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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate
State
State

At room temperature, carbaryl is typically in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2190g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white crystalline solid. In its pure form, it is a colorless or white powder and is often sold in a variety of forms including powders, dusts, and granules when used as a pesticide.

Comment on solubility

Solubility of [3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate

The solubility of [3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate can be quite intriguing due to the various factors that influence it. This compound, being an organic carbamate, presents characteristics that affect its interaction with solvents.

Factors Influencing Solubility:

  • Molecular Structure: The presence of the dimethylamino group can enhance solubility in polar solvents due to its ability to form hydrogen bonds.
  • Polarity: As a moderately polar compound, the solubility of this carbamate is generally higher in polar solvents like water compared to non-polar solvents.
  • Temperature: Increased temperature often aids in the dissolution process, allowing more of the compound to interact with the solvent.

Moreover, it is essential to consider the following:

  • The solubility may be significantly affected by the pH of the solution, determining the ionization state of the molecule.
  • Common solvents for organic compounds, like ethanol or acetone, may also dissolve this carbamate, yet the degree of solubility will vary.

In conclusion, the solubility of [3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate is influenced by its chemical structure, polarity, and the environmental conditions, making it a compound of interest for further studies in solubility behavior.

Interesting facts

Interesting Facts About [3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate

[3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate, typically referred to in scientific circles as a versatile chemical compound, is notable for its various applications in both agricultural and pharmaceutical fields. Here are some engaging insights into this compound:

  • Biological Activity: This compound is closely related to certain pesticides and herbicides, showcasing its significant role in agricultural chemistry by helping to increase crop yields effectively.
  • Mechanism of Action: It operates by inhibiting acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system, making it valuable in the study of neurochemistry.
  • Research Importance: The compound is often utilized in various studies assessing the impact of chemical exposure on ecosystems, particularly concerning its potential environmental effects.
  • Synthetic Utility: Its structure allows for modifications to create various derivatives, which are extensively explored for developing new compounds with improved properties.
  • Safety and Regulation: Given its biological activity, [3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate is subject to strict regulatory scrutiny, highlighting the importance of understanding chemical safety and risk assessment.

In the words of a renowned chemist, "The study of chemicals like [3-(dimethylamino)-4-methyl-phenyl] N-methylcarbamate is not just about their reactive capabilities; it's about understanding their broader impact on health and the environment."

This compound exemplifies the balance between utility and safety in chemical applications, urging scientists to innovate responsibly while considering ecological and health implications.

Synonyms
14144-91-3
[3-(dimethylamino)-4-methylphenyl] N-methylcarbamate
N-Methylcarbamic acid 3-(dimethylamino)-4-methylphenyl ester
Bayer 42696
BAY 42696
TL-1187
BRN 2731714
AI3-27108
CARBAMIC ACID, METHYL-, 3-(DIMETHYLAMINO)-p-TOLYL ESTER
Carbamic acid, N-methyl-, 4-methyl-3-dimethylaminophenyl ester
3-13-00-01573 (Beilstein Handbook Reference)
DTXSID80931101
Phenol, 3-(dimethylamino)-4-methyl-, methylcarbamate (ester)
3-(Dimethylamino)-4-methylphenyl hydrogen methylcarbonimidate