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Methomyl

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Identification
Molecular formula
C8H7Cl2NO2
CAS number
101-21-3
IUPAC name
methyl N-(3,5-dichlorophenyl)carbamate
State
State

It is a solid at room temperature, offering stability under standard storage conditions. Crystalline in appearance, it maintains a solid form unless exposed to high temperatures.

Melting point (Celsius)
94.00
Melting point (Kelvin)
367.15
Boiling point (Celsius)
313.00
Boiling point (Kelvin)
586.15
General information
Molecular weight
234.05g/mol
Molar mass
234.0520g/mol
Density
1.4982g/cm3
Appearence

Methyl N-(3,5-dichlorophenyl)carbamate is a crystalline solid that appears as white to off-white. It is odorless and tends to be a stable compound under normal environmental conditions.

Comment on solubility

Solubility of Methyl N-(3,5-dichlorophenyl)carbamate

The solubility of methyl N-(3,5-dichlorophenyl)carbamate (often referred to as a type of carbamate) in various solvents is an important aspect that influences its applications in fields like agrochemicals and pharmaceuticals. Overall, the solubility characteristics of such compounds can be summarized as follows:

  • Polar Solvents: Methyl N-(3,5-dichlorophenyl)carbamate is generally soluble in polar solvents such as methanol and ethanol due to the presence of its carbamate functional group, which can engage in hydrogen bonding.
  • Non-polar Solvents: In contrast, this compound tends to show much lower solubility in non-polar solvents like hexane. The hydrophobic 3,5-dichlorophenyl ring contributes to this phenomenon.
  • Temperature Influence: Like many organic compounds, solubility can be affected by temperature; increasing the temperature often leads to an increase in solubility.
  • pH Sensitivity: The solubility may also be influenced by the pH of the solution, as the ionization of the carbamate group can vary, impacting its solubility in aqueous environments.

In conclusion, understanding the solubility behaviors of methyl N-(3,5-dichlorophenyl)carbamate is critical for its practical applications, particularly in developing formulations where solubility is a key factor. A thorough knowledge of how and in what conditions this compound dissolves can inform proper handling, effectiveness, and environmental impact considerations.

Interesting facts

Interesting Facts about Methyl N-(3,5-Dichlorophenyl)carbamate

Methyl N-(3,5-dichlorophenyl)carbamate is a fascinating compound with a range of applications, primarily recognized for its role in the field of agrochemicals. Here are some intriguing aspects of this compound:

  • Pesticide Properties: This compound is often used as an active ingredient in various pesticides and herbicides. Its effectiveness in warding off pests makes it invaluable to agricultural practices globally.
  • Mechanism of Action: Methyl N-(3,5-dichlorophenyl)carbamate functions by disrupting the normal functioning of the nervous system in insects, leading to their eventual demise. This illustrates a key principle of pesticide design, where selectivity for pests is critical.
  • Synthesis: The preparation of this carbamate can be achieved through a series of chemical reactions that typically involve the reaction of 3,5-dichloroaniline with methyl chloroformate. This exemplifies the beauty of organic chemistry and its synthetic pathways.
  • Environmental Impact: As with many pesticides, studies have been conducted to evaluate the environmental impact of this compound. Understanding its degradation and persistence in the environment is essential for ensuring ecological safety.
  • Research and Development: Ongoing research into modifying the structure of methyl N-(3,5-dichlorophenyl)carbamate aims to enhance its efficacy and reduce any potential adverse effects. Such innovations in chemistries can lead to more sustainable agricultural practices.
  • Potential Health Effects: Safety assessments have been performed to evaluate its toxicity to humans and non-target organisms. Awareness of its safety profile is crucial for regulatory approvals and usage guidelines.

In summary, methyl N-(3,5-dichlorophenyl)carbamate is more than just an effective pesticide; it serves as a fascinating study in the intersection of chemistry, biology, and environmental science. Its development, use, and impact illustrate the intricate balance required in modern agricultural practices.

Synonyms
Methyl (3,5-dichlorophenyl)carbamate
25217-43-0
Methyl N-(3,5-dichlorophenyl)carbamate
Methyl 3,5-dichlorocarbanilate
3,5-Dichlorocarbanilic acid methyl ester
BRN 2101855
Carbamic acid, (3,5-dichlorophenyl)-, methyl ester
DTXSID50179876
CARBANILIC ACID, 3,5-DICHLORO-, METHYL ESTER
Carbamic acid, (3,5-dichlorophenyl)-, methyl ester (9CI)
RefChem:123378
DTXCID10102367
MFCD00126402
Carbamic acid,(3,5-dichlorophenyl)-, methyl ester (9CI)
MDPC
N-(3,5-dichlorophenyl)methoxycarboxamide
Maybridge1_000169
MixCom1_000323
SCHEMBL2095413
SCHEMBL2095417
CHEMBL2285815
FRSRGACXHCLBTC-UHFFFAOYSA-N
SBB095878
AKOS003442079
SB79662
methyl N-(3,5-dichlorophenyl) carbamate
methyl N-(3,5-dichlorophenyl)-carbamate
DS-11510
3,5-Dichlorocarbanilic acid methyl ester,
DB-067349
CS-0150651
ST50825703
Y10980
Carbamic acid, N-(3,5-dichlorophenyl)-, methyl ester