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1,2,2,3,3,4-Hexachlorobutane

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Identification
Molecular formula
C4H6Cl6
CAS number
109-68-2
IUPAC name
1,2,2,3,3,4-hexachlorobutane
State
State

It is generally found as a liquid at room temperature due to its relatively low melting point.

Melting point (Celsius)
-24.10
Melting point (Kelvin)
249.10
Boiling point (Celsius)
273.10
Boiling point (Kelvin)
546.30
General information
Molecular weight
252.77g/mol
Molar mass
252.7650g/mol
Density
1.6537g/cm3
Appearence

1,2,2,3,3,4-Hexachlorobutane typically appears as a colorless to light yellow liquid. Its appearance may vary slightly depending on purity and environmental conditions.

Comment on solubility

Solubility of 1,2,2,3,3,4-Hexachlorobutane

1,2,2,3,3,4-Hexachlorobutane, with the chemical formula C6Cl6, exhibits notable characteristics regarding its solubility:

  • Non-Polar Nature: Due to the presence of multiple chlorine substituents, this compound displays a largely non-polar character, which influences its solubility properties significantly.
  • Solubility in Organic Solvents: 1,2,2,3,3,4-Hexachlorobutane is typically soluble in non-polar organic solvents such as:
    • Hexane
    • Chloroform
    • Benzene
  • Water Insolubility: This compound is insoluble in water due to its non-polar characteristics, which prevent it from interacting favorably with polar water molecules.
  • Impact of Chlorination: The extensive chlorination increases the compound's molecular weight and decreases its solubility in polar solvents, further establishing its preference for organic environments.

In summary, the solubility of 1,2,2,3,3,4-Hexachlorobutane is dictated by its chemical structure, emphasizing its compatibility with non-polar solvents while remaining largely insoluble in polar solvents like water.

Interesting facts

Interesting Facts About 1,2,2,3,3,4-Hexachlorobutane

1,2,2,3,3,4-hexachlorobutane is a fascinating compound primarily known for its industrial applications and its role in environmental studies. Here are some captivating insights into this compound:

  • Historical Significance: This compound is part of the chlorinated hydrocarbon family, which gained prominence in the 20th century due to its various applications in agriculture and industry, particularly as a pesticide and a solvent.
  • Complex Structure: Its unique molecular structure, featuring numerous chlorine substituents, makes it an intriguing subject for chemists studying chemical reactivity and environmental persistence.
  • Environmental Impact: As a persistent organic pollutant (POP), 1,2,2,3,3,4-hexachlorobutane has raised concerns about its effects on wildlife and human health, contributing to research efforts aimed at understanding and mitigating pollution.
  • Regulatory Limits: Due to its associated risks, many countries have imposed strict regulations on its use, showcasing how chemistry intersects with public health and environmental protection.
  • Analytical Methods: Chemists utilize various analytical techniques such as gas chromatography and mass spectrometry to detect and quantify this compound in environmental samples, highlighting the importance of modern analytical chemistry in monitoring ecological health.
  • Reactivity Insights: The presence of chlorine atoms in its structure often leads to unique reactivity patterns, allowing chemists to explore fascinating mechanisms of substitution and elimination reactions.

In summary, 1,2,2,3,3,4-hexachlorobutane serves as an excellent case study in the balance between industrial utility and environmental responsibility. As we continue to learn more about chemical compounds like this, we advance our understanding of both chemistry and its profound impact on the world around us.

Synonyms
1,2,2,3,3,4-HEXACHLOROBUTANE
1573-57-5
DTXSID70166243
DTXCID7088734
1,2,2,3,3,4-HEXACHLORO-BUTANE
SCHEMBL17504240
AKOS024331687