Skip to main content

Propoxur

ADVERTISEMENT
Identification
Molecular formula
C11H15ClNO2
CAS number
114-26-1
IUPAC name
(2-chloro-5-isopropyl-phenyl) N-methylcarbamate
State
State

At room temperature, propoxur is typically found in a solid state. It is often handled as a powder or in crystalline form for its use in various pesticidal applications.

Melting point (Celsius)
91.50
Melting point (Kelvin)
364.65
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
209.24g/mol
Molar mass
209.2370g/mol
Density
1.1700g/cm3
Appearence

Propoxur appears as an off-white to pale brown crystalline solid. It is often presented in powdered form for use as an insecticide. The compound may have a faintly aromatic odor and is generally considered to be stable at room temperature.

Comment on solubility

Solubility of (2-chloro-5-isopropyl-phenyl) N-methylcarbamate

The solubility of (2-chloro-5-isopropyl-phenyl) N-methylcarbamate is influenced by several factors, making it an interesting compound to consider in various applications.

Key Factors Affecting Solubility:

  • Polarity: The structure of the compound contains both polar and nonpolar regions, which affects its solubility in different solvents.
  • Hydrogen Bonding: The presence of the N-methylcarbamate group allows for potential hydrogen bonding with solvents like water, enhancing its solubility in polar solvents.
  • Steric Hindrance: The bulky isopropyl group may limit interactions with certain solvents, affecting solubility profiles.

It is often noted that:

  • Compounds of this nature typically show better solubility in organic solvents (e.g., acetone, chloroform).
  • They may exhibit limited solubility in water, primarily due to their hydrophobic characteristics.

In summary, the solubility of (2-chloro-5-isopropyl-phenyl) N-methylcarbamate can be described as:

  • Moderately soluble in polar organic solvents.
  • Poorly soluble in water, owing to steric hindrance and hydrophobicity.

This solubility behavior plays a crucial role in its usability and effectiveness in chemical applications, particularly in formulations where specific solvent interactions are vital.

Interesting facts

Interesting Facts about (2-chloro-5-isopropyl-phenyl) N-methylcarbamate

(2-chloro-5-isopropyl-phenyl) N-methylcarbamate is a fascinating compound that finds its place in the world of chemistry due to its unique properties and applications. Here are some intriguing details about this compound:

  • Structure Insight: This compound features a carbamate functional group, which is derived from carbamic acid. The presence of a chlorine atom and an isopropyl group adds layers of complexity to its structure, influencing its reactivity and interactions with other molecules.
  • Entry into Agrochemicals: Often, compounds like N-methylcarbamates are prized for their role as pesticides. Their chemical structure can enhance activity against various pests while being designed to minimize environmental impact.
  • Reactivity and Stability: The unique combination of functional groups in this compound can lead to varied chemical behavior, resulting in different reactivity patterns. Understanding these patterns is crucial for chemists when developing safer and more effective agricultural products.
  • Research and Development: Scientists are continuously exploring the interactions of carbamate compounds with biological systems, making this compound a subject of interest for studies in toxicology and environmental science.
  • Analytical Methods: Due to its potential applications and importance in agriculture, effective methods for detecting and analyzing (2-chloro-5-isopropyl-phenyl) N-methylcarbamate are essential to ensure safe usage. Advanced techniques like chromatography play a key role in this area.

As chemists delve deeper into the study of (2-chloro-5-isopropyl-phenyl) N-methylcarbamate, they gain insights not only into its structure and properties but also into the broader implications of carbamate chemistry in sustainability and agrochemical innovation.

Synonyms
Hercules 7522-H
2752-81-0
2-Chloro-5-(1-methylethyl)phenol methylcarbamate
9G8V797HLH
Phenol, 2-chloro-5-(1-methylethyl)-, methylcarbamate
CARBAMIC ACID, METHYL-, 6-CHLORO-m-CUMENYL ESTER
BRN 2270033
ENT 25,763
AI3-25763
HERCULES 7522H
UNII-9G8V797HLH
SCHEMBL11508267
DTXSID10950204
Q27272522
2-Chloro-5-(1-methylethyl)phenol 1-(N-methylcarbamate)
PHENOL, 2-CHLORO-5-ISOPROPYL-, METHYLCARBAMATE
2-Chloro-5-(propan-2-yl)phenyl hydrogen methylcarbonimidate
PHENOL, 2-CHLORO-5-(1-METHYLETHYL)-, 1-(N-METHYLCARBAMATE)