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Ethyl 16-fluoropalmitate

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Identification
Molecular formula
C18H35FO2
CAS number
378-44-3
IUPAC name
ethyl 16-fluorohexadecanoate
State
State

At room temperature, ethyl 16-fluoropalmitate is present as a liquid.

Melting point (Celsius)
3.50
Melting point (Kelvin)
276.70
Boiling point (Celsius)
332.50
Boiling point (Kelvin)
605.70
General information
Molecular weight
318.48g/mol
Molar mass
318.4750g/mol
Density
0.9012g/cm3
Appearence

Ethyl 16-fluoropalmitate is typically a colorless to pale yellow liquid that is oily in nature.

Comment on solubility

Solubility of Ethyl 16-Fluorohexadecanoate

Ethyl 16-fluorohexadecanoate, with its unique structure, exhibits interesting solubility characteristics. Here are some key points to consider:

  • Polarity: The presence of the fluoro group contributes to the overall polarity of the compound, which can influence its solubility behavior differently compared to non-fluorinated analogs.
  • Aqueous Solubility: Generally, esters like ethyl esters are less soluble in water due to their hydrophobic alkyl chains. The larger the hydrophobic portion, the lower the solubility in water.
  • Organic Solvents: Ethyl 16-fluorohexadecanoate is likely to be well-soluble in organic solvents such as ethanol and diethyl ether, which can stabilize its molecule through favorable interactions.
  • Temperature Effects: Like most organic compounds, its solubility can change with temperature; higher temperatures often increase solubility in organic solvents.

In summary, while ethyl 16-fluorohexadecanoate may show limited solubility in water due to its hydrophobic characteristics, it is expected to dissolve effectively in organic solvents, making it versatile for use in various chemical formulations. Understanding these solubility traits can significantly aid in the practical applications of this compound.

Interesting facts

Interesting Facts About Ethyl 16-Fluorohexadecanoate

Ethyl 16-fluorohexadecanoate is an intriguing chemical compound with a diverse array of applications and interesting properties. Here are some notable points about this compound:

  • Structure and Composition: The compound features a long carbon chain, making it a fatty acid ester. The presence of a fluorine atom in the chain significantly influences its physical and chemical properties, such as increasing lipophilicity and altering reactivity.
  • Biological Significance: Compounds like ethyl 16-fluorohexadecanoate can serve as valuable intermediates in the synthesis of pharmaceuticals and agrochemicals. The introduction of fluorine often enhances the biological activity or stability of organic molecules.
  • Applications in Research: Ethyl 16-fluorohexadecanoate is often explored for its utility in materials science and nanotechnology. Its unique properties open doors to the development of advanced functional materials.
  • Fluorinated Compounds: The introduction of fluorine atoms can have drastic effects on a compound's characteristics. They exhibit improved metabolic stability and bioavailability, making them particularly attractive in drug design.
  • Green Chemistry: Understanding the behavior and degradation of fluorinated compounds like ethyl 16-fluorohexadecanoate is essential from an environmental perspective. Researchers are continuously seeking greener alternatives to produce these substances to minimize the ecological footprint.

As a chemistry student, exploring compounds like ethyl 16-fluorohexadecanoate not only enhances your knowledge of organic chemistry but also provides insight into practical applications in various fields. The fascinating balance of **structure and functionality** in such compounds demonstrates the complexity and beauty of chemical science. Remember, each molecule tells a story of its journey from synthesis to application!

Synonyms
Ethyl 16-fluorohexadecanoate
408-07-1
BRN 1789807
HEXADECANOIC ACID, 16-FLUORO-, ETHYL ESTER
DTXSID40193783
4-02-00-01184 (Beilstein Handbook Reference)
DTXCID80116274