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Metolcarb

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Identification
Molecular formula
C9H11NOS
CAS number
1129-41-5
IUPAC name
S-(p-tolyl) N-methylcarbamothioate
State
State

At room temperature, Metolcarb is in a solid state.

Melting point (Celsius)
93.00
Melting point (Kelvin)
366.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
181.26g/mol
Molar mass
181.2550g/mol
Density
1.1500g/cm3
Appearence

Metolcarb appears as a white crystalline solid. It is commonly used as a pesticide due to its effectiveness and physical stability.

Comment on solubility

Solubility of S-(p-tolyl) N-methylcarbamothioate

S-(p-tolyl) N-methylcarbamothioate, a compound known for its distinctive properties, exhibits intriguing solubility characteristics that are of interest to chemists and researchers alike.

General Solubility Profile

When considering the solubility of S-(p-tolyl) N-methylcarbamothioate, it is essential to take into account the following factors:

  • Polarity: The presence of functional groups such as carboxyl and thiol units may influence its solubility in different solvents.
  • Temperature: Like many organic compounds, solubility can increase with temperature, making heating a useful technique for dissolving the compound.
  • Solvent Type: S-(p-tolyl) N-methylcarbamothioate tends to be soluble in organic solvents such as ethanol and acetone, but may be poorly soluble in water due to its hydrophobic aromatic structure.

Important Considerations

Any attempts to dissolve S-(p-tolyl) N-methylcarbamothioate should take into account:

  • Testing in various solvents may yield differing results.
  • Stability: Prolonged solubility tests should evaluate the stability of the compound to ensure no degradation occurs.
  • Understanding the application context can help in choosing the right solvent for optimal solubility.

Overall, the solubility of S-(p-tolyl) N-methylcarbamothioate reflects its unique chemical nature and prompts a deeper exploration into suitable solvents for various applications.

Interesting facts

Interesting Facts About S-(p-tolyl) N-methylcarbamothioate

S-(p-tolyl) N-methylcarbamothioate is a fascinating compound that belongs to the class of carbamates, which are known for their diverse applications and biological significance. This compound has drawn attention due to its unique structure and properties. Here are some noteworthy points:

  • Structure and Functionality: The compound contains a thiol group, which enhances its reactivity and potential as a pesticide. Its structural components contribute to its role as a potent molecular agent.
  • Biological Relevance: Carbamates like S-(p-tolyl) N-methylcarbamothioate are often investigated for their effects on enzymatic activity in living organisms, especially concerning acetylcholinesterase inhibition. This can inform studies related to neurotoxicity.
  • Application in Agriculture: Its ability to act as a pesticide means that it can be instrumental in managing pest populations, thus aiding in agricultural productivity. Chemical innovations in recent years have highlighted its utility in Integrated Pest Management (IPM).
  • Environmental Considerations: As with many chemical compounds, the environmental impact of S-(p-tolyl) N-methylcarbamothioate is of great concern. Researchers are continually assessing its fate in ecosystems and potential effects on non-target species.
  • Research and Developments: The ongoing research into the synthesis and enhancement of this compound aims to improve its efficacy and reduce any adverse environmental impacts associated with its use.

In conclusion, S-(p-tolyl) N-methylcarbamothioate is not just a chemical compound but a subject of extensive research with implications ranging from agricultural practices to environmental safety. As the scientific community continues to explore its potential, it remains an intriguing example of the intersection between chemistry and real-world applications.

Synonyms
16066-90-3
TL-1218
BRN 1942907
CARBAMIC ACID, METHYLTHIO-, S-(p-TOLYL) ESTER
Carbamthiolic acid, N-methyl-, p-tolyl ester
DTXSID90166962
DTXCID3089453
S-(4-methylphenyl) N-methylcarbamothioate
Methylthiocarbamic acid S-(4-methylphenyl) ester
Methylthiocarbamic acid s-(4-methylphenyl)ester