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Carbaryl

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Identification
Molecular formula
C12H11NO3
CAS number
63-25-2
IUPAC name
(3-nitrophenyl) N,N-dimethylcarbamate
State
State

At room temperature, carbaryl is typically found in a solid state.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2190g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white crystalline solid. It is known for its insecticidal properties and is often used in gardening and agriculture.

Comment on solubility

Solubility of (3-nitrophenyl) N,N-dimethylcarbamate

The solubility of (3-nitrophenyl) N,N-dimethylcarbamate, a compound characterized by its nitrophenyl group, exhibits some intriguing properties:

  • Polarity: This compound has polar functional groups, which generally enhances its ability to dissolve in polar solvents.
  • Solvent Compatibility: It is **likely soluble** in organic solvents like methanol and ethanol, while its solubility in aqueous solutions might be limited due to its hydrophobic carbon skeleton.
  • Temperature Effect: As with many compounds, solubility can increase with temperature, meaning elevated conditions may aid in dissolving this carbamate.
  • pH Dependency: The solubility can also be influenced by the pH of the solution, potentially altering the ionization of functional groups.

In summary, while (3-nitrophenyl) N,N-dimethylcarbamate is expected to have good solubility in certain organic solvents, its behavior in water may not be as favorable. A proper assessment would necessitate experimental data to confirm these expectations.

Interesting facts

Interesting Facts about (3-nitrophenyl) N,N-dimethylcarbamate

(3-nitrophenyl) N,N-dimethylcarbamate is a fascinating compound that falls under the category of carbamate derivatives. Here are some engaging insights into this compound:

  • Applications in Agriculture: This compound is often utilized as a pesticide, specifically acting effective against a variety of agricultural pests. Its efficacy makes it a vital component in modern agricultural practices to enhance crop yields.
  • Mechanism of Action: It operates through a mechanism that inhibits acetylcholinesterase, an essential enzyme in the nervous system of insects, leading to their eventual paralysis and death. This mode of action is a crucial aspect of many insecticides.
  • Environmental Considerations: Being a nitrophenyl compound, it raises concerns regarding its environmental impact. Scientists meticulously study how it degrades in the environment to minimize adverse effects on non-target organisms and ecosystems.
  • Synthetic Routes: The synthesis of (3-nitrophenyl) N,N-dimethylcarbamate involves interesting chemical transformations, making use of various reagents and conditions. This aspect can be a great discussion point in organic chemistry courses.
  • Reactivity: Due to the presence of the nitro group, the compound exhibits distinctive reactivity patterns in organic reactions, making it a subject of study in synthetic organic chemistry laboratories.
  • Potential for Research: Ongoing research is aimed at discovering new derivatives with enhanced properties, which could lead to more effective and safer agricultural solutions. Scientists are constantly seeking to optimize its effectiveness while reducing toxicity.

In conclusion, (3-nitrophenyl) N,N-dimethylcarbamate is more than just a chemical compound; it combines fascinating chemistry with real-world applications in agriculture, environmental science, and research. The interplay of its properties makes it a captivating subject for both chemistry students and seasoned scientists alike.

Synonyms
3-nitrophenyl dimethylcarbamate
7304-99-6
(3-nitrophenyl) N,N-dimethylcarbamate
Carbamic acid, dimethyl-, 3-nitrophenyl ester
AI3-33125
CHEMBL2288489
DTXSID20223315
AKOS002244008
Carbamic acid, dimethyl-, m-nitrophenyl ester
AL-398/40365520
SR-01000261394
SR-01000261394-1
F1318-0213
Z274554972