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Carbaryl

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

Carbaryl is typically a solid at room temperature. It is utilized in various formulations including powders, granules and liquid concentrates.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2340g/cm3
Appearence

Carbaryl is a white crystalline solid. It may appear as a colorless to white powder. It is often found as a solid in its pure form, but it can also be present in some commercial products as a wettable powder or dust. It has a faint chemical odor.

Comment on solubility

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

(4-amino-3-methyl-phenyl) N-methylcarbamate, with the chemical formula C12H11NO2, exhibits unique solubility characteristics primarily influenced by its molecular structure. Understanding these characteristics is essential for applications in pharmaceuticals and agrochemicals.

Solubility Characteristics:

  • Polarity: The presence of the amino group and the carbamate functionality contributes to the polar nature of the molecule, enhancing its interaction with polar solvents.
  • Water Solubility: Generally, compounds containing amino groups exhibit moderate solubility in water due to hydrogen bonding; however, the overall solubility depends on the balance between hydrophilic and hydrophobic parts of the molecule.
  • Solvent Compatibility: This compound is likely to show greater solubility in organic solvents such as ethanol or dimethyl sulfoxide (DMSO), which can better stabilize its polar domains.

In summary, the solubility of (4-amino-3-methyl-phenyl) N-methylcarbamate is contingent upon its structural features, particularly its polar functional groups. Understanding these interactions is crucial for effectively applying this compound in various industrial and research settings.

Interesting facts

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

(4-amino-3-methyl-phenyl) N-methylcarbamate is a fascinating chemical compound that offers a unique intersection of organic chemistry and applications in various fields. Here are some noteworthy aspects:

  • Pesticide Potential: This compound is structurally related to carbamate pesticides, making it of interest in agricultural chemistry for its potential effectiveness in pest control.
  • Mechanism of Action: Like other carbamate compounds, it is believed to influence the activity of the enzyme acetylcholinesterase, which plays a critical role in neurotransmission. This insight opens up discussions about its effects on flora and fauna.
  • Synthesis Appeal: The synthesis of this compound can serve as an excellent educational example in organic synthesis classes, demonstrating key reactions such as condensation and substitution.
  • Bioactivity Studies: The compound has been studied for its biological activities, including anti-inflammatory and analgesic properties, leading to its potential application in pharmaceuticals.
  • Structure-Activity Relationship (SAR): Researchers often explore the SAR of such compounds, aiming to modify the structure to improve efficacy and reduce toxicity, making it a topic of interest in medicinal chemistry.

Furthermore, as an interdisciplinary subject, (4-amino-3-methyl-phenyl) N-methylcarbamate exemplifies how chemistry can inform both environmental practices and therapeutic developments. As one scientist puts it, "The lines between chemistry and real-world applications blur, demonstrating the power of molecules in shaping our lives."

Overall, this compound serves as a captivating case study for students and professionals alike, encompassing a broad range of scientific principles and real-world applications.

Synonyms
Aminomatacil
4-Amino-3-cresyl methylcarbamate
BRN 2096255
Methylcarbamic acid 4-amino-m-tolyl ester
10233-97-3
CARBAMIC ACID, METHYL-, 4-AMINO-m-TOLYL ESTER
DTXSID80144911
DTXCID2067402
SCHEMBL11719841
OCYWBKLVMHFSSX-UHFFFAOYSA-N
3-methyl-4-aminophenyl N-methylcarbamate
4-amino-3-methylphenyl N-methylcarbamate