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Carbaryl

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

Carbaryl is typically found as a solid at room temperature.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.00
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.00
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid. It is odorless and tends to appear as colorless crystals at room temperature.

Comment on solubility

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

The solubility of the compound [4-(dimethylaminomethyleneamino)-3-methyl-phenyl] N-methylcarbamate can be influenced by a variety of factors. As an organic molecule, its solubility is typically examined in both polar and non-polar solvents. Here are some key aspects to consider:

  • Polarity: Due to the presence of polar functional groups such as the carbamate moiety, this compound may exhibit higher solubility in polar solvents like water or methanol.
  • Hydrophobic interactions: The aromatic ring in the structure can cause hydrophobic interactions, which suggest that the compound may also dissolve well in non-polar solvents.
  • Temperature dependence: Solubility can change with temperature; generally, an increase in temperature can enhance solubility for many compounds.
  • pH sensitivity: The pH of the solvent can affect the ionization of the amine groups in the structure, further influencing solubility.
  • Complexation: If this compound forms stable complexes with metal ions or other molecules, its solubility could significantly alter in those specific environments.

To summarize, while the solubility of [4-(dimethylaminomethyleneamino)-3-methyl-phenyl] N-methylcarbamate is likely substantial in both polar and non-polar solvents, precise solubility data should be obtained from experimental studies to guide practical applications.

Interesting facts

Interesting Facts about [4-(dimethylaminomethyleneamino)-3-methyl-phenyl] N-methylcarbamate

[4-(dimethylaminomethyleneamino)-3-methyl-phenyl] N-methylcarbamate is a fascinating compound that exemplifies the intricate world of organic chemistry, particularly in the realm of carbamate derivatives. These compounds are notably recognized for their diverse applications in pharmaceuticals and agriculture, primarily due to their role as effective pesticides and herbicides.

Key Characteristics:

  • Mechanism of Action: Carbamates work by inhibiting the enzyme acetylcholinesterase, which is crucial for the proper functioning of the nervous system in both pests and humans, leading to their effectiveness as pesticides.
  • Structural Significance: The presence of the dimethylaminomethyleneamino group contributes to the compound's biological activity, enhancing its interaction with target organisms.
  • Diversity: The variations in the side groups of carbamates, like the methyl and dimethylamine substitutions in this compound, can significantly alter their properties and applications.

This compound is not only of interest for its potential applications but also for its place in synthetic organic chemistry. It showcases how slight modifications in molecular structure can lead to profound changes in functionality. As scientists continue to explore structure-activity relationships, compounds like [4-(dimethylaminomethyleneamino)-3-methyl-phenyl] N-methylcarbamate serve as vital tools in developing new agrochemicals and medications.

Quote:

As the chemist Richard Feynman once said, “What I cannot create, I do not understand.” The exploration of such complex molecules allows us to deepen our understanding of chemistry and its practical applications.

In conclusion, [4-(dimethylaminomethyleneamino)-3-methyl-phenyl] N-methylcarbamate represents a small yet significant piece of the puzzle in the vast landscape of chemical compounds, illustrating the vital link between molecular structure and biological effectiveness.

Synonyms
FORMPARANATE
Schering 36103
Caswell No. 359DD
Formparanate [ISO:BSI]
Union carbide UC-25074
HSDB 6448
UC-25074
ENT 27,305
EPA Pesticide Chemical Code 359700
UNII-76S03Y009F
AI3-27305
FORMPARANATE [ISO]
76S03Y009F
FORMPARANATE [HSDB]
UC-34096
N,N-Dimethyl-N'-(2-methyl-4-(((methylamino)carbonyl)oxy)phenyl)methanimidamide
4-(((Dimethylamino)methylene)amino)-m-tolylmethylcarbamate
DTXSID9041992
Carbamic acid, methyl-, ester with N'-(4-hydroxy-o-tolyl)-N,N-dimethylformamidine
Carbamic acid, methyl-, 4-(((dimethylamino)methylene)amino)-m-tolyl ester
Methanimidamide, N,N-dimethyl-N'-(2-methyl-4-(((methylamino)carbonyl)oxy)phenyl)-
4-((EZ)-DIMETHYLAMINOMETHYLENEAMINO)-M-TOLYL METHYLCARBAMATE
Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]-
UC 34096
4-((DIMETHYLAMINO)METHYLENE)AMINO-M-TOLYL METHYLCARBAMATE
4-[(DIMETHYLAMINO)METHYLENE]AMINO-M-TOLYL METHYLCARBAMATE
Formparanic acid
CARBAMIC ACID, METHYL-, 4-[[(DIMETHYLAMINO)METHYLENE]AMINO]-M-TOLYL ESTER
dimethyl(((2-methyl-4-((methylcarbamoyl)oxy)phenyl)imino)methyl)azanium chloride
DIMETHYL[({2-METHYL-4-[(METHYLCARBAMOYL)OXY]PHENYL}IMINO)METHYL]AZANIUM CHLORIDE
Union carbide UC25074
DTXCID7021992
UC25074
4(((Dimethylamino)methylene)amino)mtolylmethylcarbamate
3-METHYL-4-DIMETHYLAMINOMETHYLENEIMINOPHENYL N-METHYLCARBAMATE
Carbamic acid, methyl, ester with N'(4hydroxyotolyl)N,Ndimethylformamidine
Methanimidamide, N,NdimethylN'(2methyl4(((methylamino)carbonyl)oxy)phenyl)
N,NDimethylN'(2methyl4(((methylamino)carbonyl)oxy)phenyl)methanimidamide
Carbamic acid, methyl-, ester with N'-(4-hydroxy-o-tolyl)-N,N-dimethylformamidine (8CI)
Methanimidamide, N,N-dimethyl-N'-(2-methyl-4-(((methylamino)carbonyl)oxy)phenyl)-(9CI)
17702-57-7
[4-(dimethylaminomethylideneamino)-3-methylphenyl] N-methylcarbamate
RCRA waste no. P197
SCHEMBL121130
SCHEMBL17505050
SCHEMBL29419153
SAA70257
Methanimidamide,N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]-
NS00123833
Q5470253