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Terbutryn

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Identification
Molecular formula
C10H19ClN6O
CAS number
886-50-0
IUPAC name
6-(4-chlorophenoxy)-N2,N4-diethyl-1,3,5-triazine-2,4-diamine
State
State

At room temperature, Terbutryn is typically in a solid state.

Melting point (Celsius)
104.50
Melting point (Kelvin)
377.65
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
241.72g/mol
Molar mass
241.7230g/mol
Density
1.2060g/cm3
Appearence

Terbutryn appears as a colorless crystalline solid. It is typically prepared in a technical grade and may have a yellowish tinge when impure.

Comment on solubility

Solubility of 6-(4-chlorophenoxy)-N2,N4-diethyl-1,3,5-triazine-2,4-diamine

The solubility of 6-(4-chlorophenoxy)-N2,N4-diethyl-1,3,5-triazine-2,4-diamine in various solvents offers intriguing insights into its chemical behavior. This compound, part of the triazine family, exhibits distinctive solvation properties. Here are some points to consider:

  • Polar Solvents: It is generally poorly soluble in water due to its substantial hydrophobic character stemming from the diethyl and phenoxy groups.
  • Non-polar Solvents: However, it is more soluble in non-polar solvents such as toluene and chloroform, where it can interact more favorably with the solvent molecules.
  • Temperature Influence: Like many organic compounds, solubility may increase with temperature, enhancing its availability in solution.
  • pH Variability: The solubility may also depend on the pH of the solution, with potential variations observed in acidic or basic environments due to the presence of amine groups.

In summary, the solubility of this compound is dictated by its structure and the nature of the solvent. Understanding these interactions can significantly enhance its application in chemical processes and formulations.

Interesting facts

Interesting Facts about 6-(4-chlorophenoxy)-N2,N4-diethyl-1,3,5-triazine-2,4-diamine

This compound is a member of the triazine family, which is known for its diverse applications in fields such as agriculture and pharmaceuticals. Here are some fascinating highlights:

  • Herbicide Properties: The unique structure of this compound allows it to act effectively as a herbicide, targeting specific plant enzymes.
  • Triazine Derivatives: The triazine ring structure is a common motif in various agrochemicals, leading to ongoing research in modifying these compounds for enhanced efficacy.
  • Pharmacological Potential: Beyond its agricultural applications, compounds with similar structures are often investigated for their potential in treating diseases, showcasing a dual-use nature.
  • Chlorophenoxy Group: The presence of the 4-chlorophenoxy moiety adds to its phytotoxicity, making it a critical feature for its function in herbicidal applications.
  • Environmental Considerations: With the rise of sustainable agriculture, there is ongoing research evaluating the environmental impact and degradation pathways of such chemical compounds.

The intricate balance between effectiveness and environmental safety in products like 6-(4-chlorophenoxy)-N2,N4-diethyl-1,3,5-triazine-2,4-diamine is crucial:

"As we develop new compounds, we must always consider their long-term effects on ecosystems."

This compound exemplifies the intersection of chemistry, agriculture, and environmental science, highlighting the importance of innovative research in creating more efficient and safer agricultural practices.