Date published: 2026-5-27

1-800-457-3801

SCBT Portrait Logo
Seach Input

Benzo[ghi]fluoranthene (CAS 203-12-3)

0.0(0)
Write a reviewAsk a question

Alternate Names:
2,13-Benzofuranthene
CAS Number:
203-12-3
Molecular Weight:
226.27
Molecular Formula:
C18H10
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Benzo[ghi]fluoranthene is a polycyclic aromatic hydrocarbon (PAH) investigated in environmental chemistry due to its presence in combustion by-products. It is frequently detected in environmental samples, such as soil and air particulates, making it a subject of interest in the study of atmospheric pollutants and their deposition. Research on Benzo[ghi]fluoranthene often focuses on its behavior in the environment, including its photodegradation, volatilization, and bioaccumulation potential. Additionally, it is used in the calibration of analytical instruments designed to measure PAHs in environmental monitoring. Studies involving Benzo[ghi]fluoranthene also delve into its interactions with other organic contaminants and the development of remediation strategies to reduce its impact on ecosystems.


Benzo[ghi]fluoranthene (CAS 203-12-3) References

  1. Product ion studies of diastereomeric benzo[ghi]fluoranthene tetraols by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and post-source decay.  |  Huffer, DM., et al. 2001. J Am Soc Mass Spectrom. 12: 376-80. PMID: 11322184
  2. Genotoxicity of polycyclic aromatic hydrocarbons in Escherichia coli PQ37.  |  Mersch-Sundermann, V., et al. 1992. Mutat Res. 278: 1-9. PMID: 1370113
  3. Structural differentiation of diastereomeric benzo[ghi]fluoranthene adducts of deoxyadenosine by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and postsource decay.  |  Chiarelli, MP., et al. 2003. Chem Res Toxicol. 16: 1236-41. PMID: 14565765
  4. What contributes to the combined effect of a complex mixture?  |  Altenburger, R., et al. 2004. Environ Sci Technol. 38: 6353-62. PMID: 15597892
  5. Bioaccumulation of cyclopenta[cd]pyrene and benzo[ghi]fluoranthene by mussels transplanted in a coastal lagoon.  |  Fabbri, D., et al. 2006. Chemosphere. 64: 1083-92. PMID: 16423379
  6. Cyclodehydrogenation reactions to cyclopentafused polycyclic aromatic hydrocarbons.  |  Violi, A. 2005. J Phys Chem A. 109: 7781-7. PMID: 16834155
  7. Aryl-aryl bond formation by flash vacuum pyrolysis of benzannulated thiopyrans.  |  Amick, AW., et al. 2008. J Org Chem. 73: 5119-22. PMID: 18510364
  8. Polycyclic aromatic hydrocarbon analysis with the Mars organic analyzer microchip capillary electrophoresis system.  |  Stockton, AM., et al. 2009. Anal Chem. 81: 790-6. PMID: 19072718
  9. Iridium-catalyzed reductive carbon-carbon bond cleavage reaction on a curved pyridylcorannulene skeleton.  |  Tashiro, S., et al. 2015. Angew Chem Int Ed Engl. 54: 5351-4. PMID: 25756834
  10. Competition between quasi-planar and cage-like structures in the B29- cluster: photoelectron spectroscopy and ab initio calculations.  |  Li, HR., et al. 2016. Phys Chem Chem Phys. 18: 29147-29155. PMID: 27730232
  11. Fine-Scale Source Apportionment Including Diesel-Related Elemental and Organic Constituents of PM2.5 across Downtown Pittsburgh.  |  Tunno, BJ., et al. 2018. Int J Environ Res Public Health. 15: PMID: 30301154
  12. Selective identification of cyclopentaring-fused PAHs and side-substituted PAHs in a low pressure premixed sooting flame by photoelectron photoion coincidence spectroscopy.  |  Mercier, X., et al. 2020. Phys Chem Chem Phys. 22: 15926-15944. PMID: 32657287
  13. Long-term spatial and temporal trends, and source apportionment of polycyclic aromatic compounds in the Athabasca Oil Sands Region.  |  Chibwe, L., et al. 2021. Environ Pollut. 268: 115351. PMID: 33152634
  14. The Influence of a Fire at an Illegal Landfill in Southern Poland on the Formation of Toxic Compounds and Their Impact on the Natural Environment.  |  Rykała, W., et al. 2022. Int J Environ Res Public Health. 19: PMID: 36294191
  15. The genotoxicity of unsubstituted and nitrated polycyclic aromatic hydrocarbons.  |  Mersch-Sundermann, V., et al. 1993. Anticancer Res. 13: 2037-43. PMID: 8297112

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Benzo[ghi]fluoranthene, 100 mg

sc-233952
100 mg
$1326.00