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trans,trans-Muconic acid

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Identification
Molecular formula
C12H18O2
CAS number
3588-17-8
IUPAC name
dodeca-2,4-dienoic acid
State
State

At room temperature, trans,trans-Muconic acid is a solid.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
364.00
Boiling point (Kelvin)
637.15
General information
Molecular weight
142.13g/mol
Molar mass
142.1260g/mol
Density
1.1930g/cm3
Appearence

Trans,trans-Muconic acid typically appears as a white crystalline solid.

Comment on solubility

Solubility of Dodeca-2,4-dienoic Acid (C12H18O2)

Dodeca-2,4-dienoic acid, a fatty acid with a unique molecular structure, exhibits interesting solubility properties due to its combination of hydrophobic alkyl chains and hydrophilic carboxylic acid functional group. Here are some key points regarding its solubility:

  • Polar Solvents: Dodeca-2,4-dienoic acid tends to have moderate solubility in polar solvents like water, though it is primarily insoluble due to its long carbon chain.
  • Non-Polar Solvents: It is readily soluble in non-polar organic solvents such as hexane and benzene, owing to its hydrophobic characteristics.
  • Acidity Influence: The presence of the carboxylic acid group enhances its ability to interact with certain polar solvents, although the overall solubility in water remains limited.
  • Temperature Dependency: Solubility may increase with temperature, which often allows for better dissolution in various media.

In summary, while dodeca-2,4-dienoic acid shows a preference for non-polar environments due to its hydrocarbon backbone, it also has some solubility in polar solvents, particularly influenced by temperature and molecular interactions. As stated, “The solubility behavior is governed by the balance between hydrophilic and hydrophobic forces.”

Interesting facts

Interesting Facts About Dodeca-2,4-dienoic Acid

Dodeca-2,4-dienoic acid, often referred to as a fatty acid, is an intriguing compound that holds a significant place in the field of organic chemistry. Here are some captivating insights about this compound:

  • Structure and Unsaturation: Dodeca-2,4-dienoic acid contains two double bonds in its carbon chain, classifying it as a conjugated diene. This unique arrangement contributes to its reactivity and potential biological activity.
  • Natural Occurrence: This compound is found in various natural sources, particularly in some plant oils. It plays a role in the flavor and fragrance profiles of these substances.
  • Biological Functions: Dodeca-2,4-dienoic acid is of interest due to its potential effects on biological systems. Research indicates it may possess anti-inflammatory properties, showing promise in the health and nutrition sectors.
  • Synthesis: Organic chemists often explore various methods to synthesize dodeca-2,4-dienoic acid, making use of techniques such as aldol condensation and other multistep reactions, allowing for its production in the laboratory.
  • Applications: Beyond its natural role, this acid is a point of interest in materials science and biotechnology. Its unique properties are being investigated for uses in biofuels and biocompatible materials.

As scientists delve deeper into the properties and applications of dodeca-2,4-dienoic acid, it serves as a prime example of how a seemingly simple compound can have complex implications in both nature and technology.

Synonyms
2,4-Dodecadienoic acid
SCHEMBL466054
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