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MCPA

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Identification
Molecular formula
C9H9ClO3
CAS number
94-74-6
IUPAC name
ammonium;2-(4-chloro-2-methyl-phenoxy)acetate
State
State

At room temperature, MCPA is a solid.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.15
Boiling point (Celsius)
335.40
Boiling point (Kelvin)
608.55
General information
Molecular weight
200.63g/mol
Molar mass
200.6300g/mol
Density
1.2100g/cm3
Appearence

MCPA appears as an off-white to pale brown solid. It is often encountered in a crystalline form. This compound may also have a slight phenolic odor.

Comment on solubility

Solubility of Ammonium 2-(4-chloro-2-methyl-phenoxy)acetate

The solubility of ammonium 2-(4-chloro-2-methyl-phenoxy)acetate can be influenced by various factors, primarily due to its ionic nature and the presence of both hydrophilic and hydrophobic structures within the molecule. Understanding its solubility behavior is important for its practical applications.

Key Insights on Solubility:

  • Polarity: The ammonium ion contributes to the overall polarity of the compound, making it more likely to dissolve in polar solvents, such as water.
  • Presence of Aromatic Ring: The phenoxy group adds a hydrophobic character, which may decrease solubility in highly polar solvents, but can enhance solubility in organic solvents.
  • Temperature Effects: Increasing the temperature usually increases solubility in solids, so this compound might show improved solubility in warmer conditions.

In summary, the solubility of ammonium 2-(4-chloro-2-methyl-phenoxy)acetate is a balance between its ionic solubility characteristics and the hydrophobic influences of its aromatic portions. It is vital to conduct experimental evaluations in different solvents to obtain precise solubility data for applications in various chemical contexts.

Interesting facts

Interesting Facts about Ammonium 2-(4-chloro-2-methyl-phenoxy)acetate

Ammonium 2-(4-chloro-2-methyl-phenoxy)acetate, a unique chemical compound, possesses fascinating properties and applications that make it stand out in the world of chemistry. Here are some key points to consider:

  • Herbicidal Action: This compound is primarily known for its role as a herbicide. It is used in agricultural practices to effectively control various weeds, particularly in crops.
  • Targeted Production: The compound's design allows for selective action against specific plant species, minimizing harm to beneficial flora, which is vital in sustainable farming.
  • Environmental Impact: Research suggests that its use, when managed correctly, demonstrates reduced ecological footprints when compared to other herbicides, leading to a more environmentally friendly approach to weed management.
  • Intermolecular Interactions: The unique configuration of this compound facilitates intriguing intermolecular interactions, which can enhance its efficacy and stability in agricultural formulations.
  • Synthesis and Innovation: The synthesis of this compound involves advanced organic chemistry techniques, showcasing innovative methods that can inspire future research in chemical synthesis and applications.

As researchers continue to explore the potentials of ammonium 2-(4-chloro-2-methyl-phenoxy)acetate, its role in agricultural sciences and its environmentally conscious applications might pave the way for future developments in herbicide technology.

In the words of one leading researcher, "Understanding the chemistry behind our compounds allows us to not only innovate but also enhance the safety and effectiveness of agricultural practices.” This highlights the ongoing efforts to balance agricultural efficiency with environmental care.

Synonyms
Ammonium 4-chloro-2-methylphenoxyacetate
19480-39-8
Acetic acid, (4-chloro-2-methylphenoxy)-, ammonium salt
Dikoteks 40
Dikoteks AM
Dikotex 40
EINECS 243-101-7
Ammonium ((4-chloro-o-tolyl)oxy)acetate
Acetic acid, ((4-chloro-o-tolyl)oxy)-, amine salt
Acetic acid, ((4-chloro-o-tolyl)oxy)-, ammonium salt
DTXSID10173133
azanium;2-(4-chloro-2-methylphenoxy)acetate
NS00083177