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Triclopyr

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Identification
Molecular formula
C7H4Cl3O3Na
CAS number
55335-06-3
IUPAC name
sodium;2-(2,3,6-trichlorophenyl)acetate
State
State
Triclopyr is primarily formulated for agricultural use and is available in various salts and esters. At room temperature, it is often found as a solid, but the specific state can depend on its formulation.
Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
256.45g/mol
Molar mass
256.4510g/mol
Density
1.4919g/cm3
Appearence

Triclopyr typically appears as a pale yellow to amber liquid or crystal depending on its formulation. Its appearance can vary from solid to liquid form depending on its temperature and formulation concentration.

Comment on solubility

Solubility of Sodium 2-(2,3,6-trichlorophenyl)acetate

Sodium 2-(2,3,6-trichlorophenyl)acetate, a sodium salt of a substituted phenyl acetate, exhibits interesting solubility properties that are crucial for its applications in various fields.

Generally speaking, the solubility of this compound can be described as follows:

  • Water Solubility: Sodium salts tend to show high solubility in water due to their ionic nature. As for sodium 2-(2,3,6-trichlorophenyl)acetate, it is likely to be readily soluble in water, which is characteristic for many sodium salts.
  • Organic Solvents: The presence of the trichlorophenyl group may influence its solubility in organic solvents. While some salts can be less soluble in organic mediums, the impact of the aromatic ring could enhance solubility in non-polar or moderately polar solvents.
  • Temperature Dependence: Like many compounds, solubility may increase with temperature. Thus, higher temperatures could facilitate greater dissolution in both water and organic solvents.

In summary, sodium 2-(2,3,6-trichlorophenyl)acetate is expected to have good water solubility, which makes it easily usable in aqueous solutions. However, the varying behavior in organic solvents can be quite complex, often requiring empirical testing to establish exact solubility limits.

Interesting facts

Interesting Facts about Sodium; 2-(2,3,6-trichlorophenyl)acetate

Sodium; 2-(2,3,6-trichlorophenyl)acetate is a fascinating chemical compound that has caught the attention of scientists and researchers due to its unique composition and potential applications. Here are some intriguing aspects:

  • Chemical Structure: This compound features a distinctive aromatic ring substituted with three chlorine atoms, which not only influences its reactivity but also its overall properties. The presence of the sodium ion in the structure allows it to be soluble in water, making it relevant in various chemical reactions.
  • Potential Applications: Due to its unusual substitution pattern, this compound may exhibit interesting biological activity. Compounds with similar structures are often investigated for their potential use in:
    • Pharmaceuticals
    • Agricultural chemicals
    • Research reagents
  • Reactivity: The unique positioning of chlorine and acetate groups can lead to reactivity that is not seen in simpler compounds. This may provide pathways for various transformations in synthetic organic chemistry.
  • Environmental Considerations: Chlorinated compounds often raise concerns regarding their environmental impact. It's crucial to study their degradation pathways to ensure safe handling and disposal methods.
  • Historical Context: Understanding compounds with complex chlorinated structures can help chemists trace back the development of synthetic methodologies over the years. They represent a significant intersection of environmental and synthetic chemistry.

In summary, sodium; 2-(2,3,6-trichlorophenyl)acetate not only presents intriguing chemical properties but also serves as a reminder of the intricate relationships between chemical structure and reactivity. As a subject of study, it encapsulates a myriad of interests for both students and seasoned chemists.