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2-Butyl-2-ethyl-1,3-dioxolan-4-yl)methanol

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Identification
Molecular formula
C10H20O3
CAS number
.
IUPAC name
(2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol
State
State

At room temperature, (2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol is in a liquid state. It remains stable under normal conditions but should be stored away from heat and open flames as with other similar organic compounds.

Melting point (Celsius)
-48.00
Melting point (Kelvin)
225.15
Boiling point (Celsius)
226.00
Boiling point (Kelvin)
499.15
General information
Molecular weight
174.25g/mol
Molar mass
174.2460g/mol
Density
0.9700g/cm3
Appearence

(2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol appears as a colorless liquid under standard conditions. It is typically clear and might have a slight odor characteristic of alcohols or ethers.

Comment on solubility

Solubility of (2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol

The solubility of (2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol is influenced by multiple factors due to its unique chemical structure. This compound, with its dioxolane ring, often exhibits a balance between polar and non-polar characteristics, leading to varied solubility profiles.

Key Considerations for Solubility:

  • Polarity: The presence of hydroxyl (-OH) groups contributes to increased polarity, enhancing solubility in polar solvents such as water.
  • Hydrophobic Components: The butyl and ethyl groups introduce hydrophobic characteristics, which can limit solubility in highly polar solvents.
  • Temperature Effects: Solubility can also vary significantly with temperature; generally, increased temperature tends to improve solubility.
  • Interactions: Hydrogen bonding capabilities of the -OH group can facilitate solubility in alcohols and other similar solvents.

In summary, while (2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol may show reasonable solubility in some organic solvents, its solubility in water could be moderate due to the competing influences of its hydrophilic and hydrophobic parts. As with many compounds, understanding the specific interactions with solvent molecules is crucial for predicting its solubility behavior.

Interesting facts

Interesting Facts about (2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol

(2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol is a fascinating compound that showcases the intricacies of organic chemistry. This compound is categorized as a dioxolane, which is known for its unique cyclic structure incorporating oxygen atoms within a five-membered ring. Here are some intriguing points to consider:

  • Structurally Unique: The presence of both butyl and ethyl groups contributes to the compound’s complexity, often influencing its chemical behavior and interactions.
  • Functional Versatility: Compounds with dioxolane rings are widely studied due to their potential applications in pharmaceuticals, polymers, and as solvents.
  • Synthetic Pathways: The synthesis of this compound often involves strategic steps to build the dioxolane ring, which can provide insights into reaction mechanisms and organic synthesis techniques.
  • Reactivity: The methanol functional group in this compound can participate in hydrogen bonding, making it an interesting subject for studying solvation and reactivity in various environments.
  • Potential Applications: Due to its unique molecular structure, this compound could find possible applications in the formulation of specialty chemicals and materials.

As you delve deeper into (2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol, consider the quote by renowned chemist Linus Pauling, who said, "The best way to have a good idea is to have lots of ideas." Exploring compounds like this can lead to innovative discoveries and advancements in multiple fields!


Studying the properties and applications of such compounds enriches our understanding of chemical science and underscores the intricate connections between molecular structure and function.

Synonyms
5694-74-6
2-Butyl-2-ethyl-1,3-dioxolane-4-methanol
BRN 0108289
(2-butyl-2-ethyl-1,3-dioxolan-4-yl)methanol
1,3-DIOXOLANE-4-METHANOL, 2-BUTYL-2-ETHYL-
SCHEMBL6113851
DTXSID50972384