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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[2-(methylcarbamoyloxy)phenyl] N-methylcarbamate
State
State

Carbaryl is typically a solid at room temperature. It can be found in different formulations, including dusts and suspensions when used as a pesticide.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a colorless crystalline solid in its pure form. It is usually available as a solid or powder and may be off-white in commercially available forms. It is often formulated into pesticide products, which can range from powders to liquid suspensions.

Comment on solubility

Solubility of [2-(methylcarbamoyloxy)phenyl] N-methylcarbamate

The solubility of [2-(methylcarbamoyloxy)phenyl] N-methylcarbamate in various solvents can provide insight into its behavior in different environments. While specific solubility data may vary, here are some general insights on its potential solubility properties:

  • Polarity: The presence of both phenolic and carbamate functional groups suggests that it may exhibit a degree of polar characteristics, likely leading to moderate solubility in polar solvents such as water and alcohols.
  • Non-Polar Solvents: In non-polar solvents like hexane or toluene, the solubility might be limited, as the molecule's structure exhibits polar regions.
  • Temperature Effect: As with many compounds, solubility can increase with temperature in a given solvent, which is particularly relevant during practical applications or synthesis processes.
  • pH Dependency: The solubility could also be affected by the pH of the solution, especially due to the potentially ionizable nature of the carbamate moiety.

In conclusion, while precise solubility data for [2-(methylcarbamoyloxy)phenyl] N-methylcarbamate might not be readily available, the combination of functional groups hints at its ability to be soluble in polar environments while remaining less soluble in non-polar scenarios. Further experimental investigation would provide clarity for its behavior in specific applications.

Interesting facts

Interesting Facts about [2-(Methylcarbamoyloxy)phenyl] N-methylcarbamate

[2-(Methylcarbamoyloxy)phenyl] N-methylcarbamate is a fascinating compound within the realm of organic chemistry, showcasing the intricate connections between structure and function.

1. Chemical Structure and Functionality

This compound features a unique structure that includes a phenyl ring substituted with both a carbamate and a methylcarbamate functional group. This configuration allows for a variety of interactions:

  • Enhanced Efficacy: The presence of the methylcarbamoyloxy group significantly influences the compound's biological activity.
  • Potential Applications: It is often researched for its application in agricultural science, particularly as a pesticide or herbicide.

2. Biological Implications

Due to its chemical composition, [2-(methylcarbamoyloxy)phenyl] N-methylcarbamate may exhibit:

  • Pesticidal Properties: Its potential to inhibit pests, contributing to agricultural sustainability.
  • Neurotoxic Effects: Like many carbamates, it may affect the nervous system of insects, making it effective in pest control.

3. Research Significance

This compound has gained attention in scientific research due to:

  • Studying Enzyme Interactions: Researchers often explore how it interacts with enzymes, providing insights into pest resistance mechanisms.
  • Environmental Impact Assessments: Understanding its degradation and bioaccumulation is crucial for assessing its ecological footprint.

4. Synthesis and Chemistry

The synthesis of [2-(methylcarbamoyloxy)phenyl] N-methylcarbamate involves multiple steps, often including:

  • Functional Group Transformations: These may include esterification and amidation reactions.
  • Targeted Design: Chemists design derivatives to improve efficacy and reduce toxicity to non-target species.

This compound stands as a testament to the sophistication of chemical synthesis and its profound implications for agriculture and environmental science, exemplifying how a thoughtful approach to molecular design can yield significant benefits in both scientific research and practical applications.

Synonyms
CARBAMIC ACID, METHYL-, o-PHENYLENE ESTER
Methylcarbamic acid o-phenylene ester
1,2-Benzenediol, bis(methylcarbamate)
18315-57-6
L08MTK7ZOM
NSC 32689
Benzene, 1,2-bis(methylcarbamyloxy)-
TL-1015
BRN 1983581
Pyrocatechol bis(methylcarbamate)
UNII-L08MTK7ZOM
NSC-32689
DTXSID50171395
1,2-BENZENEDIOL, 1,2-BIS(N-METHYLCARBAMATE)
DTXCID1093886
NSC32689