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Butachlor

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Identification
Molecular formula
C17H26Cl2NO2
CAS number
23184-66-9
IUPAC name
2-(diethylamino)ethyl N-(4-butoxy-2,6-dichloro-phenyl)carbamate
State
State

At room temperature, butachlor is a liquid. This state facilitates its use as a herbicide, enabling it to be easily mixed with water or other solvents for application in agricultural fields.

Melting point (Celsius)
-3.00
Melting point (Kelvin)
270.15
Boiling point (Celsius)
369.00
Boiling point (Kelvin)
642.15
General information
Molecular weight
311.21g/mol
Molar mass
311.2140g/mol
Density
1.1320g/cm3
Appearence

Butachlor is typically a viscous, colorless to pale yellow liquid. It is known for being used in agricultural settings, where its appearance is crucial for easy application and identification.

Comment on solubility

Solubility of 2-(diethylamino)ethyl N-(4-butoxy-2,6-dichloro-phenyl)carbamate

The solubility of 2-(diethylamino)ethyl N-(4-butoxy-2,6-dichloro-phenyl)carbamate, often abbreviated as an N-carbamate compound, presents unique characteristics that can be influenced by various factors. Understanding these solubility traits can be crucial in applications ranging from pharmaceuticals to agrochemicals.

Key Factors Affecting Solubility:

  • Chemical Structure: The presence of the diethylamino group contributes to a moderate solubility profile in polar solvents due to its ability to form hydrogen bonds.
  • Solvent Dynamics: Solubility can vary significantly depending on the solvent. It tends to dissolve better in organic solvents compared to water because of its larger hydrophobic regions.
  • Temperature: Increased temperature generally enhances solubility as molecular movements become more vigorous, helping to overcome lattice energy.

It is important to note that, like many organic compounds, 2-(diethylamino)ethyl N-(4-butoxy-2,6-dichloro-phenyl)carbamate may exhibit the following behavior:

  1. Moderate to Low Water Solubility: Many N-carbamate derivatives demonstrate limited solubility in water, which may pose challenges in formulations requiring aqueous environments.
  2. Good Solubility in Organic Solvents: It is likely to dissolve readily in solvents such as ethanol or DMSO, which enhances its functionality in organic reactions.

Overall, the solubility characteristics of this compound are influenced by its complex structure and the balance of hydrophobic and hydrophilic groups. Understanding these factors is critical for optimizing its application in various fields.

Interesting facts

Interesting Facts about 2-(diethylamino)ethyl N-(4-butoxy-2,6-dichloro-phenyl)carbamate

This fascinating compound, commonly known for its application in the field of chemistry, has several noteworthy characteristics that make it a subject of interest for researchers and students alike. Here are some engaging insights:

  • Unique Structure: Its structure features multiple functional groups, including a carbamate and a dichloro-phenyl moiety, which contribute to its reactivity and functionality in various chemical reactions.
  • Pharmacological Relevance: Often studied in the context of drug design, this compound's interactions at the molecular level can provide crucial insights into pharmacodynamics and pharmacokinetics.
  • Environmental Impact: Compounds like this one are evaluated for their environmental stability and potential effects on ecosystems, making their study vital in the context of sustainable chemistry.
  • Applications: Typically utilized in agricultural chemistry, this compound can act as a pesticide or herbicide, highlighting its importance in food production and pest management systems.
  • Synthetic Pathways: The synthesis of this compound involves intricate multi-step processes, showcasing the creativity and problem-solving skills required in organic chemistry labs.

As Albert Einstein famously said, "The important thing is not to stop questioning. Curiosity has its own reason for existing." This compound is a perfect illustration of how curiosity drives scientific inquiry, leading to potential innovations and advancements in both chemistry and related fields.

In conclusion, 2-(diethylamino)ethyl N-(4-butoxy-2,6-dichloro-phenyl)carbamate represents a remarkable intersection of structure, function, and application, illustrating the broad scope of possibilities within the realm of chemical compounds.

Synonyms
K 913
BRN 2770368
CARBANILIC ACID, 4-BUTOXY-2,6-DICHLORO-, 2-(DIETHYLAMINO)ETHYL ESTER
15483-08-6
2-(Diethylamino)ethyl 4-butoxy-2,6-dichlorocarbanilate
4-Butoxy-2,6-dichlorocarbanilic acid 2-(diethylamino)ethyl ester
DTXSID40165743
DTXCID2088234