Skip to main content

Carbaryl

ADVERTISEMENT
Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
2-(1-piperidyl)ethyl N-(2,6-dichloro-4-pentoxy-phenyl)carbamate
State
State

At room temperature, Carbaryl is in a solid state. It is commonly found in powder or crystalline form, which is typical for many organophosphate insecticides.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2180g/mol
Density
1.2500g/cm3
Appearence

Carbaryl appears as a white crystalline solid. Its crystalline structure and bright white color are characteristic for identification purposes.

Comment on solubility

Solubility of 2-(1-piperidyl)ethyl N-(2,6-dichloro-4-pentoxy-phenyl)carbamate

The solubility of 2-(1-piperidyl)ethyl N-(2,6-dichloro-4-pentoxy-phenyl)carbamate can be influenced by several factors, including its chemical structure and the nature of the solvent used. Here are some key points to consider:

  • Polarity: The presence of polar functional groups may enhance solubility in polar solvents like water, while more hydrophobic portions may favor solubility in organic solvents such as ethanol or methanol.
  • Hydrogen Bonding: The ability of the compound to engage in hydrogen bonding can significantly affect its solubility. Increased hydrogen bond donors or acceptors often lead to better solubility in water.
  • Temperature: Generally, higher temperatures can increase solubility. Thus, evaluating this compound's solubility at varying temperatures would be beneficial.

Ultimately, experimental data would be necessary to ascertain its exact solubility characteristics. It is essential to consider individual conditions under which solubility is tested, as small changes in environmental factors can lead to surprisingly different results. As the saying goes, “The devil is in the details.”

Interesting facts

Exploring 2-(1-piperidyl)ethyl N-(2,6-dichloro-4-pentoxy-phenyl)carbamate

This intriguing compound, known as a carbamate, is notable for its potential applications in various fields, particularly in medicinal chemistry and agriculture. Here are some fascinating aspects to consider:

  • Structural Complexity: The presence of a piperidine ring in its structure provides unique properties that influence its interactions with biological systems.
  • Biological Activity: Carbamates are known for their ability to inhibit certain enzymes, making this compound a topic of interest in drug development, especially in treating neurological disorders.
  • Versatile Applications: Beyond pharmacology, it has potential uses in agriculture, functioning as a pesticide or herbicide due to its chemical stability.
  • Halogen Influence: The incorporation of chlorine atoms in its molecular structure enhances its biological activity and also may increase lipophilicity, affecting how the compound interacts with cell membranes.
  • Safety Considerations: As with many chemical compounds, understanding the safety profile is critical, especially considering its applications in pesticides and the potential environmental impact.

This compound exemplifies the intersection of chemistry and application, showcasing how structural variations can lead to diverse functionalities. The study of such compounds not only enhances our understanding of chemical interactions but also opens pathways for innovation in drug design and agricultural practices.

As noted by chemists, “The design of a compound often determines its destiny.” This highlights the importance of structural analysis in predicting the behavior and utility of chemical substances.

Synonyms
K 924
BRN 1267455
CARBANILIC ACID, 2,6-DICHLORO-4-(PENTYLOXY)-, 2-PIPERIDINOETHYL ESTER
2-Piperidinoethyl 2,6-dichloro-4-(pentyloxy)carbanilate
15483-07-5
DTXSID80165742
2,6-Dichloro-4-(pentyloxy)carbanilic acid 2-piperidinoethyl ester
DTXCID7088233