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Metolcarb

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Identification
Molecular formula
C11H14ClNO2
CAS number
1129-41-5
IUPAC name
(4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate
State
State

At room temperature, Metolcarb is in a solid state.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.15
General information
Molecular weight
213.69g/mol
Molar mass
213.6670g/mol
Density
1.1839g/cm3
Appearence

Metolcarb appears as a white solid. It is typically available in technical grade as an off-white to light beige powder.

Comment on solubility

Solubility of (4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate

(4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate is a compound that exhibits interesting solubility characteristics. Understanding its solubility behavior is essential for various applications, including formulation in different chemical environments. The factors affecting its solubility include:

  • Polarity: The presence of both polar (e.g., N-methyl group) and non-polar (e.g., chloro and methyl groups) elements within the molecule contributes to its unique solubility in various solvents.
  • Solvent Interaction: It is more likely to be soluble in organic solvents such as ethers and alcohols due to its hydrophobic character, while being less soluble in water.
  • Temperature: As with many organic compounds, increasing the temperature may enhance solubility due to increased molecular motion, allowing for better interaction with solvent molecules.

In summary, (4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate is generally poorly soluble in water, but may have decent solubility in organic solvents. The balance of hydrophilic and hydrophobic regions within its structure significantly influences its overall solubility behavior. This duality underlines the importance of selecting the right solvent for optimal dissolution and application purposes.

Interesting facts

Interesting Facts about (4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate

(4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate, commonly referred to in various scientific circles, is a fascinating compound that serves multiple roles in the field of chemistry and beyond. Here are some key insights:

  • Versatile Applications: This compound is primarily known for its use as a pesticide. It plays a crucial role in agricultural settings to protect crops from pests, particularly in systems that require high specificity to reduce the impact on non-target species.
  • Mechanism of Action: It acts by inhibiting acetylcholinesterase, an essential enzyme that breaks down neurotransmitters. This leads to an accumulation of acetylcholine at nerve synapses, ultimately resulting in pest paralysis and death.
  • Environmental Considerations: While effective, the use of such compounds raises important discussions about environmental safety and sustainability. Researchers are continually evaluating its biodegradability and potential impacts on non-target organisms.
  • Structure-Activity Relationship: The specific substitutions on the phenyl ring, like the chlorine and methyl groups, greatly influence the compound's biological activity. Studying these relationships enhances our understanding of how molecular modifications can affect pesticide efficacy and safety.
  • Regulatory Status: As a widely used chemical in pest control, it is subject to stringent regulations and evaluations by various health and environmental organizations. Compliance with these standards is critical for its continued use.

In summary, (4-chloro-3,5-dimethyl-phenyl) N-methylcarbamate represents a remarkable intersection of chemistry, agriculture, and environmental science. Its ongoing study is essential for improving agricultural practices and ensuring safety for both humans and ecosystems.

Synonyms
DRC 3342
673-00-7
CARBAMIC ACID, METHYL-, 4-CHLORO-3,5-XYLYL ESTER
BRN 2332797
Methylcarbamic acid 4-chloro-3,5-xylyl ester
Carbamic acid, methyl-, 4-chloro-3,5-dimethylphenyl ester
DTXSID50217666
DTXCID00140157
4-Chloro-3
4-chloro-3,5-dimethylphenyl methylcarbamate
CARBAMICACID,METHYL-,4-CHLORO-3,5-XYLYLESTER
UVPPWESDRAKSEO-UHFFFAOYSA-N