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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
phenyl N-methylcarbamate
State
State

At room temperature, carbaryl is typically a solid. It is commercially available in granules, dust, and suspension concentrate forms.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
376.90
Boiling point (Kelvin)
650.05
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid known for its use as an insecticide. It has a slightly sweet odor and often appears in powdered form for application purposes.

Comment on solubility

Solubility of Phenyl N-methylcarbamate

The solubility of phenyl N-methylcarbamate, a synthetic compound with the formula C9H10N2O2, can be influenced by various factors including temperature and the nature of the solvent used. Here are some key points to consider:

  • Polar vs. Nonpolar Solvents: Phenyl N-methylcarbamate generally demonstrates greater solubility in polar solvents such as water compared to nonpolar solvents. This is due to its ability to engage in hydrogen bonding with polar molecules.
  • Temperature Dependency: Like many organic compounds, the solubility of phenyl N-methylcarbamate increases with temperature. Thus, heating the solvent may enhance the dissolution process.
  • Saturation Levels: The maximum concentration at which phenyl N-methylcarbamate can dissolve in a solvent is termed its saturation point. It varies by solvent and temperature, and once this point is reached, any additional compound will remain undissolved.
  • Application in Solutions: This compound's solubility characteristics make it suitable for various applications in chemical processes, particularly in formulations requiring precise solubility profiles.

Overall, understanding the solubility of phenyl N-methylcarbamate is essential for its effective application in chemical synthesis and formulation. As with many organic compounds, careful consideration of solvent choices and conditions will lead to optimal results in dissolution.

Interesting facts

Interesting Facts about Phenyl N-methylcarbamate

Phenyl N-methylcarbamate is a fascinating compound in the realm of organic chemistry. It belongs to the class of carbamates, which are derived from carbamic acid. This compound has piqued the interest of researchers due to its diverse applications and unique properties. Here are some noteworthy aspects:

  • Biological Relevance: Phenyl N-methylcarbamate is often studied for its role in the inhibition of certain enzymes. Its ability to interact with biological molecules makes it a potential candidate for medicinal chemistry.
  • Pesticidal Properties: This compound is recognized for its effectiveness as a pesticide, demonstrating insecticidal properties that could aid in agricultural practices.
  • Versatile Applications: Beyond its uses in agriculture, phenyl N-methylcarbamate is also explored in the synthesis of various chemicals and pharmaceuticals, showcasing its versatility in both industrial and laboratory settings.
  • Structure-Activity Relationship: Researchers are intrigued by the relationship between its chemical structure and biological activity, which helps in designing new derivatives with improved efficacy.
  • Environmental Impact: As with many chemical compounds, understanding the environmental fate of phenyl N-methylcarbamate is crucial. Its breakdown products and potential ecological effects are essential areas of study.

The exploration of phenyl N-methylcarbamate emphasizes the connection between structure, function, and application in various fields. As Albert Einstein once said, “Scientific research is one of the most exciting and rewarding of enterprises,” and compounds like this one reflect the wonders of chemistry in action.

In summary, phenyl N-methylcarbamate embodies the spirit of discovery in chemical science, opening doors to new research avenues and practical applications.

Synonyms
PHENYL METHYLCARBAMATE
1943-79-9
Phenyl N-methylcarbamate
Methylcarbamic acid phenyl ester
Phenmec
N-Methylphenylcarbamate
Phenyl monomethylcarbamate
Carbamic acid, methyl-, phenyl ester
Phenol, methylcarbamate
Phenyl-N-methylcarbamate
DRC 3345
Methyl carbamic acid phenyl ester
CCRIS 1835
HSDB 2598
NSC 128138
BRN 2045075
AI3-33080
19U7Y0R088
NSC-128138
Carbamic acid, N-methyl-, phenyl ester
DTXSID1073282
4-06-00-00630 (Beilstein Handbook Reference)
N-METHYLPHENYLCARBAMATE [HSDB]
NMethylphenylcarbamate
Phenyl Nmethylcarbamate
DTXCID7036088
Carbamic acid, methyl, phenyl ester
815-597-0
Carbamic acid,N-methyl-, phenyl ester
MFCD01738783
methyl-carbamic acid phenyl ester
UNII-19U7Y0R088
Phenylmethylcarbamate
phenyl(methyl)carbamate
WLN: 1MVOR
SCHEMBL78497
CHEMBL2046815
ALBB-037526
BDBM50004688
NSC128138
AKOS006242248
MS-20800
SY269947
DB-065852
CS-0160301
NS00125245
C10489
Q27252134