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Carbaryl

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

Carbaryl is typically found in a solid state at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid with a faint aromatic odor.

Comment on solubility

Solubility of [3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate

The solubility of [3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate can be quite interesting due to its unique chemical structure. This compound exhibits characteristics that can affect its solubility in different solvents. It is important to consider the following factors:

  • Polarity: The solubility may be influenced by the polar and nonpolar groups within the molecule. The presence of the N-methyl carbamate group suggests potential interactions with polar solvents.
  • Hydrogen Bonding: Compounds that can engage in hydrogen bonding tend to have higher solubility in polar solvents like water. This feature can enhance its interaction with solvent molecules.
  • Temperature: Solubility is also temperature-dependent; mixing this compound with solvents at varied temperatures might yield different results in terms of how well it dissolves.
  • Solvent Choice: The choice of solvent can be crucial. For instance, this compound might dissolve better in organic solvents compared to aqueous solutions, due to its hydrophobic characteristics.

In summary, the solubility of [3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate is influenced by its molecular structure and the nature of the solvent. Considering these factors is essential when predicting its solubility in various environments.

Interesting facts

Interesting Facts about [3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate

[3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate is a complex organic compound that falls within the category of carbamates. Carbamates are important in various fields, particularly in agriculture and pharmaceuticals, due to their diverse applications. Here, we explore some fascinating aspects of this compound:

  • Biological Activity: This compound has been studied for its potential biological activity. Carbamates often act as inhibitors of certain enzymes, which can be crucial in the development of pesticides or therapeutic agents.
  • Mechanism of Action: Its structure suggests that it could have specific interactions with the biological targets, potentially affecting neurotransmitter activity or metabolic pathways.
  • Synthesis: The synthesis of this compound typically involves methods of organic chemistry, which include the reaction of amines with isocyanates. This process can be a teaching point for students learning the nuances of organic synthesis.
  • Relevance in Industry: Compounds of this nature are often components in the development of herbicides and insecticides, making them crucial in modern agriculture. Their ability to modulate biochemical processes is what makes them effective.

In the field of environmental science, the persistence and breakdown products of carbamates can be subjects of extensive study, leading to a deeper understanding of their environmental impact. Understanding such compounds prepares students and chemists for innovations in sustainable chemistry practices.

Moreover, the study of such compounds underscores the necessity of thorough toxicological evaluations, contributing to safer products for both agriculture and consumer use. As noted by prominent chemists, "The development of safe and effective chemical solutions is essential for the progress of society."

Conclusion

The exploration of [3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate highlights the intricate connection between organic chemistry and its practical applications. By delving into its synthesis, activity, and industry relevance, chemists can pave the way for advancements that align with both scientific integrity and societal needs.

Synonyms
17798-17-3
BUTYRANILIDE, 2,2-DIMETHYL-3'-HYDROXY-, METHYLCARBAMATE (ester)
m-(2,2-Dimethylbutyramido)phenyl methylcarbamate
NSC 222517
3'-(Methylcarbamoyloxy)-2,2-dimethylbutyranilide
BRN 2142140
6T6BS6S4W6
NSC-222517
Butyranilide, 3'-hydroxy-2,2-dimethyl-, methylcarbamate (ester)
Butanamide, 2,2-dimethyl-N-(3-(((methylamino)carbonyl)oxy)phenyl)-
Carbamic acid, methyl-, ester with 3'-hydroxy-2,2-dimethylbutyranilide
UNII-6T6BS6S4W6
DTXSID30170407
DTXCID3092898
Butanamide, 2,2-dimethyl-N-(3-(((methylamino)carbonyl)oxy)phenyl)-(9CI)
[3-(2,2-dimethylbutanoylamino)phenyl] N-methylcarbamate
NSC222517
orb1986349
N-Methylcarbamic acid 3-[(2,2-dimethylbutyryl)amino]phenyl ester
AKOS040750947
Butyranilide,2-dimethyl-, methylcarbamate (ester)
Butyranilide,2-dimethyl-3'-hydroxy-, methylcarbamate (ester)
Carbamic acid, ester with 3'-hydroxy-2,2-dimethylbutyranilide
Butanamide,2-dimethyl-N-[3-[[(methylamino)carbonyl]oxy]phenyl]-