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Carbaryl

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Identification
Molecular formula
C12H13NO2
CAS number
63-25-2
IUPAC name
(3,4-dimethylphenyl) N-methylcarbamate
State
State

At room temperature, Carbaryl is in a solid state. It is generally handled as a powder in commercial and laboratory settings.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
201.24g/mol
Molar mass
201.2240g/mol
Density
1.2320g/cm3
Appearence

Carbaryl appears as a white crystalline solid. It is typically found in powder form and may emit a mild characteristic odor. The solid is stable under standard conditions but should be handled carefully to avoid degradation or reaction with incompatible materials.

Comment on solubility

Solubility of (3,4-dimethylphenyl) N-methylcarbamate

(3,4-dimethylphenyl) N-methylcarbamate exhibits distinct solubility characteristics that are essential for understanding its behavior in various chemical environments.

Generally, the solubility of this compound is influenced by factors such as:

  • Polarity: The presence of the carbamate functional group enhances its ability to interact with polar solvents.
  • Hydrophobicity: The dimethylphenyl group introduces a hydrophobic character, which may decrease solubility in water.
  • pH Levels: The solubility may be affected by the pH of the solution, as ionization can occur under certain conditions.

In general, (3,4-dimethylphenyl) N-methylcarbamate tends to be more soluble in organic solvents such as:

  • Acetone
  • Ethyl acetate
  • Dichloromethane

However, it is reported to have *limited solubility* in water, making it essential to consider solvent choice when utilizing this compound in chemical reactions or formulations. As a guiding principle, it is always advisable to conduct preliminary solubility tests to confirm the behavior of this compound in a specific solvent system.

Interesting facts

Interesting Facts About (3,4-Dimethylphenyl) N-methylcarbamate

(3,4-dimethylphenyl) N-methylcarbamate, often referred to in scientific literature due to its interesting properties and applications, is a member of the carbamate family of compounds. These compounds are generally recognized for their versatile biological activities.

Key Characteristics

  • Agricultural Use: This compound acts as a pesticide and is commonly utilized in agricultural settings to protect crops from pests.
  • Biochemical Interaction: Like many carbamates, it interacts with the enzyme acetylcholinesterase, which is vital for the proper functioning of the nervous system. This interaction can lead to increased synaptic activity.
  • Research Relevance: The study of N-methylcarbamates contributes significantly to neuropharmacology. Researchers often investigate their effects and mechanisms of action, making them pivotal in understanding neurological disorders.

Safety and Environmental Impact

The safety profile of (3,4-dimethylphenyl) N-methylcarbamate raises some concerns:

  • It is essential to handle this compound with care, as exposure can lead to toxic effects, particularly on the neurological system.
  • Environmental studies are crucial to assess the impact of its usage in agriculture, highlighting the need for sustainable practices to mitigate potential harm to non-target species.

Application in Synthesis

In organic synthesis, (3,4-dimethylphenyl) N-methylcarbamate serves as a valuable intermediate:

  • It can be used in the preparation of other complex molecules, demonstrating its utility in synthetic chemistry.
  • Researchers often explore its transformations, which can lead to the discovery of new compounds with enhanced properties.

As a reaffirmation of its significance, it is often noted, "The study of carbamates is a window into the intricacies of life sciences, merging chemistry with biology in intriguing ways."

Overall, (3,4-dimethylphenyl) N-methylcarbamate exemplifies the fascinating interplay between chemical composition and biological activity, making it an important topic of discussion in both academic and practical chemistry contexts.

Synonyms
Xylylcarb
Meobal
3,4-Xylyl methylcarbamate
2425-10-7
3,4-Dimethylphenyl Methylcarbamate
3,4-Dimethylphenyl N-methylcarbamate
Phenol, 3,4-dimethyl-, methylcarbamate
Methylcarbamic acid 3,4-xylyl ester
Carbamic acid, methyl-, 3,4-xylyl ester
Xylylcarb [BSI:ISO]
3,4-DIMETHYLPHENOL METHYLCARBAMATE
V 17004
XYLYLCARB [ISO]
EINECS 219-364-9
2999840EDW
BRN 2047375
Carbamic acid, N-methyl-, (3,4-dimethylphenyl) ester
3,4-Xylylester kyseliny methylkarbaminove
AI3-27693
DTXSID3058032
CHEBI:35048
3,4-dimethylphenylmethylcarbamate
Phenol, 3,4-dimethyl-, 1-(N-methylcarbamate)
3,4-Xylylester kyseliny methylkarbaminove [Czech]
3,4-DIMEPHENYL N-METHYLCARBAMATE
DTXCID9031800
3,4-Dimethylphenyl methylcarbamate (9CI)
219-364-9
MPMC
(3,4-dimethylphenyl) N-methylcarbamate
S 1042
Xylecarb
SCHEMBL63141
3,4-Xylyl N-methylcarbamate
BIDD:ER0428
UNII-2999840EDW
WCJYTPVNMWIZCG-UHFFFAOYSA-
AKOS006273043
NS00021912
S-1042
Carbamic acid, 3,4-dimethylphenyl ester, N-methyl
Q2598558
InChI=1/C10H13NO2/c1-7-4-5-9(6-8(7)2)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)