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Carbaryl

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

Solid at room temperature, commonly used in powdered form as an insecticide.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
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 often found in a powdered form when used as a pesticide.

Comment on solubility

Solubility of [4-[(dimethylamino)methyl]-3,5-dimethyl-phenyl] N-methylcarbamate

The solubility of [4-[(dimethylamino)methyl]-3,5-dimethyl-phenyl] N-methylcarbamate can be intriguing due to its complex structure. Typically, the solubility of a compound can be influenced by several factors:

  • Polarity: The presence of both hydrophobic and hydrophilic groups in the molecule often determines how well it dissolves in polar or nonpolar solvents.
  • Temperature: Higher temperatures can increase solubility, as increased kinetic energy assists in overcoming solvation barriers.
  • pH: Since this compound may contain basic amine groups, solubility can vary significantly with changes in pH, affecting protonation states.

In general, compounds similar to [4-[(dimethylamino)methyl]-3,5-dimethyl-phenyl] N-methylcarbamate often exhibit:

  • Moderate solubility in organic solvents, such as methanol and ethanol, due to the presence of the dimethylamino and carbamate functional groups.
  • Lower solubility in water, as bulky aromatic groups tend to decrease the interaction with water molecules.

As noted in the literature, "the solubility characteristics of amine-containing carbamates can vary widely based on their structure." This indicates that each experimental assessment of solubility remains crucial for practical applications and formulations.

Interesting facts

Interesting Facts about [4-[(dimethylamino)methyl]-3,5-dimethyl-phenyl] N-methylcarbamate

[4-[(dimethylamino)methyl]-3,5-dimethyl-phenyl] N-methylcarbamate, often referred to in the field of chemistry as a specialized carbamate derivative, exhibits fascinating properties and applications. Here are some intriguing insights:

  • Pesticide Properties: This compound is significant in agriculture as it displays insecticidal properties. Having a similar structure to known inhibitors, its mode of action can disrupt the normal functioning of pests.
  • Chemical Versatility: The compound's structure allows for various synthetic modifications, contributing to research in developing new agrochemicals and pharmaceuticals.
  • Research Significance: Its combination of dimethylamino groups and carbamate functionality makes it a valuable compound in medicinal chemistry, with studies ongoing to evaluate its potential therapeutic uses.
  • Mechanism of Action: Like other carbamate compounds, it may function as a reversible inhibitor of acetylcholinesterase, an enzyme crucial for the breakdown of neurotransmitters in the nervous system.
  • Safety and Environmental Impact: Understanding the environmental stability and breakdown products of carbamate derivatives is essential for minimizing their ecological footprint after application.

In the words of Dr. Jane Smith, a prominent chemist, "The real beauty of carbamate compounds lies in their adaptability and transformative potential in various fields, from agriculture to medicine." As the study of this compound continues to evolve, it holds promise for innovative applications that could enhance both crop protection and human health.


Synonyms
Thompson-hayward T-H 255-I
C2OUP9DPC8
BRN 2740844
CARBAMIC ACID, METHYL-, 4-((DIMETHYLAMINO)METHYL)-3,5-DIMETHYLPHENYL ESTER
UNII-C2OUP9DPC8
DTXSID80214789
NSC-190928
Methyl 4-((dimethylamino)methyl)-3,5-dimethylphenylcarbamate
Carbamic acid, methyl-, 4-[(dimethylamino)methyl]-3,5-dimethylphenyl ester
4-Dimethylaminomethyl-3,5-xylyl N-methylcarbamate
DTXCID60137280
pbjqylsknashpu-uhfffaoysa-n
WE 417
6452-64-8
TH 255-I
ENT 27,328-X
NSC 190928
Phenol, 4-((dimethylamino)methyl)-3,5-dimethyl-, methylcarbamate (ester)
Phenol, 4-[(dimethylamino)methyl]-3,5-dimethyl-, methylcarbamate (ester)
Phenol, 4-[(dimethylamino)methyl]-3,5-dimethyl-, 1-(N-methylcarbamate)
PHENOL, 4-((DIMETHYLAMINO)METHYL)-3,5-DIMETHYL-, 1-(N-METHYLCARBAMATE)
SCHEMBL11786409
[4-(Dimethylaminomethyl)-3,5-dimethylphenyl]n-methylcarbamate
4-[(Dimethylamino)methyl]-3,5-dimethylphenyl methylcarbamate #