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Triethylene glycol monoethyl ether acrylate

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Identification
Molecular formula
C10H16O6
CAS number
2478-10-6
IUPAC name
4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid
State
State

At room temperature, this compound is in a liquid state.

Melting point (Celsius)
-62.00
Melting point (Kelvin)
211.15
Boiling point (Celsius)
470.00
Boiling point (Kelvin)
743.15
General information
Molecular weight
204.21g/mol
Molar mass
204.2090g/mol
Density
1.2541g/cm3
Appearence

The compound is typically a colorless liquid, often slightly viscous, and has a faint, characteristic acrid odor.

Comment on solubility

Solubility of 4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid (C10H16O6)

The solubility of 4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid is an interesting topic due to its complex structure. This compound exhibits several solubility characteristics:

  • Polar Functional Groups: The presence of multiple hydroxyl (-OH) groups contributes to its overall polarity, enhancing its interaction with water molecules.
  • Solvent Interaction: Its ability to hydrogen bond with solvents like water and alcohols makes it likely to be soluble in such polar solvents.
  • Potential Limitations: Despite its polar nature, the hydrocarbon chain may make complete solubility in non-polar solvents less favorable.

In terms of actual behavior in solution, we can expect:

  1. High solubility in aqueous environments: Due to its polar groups, it can easily dissolve in water.
  2. Reduced solubility in non-polar solvents: As a result of hydrophobic interactions from the longer carbon chain.

In conclusion, the solubility of C10H16O6 underscores the influence of structural functionality on its interaction with solvents, making it a unique substance in chemical applications.

Interesting facts

Interesting Facts about 4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid

4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid is a fascinating compound that showcases the beauty of organic chemistry through its structural complexity and functional diversity. Here are some compelling points that highlight the significance of this compound:

  • Functional Groups: This compound features multiple functional groups including hydroxyl (-OH) and keto (C=O), which contribute to its chemical reactivity and potential applications in various fields.
  • Synthetic Utility: The presence of the but-2-enoic acid backbone makes this compound a potential intermediate in the synthesis of other organic molecules, paving the way for innovative chemical transformations.
  • Biological Relevance: Compounds with similar structures are often studied for their biological activities, making them important in drug discovery and development processes.
  • Solvent Properties: The hydroxyethoxy groups can enhance the solubility of this compound in aqueous environments, which is advantageous for formulation in biological systems.

Quote from an organic chemist: "The intricate design of organic structures reflects nature's complexity, and compounds like 4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid exemplify this in their potential uses and interactions."

Overall, 4-[2-(2-hydroxyethoxy)ethoxy]-4-oxo-but-2-enoic acid stands as a prime example of how organic compounds can hold keys to understanding chemical behavior, biological interactions, and innovative synthesis pathways in chemistry.