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Deltamethrin

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Identification
Molecular formula
C22H19Br2NO3
CAS number
52918-63-5
IUPAC name
[(1S)-2-methyl-4-oxo-3-penta-2,4-dienyl-cyclopent-2-en-1-yl] (1R,3R)-3-(3-methoxy-2-methyl-3-oxo-prop-1-enyl)-2,2-dimethyl-cyclopropanecarboxylate
State
State

At room temperature, deltamethrin is in a solid state. It is commonly used in its solid, crystalline form for various applications, especially in pest control products.

Melting point (Celsius)
98.50
Melting point (Kelvin)
371.65
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
505.22g/mol
Molar mass
505.2190g/mol
Density
1.5000g/cm3
Appearence

Deltamethrin appears as a colorless to off-white solid. It is usually available in crystalline powder form. It does not have a notable odor, making it relatively easy to handle in industrial and laboratory settings.

Comment on solubility

Solubility of [(1S)-2-methyl-4-oxo-3-penta-2,4-dienyl-cyclopent-2-en-1-yl] (1R,3R)-3-(3-methoxy-2-methyl-3-oxo-prop-1-enyl)-2,2-dimethyl-cyclopropanecarboxylate

The solubility of the compound [(1S)-2-methyl-4-oxo-3-penta-2,4-dienyl-cyclopent-2-en-1-yl] (1R,3R)-3-(3-methoxy-2-methyl-3-oxo-prop-1-enyl)-2,2-dimethyl-cyclopropanecarboxylate can be influenced by several factors due to its complex structure. Here are some key points regarding its solubility:

  • Polarity: The presence of polar functional groups, such as the methoxy (-OCH3) and carbonyl (C=O) groups, may enhance solubility in polar solvents like water. Conversely, the hydrocarbon framework may impart non-polar characteristics, affecting solubility in organic solvents.
  • Solvent Interaction: The solubility can vary significantly depending on the solvent used. For example:
    • Highly polar solvents: May exhibit improved solubility due to hydrogen bonding.
    • Non-polar solvents: May show lower solubility due to poor interactions with the compound.
  • Concentration Effects: As with many organic compounds, solubility may be concentration-dependent, where higher concentrations could lead to saturation and precipitation out of the solution.
  • Temperature Influence: Solubility typically increases with temperature for many compounds, suggesting that heating the solvent could enhance the dissolution process.

In conclusion, the solubility of this compound is quite nuanced, relying on the specific balance of its structural elements and environmental conditions. Further experimental validation in various solvents would provide clarifying insights into its solubility profile.

Interesting facts

Interesting Facts about [(1S)-2-methyl-4-oxo-3-penta-2,4-dienyl-cyclopent-2-en-1-yl] (1R,3R)-3-(3-methoxy-2-methyl-3-oxo-prop-1-enyl)-2,2-dimethyl-cyclopropanecarboxylate

This compound boasts a complex structure that is a fascinating subject for chemists who appreciate the beauty of organic synthesis and molecular diversity. Here are some engaging aspects of this intriguing compound:

  • Synthetic Pathways: The synthesis of this compound can involve intricate multi-step reactions that showcase the creativity involved in organic chemistry. Chemists often utilize techniques such as coupling reactions and stereocontrol methods to achieve the desired stereochemistry.
  • Biological Importance: Compounds with similar structures have been investigated for their potential applications in the pharmaceutical industry. Many natural products derived from plants exhibit similar frameworks, suggesting that this compound could hold biological significance or pharmacological properties worth exploring.
  • Cyclopropane Chemistry: The presence of cyclopropane rings is notable; these three-membered rings are known for their strain and unique chemical reactivity. Chemists harness their reactivity to develop new chemical transformations and materials.
  • Material Applications: Understanding compounds like this can contribute to advances in material science, especially in the development of polymers or coatings that require specific properties due to their structural intricacies.
  • Regio- and Stereochemistry: The specific stereochemical arrangement in this compound highlights the importance of chirality in chemistry. The (1S,3R) notation indicates that understanding the optical activity of compounds is crucial in many chemical applications, including drug design and synthesis.

This compound exemplifies the universe of organic chemistry, where even a single molecule can lead to vast avenues of chemical inquiry and application. As scientists study this compound further, they may uncover even more fascinating properties and potential uses that contribute to our understanding of chemistry and its role in various industries.