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Tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate

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Identification
Molecular formula
C19H34O5
CAS number
52904-15-5
IUPAC name
tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate
State
State

The compound is typically in a liquid state at room temperature due to its molecular structure, which influences its relatively low melting point.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
368.57g/mol
Molar mass
368.5710g/mol
Density
0.9125g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid. It is known for its oily consistency and is often used in formulations for its smooth texture. Being an ester, it has a faint pleasant odor typical of many esters.

Comment on solubility

Solubility Insights for Tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate (C19H34O5)

Understanding the solubility of tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate is crucial for its applications in various fields, including pharmaceuticals and cosmetics. This compound exhibits a unique structural composition that influences its solubility characteristics.

Factors Influencing Solubility

The solubility of this compound can be addressed through several key factors:

  • Hydrocarbon Chain: With a long tridecyl (C13) chain, the compound may show limited solubility in polar solvents, making it more favorable in organic solvents.
  • Functional Groups: The presence of hydroxymethyl and carboxylate groups enhances its interaction with polar solvents, creating a potential for improved solubility in aqueous environments.
  • Molecular Size and Weight: The substantial molecular weight of C19H34O5 may hinder the dissolution rate in some solvents due to increased van der Waals interactions.

Predicted Solubility Behavior

Given these factors, one might predict:

  • This compound could exhibit low to moderate solubility in water but is likely to be more soluble in organic solvents such as ethanol and acetone.
  • Its dual nature allows it to potentially form micelles or aggregates in solution, especially in surfactant applications.

In conclusion, due to its complex structure, the solubility of tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate can vary significantly based on the solvent used, emphasizing the importance of selecting the appropriate medium for its intended use.

Interesting facts

Interesting Facts about Tridecyl 2-(Hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate

Tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate is a fascinating compound that highlights the diverse functionalities of ester derivatives. Here are some intriguing facts:

  • Structural Features: This compound features a tetrahydropyran ring, which is a six-membered cyclic ether that is known for its stability and versatility in organic chemistry.
  • Functional Groups: The presence of a carboxylate group adds acidic properties, while the hydroxymethyl substituent can participate in hydrogen bonding, influencing solubility and reactivity.
  • Natural Occurrences: Similar compounds are often found in nature, particularly in various plant-derived oils, which can have applications in flavoring and fragrance industries.
  • Synthesis Insight: Chemists might explore this compound through methods like esterification or ring-opening reactions, providing valuable experience in synthetic organic chemistry.
  • Potential Applications: The unique structure of this compound suggests potential utility in pharmaceuticals and agrochemicals, particularly as intermediates in the synthesis of bioactive molecules.
  • Environmental Considerations: Understanding the biodegradability and environmental impact of such compounds is essential, especially as industries push for more sustainable chemical practices.

With the continuous exploration of chemical properties and applications, tridecyl 2-(hydroxymethyl)-6-oxo-tetrahydropyran-3-carboxylate showcases the intricate interplay of structure and function in the realm of organic compounds.