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Lauroyl chloride

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Identification
Molecular formula
C12H23ClO
CAS number
16482-36-7
IUPAC name
(2,2,2-trichloro-1-dimethoxyphosphoryl-ethyl) dodecanoate
State
State

At room temperature, lauroyl chloride is in a liquid state.

Melting point (Celsius)
17.00
Melting point (Kelvin)
290.15
Boiling point (Celsius)
117.00
Boiling point (Kelvin)
390.15
General information
Molecular weight
296.70g/mol
Molar mass
296.6970g/mol
Density
1.0830g/cm3
Appearence

Lauroyl chloride appears as a colorless to pale yellow liquid with a pungent odor. It is a lachrymator, meaning it can cause tears to form in the eyes.

Comment on solubility

Solubility of (2,2,2-trichloro-1-dimethoxyphosphoryl-ethyl) dodecanoate

The solubility of (2,2,2-trichloro-1-dimethoxyphosphoryl-ethyl) dodecanoate is an intriguing characteristic that speaks to its potential applications. This compound, with its unique structure, can exhibit varying solubility depending on the solvent used. Here are some important points to consider regarding its solubility:

  • Polarity: The presence of the dimethoxyphosphoryl group introduces some polar characteristics, potentially enhancing solubility in polar solvents.
  • Hydrophobic Tail: The long dodecanoate chain is hydrophobic, which tends to promote solubility in organic solvents like diethyl ether or hexane.
  • Solvent Compatibility: This compound might be expected to show enhanced solubility in solvents that can accommodate both polar and nonpolar characteristics, such as dichloromethane.
  • Temperature Effects: As with many compounds, solubility may also increase with temperature, providing further opportunities for its use in various applications.

In conclusion, the solubility of (2,2,2-trichloro-1-dimethoxyphosphoryl-ethyl) dodecanoate is nuanced, influenced by its unique structural features and the solvents employed. Understanding these interactions is crucial for its application in chemical formulations and processes.

Interesting facts

Interesting Facts about (2,2,2-Trichloro-1-dimethoxyphosphoryl-ethyl) Dodecanoate

(2,2,2-Trichloro-1-dimethoxyphosphoryl-ethyl) dodecanoate is a fascinating compound that showcases the interplay between organic chemistry and biochemistry. Here are some engaging facts about this intriguing molecule:

  • Versatile Applications: This compound serves as a key intermediate in the synthesis of various chemical entities, which can be utilized in agriculture, pharmaceuticals, and materials science.
  • Chlorine Atoms: The presence of three chlorine atoms in its structure enhances its reactivity, making it a valuable building block in chlorinated compound synthesis.
  • Phosphorylation: The dimethoxyphosphoryl group allows this compound to participate in phosphorylation reactions, a crucial process in biochemical pathways, including energy transfer and signal transduction.
  • Fatty Acid Derivative: As a dodecanoate, it is derived from lauric acid, a fatty acid known for its antimicrobial properties, which may contribute to the compound's effectiveness in various applications.

In particular, the incorporation of such elements can lead to innovative solutions in fields such as drug delivery and agrochemical formulations. Chemists often remark that the "synergy of functionality and reactivity" in compounds like this one opens new avenues for research and development. The continuous exploration of such compounds sheds light on the vast potential of chemical science to address real-world challenges.

In summary, (2,2,2-trichloro-1-dimethoxyphosphoryl-ethyl) dodecanoate exemplifies how chemical ingenuity can lead to multifaceted applications by leveraging unique structural features. Its significance stretches beyond the laboratory, impacting sectors that aim to improve human health and agricultural productivity.

Synonyms
4414-15-7
Dodecanoic acid, 2,2,2-trichloro-1-(dimethoxyphosphinyl)ethyl ester
Lauroyltrichlorofon
DTXSID50963176
2,2,2-trichloro-1-(dimethoxyphosphoryl)ethyl dodecanoate