Skip to main content

Chlorfenapyr

ADVERTISEMENT
Identification
Molecular formula
C15H11BrClF3N2O
CAS number
122453-73-0
IUPAC name
(2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate
State
State

At room temperature, Chlorfenapyr is typically in a solid state. It is stable under normal temperatures and pressures.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
425.40
Boiling point (Kelvin)
698.60
General information
Molecular weight
409.81g/mol
Molar mass
409.8050g/mol
Density
1.4991g/cm3
Appearence

Chlorfenapyr is usually found as a white to beige colored crystalline solid. It's often supplied as a technical grade material or formulated as a liquid concentrate for insecticidal activities.

Comment on solubility

Solubility of (2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate

The solubility of (2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate can be influenced by various factors, including its molecular structure and the nature of the solvent. Generally, the solubility of organic compounds like this carbamate can vary significantly between different solvents.

  • Polarity: The presence of chlorine and carbamate functional groups can affect polarity, which in turn can influence solubility. Compounds with polar functional groups tend to dissolve better in polar solvents.
  • Temperature: As is common with many chemical compounds, an increase in temperature usually enhances solubility. Therefore, testing solubility at various temperatures might yield more insights.
  • pH Level: The solubility of carbamates may change significantly with pH, particularly if they can ionize under certain conditions.

In general, you might find that this compound exhibits limited solubility in water, often favoring organic solvents such as acetone, ethanol, or chloroform. It is essential to conduct specific solubility tests to confirm these observations, as solubility can vary based on experimental conditions.

In summary, while the solubility characteristics of (2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate may be broadly understood, the specific conditions and solvent used can greatly impact the extent to which this compound can dissolve. Therefore, thorough testing and consideration are essential.

Interesting facts

Interesting Facts about (2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate

(2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate is a fascinating compound that falls into the category of carbamate pesticides. Here are some intriguing aspects that highlight its significance in both chemistry and agriculture:

  • Versatile Applications: This compound is primarily utilized in agricultural practices as a pesticide, showcasing its importance in pest management and crop protection.
  • Mechanism of Action: Like many carbamates, it works by inhibiting the enzyme acetylcholinesterase, which is essential for nerve function in pests. This leads to the accumulation of neurotransmitters, ultimately causing paralysis and death of the pest.
  • Environmental Impact: While effective in pest control, it is crucial to consider the environmental implications. The use of this compound should be managed carefully to minimize potential risks to non-target organisms and ecosystems.
  • Design and Synthesis: The synthesis of this compound showcases advanced organic chemistry techniques, including the introduction of chlorine atoms for enhanced biological activity. The presence of the chlorophenyl moiety contributes to its effective binding properties.
  • Research Insight: Ongoing research investigates its efficacy and potential alternatives, enhancing sustainable agricultural practices while ensuring food security.

In summary, (2-chloro-1-methyl-ethyl) N-(3-chlorophenyl)carbamate is more than just a chemical compound; it plays a vital role in modern agriculture. As agricultural scientists and chemists continue to explore its characteristics, they must also weigh its benefits against environmental considerations, fostering a balanced approach to pest management.

Synonyms
2150-32-5
1-chloropropan-2-yl N-(3-chlorophenyl)carbamate
CPPC
SCHEMBL1412398
DTXSID80944110
1-Chloropropan-2-yl hydrogen (3-chlorophenyl)carbonimidate
Carbamic acid, (3-chlorophenyl)-, 2-chloro-1-methylethyl ester
Carbamic acid,(3-chlorophenyl)-,2-chloro-1-methylethyl ester(9ci)