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Carbaryl

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Identification
Molecular formula
C12H11Cl2NO3
CAS number
63-25-2
IUPAC name
2-(dimethylamino)ethyl N-(2,6-dichloro-4-ethoxy-phenyl)carbamate
State
State

Carbaryl is typically in a solid crystalline state at room temperature. It is stable under normal conditions but should be kept in a tightly sealed container to prevent moisture absorption and decomposition.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2780g/cm3
Appearence

Carbaryl appears as a white crystalline solid. It may appear as a powder or as large crystals depending on the form it is found in. The compound is noted for its absence of odor.

Comment on solubility

Solubility of 2-(dimethylamino)ethyl N-(2,6-dichloro-4-ethoxy-phenyl)carbamate

The solubility of 2-(dimethylamino)ethyl N-(2,6-dichloro-4-ethoxy-phenyl)carbamate, often referred to as a complex organic compound, is influenced by several key factors:

  • Polarity: The presence of both polar and nonpolar functional groups in this compound affects its solubility in different solvents. Compounds with polar functional groups tend to be more soluble in polar solvents, while nonpolar groups favor solubility in nonpolar solvents.
  • Temperature: Like many organic compounds, solubility can increase with temperature. As temperature rises, the kinetic energy of molecules increases, often resulting in enhanced solubility.
  • pH Levels: The solubility of this compound may also be impacted by the surrounding pH, especially because it contains an amine group, which could be protonated under acidic conditions, thus improving its solubility in aqueous solutions.

In general, the solubility of such compounds varies significantly, often requiring empirical testing to determine specific solubility parameters in given solvents or conditions. As a rule of thumb, “like dissolves like” applies, meaning that polar compounds dissolve well in polar solvents and vice versa. Therefore, understanding the nature of the individual components of 2-(dimethylamino)ethyl N-(2,6-dichloro-4-ethoxy-phenyl)carbamate is crucial for predicting its solubility behavior in various environments.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl N-(2,6-Dichloro-4-ethoxy-phenyl)carbamate

2-(Dimethylamino)ethyl N-(2,6-dichloro-4-ethoxy-phenyl)carbamate is a fascinating compound that showcases an intriguing blend of function and application in the field of chemistry. Here are some insightful points about this compound:

  • Biological Activity: This compound is often analyzed for its potential pharmacological properties, making it of particular interest in medicinal chemistry. Its structure suggests that it may play a role as a drug candidate or have applications in targeted therapies.
  • Synthetic Versatility: The presence of both dimethylamino and carbamate functional groups in its structure opens up various pathways for further chemical modification, enhancing its appeal in synthetic organic chemistry. It can serve as a versatile building block for developing more complex molecules.
  • Environmental Impact: Due to its chlorine substituents, the compound’s environmental persistence and effects on ecosystems are crucial areas of study. Understanding its degradation pathways can lead to better insights into managing its ecological risks.
  • Structure-Activity Relationships (SAR): Researchers are keen to explore how modifications to both the carbamate and the aromatic ring can affect the compound's biological activity. This highlights the importance of SAR studies in drug development.
  • Regulatory Aspects: As with many compounds that exhibit potential biological activity, this compound may fall under scrutiny for its use in pharmaceuticals, requiring careful evaluation against regulatory standards.

In summary, 2-(Dimethylamino)ethyl N-(2,6-dichloro-4-ethoxy-phenyl)carbamate is more than just a chemical entity; it embodies a rich tapestry of research possibilities across biology, synthesis, and environmental science. Scientists continue to investigate its properties to unlock its full potential.

Synonyms
K 901
BRN 2758939
CARBANILIC ACID, 2,6-DICHLORO-4-ETHOXY-, 2-(DIMETHYLAMINO)ETHYL ESTER
16770-84-6
2-(Dimethylamino)ethyl 2,6-dichloro-4-ethoxycarbanilate
DTXSID70168363
2,6-Dichloro-4-ethoxycarbanilic acid 2-(dimethylamino)ethyl ester
DTXCID3090854