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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
1-naphthyl N,N-dimethylcarbamate
State
State

Carbaryl is a solid at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.00
Boiling point (Celsius)
374.00
Boiling point (Kelvin)
647.00
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white crystalline solid with a slight odor. It is typically found in powdered form for ease of use. The crystals may appear slightly off-white depending on purity and environmental conditions.

Comment on solubility

Solubility of 1-naphthyl N,N-dimethylcarbamate

1-naphthyl N,N-dimethylcarbamate is a compound that demonstrates variable solubility characteristics depending on its environment.

General observations about its solubility include:

  • Solvent Polarity: This compound is generally more soluble in non-polar solvents such as hexane or ether, due to its non-polar naphthalene ring structure.
  • Water Solubility: It exhibits limited solubility in water, primarily because of the hydrophobic nature of the naphthyl group, which tends to resist interactions with polar water molecules.
  • Effect of Temperature: As with many organic compounds, increased temperature can enhance solubility, making it more appreciable in certain solvents.

In summary, while 1-naphthyl N,N-dimethylcarbamate finds itself well-dissolved in various organic solvents, its interaction with water remains minimal, highlighting the influence of molecular structure on solubility.

Interesting facts

Interesting Facts about 1-naphthyl N,N-dimethylcarbamate

1-naphthyl N,N-dimethylcarbamate is an intriguing organic compound that garners attention in both academia and industry for various reasons. Here are some fascinating insights:

  • Herbicide Potential: This compound is notably recognized for its herbicidal properties. It serves as a vital ingredient in the formulation of certain herbicides that help in weed management, showcasing its importance in agriculture.
  • Insecticidal Activity: In addition to its role in weed control, 1-naphthyl N,N-dimethylcarbamate exhibits potential insecticidal activity, making it a compound of interest for pest management solutions.
  • Research Applications: The compound has been the subject of numerous studies aimed at exploring its mechanism of action and effectiveness, providing valuable insights for future enhancements in pest control strategies.
  • Biochemical Pathway: As a carbamate, it interacts with the biochemical pathways of pests by inhibiting the activity of specific enzymes, which can lead to their mortality—highlighting the compound’s mechanism at a molecular level.
  • Environmental Impact: Owing to its use in agriculture, understanding the environmental impact of 1-naphthyl N,N-dimethylcarbamate is crucial. Research continues to evaluate its degradation products and ecotoxicological effects, ensuring safe use in eco-friendly practices.
  • Structure-Activity Relationship: Chemists study the structure-activity relationship (SAR) of this compound to modify its properties for enhanced efficacy or reduced toxicity, a fundamental aspect of drug discovery and development.

In conclusion, 1-naphthyl N,N-dimethylcarbamate is more than just a chemical name; it represents a significant contribution to modern agricultural practices, pest management, and biochemical research. Its multifunctional properties and ongoing studies make it a captivating subject for chemistry enthusiasts.

Synonyms
1-Naphthyl dimethylcarbamate
2619-00-3
91384-85-9
1-Naphthyl N,N-dimethylcarbamate
Carbamic acid, dimethyl-, 1-naphthalenyl ester
Naphthyl N,N-dimethylcarbamate
AI3-27522
Carbamic acid, dimethyl-, 1-naphthyl ester
Carbamic acid, dimethyl-, naphthalenyl ester
CHEMBL2288466
DTXSID10919775
Naphthalen-1-yl dimethylcarbamate
QNLGINLKNITHFX-UHFFFAOYSA-N
.alpha.-Naphthyl dimethylcarbamate
1-naphthyl-N,N-dimethyl carbamate
NS00124722