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Carbaryl

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Identification
Molecular formula
C12H11Cl2NO2
CAS number
63-25-2
IUPAC name
(2,4-dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate
State
State

Solid at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.00
Boiling point (Celsius)
344.00
Boiling point (Kelvin)
617.00
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid.

Comment on solubility

Solubility of (2,4-dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate

(2,4-dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate is a compound that exhibits interesting solubility characteristics. Understanding its solubility is essential for various applications, including formulation and environmental impact assessments.

Solubility Characteristics

Key factors affecting the solubility of this compound include:

  • Polarity: The presence of multiple functional groups influences the overall polarity, thus impacting its interaction with solvents.
  • Hydrogen bonding: The N-methylcarbamate moiety can engage in hydrogen bonding, enhancing solubility in polar solvents.
  • Temperature: As with many organic compounds, solubility typically increases with temperature, potentially leading to greater dissolution in warmer solvents.

“Like dissolves like” is a common phrase in chemistry, suggesting that the solubility of (2,4-dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate in solvents can vary significantly based on their polarity.

Solvent Compatibility

In terms of solvent compatibility:

  • Polar solvents: This compound is likely to show better solubility in polar solvents like methanol and ethanol.
  • Non-polar solvents: Limited solubility may be expected in non-polar solvents, such as hexane.

Understanding the solubility of (2,4-dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate is critical for its use in various applications, from agricultural to environmental sciences.

Interesting facts

Interesting Facts about (2,4-Dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate

(2,4-Dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate is a fascinating compound with a variety of applications and notable characteristics. Here are some intriguing facts about it:

  • Pesticide Action: This compound is commonly used as a pesticide, particularly targeting insects and pests in agricultural settings. Its effectiveness is largely due to its ability to interfere with the normal functioning of the pest's nervous system.
  • Mechanism of Action: As a carbamate, it works by inhibiting the activity of the enzyme acetylcholinesterase. This leads to an accumulation of acetylcholine in synapses, causing continuous stimulation of nerve cells, which ultimately results in the pest's demise.
  • Environmental Considerations: While it is effective as a pesticide, there are significant concerns regarding its environmental impact. The persistence of such compounds in ecosystems can lead to harmful effects on non-target organisms, including beneficial insects, birds, and aquatic life.
  • Regulatory Status: Due to environmental and health concerns, the use of certain carbamate derivatives is heavily regulated in many countries. Understanding and adhering to these regulations is crucial for sustainable agricultural practices.
  • Research and Development: Scientists continue to explore ways to improve the efficacy and reduce the toxicity of carbamate-based pesticides. Innovations in formulations and delivery methods are ongoing areas of research aimed at minimizing ecological disruptions.

In conclusion, the compound (2,4-dichloro-5-ethyl-3-methyl-phenyl) N-methylcarbamate is a prime example of how chemical compounds play a critical role in modern agriculture. However, its use must be balanced with environmental sustainability and safety considerations. As future chemists and scientists, understanding such compounds paves the way for developing safer and more effective agricultural solutions.

Synonyms
DRC 3321
672-06-0
CARBAMIC ACID, METHYL-, 2,4-DICHLORO-5-ETHYL-m-TOLYL ESTER
2,4-Dichloro-5-ethyl-3-methylphenol methylcarbamate
(2,4-dichloro-5-ethyl-3-methylphenyl) N-methylcarbamate
Phenol, 2,4-dichloro-5-ethyl-3-methyl-, 1-(N-methylcarbamate)
U 17556
BRN 2130792
m-Cresol-2,4-dichloro-5-ethyl N-methylcarbamate
Phenol, 2,4-dichloro-5-ethyl-3-methyl-, methylcarbamate
DTXSID60217475
AKOS040751640