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Bendiocarb

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Identification
Molecular formula
C11H13NO4S
CAS number
22781-23-3
IUPAC name
[2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate
State
State

At room temperature, bendiocarb is in a solid state. It does not sublimate and maintains its solid form unless it's exposed to higher temperatures that exceed its melting point.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.00
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
223.29g/mol
Molar mass
223.2900g/mol
Density
1.2300g/cm3
Appearence

Bendiocarb is a white crystalline solid. It may also appear as a colorless crystalline powder under different conditions. The compound is known for its stability in solid form, though it may have a slight odor characteristic of carbamates.

Comment on solubility

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

The solubility of [2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate is influenced by its structural features, which include both hydrophobic and hydrophilic functional groups. Such a compound presents a unique solubility profile that can be summarized in several key points:

  • Polar Characteristics: The presence of the carbamate functional group enhances the compound's water solubility due to its ability to form hydrogen bonds with water molecules.
  • Hydrophobic Regions: The 3-methylsulfanylpropyl chain contributes to hydrophobic interactions, which can hinder complete solubility in polar solvents.
  • Solvent Dependency: This compound is expected to be more soluble in organic solvents such as ethanol and acetone compared to water, which aligns with the trends observed in similar carbamate derivatives.
  • Concentration Effect: As the concentration of the compound increases, solubility may be affected due to potential aggregation of hydrophobic regions, which could limit interaction with the solvent.

In conclusion, while [2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate has some solubility in polar solvents, its overall solubility behavior is modulated by the interplay between its hydrophilic and hydrophobic components. Understanding these solubility characteristics is crucial for applications in pharmaceuticals and agrochemicals where bioavailability is essential.

Interesting facts

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

[2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate is a fascinating compound with unique properties and applications in the field of chemistry. Here are several intriguing aspects that highlight its significance:

  • Pesticidal Properties: This compound is primarily known for its role as a pesticide. It effectively acts against various pests by disrupting their nerve function, making it invaluable in agricultural practices.
  • Structural Complexity: The presence of both a phenyl group and a carbamate functional group in its structure demonstrates its versatility. This complexity allows for a wide range of interactions with biological systems, enhancing its efficacy as an agrochemical.
  • Mechanism of Action: The compound operates by inhibiting the enzyme acetylcholinesterase, which is crucial in the nervous system of insects. This inhibition leads to the accumulation of acetylcholine, eventually causing paralysis and death of the pest.
  • Synthetic Pathways: The synthesis of [2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate often involves multistep reactions, showcasing the ingenuity required in synthetic organic chemistry. Researchers continuously work to optimize these pathways to improve yield and reduce environmental impact.
  • Regulatory Considerations: As with many pesticides, it is essential to consider the regulatory landscape surrounding its use. Safety assessments and environmental impact studies are vital in determining its application in agricultural settings.

In conclusion, [2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate exemplifies the dynamic nature of chemical compounds in agriculture and highlights the ongoing need for research that balances efficacy with environmental safety. As chemistry students or researchers delve into the nuances of such compounds, it becomes evident how crucial they are in addressing global food production challenges.

Synonyms
Hooker hrs-1667
16637-86-8
HRS 1667
CARBAMIC ACID, METHYL-, o-(3-(METHYLTHIO)PROPYL)PHENYL ESTER
2-(3-(Methylthio)propyl)phenyl methylcarbamate
ENT 27,173
BRN 2113005
AI3-27173
Carbamic acid, methyl-, 2-(3-(methylthio)propyl)phenyl ester
DTXSID60168094
Phenol, 2-(3-(methylthio)propyl)-, methylcarbamate
DTXCID1090585
[2-(3-methylsulfanylpropyl)phenyl] N-methylcarbamate
SCHEMBL11509338
[2-(3-Methylsulfanylpropyl)phenyl]n-methylcarbamate