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Butoxyethyl triclopyr

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Identification
Molecular formula
C15H20Cl3O4
CAS number
64700-56-7
IUPAC name
3-(2-butoxyethoxy)propyl 2-(2,4,5-trichlorophenoxy)acetate
State
State

At room temperature, butoxyethyl triclopyr is in a liquid state, typically used in its emulsified form for various herbicidal applications.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
327.40
Boiling point (Kelvin)
600.55
General information
Molecular weight
387.68g/mol
Molar mass
387.6800g/mol
Density
1.2700g/cm3
Appearence

Butoxyethyl triclopyr is generally a colorless to pale yellow liquid. It is often used as a herbicide and may form emulsions when mixed with water solutions.

Comment on solubility

Solubility of 3-(2-butoxyethoxy)propyl 2-(2,4,5-trichlorophenoxy)acetate

The solubility of 3-(2-butoxyethoxy)propyl 2-(2,4,5-trichlorophenoxy)acetate is influenced by its distinct molecular structure and the presence of functional groups within its composition. Understanding its solubility characteristics can be quite pertinent in both laboratory and environmental contexts. Here are some key aspects to consider:

  • Polarity: This compound contains both polar and non-polar functional groups, which results in varying solubility in different solvents.
  • Solvent Compatibility: The ether and acetate groups may enhance solubility in organic solvents such as ethanol and acetone while being less soluble in water.
  • Lipophilicity: The presence of chlorinated phenoxy groups tends to increase lipophilicity, contributing to solubility in non-polar organic solvents.
  • Environmental Concerns: Given its chemical nature, this compound may exhibit limited biodegradability, affecting its behavior in aquatic environments.

In practical applications, when evaluating the potential uses of 3-(2-butoxyethoxy)propyl 2-(2,4,5-trichlorophenoxy)acetate, the solubility profile should always be assessed to predict its reactivity and interactions with other substances.

Interesting facts

Interesting Facts about 3-(2-butoxyethoxy)propyl 2-(2,4,5-trichlorophenoxy)acetate

This compound, often recognized for its applications in both agriculture and pharmaceuticals, is a fascinating example of organic chemistry in action. Below are some intriguing details:

  • Agricultural Applications: This compound is frequently used as a herbicide. Its efficacy in controlling a wide spectrum of weeds makes it invaluable in crop management, promoting growth in desirable plants while suppressing unwanted vegetation.
  • Complex Structure: The chemical structure features a combination of ether and ester linkages, contributing to its unique properties. The presence of a trichlorophenoxy group significantly enhances its herbicidal activity.
  • Mechanism of Action: Its mechanism involves the disruption of plant growth processes, specifically by interfering with hormonal balance and essential metabolic pathways in targeted plants.
  • Environmental Considerations: Given its use in agriculture, understanding its environmental impact is crucial. Research is ongoing to evaluate its persistence in soil and aquatic environments to mitigate any potential risks.
  • Biochemical Importance: Besides its agricultural relevance, compounds with similar structures are also studied for potential pharmaceutical benefits; they may exhibit various biological activities, including anti-inflammatory properties.

In essence, 3-(2-butoxyethoxy)propyl 2-(2,4,5-trichlorophenoxy)acetate represents a key intersection of chemistry and environmental science, demonstrating both the opportunities and challenges presented by synthetic compounds in our modern world.

Synonyms
2,4,5-t Butoxyethoxypropanol ester
2,4,5-T 3-(2-butoxyethoxy)propyl ester
1928-58-1
UNII-5VZN5B948N
5VZN5B948N
DTXSID8074994
Acetic acid, (2,4,5-trichlorophenoxy)-, 3-(2-butoxyethoxy)propyl ester
DTXCID5036050
NS00123205
Q27262939