Cas no 13345-26-1 (Benzoapyren-8-ol)

Benzoapyren-8-ol structure
Benzoapyren-8-ol structure
Product Name:Benzoapyren-8-ol
CAS No:13345-26-1
MF:C20H12O
MW:268.308685302734
CID:182211
PubChem ID:25893
Update Time:2025-05-19

Benzoapyren-8-ol Chemical and Physical Properties

Names and Identifiers

    • Benzo[a]pyren-8-ol
    • 8-HYDROXYBENZO[A]PYRENE
    • 8-Hydroxy-benzo(a)pyrene
    • Benzo(a)pyren-8-ol
    • Benzo(a)pyrene, 8-hydroxy-
    • benzo[pqr]tetraphen-8-ol
    • BRN 2379758
    • 8-Hydroxy benzo[a]pyrene
    • BIDD:ER0355
    • 8-HYDROXYBENZO(A)PYRENE
    • Q27116106
    • 13345-26-1
    • AKOS015905883
    • pentacyclo[10.6.2.0?,?.0?,??.0??,??]icosa-1(18),2,4,6,8,10,12,14,16,19-decaen-5-ol
    • DTXSID00158116
    • 8-Hydroxy-3,4-benzopyrene
    • CHEMBL1908057
    • CHEBI:34493
    • NS00124225
    • CS-0098958
    • Benzoapyren-8-ol
    • Inchi: 1S/C20H12O/c21-16-7-9-17-15(11-16)10-14-5-4-12-2-1-3-13-6-8-18(17)20(14)19(12)13/h1-11,21H
    • InChI Key: OWEZWMDNHHTXJU-UHFFFAOYSA-N
    • SMILES: OC1C=CC2=C(C=1)C=C1C=CC3=CC=CC4=CC=C2C1=C43

Computed Properties

  • Exact Mass: 268.08886
  • Monoisotopic Mass: 268.088815
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 0
  • Complexity: 405
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 5.8
  • Topological Polar Surface Area: 20.2

Experimental Properties

  • Density: 1.379
  • Boiling Point: 527.2°Cat760mmHg
  • Flash Point: 252.9°C
  • Refractive Index: 1.924
  • PSA: 20.23

Benzoapyren-8-ol Pricemore >>

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Additional information on Benzoapyren-8-ol

Exploring Benzoapyren-8-ol (CAS No. 13345-26-1): Properties, Applications, and Environmental Impact

Benzoapyren-8-ol (CAS No. 13345-26-1) is a hydroxylated derivative of benzo[a]pyrene, a polycyclic aromatic hydrocarbon (PAH). This compound has garnered significant attention in environmental and biochemical research due to its unique properties and potential applications. In this article, we delve into the chemical characteristics, uses, and current research trends surrounding Benzoapyren-8-ol, while addressing common queries from researchers and industry professionals.

The molecular structure of Benzoapyren-8-ol features a hydroxyl group attached to the eighth carbon of the benzo[a]pyrene skeleton. This modification significantly alters its solubility and reactivity compared to its parent compound. Researchers often investigate Benzoapyren-8-ol metabolism and Benzoapyren-8-ol toxicity to understand its environmental persistence and biological effects. Recent studies have shown that this compound may play a role in advanced material synthesis and environmental remediation technologies.

One of the most searched questions about Benzoapyren-8-ol relates to its environmental fate and degradation. As concerns about PAH pollution grow, scientists are examining how hydroxylated derivatives like Benzoapyren-8-ol behave in different ecosystems. The compound's photodegradation pathways and microbial transformation are particularly interesting topics in current environmental chemistry research. These studies help develop more effective strategies for PAH contamination cleanup and pollution prevention.

In biochemical applications, Benzoapyren-8-ol serves as an important reference standard for analyzing PAH metabolites in biological samples. Laboratories worldwide use it to develop more accurate biomonitoring methods for assessing human exposure to aromatic hydrocarbons. The compound's unique fluorescence properties also make it valuable in analytical chemistry techniques and sensor development.

The synthesis and purification of Benzoapyren-8-ol require specialized expertise in organic chemistry. Many researchers search for information about Benzoapyren-8-ol synthesis methods and purification protocols. Current best practices involve controlled oxidation reactions followed by careful chromatographic separation to obtain high-purity material suitable for research applications.

From a regulatory perspective, Benzoapyren-8-ol is primarily studied as a reference compound rather than being produced or used in large quantities. This distinction is important when considering chemical safety guidelines and laboratory handling procedures. Proper storage conditions typically recommend protection from light and moisture to maintain stability.

Emerging research areas involving Benzoapyren-8-ol include its potential role in advanced oxidation processes for water treatment and its interactions with nanomaterials in environmental systems. These cutting-edge applications demonstrate how fundamental research on PAH derivatives can lead to innovative solutions for pressing environmental challenges.

The analytical detection of Benzoapyren-8-ol typically employs techniques such as high-performance liquid chromatography (HPLC) coupled with mass spectrometry or fluorescence detection. These methods allow for sensitive quantification even in complex matrices, addressing another common search query about Benzoapyren-8-ol analysis methods.

As research continues, the scientific community maintains interest in understanding the structure-activity relationships of Benzoapyren-8-ol and similar PAH derivatives. This knowledge contributes to better predictive models for environmental behavior and biological interactions, supporting more informed decisions in environmental management and public health protection.

For researchers working with Benzoapyren-8-ol, proper chemical characterization and analytical validation remain crucial. Recent advancements in spectroscopic techniques have improved our ability to study this compound's molecular interactions and transformation products in various environments.

The study of Benzoapyren-8-ol exemplifies how detailed investigation of specific chemical compounds can yield insights with broad implications. From environmental chemistry to analytical method development, this hydroxylated PAH derivative continues to be a valuable subject of scientific inquiry, addressing both fundamental questions and practical applications in modern chemistry.

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