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2,2-Dichlorosuccinic acid

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Identification
Molecular formula
C4H4Cl2O4
CAS number
14091-99-1
IUPAC name
2,2-dichlorobutanedioic acid
State
State

At room temperature, 2,2-Dichlorosuccinic acid is a solid.

Melting point (Celsius)
106.00
Melting point (Kelvin)
379.00
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
-1.00
General information
Molecular weight
173.95g/mol
Molar mass
173.9510g/mol
Density
1.6700g/cm3
Appearence

2,2-Dichlorosuccinic acid appears as a white or off-white crystalline solid. It is commonly found in powder or crystalline form.

Comment on solubility

Solubility of 2,2-Dichlorobutanedioic Acid

2,2-Dichlorobutanedioic acid, with the chemical formula C4H4Cl2O4, shows interesting solubility characteristics:

  • Water Solubility: This compound is typically highly soluble in water due to its two carboxylic acid groups, which can form hydrogen bonds with water molecules.
  • Solvent Compatibility: In addition to water, it is also soluble in many polar organic solvents, such as methanol and ethanol, which enhances its versatility in various chemical applications.
  • Influence of Cl Atoms: The presence of chlorine atoms can affect the solubility; however, the overall hydrophilicity of the acid outweighs the hydrophobic character introduced by these groups.

"The solubility in different solvents can be influenced by factors such as temperature and pH." Thus, altering these conditions can lead to variations in solubility behavior.

In summary, 2,2-dichlorobutanedioic acid is a water-soluble compound that can interact favorably with various solvents, making it a potentially valuable substance in chemical syntheses and formulations.

Interesting facts

Interesting Facts about 2,2-Dichlorobutanedioic Acid

2,2-Dichlorobutanedioic acid is an intriguing compound known for its unique molecular structure and significant applications in various fields. Here are some interesting insights:

  • Chemical Structure: This compound features a butanedioc acid backbone with two chlorine atoms attached to the second carbon atom. This dual substitution can greatly influence its chemical reactivity and stability, making it a valuable compound for chemists.
  • Applications: 2,2-Dichlorobutanedioic acid has been utilized in the synthesis of various pharmaceuticals and agricultural chemicals. Its properties enable the development of substances with specific biological activities.
  • Role in Research: Owing to its unique structure, this compound is often studied in research to understand substitution effects on physical and chemical properties, paving the way for innovations in organic chemistry.
  • Environmental Considerations: Like many chlorinated compounds, 2,2-dichlorobutanedioic acid may have environmental implications. Researchers are actively investigating its degradation pathways and the implications of its use in various industries.
  • Toxicity and Safety: Being chlorinated, it may pose certain risks. It's crucial for chemists and users to handle this compound with caution, following appropriate safety protocols to avoid contamination or harmful exposure.

In summary, 2,2-dichlorobutanedioic acid stands out in the realm of organic compounds for its structure and diverse applications. Its study not only enriches our understanding of chemical behavior but also enhances our ability to innovate in chemical synthesis.

Synonyms
Butanedioic acid, 2,2-dichloro-
2,2-Dichlorobutandioic acid
15519-38-7
DTXSID30165853
DTXCID9088344
Dichlorbernsteinsaure
SCHEMBL4304729
NS00133618