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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(4-aminophenyl) N-methylcarbamate
State
State

At room temperature, carbaryl is in a solid state. It is typically found in crystalline powder form, making it easy to handle for industrial and commercial use.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a colorless or white crystalline solid. It is known for its odorless nature and has a crystalline powder appearance.

Comment on solubility

Solubility of (4-aminophenyl) N-methylcarbamate

(4-aminophenyl) N-methylcarbamate, a compound characterized by its unique chemical structure, exhibits specific solubility properties that can be quite informative. The solubility of this compound is influenced by various factors, which include:

  • Molecular Structure: The presence of both the amino and carbamate functional groups significantly affects solubility.
  • Polarity: Due to the polar nature of the functional groups, (4-aminophenyl) N-methylcarbamate is likely to be soluble in polar solvents like water.
  • Temperature: Solubility can increase with temperature, which is common for many organic compounds.

In general, compounds like (4-aminophenyl) N-methylcarbamate tend to show a greater solubility in:

  • Alcohols
  • Aqueous solutions
However, solubility in non-polar solvents is generally low.

Understanding the solubility of this compound can be crucial for applications in pharmaceuticals and related fields. As noted, “Every compound has its unique properties, and solubility is often a key to unlocking its potential.”

Interesting facts

Interesting Facts about (4-aminophenyl) N-methylcarbamate

(4-aminophenyl) N-methylcarbamate, often referred to in the scientific community as a derivative of carbamate, combines the amine functionality with a carbamate structure. This compound is noteworthy for several reasons:

  • Biological Activity: The primary significance of (4-aminophenyl) N-methylcarbamate lies in its potential biological activities. It has been studied for its effects on acetylcholinesterase, an enzyme critical for neurotransmitter regulation.
  • Pesticide Development: Compounds in the carbamate family, including this one, are frequently utilized in the development of pesticides due to their ability to inhibit cholinesterase, leading to increased effectiveness in pest control.
  • Synthesis Roadmap: The synthesis of (4-aminophenyl) N-methylcarbamate can involve several chemical transformations, making it an excellent subject for students learning about organic synthesis pathways. The typical steps include aminolysis and carbamoylation.
  • Research Potential: Ongoing research indicates that compounds like this one could pave the way for novel therapeutics in treating conditions associated with neurotransmitter dysregulation.

As with all chemical entities, proper handling and understanding of its properties are crucial. Research into (4-aminophenyl) N-methylcarbamate not only broadens our knowledge of organic chemistry but also highlights the importance of such compounds in practical applications.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This encapsulates the spirit of exploring compounds like (4-aminophenyl) N-methylcarbamate, urging scientists to delve deeper into its potential!

Synonyms
Methylcarbamic acid 4-aminophenyl ester
BRN 2209618
20120-72-3
CARBAMIC ACID, METHYL-, 4-AMINOPHENYL ESTER
DTXSID20173942
DTXCID0096433
RefChem:332551
SCHEMBL11675308