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Propoxur

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Identification
Molecular formula
C11H13Cl2NO3
CAS number
114-26-1
IUPAC name
isopropyl N-(2,4-dichlorophenyl)carbamate
State
State

Propoxur is typically solid at room temperature.

Melting point (Celsius)
91.00
Melting point (Kelvin)
364.15
Boiling point (Celsius)
537.00
Boiling point (Kelvin)
810.15
General information
Molecular weight
209.14g/mol
Molar mass
209.0980g/mol
Density
1.2600g/cm3
Appearence

Propoxur is a white crystalline solid. It is tasteless and odorless.

Comment on solubility

Solubility of Isopropyl N-(2,4-dichlorophenyl)carbamate (C11H13Cl2NO3)

The solubility of isopropyl N-(2,4-dichlorophenyl)carbamate is influenced by its chemical structure and the presence of polar and non-polar functional groups. Here are some key points to consider:

  • Polarity: The compound contains a carbamate functional group, which is polar and can interact favorably with water molecules.
  • Hydrophobic Regions: The presence of the 2,4-dichlorophenyl moiety adds a hydrophobic character that can reduce overall solubility in aqueous environments.
  • Solvent Dependence: This compound may exhibit different solubility profiles in various solvents. For example, it might be more soluble in organic solvents like ethanol or acetone compared to water.
  • Temperature Influence: As with many organic compounds, an increase in temperature can enhance solubility due to increased molecular motion and interaction.
  • Environmental Considerations: The solubility of this compound can have implications for its environmental behavior, particularly in terms of bioavailability and degradation in water systems.

Overall, while isopropyl N-(2,4-dichlorophenyl)carbamate possesses some polar characteristics, its hydrophobic regions suggest that it may have limited solubility in water but could be more soluble in organic solvents. It's essential to test its solubility empirically for precise applications.

Interesting facts

Exploring Isopropyl N-(2,4-Dichlorophenyl)carbamate

Isopropyl N-(2,4-dichlorophenyl)carbamate is a fascinating compound with significant applications in the realm of agricultural chemicals. Known primarily for its use as an herbicide, this compound offers various attributes that make it invaluable to farmers and researchers alike.

Key Features:

  • Mechanism of Action: As a herbicide, it works by inhibiting specific enzymes involved in amino acid synthesis, thus preventing the growth of unwanted plants in agricultural settings.
  • Selectivity: One notable characteristic is its selective action, allowing it to target specific weed species while leaving desirable crops unharmed.
  • Environmental Impact: Research is ongoing to understand its environmental fate, making it crucial for ensuring sustainable agricultural practices.
  • Safety: Safety assessments are essential. Scientists continually evaluate its toxicology and degradation products to ensure minimal risk to non-target organisms.

In addition to its herbicidal properties, isopropyl N-(2,4-dichlorophenyl)carbamate’s structure presents an intriguing case for synthetic chemists. The presence of the dichlorophenyl moiety not only enhances its biological activity but also contributes to the study of structure-activity relationships (SAR) in pesticide development. As noted by chemist Richard Feynman, "What I cannot create, I do not understand," signaling the importance of studying and understanding such compounds for innovation in agricultural technologies.

Overall, the ongoing exploration of isopropyl N-(2,4-dichlorophenyl)carbamate contributes to our understanding of herbicides and their role in modern agriculture while upholding safety and environmental stewardship.

Synonyms
ISOPROPYL N-(2,4-DICHLOROPHENYL)CARBAMATE
666-773-7
2150-25-6
propan-2-yl N-(2,4-dichlorophenyl)carbamate
NSC83153
NCIOpen2_004498
SCHEMBL11794832
DTXSID30274575
NSC-83153
AKOS024334739
Carbamic acid, N-(2,4-dichlorophenyl)-, 1-methylethyl ester