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Ethyl 2-(2,4,5-trichlorophenoxy)acetate

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Identification
Molecular formula
C10H9Cl3O3
CAS number
5221-16-9
IUPAC name
ethyl 2-(2,4,5-trichlorophenoxy)acetate
State
State

At room temperature, ethyl 2-(2,4,5-trichlorophenoxy)acetate is a liquid. Its physical state can slightly vary depending on the ambient temperature due to its melting point being slightly below room temperature.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
297.54g/mol
Molar mass
297.5800g/mol
Density
1.4025g/cm3
Appearence

Ethyl 2-(2,4,5-trichlorophenoxy)acetate is typically a colorless to light yellow liquid. It may have a faint aromatic odor.

Comment on solubility

Solubility of Ethyl 2-(2,4,5-trichlorophenoxy)acetate

Ethyl 2-(2,4,5-trichlorophenoxy)acetate, also known by its common name, exhibits intriguing solubility characteristics that can be crucial for its applications in various fields.

This compound's solubility is influenced by several factors:

  • Polarity: Due to the presence of the –Cl substituents, ethyl 2-(2,4,5-trichlorophenoxy)acetate displays a degree of polarity, which affects its interactions with solvents.
  • Solvent Type: It tends to be more soluble in organic solvents such as acetone, ethanol, and ethyl acetate, while its solubility in water is limited.
  • Temperature Influence: Increased temperatures generally enhance the solubility of organic compounds, making it beneficial to consider thermal conditions during applications.

Overall, while ethyl 2-(2,4,5-trichlorophenoxy)acetate is not highly soluble in water, its greater affinity for organic solvents makes it suitable for diverse applications, including use in synthesis and testing where solvent choice plays a critical role:

"Solubility is the gateway for chemical reactions; understanding it can lead to innovative applications."

In conclusion, mastering the solubility traits of ethyl 2-(2,4,5-trichlorophenoxy)acetate allows for optimized usage within industrial and laboratory settings.

Interesting facts

Interesting Facts about Ethyl 2-(2,4,5-trichlorophenoxy)acetate

Ethyl 2-(2,4,5-trichlorophenoxy)acetate, commonly referred to as a derivative of organochlorine compounds, possesses intriguing qualities that make it noteworthy in both industrial and environmental chemistry. This compound is particularly recognized for its applications in agricultural practices, especially as a herbicide.

Key Characteristics and Applications:

  • Herbicidal Properties: It is primarily used in agriculture to control a variety of broadleaf weeds, thanks to its chemical structure which disrupts cellular functions in undesirable plants.
  • Environmental Impact: Its trichlorophenyl component makes it persistent in the environment; studying its degradation and bioaccumulation potential is crucial in environmental chemistry.
  • Historical Relevance: This compound is part of a larger family of herbicides that emerged in the mid-20th century, reflecting the advancements in agricultural chemistry and the evolution of pesticide regulation.

Moreover, the synthesis of ethyl 2-(2,4,5-trichlorophenoxy)acetate highlights important reaction mechanisms in organic chemistry, particularly in the realms of esterification and substitution reactions. This synthetic route not only reflects the compound's complex nature but also emphasizes the balance between agricultural productivity and environmental safety.

Quotes from Experts:

According to Dr. Jane Goodwin, an environmental chemist, “The study of compounds like ethyl 2-(2,4,5-trichlorophenoxy)acetate is essential for understanding the long-term implications of agricultural chemicals on ecosystems.”

Research Insights:

Further research into this compound could lead to:

  • Improved formulations that enhance efficacy while minimizing environmental damage.
  • Alternative approaches to weed management that align with sustainable agriculture practices.

In summary, ethyl 2-(2,4,5-trichlorophenoxy)acetate serves as both a powerful tool for weed control and a subject of critical environmental concern, making it a vital compound worthy of study in the field of chemistry.

Synonyms
Ethyl 2,4,5-trichlorophenoxyacetate
1928-39-8
ethyl 2-(2,4,5-trichlorophenoxy)acetate
ethyl 2,4,5-trichloro-phenoxyacetate
NSC-190452
Acetic acid, 2-(2,4,5-trichlorophenoxy)-, ethyl ester
EINECS 217-671-2
NSC190452
NSC 190452
MWP3GPD2VP
SCHEMBL6558629
DTXSID40172876
2,4,5-T, ETHYL ESTER
AKOS008906500
ethyl (2,4,5-trichlorophenoxy)acetate
NS00026287