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Carbaryl

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

Carbaryl is commonly a solid at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
201.22g/mol
Molar mass
201.2190g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid, often observed as a fine powder. It is odourless to those sensitive to it, but might hold a mild characteristic odour in large amounts.

Comment on solubility

Solubility of [3-(hexanoylamino)-2-methyl-phenyl] N-methylcarbamate

The solubility of the compound [3-(hexanoylamino)-2-methyl-phenyl] N-methylcarbamate can be significantly influenced by its structural features. This compound, known for its unique functional groups, presents various solubility characteristics:

  • Polarity: The presence of both hydrophilic (the carbamate group) and hydrophobic (hexanoyl chain) elements suggests that the solubility can vary dramatically in different solvents.
  • Solvent Type: Generally, polar solvents such as water may show limited solubility due to the bulky nature of the hexanoyl chain, while non-polar solvents could enhance solubility due to favorable interactions.
  • Temperature Effects: Increased temperature often improves solubility for many organic compounds, which could be the case here as well.
  • pH Influence: The pH of the solution may also play a critical role in solubility, particularly due to the presence of amine functionality that can participate in protonation reactions.

To summarize, the solubility of [3-(hexanoylamino)-2-methyl-phenyl] N-methylcarbamate is affected by a combination of polar and non-polar interactions, solvent choices, temperature, and possibly the pH of the environment. Understanding these factors is crucial for predicting behavior in different chemical contexts.

Interesting facts

Exploring [3-(Hexanoylamino)-2-methyl-phenyl] N-methylcarbamate

[3-(Hexanoylamino)-2-methyl-phenyl] N-methylcarbamate is a fascinating compound, primarily recognized for its role in various chemical and biological applications. Here are some interesting facts about this compound:

  • Insecticidal Properties: This compound is known to demonstrate potent insecticidal activity, making it a candidate for pest control formulations.
  • Mechanism of Action: It operates by disrupting key biological pathways in insects, which is crucial for developing effective insecticides with minimal environmental impact.
  • Synthetic Utility: The synthesis of this compound involves multiple steps, showcasing the creativity and precision required in organic chemistry. Its structure allows for modifications that can lead to derivatives with varying properties.
  • Research Applications: Ongoing research on this compound explores its effectiveness and safety, aiming to enhance agricultural outputs while reducing chemical residues.
  • Structural Features: The unique combination of a hexanoylamino group and a carbamate moiety underscores the complexity and versatility of this compound, highlighting how structure influences function.

As a rapidly evolving area in chemistry, the study of this compound exemplifies the intersection between chemical research and practical applications. Scientists strive to uncover new insights and optimize its use in sustainable agriculture. In words of one researcher, "Innovation in chemistry is about finding balance—between efficacy, safety, and sustainability."

From its insecticidal properties to its synthetic potential, [3-(Hexanoylamino)-2-methyl-phenyl] N-methylcarbamate continues to be a subject of great interest in the scientific community.

Synonyms
m-(2-Methylhexanamido)phenyl methylcarbamate
BRN 2143516
DTXSID50170404
DTXCID8092895
17795-81-2
Hexananilide, 3'-hydroxy-2-methyl-, methylcarbamate (ester)