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Diuron

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Identification
Molecular formula
C9H10Cl2N4O
CAS number
330-54-1
IUPAC name
1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea
State
State

At room temperature, Diuron is typically found as a solid due to its crystalline nature.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
233.10g/mol
Molar mass
233.0950g/mol
Density
1.4820g/cm3
Appearence

Diuron is an off-white crystalline solid. It is available in the form of wettable powders or granules for agricultural use. The solid form may have a faint chemical odor.

Comment on solubility

Solubility of 1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea

The solubility of 1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea, often referred to as a complex organic compound, is a topic of interest due to its unique structural characteristics. Here are some key points to consider:

  • Polar and Non-Polar Interactions: The presence of both polar urea and non-polar isopropyl groups indicates that its solubility may vary significantly in different solvents.
  • Solvent Compatibility: This compound is generally soluble in:
    • Polar solvents: Such as water and alcohols, due to hydrogen bonding capabilities.
    • Non-polar solvents: Poor solubility, likely leading to a limited application in these environments.
  • Temperature Dependence: Like many organic compounds, solubility can often increase with temperature, facilitating better dissolution in warm solvents.

In summary, while 1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea exhibits good solubility in polar solvents, its solubility in non-polar solvents remains minimal. Therefore, this compound's versatility in solution is heavily reliant on the solvent's properties.

Interesting facts

Interesting Facts about 1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea

1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea, commonly referred to as a selective herbicide, is a fascinating compound with unique characteristics and applications in the field of agriculture. Here are some intriguing points to note:

  • Mechanism of Action: This compound functions primarily by inhibiting photosynthesis in target plants. It acts on specific biochemical pathways, effectively disrupting the growth of unwanted vegetation while being less harmful to desired crops.
  • Environmental Impact: Due to its selective nature, its application can lead to a reduction in the overall usage of harsher chemical herbicides, promoting a more sustainable approach to weed management.
  • History of Use: Developed in the mid-20th century, this compound has been integral in advancing herbicide technology, marking a significant milestone in agrochemical innovation.
  • Resistance Management: The incorporation of this compound in agricultural practice assists in managing herbicide resistance, as it can be rotated with other treatment methods to minimize resistance development in weed populations.
  • Synthesis: The synthesis involves multi-step chemical reactions, often requiring careful control of reaction conditions to yield a high-purity product.

As noted by chemists, "The development of selective herbicides like this compound represents a crucial advancement in our ability to manage agricultural ecosystems." With ongoing research, the potential of 1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-isopropyl-urea continues to expand in various applications, pushing the boundaries of effective weed control and agricultural productivity.

Synonyms
1-(4,6-dichloro-1,3,5-triazin-2-yl)-3-propan-2-ylurea
5097-54-1
DTXSID10274694