Date published: 2025-9-16

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Naphthalene (CAS 91-20-3)

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Application:
Naphthalene is a ubiquitous aromatic hydrocarbon compound
CAS Number:
91-20-3
Molecular Weight:
128.17
Molecular Formula:
C10H8
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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Naphthalene is a chemical compound that functions as a precursor in the synthesis of various organic compounds. It acts as a starting material for the production of phthalic anhydride, which is used in the manufacturing of plasticizers, dyes, and resins. Naphthalene also serves as a reagent in the preparation of insecticides and fungicides, contributing to the development of these chemical compounds. At the molecular level, naphthalene undergoes various chemical reactions, including aromatic substitution and oxidation, to form the desired end products. Its mechanism of action involves participating in these chemical transformations, enabling the synthesis of a range of organic compounds with diverse industrial applications.


Naphthalene (CAS 91-20-3) References

  1. Naphthalene, an insect repellent, is produced by Muscodor vitigenus, a novel endophytic fungus.  |  Daisy, BH., et al. 2002. Microbiology (Reading). 148: 3737-3741. PMID: 12427963
  2. Naphthalene-induced respiratory tract toxicity: metabolic mechanisms of toxicity.  |  Buckpitt, A., et al. 2002. Drug Metab Rev. 34: 791-820. PMID: 12487150
  3. Genetic toxicity of naphthalene: a review.  |  Schreiner, CA. 2003. J Toxicol Environ Health B Crit Rev. 6: 161-83. PMID: 12554433
  4. Naphthalene analogues of lignans.  |  Madrigal, B., et al. 2003. J Org Chem. 68: 854-64. PMID: 12558407
  5. Naphthalene--an environmental and occupational toxicant.  |  Preuss, R., et al. 2003. Int Arch Occup Environ Health. 76: 556-76. PMID: 12920524
  6. Depurinating naphthalene-DNA adducts in mouse skin related to cancer initiation.  |  Saeed, M., et al. 2009. Free Radic Biol Med. 47: 1075-81. PMID: 19619639
  7. A critical review of naphthalene sources and exposures relevant to indoor and outdoor air.  |  Jia, C. and Batterman, S. 2010. Int J Environ Res Public Health. 7: 2903-39. PMID: 20717549
  8. [Recent advances in bacterial biodegradation of naphthalene, phenanthrene by bacteria: a review].  |  Zhang, D., et al. 2010. Sheng Wu Gong Cheng Xue Bao. 26: 726-34. PMID: 20815251
  9. Radiolytic studies of naphthalene in the presence of water.  |  Keheyan, Y. and ten Kate, IL. 2012. Orig Life Evol Biosph. 42: 179-86. PMID: 22660983
  10. Identification of naphthalene metabolism by white rot fungus Armillaria sp. F022.  |  Hadibarata, T., et al. 2012. J Environ Sci (China). 24: 728-32. PMID: 22894109
  11. Removal of naphthalene and phenanthrene using aerobic membrane bioreactor.  |  Mijaylova Nacheva, P. and Esquivel Sotelo, A. 2016. Biodegradation. 27: 83-93. PMID: 26895256
  12. Naphthalene, a versatile platform in medicinal chemistry: Sky-high perspective.  |  Makar, S., et al. 2019. Eur J Med Chem. 161: 252-276. PMID: 30366253
  13. Detection of naphthalene in sea-water by a label-free plasmonic optical fiber biosensor.  |  Cennamo, N., et al. 2019. Talanta. 194: 289-297. PMID: 30609533
  14. Metal Complexes with Naphthalene-Based Acetic Acids as Ligands: Structure and Biological Activity.  |  Lazou, M., et al. 2023. Molecules. 28: PMID: 36903416
  15. Metabolism and toxicity of diisopropylnaphthalene as compared to naphthalene and monoalkyl naphthalenes: a minireview.  |  Höke, H. and Zellerhoff, R. 1998. Toxicology. 126: 1-7. PMID: 9585087

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Naphthalene, 250 mg

sc-215533
250 mg
$20.00

Naphthalene, 5 g

sc-215533A
5 g
$36.00