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1,2,3,4-Tetrachloronaphthalene

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Identification
Molecular formula
C10H4Cl4
CAS number
7071-47-2
IUPAC name
1,2,3,4-tetrachloronaphthalene
State
State
At room temperature, 1,2,3,4-Tetrachloronaphthalene is typically in a solid state.
Melting point (Celsius)
107.00
Melting point (Kelvin)
380.15
Boiling point (Celsius)
373.00
Boiling point (Kelvin)
646.15
General information
Molecular weight
255.98g/mol
Molar mass
255.9760g/mol
Density
1.4632g/cm3
Appearence

1,2,3,4-Tetrachloronaphthalene appears as a white crystalline solid. It may have a distinct odor, characteristic of chlorinated aromatic hydrocarbons.

Comment on solubility

Solubility of 1,2,3,4-tetrachloronaphthalene

1,2,3,4-tetrachloronaphthalene (C10H4Cl4) exhibits some interesting characteristics regarding its solubility. Here are key points to consider:

  • Solvent Dependency: This compound is largely insoluble in water, which is common for many chlorinated compounds. However, it can dissolve in organic solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Nonpolar Nature: The nonpolar nature of 1,2,3,4-tetrachloronaphthalene limits its solubility in polar solvents like water, adhering to the principle of "like dissolves like."
  • Practical Implications: Its limited solubility in water has ramifications in environmental contexts, particularly concerning its behavior in aquatic systems and potential bioaccumulation.

In summary, 1,2,3,4-tetrachloronaphthalene showcases a clear divide in solubility profiles, reflecting the intricate balance of chemical properties and environmental effects. As noted, it's crucial to choose the right solvent for effective dissolution!

Interesting facts

Interesting Facts about 1,2,3,4-Tetrachloronaphthalene

1,2,3,4-tetrachloronaphthalene is a fascinating chemical compound with several notable characteristics and applications. This polyhalogenated aromatic compound has been the subject of much study due to its unique chemical properties.

Chemical Structure and Properties

  • Polyhalogenation: The introduction of four chlorine atoms enhances the compound's reactivity and stability compared to naphthalene.
  • Environmental Impact: Due to its persistence in the environment, 1,2,3,4-tetrachloronaphthalene poses potential ecological concerns.
  • Isomerism: As part of the naphthalene series, it displays isomeric forms and their various chemical behaviors, leading to interesting studies in the field of chemistry.

Applications

This compound has various applications in different industries:

  • Industrial Solvent: Used as a solvent in the synthesis of pesticides and dyes.
  • Research Tool: It serves as a reagent in organic synthesis, allowing chemists to explore diverse reaction pathways.

Health and Safety Considerations

When handling this compound, safety precautions are vital due to its toxicity and potential environmental hazards. Always adhere to proper disposal methods to mitigate harm.

A Final Thought

As a compound derived from the natural hydrocarbon naphthalene, 1,2,3,4-tetrachloronaphthalene illustrates the intricate balance between organic chemistry and environmental science. Understanding its properties enhances our ability to develop safer and more effective chemical processes.

Synonyms
1,2,3,4-TETRACHLORONAPHTHALENE
20020-02-4
Naphthalene, 1,2,3,4-tetrachloro-
CCRIS 5937
HSDB 4283
Napthalene, 1,2,3,4-tetrachloro-
NSC 524443
UNII-365DE4737Q
AI3-26504
365DE4737Q
NSC-524443
DTXSID5026095
TETRACHLORONAPHTHALENE, 1,2,3,4-
1,2,3,4-TETRACHLORONAPHTHALENE [HSDB]
DTXCID306095
Naphthalene, 1,2,3,4tetrachloro
1,2,3,4-TETRACHLORONAPTHALENE
622-398-0
InChI=1/C10H4Cl4/c11-7-5-3-1-2-4-6(5)8(12)10(14)9(7)13/h1-4
NAQWICRLNQSPPW-UHFFFAOYSA-N
RefChem:71291
1335-88-2
PCN 27
1,2,3,4-Tetrachloronaphthalene 10 microg/mL in Isooctane
1,2,3,4-Tetrachloronaphthalene 100 microg/mL in Nonane
1,2,3,4-Tetrachloronaphthalene 100 microg/mL in Cyclohexane
C10H4Cl4
SCHEMBL526943
SCHEMBL29494607
NSC524443
AKOS015849892
NS00098503
Q27256527