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Butyl ethyl sulfide

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Identification
Molecular formula
C6H14S
CAS number
5925-66-0
IUPAC name
1-ethylsulfanylbutane
State
State

At room temperature, Butyl ethyl sulfide is a liquid. It is not very volatile, making it relatively stable under standard conditions.

Melting point (Celsius)
-105.00
Melting point (Kelvin)
168.15
Boiling point (Celsius)
142.80
Boiling point (Kelvin)
415.95
General information
Molecular weight
118.24g/mol
Molar mass
118.2360g/mol
Density
0.8271g/cm3
Appearence

Butyl ethyl sulfide is a clear, colorless liquid with a characteristic sulfide odor. It is typically used as a flavor or fragrance intermediate.

Comment on solubility

Solubility of 1-ethylsulfanylbutane

1-ethylsulfanylbutane, a compound characterized by its unique structure, exhibits distinct solubility properties that are largely influenced by its alkyl and sulfanyl functional groups.

Solubility in Different Solvents

This compound demonstrates:

  • Moderate solubility in organic solvents, such as ethanol and acetone, due to its non-polar to moderately polar nature.
  • Poor solubility in water, attributed to the hydrophobic characteristics of the long carbon chain and the relatively low polarity of the sulfanyl group.
  • Variable solubility in aromatic solvents, which can facilitate interactions with the compound's functional groups.

Factors Affecting Solubility

The solubility behavior of 1-ethylsulfanylbutane can be affected by several factors, including:

  • Temperature: Increased temperature often enhances solubility in organic solvents.
  • Presence of functional groups: The interactions between solutes and solvents greatly impact solubility.
  • Chain length: Larger alkyl groups may hinder solubility in polar environments.

In conclusion, the solubility of 1-ethylsulfanylbutane is a balance between its non-polar characteristics pushing it away from polar solvents and its ability to interact with non-polar organic compounds. Understanding these solubility properties is crucial for applications in organic synthesis and chemical engineering.

Interesting facts

Interesting Facts about 1-Ethylsulfanylbutane

1-Ethylsulfanylbutane is a fascinating organic compound that belongs to the class of thioethers, characterized by the presence of sulfur atoms. This compound is particularly notable for several reasons:

  • Structural Uniqueness: The presence of the ethylsulfanyl group provides unique chemical properties and reactivity that differ from typical alkanes.
  • Applications: This compound serves as an important precursor in organic synthesis. Its reactivity makes it valuable in the development of pharmaceuticals and agricultural chemicals.
  • Odor Profile: Many thioethers, including compounds in the same family, are known for their distinctive odors, often reminiscent of rotten eggs or garlic, which can have environmental implications.
  • Biological Activity: Some studies suggest that compounds containing sulfur might exhibit biological activity, including antioxidant properties, which are essential for research in health and nutrition.
  • Environmental Impact: As sulfur-containing organic compounds can be volatile, it raises questions about their behavior and fate in the environment, particularly regarding atmospheric reactions.

In conclusion, 1-ethylsulfanylbutane highlights the intricate interplay of structure and function in organic chemistry. As “the key to understanding lies in the details,” delving deeper into its properties and applications continues to reveal crucial insights into this dynamic field.

Synonyms
n-Butyl Ethyl Sulfide
Butyl ethyl sulfide
638-46-0
1-ethylsulfanylbutane
Sulfide, butyl ethyl
Butane, 1-(ethylthio)-
3-Thiaheptane
1-(Ethylsulfanyl)butane
Ethyl butyl sulfide
Ethyl butyl sulphide
1-(Ethylthio)butane
Ethyl n-butyl sulfide
2RYB65Z11E
NSC-19
ETHYL BUTYLSULFIDE
UNII-2RYB65Z11E
n-Butylethylsulfide
AI3-32577
1-(Ethylsulfanyl)butane #
NSC19
SCHEMBL199217
NSC 19
XJIRSLHMKBUGMR-UHFFFAOYSA-
DTXSID80862340
MFCD00039958
AKOS006229965
BS-23728
DB-054562
G77547
EN300-6491153
Q27255519
InChI=1/C6H14S/c1-3-5-6-7-4-2/h3-6H2,1-2H3