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Azinphos-methyl

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Identification
Molecular formula
C10H12NO5PS
CAS number
86-50-0
IUPAC name
[diethylamino(methoxy)phosphoryl] diethyl phosphate
State
State

Solid at room temperature with a crystalline texture.

Melting point (Celsius)
72.00
Melting point (Kelvin)
345.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
317.28g/mol
Molar mass
317.2800g/mol
Density
1.4588g/cm3
Appearence

A colorless to white crystalline solid.

Comment on solubility

Solubility of [diethylamino(methoxy)phosphoryl] diethyl phosphate

The solubility of the compound [diethylamino(methoxy)phosphoryl] diethyl phosphate, characterized by its complex structure, hinges on a variety of factors:

  • Polarity: This compound contains polar functional groups, which may enhance its solubility in polar solvents such as water.
  • Hydrogen Bonding: The presence of amino and methoxy groups suggests the potential for hydrogen bonding, further aiding solubility in aqueous environments.
  • Solvent Interactions: The ability of the compound to dissolve in organic solvents could be influenced by its diethyl groups, which tend to promote solubility in less polar organic media.
  • Concentration and Temperature: As with many chemical compounds, solubility may also vary with changes in concentration and temperature, necessitating empirical testing for precise quantification.

In summary, while the exact solubility of [diethylamino(methoxy)phosphoryl] diethyl phosphate may require additional empirical data, factors such as polarity, hydrogen bonding, and solvent choice are critical in evaluating its dissolution behavior.

Interesting facts

Interesting Facts about [diethylamino(methoxy)phosphoryl] diethyl phosphate

[diethylamino(methoxy)phosphoryl] diethyl phosphate is an intriguing compound that falls within the category of organophosphorus compounds. Known for its unique chemical structure and properties, it plays a significant role in various fields of study.

1. Chemical Significance

This compound features a phosphorus center bonded to different functional groups, including:

  • Diethylamino group: This contributes to the compound's basicity and potential biological activity.
  • Methoxy group: This influences both the electronic characteristics and the reactivity of the compound.

2. Applications in Research

[diethylamino(methoxy)phosphoryl] diethyl phosphate is particularly noteworthy for its applications in:

  • Pesticide Development: Its phosphoric acid derivatives are studied for use as insecticides and herbicides due to their efficacy in disrupting biological processes.
  • Pharmaceutical Chemistry: The compound's structure can be utilized for drug design, particularly for agents targeting nervous system disorders.

3. Toxicological Aspects

Like many organophosphates, this compound's derivatives may exhibit neurotoxic properties. Caution is essential as they can influence neurotransmitter activity by inhibiting acetylcholinesterase. The following points are relevant in toxicology:

  • Mechanism of Action: Inhibition of acetylcholinesterase leads to an accumulation of acetylcholine at synaptic junctions.
  • Safety Measures: Proper handling and use of protective equipment are critical when working with such compounds in research settings.

4. Future Research Directions

Ongoing studies are exploring the potential for less harmful analogs to be developed from [diethylamino(methoxy)phosphoryl] diethyl phosphate, aiming to enhance safety while retaining effectiveness in its applications.

In conclusion, [diethylamino(methoxy)phosphoryl] diethyl phosphate is not just a chemical compound but a fascinating subject of study, bridging various disciplines from agricultural sciences to pharmacology. Its multifunctional nature inspires continued research and innovation within the scientific community.

Synonyms
625-13-8
AMIDODIPHOSPHORIC ACID, DIETHYL-, P',P'-DIETHYL P-METHYL ESTER
4035 HC
BRN 2382431
Amidopyrophosphoric acid, diethyl-, P',P'-diethyl P-methyl ester
DTXSID10978089
Diethyl methyl diethylamidodiphosphate