Skip to main content

Carbaryl

ADVERTISEMENT
Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(4-formamido-3-methyl-phenyl) N-methylcarbamate
State
State

At room temperature, carbaryl is in a solid state. It typically has a crystalline structure, which is typical of many carbamate insecticides.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
323.60
Boiling point (Kelvin)
596.75
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2345g/cm3
Appearence

Carbaryl is a white crystalline solid. It is often encountered as a solid that can form crystals but may also appear as a powder. Its appearance is quite typical for many organic chemicals used in agricultural applications.

Comment on solubility

Solubility of (4-formamido-3-methyl-phenyl) N-methylcarbamate

The solubility of (4-formamido-3-methyl-phenyl) N-methylcarbamate, with the chemical formula C12H11NO2, can be quite intriguing due to its unique structure. Solubility in solvents is influenced by several factors including polarity, temperature, and molecular interactions.

Factors Affecting Solubility:

  • Polarity: The presence of functional groups, such as amides and carbamates, can enhance hydrogen bonding capabilities, which may increase solubility in polar solvents.
  • Temperature: Generally, increased temperature leads to higher solubility for many compounds; however, specific behaviors can vary based on the compound.
  • Molecular Interactions: Interactions with the solvent can dictate whether a compound dissolves. For example, strong interactions with water would suggest good solubility in aqueous environments.

In practice, the solubility of this compound may be moderate in common organic solvents such as methanol or ethanol, but it could exhibit limited solubility in non-polar solvents. As a point of interest, many carbamate derivatives often show enhanced solubility in polar protic solvents due to their ability to form hydrogen bonds.

This compound's solubility can also be critical in various applications, impacting its utility in chemical reactions, biological systems, and pharmaceutical formulations. To summarize, understanding the solubility of (4-formamido-3-methyl-phenyl) N-methylcarbamate is essential for predicting its behavior in different environments and functional applications.

Interesting facts

Interesting Facts about (4-formamido-3-methyl-phenyl) N-methylcarbamate

(4-formamido-3-methyl-phenyl) N-methylcarbamate, a fascinating compound in the field of organic chemistry, exhibits unique characteristics and potential applications. Here are some engaging facts about this compound:

  • Amide Functionality: The presence of the amide group in the structure indicates that this compound can engage in hydrogen bonding, contributing to its reactivity and solubility in certain solvents.
  • Methyl Substituents: The methyl groups in the structure can enhance lipophilicity, meaning that the compound may interact effectively with lipid membranes, which is crucial for biological activity.
  • Pharmaceutical Applications: Compounds with similar structures are often found in the field of medicinal chemistry, where they may serve as precursors or active agents in drug design. This opens up possibilities for therapeutic uses.
  • Mechanism of Action: The interactions of this compound at the molecular level may involve enzymatic processes, potentially influencing metabolic pathways within biological systems.
  • Synthetic Pathways: The synthesis of this compound could involve multi-step organic reactions, often including methods such as substitution or condensation reactions, showcasing the ingenuity of synthetic organic chemistry.

In summary, (4-formamido-3-methyl-phenyl) N-methylcarbamate stands out for its distinct structural features and potential implications in various fields, particularly in pharmaceuticals. The exploration of its properties and applications highlights the dynamic nature of organic chemistry.

Synonyms
Formamido matacil
4-Formamido-3-cresyl methylcarbamate
10234-35-2
BRN 2734896
Methylcarbamic acid ester with 4'-hydroxy-o-formotoluidide
DTXSID90144927
CARBAMIC ACID, METHYL-, ESTER with 4'-HYDROXY-o-FORMOTOLUIDIDE
DTXCID6067418