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4-Ethoxybutan-1-ol

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Identification
Molecular formula
C6H14O2
CAS number
6312-29-6
IUPAC name
4-ethoxybutan-1-ol
State
State

At room temperature, 4-ethoxybutan-1-ol is a liquid. It is often used as an intermediate in chemical reactions and as a solvent in various industrial applications.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
189.60
Boiling point (Kelvin)
462.75
General information
Molecular weight
118.17g/mol
Molar mass
118.1740g/mol
Density
0.8978g/cm3
Appearence

4-Ethoxybutan-1-ol is a colorless liquid that features a mild odor. It appears transparent and is fully miscible in water and various organic solvents.

Comment on solubility

Solubility of 4-ethoxybutan-1-ol

4-ethoxybutan-1-ol, with the chemical formula C6H14O, exhibits notable solubility characteristics that are important for various applications. Understanding its solubility helps in predicting how this compound behaves in different environments.

Water Solubility

This compound is soluble in water due to the presence of the hydroxyl (-OH) group that can form hydrogen bonds with water molecules. The solubility can be further understood through the following:

  • The ethoxy group (-OCH2CH3) helps to enhance solubility due to its moderate polar nature.
  • As the hydrocarbon chain increases in length, the hydrophobic character may limit solubility, but in the case of 4-ethoxybutan-1-ol, it remains sufficiently soluble.

Solvent Compatibility

4-ethoxybutan-1-ol is also soluble in organic solvents, allowing it to dissolve in various polar and non-polar solvents. This property makes it valuable in applications such as:

  • Cosmetic formulations
  • Pharmaceuticals

Overall, the solubility of 4-ethoxybutan-1-ol can be summarized by the following points:

  • Moderate water solubility due to the -OH functional group.
  • Good solubility in a range of organic solvents.
  • Versatile applications stemming from its solubility properties.

In conclusion, the solubility characteristics of 4-ethoxybutan-1-ol make it a valuable compound across various fields, highlighting its importance in chemical formulations.

Interesting facts

Interesting Facts about 4-ethoxybutan-1-ol

4-ethoxybutan-1-ol is an intriguing compound that belongs to the family of alcohols, specifically butanol derivatives. As a scientist or chemistry student, you may find several noteworthy points about this compound:

  • Functional Groups: 4-ethoxybutan-1-ol contains an ethoxy group (-OCH2CH3) attached to a butanol skeleton. This combination enhances its properties and applications.
  • Applications: This compound is used in various applications, particularly in the formulation of solvents, fragrances, and flavoring agents. Its unique structure allows it to interact favorably in these mixtures.
  • Reactivity: The presence of both ether (from the ethoxy) and alcohol functional groups gives this compound unique reactivity. It can participate in diverse chemical reactions, such as esterification and ether cleavage, making it valuable in organic synthesis.
  • Biological Significance: Studies have shown that alcohols, including 4-ethoxybutan-1-ol, can influence biological systems. Understanding its interactions can lead to insights in pharmacology or toxicology.
  • Environmental Impact: As with many chemicals, it’s essential to assess the environmental impact of 4-ethoxybutan-1-ol. Its biodegradability and potential toxicity should be evaluated, especially if used in consumer products.

Overall, 4-ethoxybutan-1-ol is a compound that bridges the realms of industrial application and academic research, showcasing the beautiful complexity of organic chemistry.

Synonyms
4-Ethoxybutan-1-ol
111-73-9
4-Ethoxy-1-butanol
Dowanol BEAT
1-BUTANOL, 4-ETHOXY-
Butylene glycol monoethyl ether
Butylene glycol ethyl ether
4-ethoxybutanol
Dowanol be
Dowanal BEAT
Butanediol, monoethyl ether
KF8FNI35PO
EINECS 203-901-9
NSC 221255
BRN 1732976
NSC-221255
DTXSID10149439
UNII-KF8FNI35PO
Butanediol, monoethyl ester
WLN: Q4O2
SCHEMBL107912
DTXCID8071930
MFCD00040194
NSC221255
AKOS008152676
SY195981
DB-367760
NS00079186
EN300-85576
G45726
Z993012560