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Propoxur

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Identification
Molecular formula
C11H13Cl2NO2
CAS number
114-26-1
IUPAC name
isopropyl N-(3,4-dichlorophenyl)carbamate
State
State

Propoxur is in a solid state at room temperature. It is stable and has low solubility in water but is more soluble in organic solvents.

Melting point (Celsius)
91.00
Melting point (Kelvin)
364.15
Boiling point (Celsius)
398.60
Boiling point (Kelvin)
671.75
General information
Molecular weight
209.14g/mol
Molar mass
209.1190g/mol
Density
1.2700g/cm3
Appearence

Propoxur is a white crystalline solid. It may appear slightly off-white or beige if impurities are present. It is typically found in a fine powder form.

Comment on solubility

Solubility of Isopropyl N-(3,4-dichlorophenyl)carbamate

The solubility of isopropyl N-(3,4-dichlorophenyl)carbamate, a carbamate compound, is influenced by several factors including its molecular structure and interactions with solvents. Here are some key points regarding its solubility:

  • Polarity: This compound exhibits moderate polarity due to the presence of the carbamate functional group, which can engage in hydrogen bonding.
  • Solvent Compatibility: Isopropyl N-(3,4-dichlorophenyl)carbamate is more soluble in organic solvents such as ethanol and acetone, rather than in polar solvents like water.
  • Temperature Effects: Increased temperature often enhances solubility for many organic compounds, suggesting that heating may improve the dissolution of this carbamate.
  • Viscosity of the Solvent: The viscosity of the solvent can also play a crucial role; lower viscosity solvents usually provide better solubility for organic compounds.

In conclusion, while isopropyl N-(3,4-dichlorophenyl)carbamate demonstrates limited water solubility, its compatibility with non-polar and moderately polar organic solvents opens a range of applications in various fields. Understanding its solubility characteristics is crucial for effective use in formulations and chemical processes.

Interesting facts

Interesting Facts about Isopropyl N-(3,4-dichlorophenyl)carbamate

Isopropyl N-(3,4-dichlorophenyl)carbamate is a fascinating chemical compound that has garnered attention in both agricultural and medicinal chemistry. Here are some intriguing highlights:

  • Pesticidal Properties: This compound is primarily recognized for its activity as a pesticide. It acts as a herbicide, effectively controlling unwanted weeds and enhancing crop yields.
  • Mechanism of Action: The efficacy of isopropyl N-(3,4-dichlorophenyl)carbamate is largely attributed to its ability to inhibit specific biochemical pathways in plants. This interferes with essential growth processes, ultimately leading to weed death.
  • Structural Significance: The presence of the 3,4-dichlorophenyl group plays a crucial role in the compound's biological activity. The electronegative chlorine atoms enhance the compound’s ability to interact with the target sites in living organisms.
  • Analytical Techniques: Researchers often employ advanced analytical methods such as gas chromatography and liquid chromatography to study the compound's presence in environmental samples, promoting safety assessments and regulatory compliance.
  • Environmental Impact: While effective against pests, the environmental ramifications of synthetic herbicides, including isopropyl N-(3,4-dichlorophenyl)carbamate, are an area of ongoing research, as scientists seek to better understand ecological consequences and develop safer alternatives.

In summary, isopropyl N-(3,4-dichlorophenyl)carbamate exemplifies the dual potential found in organic compounds—it serves both agricultural purposes and presents challenges that demand responsible stewardship and innovation. Its continual study not only advances the field of chemistry but also contributes to sustainable practices in agriculture.

Synonyms
2150-28-9
Isopropyl N-(3,4-dichlorophenyl)carbamate
ISOPROPYL 3,4-DICHLOROCARBANILATE
DTXSID90175837
DTXCID2098328
665-636-9
propan-2-yl N-(3,4-dichlorophenyl)carbamate
Carbamic acid,(3,4-dichlorophenyl)-, 1-methylethyl ester (9CI)
SCHEMBL10608407
NLBTXMFJUAESAC-UHFFFAOYSA-N
Isopropyl 3,4-dichlorophenylcarbamate
AKOS024334511
CCG-255225
Isopropyl 3,4-dichlorophenylcarbamate #
isopro-pyl-N-(3,4-dichlorophenyl)carbamate