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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[4-[formyl(methyl)amino]-3,5-dimethyl-phenyl] N-methylcarbamate
State
State
Carbaryl is typically found as a crystalline solid at room temperature.
Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
306.00
Boiling point (Kelvin)
579.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.1800g/cm3
Appearence
Carbaryl is a white crystalline solid. It may have a faint odor.
Comment on solubility

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

The solubility of [4-[formyl(methyl)amino]-3,5-dimethyl-phenyl] N-methylcarbamate in various solvents can be quite complex due to its unique molecular structure.

Here are some key points regarding its solubility:

  • Polarity: The presence of the carbamate functional group suggests that it might have moderate polarity, which typically increases solubility in polar solvents.
  • Solvents: It is likely soluble in water and alcohols (like methanol or ethanol) while showing limited solubility in non-polar organic solvents (such as hexane or toluene).
  • pH Dependency: The solubility could be affected by the pH of the solution, as changes in pH can influence the ionization state of the compound.
  • Temperature Effects: Increased temperature might enhance solubility, as is common with many organic compounds.

Overall, empirical studies would be essential to determine the exact solubility profile due to the intricate nature of this compound. In practical applications, understanding this solubility behavior is pivotal for improving the efficacy of the compound in various fields such as pharmaceuticals and agriculture.

Interesting facts

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

This compound, with a complex structure, falls under the category of carbamates, which are esters or salts formed from carbamic acid. Here are some engaging insights about this intriguing substance:

  • Biological Relevance: Carbamates are of significant interest in pharmacology and agriculture. They often exhibit biological activities such as acting as insecticides or even as potential therapeutic agents.
  • Molecular Intricacy: The presence of multiple functional groups in this compound, including a formyl group and an amino group, contributes to its versatility and potential reactivity in various chemical reactions.
  • Structure-Activity Relationship: Understanding the relationship between the chemical structure and biological activity of carbamates can help guide the design of new compounds with enhanced efficacy and reduced toxicity.
  • Synthetic Pathways: The synthesis of such compounds often involves sophisticated organic reactions, showcasing the advanced methods employed in modern organic chemistry, such as microwave-assisted synthesis and multistep reactions.
  • Environmental Impact: While carbamate compounds are useful, some can be harmful to non-target organisms in the environment. Research is ongoing to create safer, more environmentally friendly alternatives.

As a chemical scientist, diving into the world of compounds like [4-[formyl(methyl)amino]-3,5-dimethyl-phenyl] N-methylcarbamate not only hones our understanding of chemistry but also opens doors to innovative developments in multiple fields, from medicine to agriculture.

Quote to ponder: "Science knows no country, because knowledge belongs to humanity, and is the torch which illuminates the world." – Louis Pasteur

Synonyms
4-(Methylformamido)-3,5-xylyl methylcarbamate
10233-94-0
Methylformamido zectran
BRN 2750027
CARBAMIC ACID, METHYL-, ESTER with 4'-HYDROXY-N-METHYL-2',6'-FORMOXYLIDIDE
DTXSID9058282
NS00127103
Formamide, N-(2,6-dimethyl-4-(((methylamino)carbonyl)oxy)phenyl)-N-methyl-