Skip to main content

Gamma-nonalactone

ADVERTISEMENT
Identification
Molecular formula
C9H16O2
CAS number
104-61-0
IUPAC name
5-octyltetrahydrofuran-2-one
State
State

At room temperature, Gamma-nonalactone is a liquid.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
266.00
Boiling point (Kelvin)
539.15
General information
Molecular weight
156.22g/mol
Molar mass
156.2650g/mol
Density
0.9509g/cm3
Appearence

Gamma-nonalactone appears as a colorless to pale yellow liquid with a coconut, peach-like aroma.

Comment on solubility

Solubility of 5-octyltetrahydrofuran-2-one

5-octyltetrahydrofuran-2-one, a cyclic compound, exhibits interesting solubility characteristics influenced by its unique molecular structure. Here are some key points about its solubility:

  • Polar vs Nonpolar: The presence of the tetrahydrofuran ring introduces some polar characteristics, while the long hydrocarbon chain (octyl group) contributes to its nonpolar nature.
  • Solvent Compatibility: This compound is likely to be soluble in nonpolar solvents such as hexane and octane, but may have limited solubility in polar solvents like water.
  • Temperature Influence: As with many organic compounds, solubility can vary with temperature; typically, higher temperatures enhance solubility, especially in organic solvents.
  • Potential Applications: Due to its solubility properties, 5-octyltetrahydrofuran-2-one may be useful in formulations requiring compatibility with nonpolar environments, potentially in pharmacological or industrial applications.

In summary, understanding the solubility of 5-octyltetrahydrofuran-2-one is crucial for its practical application and utilization. The *balance between polar and nonpolar features* plays a significant role in defining its behavior in various solvents.

Interesting facts

Interesting Facts about 5-Octyltetrahydrofuran-2-one

5-Octyltetrahydrofuran-2-one is a fascinating compound that has garnered attention in various scientific fields due to its unique structure and properties. Here are some noteworthy points about this intriguing molecule:

  • Natural Occurrence: This compound is often found in natural sources, especially in certain essential oils and plant extracts. Its presence contributes to the aroma and flavor profiles of these substances.
  • Synthesis Potential: The synthesis of 5-octyltetrahydrofuran-2-one can be achieved through various methods, including aldol condensation and other chemical transformations, making it a versatile compound for chemists to study.
  • Applications: This molecule shows promise as a flavoring agent or fragrance chemical, often utilized in the food and cosmetic industries to enhance sensory experiences.
  • Research Implications: Studies investigating the biological activities of 5-octyltetrahydrofuran-2-one have suggested potential health benefits, including antimicrobial properties.

Key Points of Interest:

  • It belongs to the class of compounds known as lactones, characterized by a cyclic ester structure. This functionality can lead to interesting reactivity patterns under certain conditions.
  • The unique alkyl chain length (octyl) may influence its physicochemical properties, making it an ideal candidate for studies related to lipid interactions and membrane fluidity.
  • The compound serves as an excellent example of how slight modifications in molecular structure can lead to significant changes in biological and physical properties.

In conclusion, 5-octyltetrahydrofuran-2-one is not just an interesting compound due to its chemical structure, but it also plays a vital role in nature and industry. Its potential applications highlight its importance in both scientific research and practical use.

Synonyms
gamma-Dodecalactone
4-Dodecanolide
5-octyloxolan-2-one
2(3H)-Furanone, dihydro-5-octyl-
.gamma.-Dodecalactone
gamma-Dodecalactone (natural)
FEMA No. 2400
Dihydro-5-octylfuran-2(3H)-one
gamma Dodecalactone
.gamma.-Dodecanolide
YX9N4581LU
DTXSID7047190
5-Octyl-dihydrofuran-2(3H)-one
EINECS 218-971-6
NSC-26511
4-Hydroxy-4-octylbutanoic acid lactone
UNII-YX9N4581LU
(GAMMA)-DODECALACTONE
DODECANO-1,4-LACTONE
4-Hydroxydodecanoic acid, .gamma.-lactone
AI3-35986
DTXCID5027190
GAMMA-DODECALACTONE [FCC]
(RS)-.GAMMA.-DODECALACTONE
2-(3H)-Furanone, 5-octyldihydro-
5-OCTYLTETRAHYDRO-2-FURANONE
.GAMMA.-DODECALACTONE [FHFI]
.GAMMA,-OCTYL-.GAMMA.-BUTYROLACTONE
4-HYDROXYDODECANOIC ACID GAMMA.-LACTONE
4-HYDROXYDODECANOIC ACID(GAMMA)-LACTONE
R-(+)-g-Dodecalactone
(RS)-GAMMA-DODECALACTONE
(+-)-GAMMA-DODECALACTONE
(+-)-.GAMMA.-DODECALACTONE
4-Hydroxydodecanoic acid, gamma-lactone
.GAMMA,-OCTYL-GAMMA-BUTYROLACTONE
148051
gamma-dodecanolide
wgpczplrvawxpw-uhfffaoysa-n
2305-05-7
GAMMA-DODECANOLACTONE
Dodecanolide-1,4
Dodecan-4-olide
4-Hydroxydodecanoic acid lactone
Dihydro-5-octyl-2(3H)-furanone
g-Dodecalactone
(+/-)-4-Dodecanolide
5-OCTYLDIHYDROFURAN-2(3H)-ONE
5-octyl-2-oxolanone
.gamma.-Dodecanolactone
MFCD00036499
NSC 26511
.gamma.-n-Octyl-.gamma.-N-butyrolactone
CHEMBL195215
.gamma.-Octyl-.gamma.-butyrolactone
xi-Dihydro-5-octyl-2(3H)-furanone
(+/-)-gamma-Octyl-gamma-butyrolactone
Dodecanoic acid, 4-hydroxy-, .gamma.-lactone
dodecalactone
gamma-Octyl-gamma-butyrolactone
gamma-Laurolactone
gamma-n-Octyl-gamma-N-butyrolactone
.gamma. Dodecalactone
gamma -Dodecanolactone
Dodecanoic acid, 4-hydroxy-, gamma-lactone
WLN: T5OVTJ E8
(+/-)-delta-dodecanolactone
5-Octyl-dihydro-furan-2-one
SCHEMBL111041
5-octyl-tetrahydro-furan-2-one
Dodecanoic acid, .gamma.-lactone
CHEBI:171837
(.+/-.)-4-n-Octylbutyrolactone
5-Octyldihydro-2(3H)-furanone #
NSC26511
Tox21_302617
BDBM50168008
LMFA07040042
AKOS015904896
(+/-)-.GAMMA.-DODECALACTONE
FG04103
(+/-)-4-N-OCTYLBUTYROLACTONE
gamma-Dodecalactone, analytical standard
gamma-Dodecalactone, >=97%, FCC, FG
NCGC00256822-01
AS-61143
(+/-)-Dihydro-5-octyl-2(3H)-furanone
CAS-2305-05-7
DB-003478
gamma-Dodecalactone, natural, >=98%, FG
CS-0320646
D1576
NS00012351
D89886
Q27294762
57084-18-1