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Pirimicarb

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Identification
Molecular formula
C11H18N4O2
CAS number
23103-98-2
IUPAC name
(6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate
State
State

Solid: Pirimicarb is typically found as a solid in its pure form at room temperature.

Melting point (Celsius)
90.00
Melting point (Kelvin)
363.00
Boiling point (Celsius)
368.00
Boiling point (Kelvin)
641.00
General information
Molecular weight
238.29g/mol
Molar mass
238.2890g/mol
Density
1.1420g/cm3
Appearence

Pirimicarb appears as a white to pale yellow crystalline solid.

Comment on solubility

Solubility of (6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate

The solubility of (6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate can be influenced by several factors including temperature, the solvent nature, and the molecular structure of the compound itself. Generally, one might note the following aspects:

  • Polarity: The presence of both polar and non-polar groups in the molecular structure can lead to complex solubility behaviors. Here, the carbamate functional group introduces polarity, which can enhance solubility in polar solvents.
  • Solvent Selection: It tends to be more soluble in organic solvents such as methanol and ethanol rather than in water, due to its hydrophobic alkyl substituents.
  • Hydrogen Bonding: The potential for hydrogen bonding with solvent molecules can greatly increase the solubility of regions within the molecule that are available for such interactions.

In summary, while (6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate may display moderate solubility in appropriate solvents, its actual solubility will need to be determined experimentally to account for variations in temperature and solvent properties, which are paramount in predicting solubility outcomes.

Interesting facts

Interesting Facts about (6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate

(6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate, a compound with significant applications in agricultural chemistry, showcases some intriguing characteristics that are worth exploring. It belongs to a class of compounds known for their role as effective pesticides and herbicides.

Key Highlights:

  • Pesticidal Properties: This compound is primarily used for its ability to control pests that threaten crops, contributing to food security.
  • Mechanism of Action: The compound acts by interfering with essential biochemical processes in pests, ultimately leading to their demise, while being designed to minimize impact on non-target species.
  • Synthesis and Structure: The molecular architecture of this compound includes a pyrimidine ring, which is crucial for its biological activity, making it a focal point of research in molecular design.
  • Environmentally Considerate: Researchers are continually working on improving the environmental impact of such derivatives, ensuring they degrade safely and do not accumulate in ecosystems.

As a testament to its utility, the compound has spurred considerable research aimed at enhancing its efficacy and selectivity. According to recent studies, “the careful manipulation of substituents on the pyrimidine ring can lead to significant improvements in pest-target interactions.” This compound not only exemplifies the intersection of chemistry and agriculture but also highlights the ongoing efforts to innovate sustainable practices in pest management.

In conclusion, (6-methyl-2-propyl-pyrimidin-4-yl) N,N-dimethylcarbamate represents a sophisticated blend of organic chemistry and practical application, underscoring the invaluable role of chemical compounds in modern agriculture.

Synonyms
Pyramat
Pyramate
2532-49-2
Geigy G-23330
6-Methyl-2-propyl-4-pyrimidinyl dimethylcarbamate
ENT 19,059
6-Methyl-2-propyl-4-pyrimidinyl dimethyl carbamate
G-23,330
2-n-Propyl 4-methylpyrimidyl-(6) N,N-dimethyl carbamate
Dimethylcarbamic acid, 6-methyl-2-propyl-4-pyrimidinyl ester
CARBAMIC ACID, DIMETHYL-, 6-METHYL-2-PROPYL-4-PYRIMIDINYL ESTER
(6-methyl-2-propylpyrimidin-4-yl) N,N-dimethylcarbamate
4-Methyl-2-propyl-6-pyrimidinylester kyseliny dimethylkarbaminove
Caswell No. 575AA
EPA Pesticide Chemical Code 575300
BRN 0177756
AI3-19059
4-Pyrimidinol, 6-methyl-2-propyl-, dimethylcarbamate (ester)
4-Methyl-2-propyl-6-pyrimidinylester kyseliny dimethylkarbaminove [Czech]
5-23-11-00186 (Beilstein Handbook Reference)
DTXSID2041549
SCHEMBL11436041
CQRUIYKYVFQBRT-UHFFFAOYSA-N
DB-415142
NS00120793
4-Pyrimidinol, 6-methyl-2-propyl-, dimethylcarbamate
6-Methyl-2-propyl-4-pyrimidinyl N,N-dimethylcarbamate