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Benzo[b]pyrene-6-carbaldehyde

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Identification
Molecular formula
C21H12O
CAS number
39785-85-8
IUPAC name
benzo[b]pyrene-6-carbaldehyde
State
State

Benzo[b]pyrene-6-carbaldehyde is typically in a solid state at room temperature, appearing as a yellow crystalline substance.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
508.00
Boiling point (Kelvin)
781.15
General information
Molecular weight
278.32g/mol
Molar mass
278.2960g/mol
Density
1.3000g/cm3
Appearence

Benzo[b]pyrene-6-carbaldehyde appears as a yellow crystalline solid. Its structure consists of several fused aromatic rings, characteristic of polycyclic aromatic hydrocarbons, giving it a distinct crystalline form.

Comment on solubility

Solubility of Benzo[b]pyrene-6-carbaldehyde

Benzo[b]pyrene-6-carbaldehyde is a polycyclic aromatic hydrocarbon (PAH) that exhibits interesting solubility characteristics.

When considering the solubility of this compound, it is essential to note the following factors:

  • Solvent Interactions: Benzo[b]pyrene-6-carbaldehyde is generally more soluble in organic solvents compared to aqueous solutions due to its hydrophobic nature.
  • Concentration: At higher concentrations, it may solubilize better in solvents like dichloromethane, acetone, or ethanol.
  • Temperature Influence: Increased temperature typically enhances solubility, allowing for better dissolution in organic media.

In summary, while benzo[b]pyrene-6-carbaldehyde may not be readily soluble in water, it demonstrates favorable solubility characteristics in various organic solvents, which makes it valuable for specific research and industrial applications.

Interesting facts

Interesting Facts about Benzo[b]pyrene-6-carbaldehyde

Benzo[b]pyrene-6-carbaldehyde is a fascinating organic compound with notable implications in both chemical research and environmental science. Here are some intriguing points about this compound:

  • Structure and Reactivity: As a derivative of benzo[b]pyrene, this compound features a fused polycyclic aromatic hydrocarbon structure. Its carbonyl group contributes to its reactivity, allowing it to undergo various chemical reactions, particularly in organic synthesis.
  • Environmental Concerns: Benzo[b]pyrene is renowned for its role as a polycyclic aromatic hydrocarbon (PAH), which can be produced from incomplete combustion processes. This means Benzo[b]pyrene-6-carbaldehyde is often studied in the context of environmental pollution and its potential carcinogenic effects.
  • Biological Significance: Notably, this compound is being researched for its interactions with biological macromolecules and potential implications in toxicology. Understanding how benzo[b]pyrene derivatives interact with DNA could shed light on cancer mechanisms.
  • Synthetic Applications: Chemists have developed various methods for synthesizing benzo[b]pyrene-6-carbaldehyde, making it a versatile building block in organic synthesis. Its unique structure allows it to be used in the construction of more complex molecules.
  • Detection Methods: Analytical techniques such as gas chromatography-mass spectrometry (GC-MS) are employed to detect and quantify this compound in environmental samples, emphasizing its relevance in monitoring pollution levels.

Overall, benzo[b]pyrene-6-carbaldehyde is an essential compound in contemporary scientific inquiries, particularly within the realms of environmental chemistry and toxicology. Its multifaceted role as both a potential contaminant and a building block for new chemical entities makes it a subject worth exploring.


Synonyms
6-Formylbenzo(a)pyrene
BENZO(a)PYRENE-6-CARBOXALDEHYDE
13312-42-0
Benzo[a]pyrene-6-carbaldehyde
BRN 2126623
Benzo[a]pyrene-6-carboxaldehyde
6-Benzo(a)pyrenecarboxaldehyde
DTXSID50157972
3-07-00-02901 (Beilstein Handbook Reference)
Benzo(a)pyrene-6-carbaldehyde
DTXCID9080463
jyhgzhpgiqqnjp-uhfffaoysa-n
3,4-Benzpyrene-5-aldehyde
benzo[b]pyrene-6-carbaldehyde
benzo[a]pyrene 6-aldehyde
SCHEMBL548870