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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[3,5-dimethyl-4-(methylamino)phenyl] N-methylcarbamate
State
State

Carbaryl is solid at room temperature. It retains a stable crystalline form under normal conditions.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white crystalline solid. It is commonly found in powdered form and may appear as a white to slightly grayish solid. This compound is generally recognized for its slightly aromatic smell.

Comment on solubility

Solubility of [3,5-Dimethyl-4-(methylamino)phenyl] N-methylcarbamate

The solubility of [3,5-dimethyl-4-(methylamino)phenyl] N-methylcarbamate is influenced by its chemical structure, which contains both polar and non-polar functional groups. This dual nature leads to solubility in a range of solvents.

Key Points on Solubility:

  • Polar Solvents: The presence of the methylamino group enhances solubility in polar solvents such as water and alcohols.
  • Non-Polar Solvents: Conversely, the hydrophobic dimethyl groups may impart some solubility in non-polar solvents like hydrocarbons.
  • Temperature Effects: Generally, solubility can increase with rising temperature, allowing this compound to dissolve more readily in hot solvents.
  • pH Dependence: The solubility may also vary with pH, influenced by the ionization of the methylamino group, highlighting the importance of conditions during dissolution.

In summary, the solubility profile of [3,5-dimethyl-4-(methylamino)phenyl] N-methylcarbamate is a clear demonstration of how functional groups affect interactions with solvents, making the study of such compounds both intriguing and essential in chemical research.

Interesting facts

Exploring [3,5-Dimethyl-4-(methylamino)phenyl] N-methylcarbamate

[3,5-Dimethyl-4-(methylamino)phenyl] N-methylcarbamate is a fascinating compound that falls into the category of carbamates, known for their applications in various fields including agriculture and pharmaceuticals. Here are some noteworthy aspects:

  • Versatile Applications: Carbamates, including this specific compound, are often utilized as insecticides and herbicides in agriculture, highlighting their importance in pest management and crop protection.
  • Biological Significance: The methylamino group present in this structure could suggest interactions with biological systems, possibly influencing neurotransmitter activities or enzyme functions.
  • Structure-Activity Relationship: The presence of dimethyl groups can enhance the lipophilicity of the molecule, potentially affecting its bioavailability and interaction with target sites.
  • Research Interest: Compounds with a similar structure are often of interest in medicinal chemistry, as researchers look for ways to modify their functionalities for improved therapeutic effects.

A fascinating trivia is that the structure of carbamates allows them to mimic the action of naturally occurring neurotransmitters, leading to a variety of biological effects. It is not uncommon for scientists to investigate such compounds to uncover new drug candidates or more effective agricultural solutions.

As we delve deeper into such compounds, understanding not only their chemical properties but also their interactions within biological systems becomes crucial. This compound exemplifies the intricate connections between chemistry, agriculture, and biology, showcasing the significance of synthetic chemistry in tackling real-world challenges.

Synonyms
Methylamino zectran
4-Methylamino-3,5-xylyl methylcarbamate
10389-50-1
CE66S51808
BRN 2733806
UNII-CE66S51808
CARBAMIC ACID, METHYL-, 4-(METHYLAMINO)-3,5-XYLYL ESTER
DTXSID9058286
Phenol, 3,5-dimethyl-4-(methylamino)-, methylcarbamate (ester)
4-methylamino-3,5-xylyl methyl-carbamate
NS00122177
4-(Methylamino)-3,5-xylyl N- methylcarbamate
METHYLAMINO)-3,5-XYLYL METHYLCARBAMATE, 4-(
Q27275419