity of enzymes participating in fatty acid metabolism by binding to their active sites, thereby impeding their function. Additionally, it acts as an inhibitor for membrane proteins involved in signal transduction, blocking their activity by binding to their active sites.


Sodium 3-Hydroxy-2-naphthoate (CAS 14206-62-3) References

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  2. Phase behavior of concentrated aqueous solutions of cetyltrimethylammonium bromide (CTAB) and sodium hydroxy naphthoate (SHN).  |  Krishnaswamy, R., et al. 2005. Langmuir. 21: 10439-43. PMID: 16262304
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  4. Structure of mesh phases in cationic surfactant systems with strongly bound counterions: influence of the surfactant headgroup and the counterion.  |  Ghosh, SK. and Raghunathan, VA. 2009. Langmuir. 25: 2622-8. PMID: 19437686
  5. Synergistic effects of mixed aromatic counterions on nanostructures and drag reducing effectiveness of aqueous cationic surfactant solutions.  |  Ge, W., et al. 2011. J Phys Chem B. 115: 5939-46. PMID: 21510683
  6. Guest-Host Chemistry with Dendrimers-Binding of Carboxylates in Aqueous Solution.  |  Ficker, M., et al. 2015. PLoS One. 10: e0138706. PMID: 26448138
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  9. Reversible phase transition between salt-free catanionic vesicles and high-salinity catanionic vesicles.  |  Shen, Y., et al. 2007. Soft Matter. 3: 1407-1412. PMID: 32900121
  10. Shear-Induced Ordering of Nanopores and Instabilities in Concentrated Surfactant Mesh Phases.  |  Bera, PK., et al. 2021. Langmuir. 37: 6874-6886. PMID: 34085836
  11. Formation and Properties of Lamellar Phases in Systems of Cationic Surfactants and Hydroxy-Naphthoate.  |  Horbaschek, K., et al. 1998. J Colloid Interface Sci. 206: 439-456. PMID: 9756656
  12. Self-assembled structures in excess and salt-free catanionic surfactant solutions  |  J Hao, H Hoffmann. 2004. Current Opinion in Colloid & Interface Science. 9: 279-293.
  13. Vesicles and Nanofibers with Krafft Transition from Cationic Surfactant-Divalent Azobenzene Dye Salt-Free Complex  |  Xuefeng Li, et al. 2011. Journal of Dispersion Science and Technology. 32.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Sodium 3-Hydroxy-2-naphthoate, 5 g

sc-487929
5 g
$248.00